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| Publications of Warren G. Hall :chronological alphabetical combined listing:
%% Journal Articles
@article{fds12117,
Author = {Due, D.L. and Huettel, S.A. and W.G. and Rubin,
D.C.},
Title = {Activation in Mesolimbic and Visuospatial Neural Circuits
Elicited by Smoking Cues: Evidence from Functional Magnetic
Resonance Imaging},
Journal = {American Journal of Psychiatry},
Volume = {159},
Pages = {954-960},
Year = {2002},
Key = {fds12117}
}
@article{fds251882,
Author = {Changizi, MA and McGeHee, R and Hall, WG},
Title = {Appetitive Responses to Dehydration and Food-Deprivation are
Learned},
Journal = {Psychological Behavior},
Volume = {75},
Pages = {295-304},
Year = {2002},
Key = {fds251882}
}
@article{fds251880,
Author = {Changizi, MA and Hall, WG},
Title = {Thirst modulates a perception.},
Journal = {Perception},
Volume = {30},
Number = {12},
Pages = {1489-1497},
Year = {2001},
Month = {January},
ISSN = {0301-0066},
url = {http://www.ncbi.nlm.nih.gov/pubmed/11817755},
Abstract = {Does thirst make you more likely to think you see water?
Tales of thirsty desert travelers and oasis mirages are
consistent with our intuitions that appetitive state can
influence what we see in the world. Yet there has been
surprisingly little scrutiny of this appetitive modulation
of perception. We tested whether dehydrated subjects would
be biased towards perceptions of transparency, a common
property of water. We found that thirsty subjects have a
greater tendency to perceive transparency in ambiguous
stimuli, revealing an ecologically appropriate modulation of
the visual system by a basic appetitive motive.},
Doi = {10.1068/p3266},
Key = {fds251880}
}
@article{fds251881,
Author = {Myers, KP and Hal, WG},
Title = {Experience with Drinking While Dehydrated is Required for
Weanling Rats to Acquire an Appetitive Response to Cellular
Dehydration},
Journal = {Development Psychobiology},
Volume = {38},
Pages = {145-153},
Year = {2001},
Key = {fds251881}
}
@article{fds251878,
Author = {Coyle, S and Arnold, HM and Goldberg-Arnold, JS and Rubin, DC and Hall,
WG},
Title = {Olfactory conditioning facilitates diet transition in human
infants.},
Volume = {37},
Number = {3},
Pages = {144-152},
Publisher = {Wiley},
Year = {2000},
Month = {November},
ISSN = {0012-1630},
url = {http://www.ncbi.nlm.nih.gov/pubmed/11044862},
Abstract = {We evaluated whether Pavlovian conditioning methods could be
used to increase the ingestion of non-preferred solutions by
formula-fed human infants. In baseline measures, 5-7 month
old infants sucked less frequently and consumed less water
than regular formula. During a 3-day olfactory conditioning
period, parents placed a small scented disk, the conditioned
stimulus, on the rim of their infants' formula bottle at
every feeding. Following this training, infants' responses
to water were tested when their water bottles had a disk
scented with the training odor, a novel odor, or no odor.
Infants tested with the training odor sucked more frequently
and consumed significantly more water than they had at
baseline. Infants tested with no odor or a novel odor
consumed water at or below baseline levels. These data
demonstrate that olfactory conditioning can be used to
enhance ingestion in infants and suggest that such methods
may be useful for infants experiencing difficulty when
making transitions from one diet to another.},
Doi = {10.1002/1098-2302(200011)37:3<144::aid-dev3>3.0.co;2-z},
Key = {fds251878}
}
@article{fds251877,
Author = {Myers, KP and Hall, WG},
Title = {Conditioned changes in appetitive and consummatory responses
to flavors paired with oral or nutrient reinforcement among
adult rats.},
Journal = {Physiology & behavior},
Volume = {68},
Number = {5},
Pages = {603-610},
Year = {2000},
Month = {March},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/10764888},
Abstract = {Recent studies of the behavioral organization of conditioned
flavor preferences have suggested the involvement of at
least two separate learning systems-an appetitive response
system sensitive to the oral hedonic properties of the
reinforcer, and a consummatory response system sensitive to
its nutrient properties. However, these prior studies were
conducted with weanling rats, that differ from adults in
terms of their prior experience with food, their learning
competencies, and the peculiar ontogenetic constraints on
their behavior. It is, therefore, unknown whether flavor
preference behaviors are similarly organized in adult rats.
In this experiment, adult rats were trained to associate a
specific CS flavor with either the sweet taste or the
postingestive nutrient effects of sucrose. Conditioned
appetitive orienting and consummatory oral responding to the
CS flavors were then measured. Unlike weanling rats, adult
rats exhibited both conditioned appetitive behavior and
conditioned consummatory behavior in response a CS that was
previously paired with either oral hedonic or nutrient
reinforcement. These results suggest a set of important
developmental changes in the neurobehavioral mechanisms of
flavor preference learning in the postweaning
period.},
Doi = {10.1016/s0031-9384(99)00209-7},
Key = {fds251877}
}
@article{fds251879,
Author = {Hall, WG and Arnold, HM and Myers, KP},
Title = {The acquisition of an appetite.},
Journal = {Psychological science},
Volume = {11},
Number = {2},
Pages = {101-105},
Year = {2000},
Month = {March},
ISSN = {0956-7976},
url = {http://www.ncbi.nlm.nih.gov/pubmed/11273415},
Abstract = {Unlike older animals, weanling-age rats do not seek water to
drink when they are dehydrated, despite the fact that a
physiological sensitivity to dehydration is present very
soon after birth. We demonstrate here that the appetitive
behaviors needed to approach and obtain water become linked
to dehydration only as a result of specific postnatal
learning experience. Preventing early experience with
dehydration retards the developmental emergence of
dehydration-induced, water-oriented behavior in young rats.
But a single pairing of water with dehydration can establish
an appetitive response. These findings reveal a critical
role of early learning in the development of goal-oriented
behavior. Such a learning process is potentially
characteristic of other behavioral systems, from the most
basic appetites to complex motives.},
Doi = {10.1111/1467-9280.00223},
Key = {fds251879}
}
@article{fds251811,
Author = {Myers, KP and Hall, WG},
Title = {Evidence that oral and nutrient reinforcers differentially
condition appetitive and consummatory responses to
flavors.},
Journal = {Physiology & behavior},
Volume = {64},
Number = {4},
Pages = {493-500},
Year = {1998},
Month = {June},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/9761223},
Abstract = {Rats tend to increase their intake of a flavor that has
previously been paired with either sweet taste or with
caloric repletion. However, it is unclear whether such a
change in intake is caused by changes in appetitive
behaviors such as orienting and approach, or changes in
consummatory behaviors and oral responsiveness. Also, it is
unclear whether oral reinforcers (sweetness) and
postingestive reinforcers (nutrients) lead to the same kinds
of behavioral change. In the current experiments, weanling
rats with oral and gastric cannulas repeatedly experienced a
flavor paired with either sweetness, high caloric density,
or neither. Rats were then tested for differences in
appetitive olfactory orienting and consummatory oral
responsiveness elicited by the flavor. Results suggest that
oral reinforcement (sweetness) produces conditioning of
appetitive responding to the flavor, while postingestive
reinforcement produces conditioning of consummatory
responding. A second experiment indicates that these
behavioral changes are specific increases in responsiveness
conditioned by flavor + unconditioned stimulus (US) pairing,
and are unlikely to be nonspecific effects of daily
unconditioned stimulus exposure.},
Doi = {10.1016/s0031-9384(98)00106-1},
Key = {fds251811}
}
@article{fds251812,
Author = {Swithers, SE and Westneat, MW and Hall, WG},
Title = {Electromyographic analysis of oral habituation in rat
pups.},
Journal = {Physiology & behavior},
Volume = {63},
Number = {2},
Pages = {197-203},
Year = {1998},
Month = {January},
ISSN = {0031-9384},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1998YK64800007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Rat pups show decreases in mouthing activity in response to
a series of repeated oral infusions of a diet. This decrease
in mouthing activity has been termed "oral habituation" and
these changes have been readily recorded with simple
behavioral observations. Oral habituation appears to be a
component of satiety in young rats. In the present study, to
more specifically characterize changes in motor response
topography during habituation in muscle groups used for
mastication, mouthing activity was recorded by implanting
fine wire electromyographic electrodes in the superficial
masseter, anterior digastric, sternohyoideus, and
genioglossus muscles of 12-day-old rat pups. During testing,
pups received a series of brief oral infusions of a 10%
sucrose diet delivered through an oral cannula. The results
demonstrated that mouthing activity as observed and scored
behaviorally was highly correlated with mouthing behavior
recorded by EMG, with oral habituation distinctly emerging
in both measures. In addition, the pattern of motor activity
in the four masticatory muscles changed during the course of
oral habituation. Within the minute following a single
infusion, the cycle frequency, duration of activity, and
relative onset time of activity in the four muscles changed.
In addition, across the course of habituation, both cycle
frequency and relative onset times of muscle activity
changed. These results demonstrate the general reliability
of behavioral observations of masticatory motor activity in
young rats and provide further information on how the
pattern of activity of muscles involved in the mouthing
motor pattern is altered during the course of oral
habituation.},
Doi = {10.1016/s0031-9384(97)00421-6},
Key = {fds251812}
}
@article{fds251813,
Author = {Myers, K and Hall, WG},
Title = {Sensitization of ingestive responding and activity in
developing rats},
Journal = {Behav. Neurosci.},
Volume = {111},
Pages = {413-423},
Year = {1997},
Key = {fds251813}
}
@article{fds251814,
Author = {Kucharski, D and Arnold, HM and Hall, WG},
Title = {Unilateral conditioning of an odor aversion in 6-day-old rat
pups.},
Journal = {Behavioral neuroscience},
Volume = {109},
Number = {3},
Pages = {563-566},
Year = {1995},
Month = {June},
ISSN = {0735-7044},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1995RC29600019&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {In young rats, several forms of olfactory memory can be
functionally localized to one side of the brain by
restricting training stimuli to one naris and corresponding
olfactory bulb. In the experiment, the analysis of
lateralized olfactory learning in 6-day-old rat pups was
extended by an evaluation of the consequences of aversive
reinforcers in a unilateral olfactory conditioning paradigm.
An olfactory aversion was conditioned by delivering a mild
footshock to animals in the presence of a novel odor.
Olfactory stimulation was confined to one naris and
corresponding olfactory bulb by inserting a soft rubber plug
into the opposite naris. This lateralization in processing
resulted in unilateral memory for the odor aversion that was
only expressed when the trained naris was open during an
odor preference test. The hypothesis that the hedonic value
(or valence) component of conditioning is represented in
structures that are unilaterally accessed during training
and testing is discussed.},
Doi = {10.1037//0735-7044.109.3.563},
Key = {fds251814}
}
@article{fds251815,
Author = {Swithers, SE and Hall, WG},
Title = {Does oral experience terminate ingestion?},
Journal = {Appetite},
Volume = {23},
Number = {2},
Pages = {113-138},
Year = {1994},
Month = {October},
ISSN = {0195-6663},
url = {http://www.ncbi.nlm.nih.gov/pubmed/7864607},
Abstract = {Using data from studies of ingestive behavior in developing
rat pups we demonstrate how oral experience can contribute
to the termination of ingestion. In rat pups, repeated oral
stimulation with sweet solutions causes a decline in oral
responsiveness. The diminished responsiveness is specific to
the flavor of the stimulus experienced orally and can
persist for several hours. We suggest that this
experience-based decrement in responsiveness is best
considered "oral habituation" and that oral habituation
largely accounts for the onset of satiety. Post-ingestive
feedback signals may have their influence through the oral
habituation process or act in the context of oral
habituation. Oral habituation is also shown to depend on the
pattern of stimulus presentation, a phenomenon that adds
considerable complexity to assessing the contributions of
oral experience to satiety. The concept of oral habituation
may be useful in understanding the immediate control of
ingestion and the moment-to-moment expression of ingestive
behavior in adult animals.},
Doi = {10.1006/appe.1994.1041},
Key = {fds251815}
}
@article{fds251816,
Author = {Swithers-Mulvey, SE and Hall, WG},
Title = {Integration of oral habituation and gastric signals in
decerebrate rat pups.},
Journal = {The American journal of physiology},
Volume = {265},
Number = {1 Pt 2},
Pages = {R216-R219},
Year = {1993},
Month = {July},
ISSN = {0002-9513},
url = {http://www.ncbi.nlm.nih.gov/pubmed/8342690},
Abstract = {During a series of oral infusions of a sweet solution, the
ingestive responses of young rat pups habituate; pups stop
responding to the infusions even when their stomachs are
empty and the infused diet is nonnutritive. The rate of this
oral habituation is enhanced by the addition of gastric fill
signals, even in decerebrate pups. In intact but not in
decerebrate pups, prior deprivation gates out the influence
of gastric fill on habituation. This oral habituation
system, responsive to multiple ingestion-related signals,
may serve as the elemental process that integrates
physiological state with ongoing behavior to control
ingestion.},
Doi = {10.1152/ajpregu.1993.265.1.r216},
Key = {fds251816}
}
@article{fds251817,
Author = {Warwick, ZS and Hall, WG and Pappas, TN and Schiffman,
SS},
Title = {Taste and smell sensations enhance the satiating effect of
both a high-carbohydrate and a high-fat meal in
humans.},
Journal = {Physiol Behav},
Volume = {53},
Number = {3},
Pages = {553-563},
Year = {1993},
Month = {March},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/8451323},
Abstract = {The effects of meal sensory properties (tasty vs. bland) and
nutrient composition [high-CHO (carbohydrate) vs. high-FAT]
on hunger ratings, blood glucose and free fatty acids (FFA),
taste perception, and subsequent food intake, were studied
in human subjects. Aspartame and vanilla were used to
augment meal palatability, yielding four isocaloric liquid
meals: bland-FAT, tasty-FAT, bland-CHO, tasty-CHO.
Normal-weight, nondieting young adults consumed each of the
meals for breakfast on separate days. The main finding was
that tasty versions of high-FAT and high-CHO meals were more
satiating than nutritionally identical bland meals, as
indicated by a greater decrease in hunger ratings following
the tasty meals. Changes in blood glucose and FFA were
related to meal nutrient composition, but not to meal
sensory properties. High-CHO meals tended to be more
satiating than high-FAT meals. Consumption of each of the
meals produced a similar decrease in pleasantness ratings of
food-related tastes. Intake of carbohydrates was
significantly higher at a self-selected lunch 5.25 h
following a tasty breakfast. These findings indicate that
hunger is decreased to a greater extent by meals flavored
with aspartame and vanilla relative to nutritionally
identical, unflavored meals. The satiety-enhancing effect of
oral stimulation was found for both high-FAT and high-CHO
meals.},
Doi = {10.1016/0031-9384(93)90153-7},
Key = {fds251817}
}
@article{fds251818,
Author = {Swithers-Mulvey, SE and Hall, WG},
Title = {Control of ingestion by oral habituation in rat
pups.},
Journal = {Behavioral neuroscience},
Volume = {106},
Number = {4},
Pages = {710-717},
Year = {1992},
Month = {August},
ISSN = {0735-7044},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1503662},
Abstract = {The role of habituation of mouthing activity in the control
of ingestion was investigated in 6-, 12-, and 18-day-old rat
pups. In pups at all ages, oral habituation to a flavored
diet inhibited ingestion of a continuous oral infusion of
that same diet. Twelve-day-old pups that had orally
habituated to a diet continued to consume less of a
continuous oral infusion of that diet both 30 min and 3 hr
later, and the duration of suppressed ingestion was shown to
be dependent on the rate of stimulus presentation during
habituation experience. These data suggest that oral
habituation may be a diet-specific influence on both intra-
and intermeal patterning.},
Doi = {10.1037//0735-7044.106.4.710},
Key = {fds251818}
}
@article{fds251822,
Author = {Westneat, MW and Hall, WG},
Title = {Ontogeny of feeding motor patterns in infant rats: an
electromyographic analysis of suckling and
chewing.},
Journal = {Behavioral neuroscience},
Volume = {106},
Number = {3},
Pages = {539-554},
Year = {1992},
Month = {June},
ISSN = {0735-7044},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1616619},
Abstract = {During mammalian ontogeny, there is a transition from
suckling to the chewing of food. The question was asked: Is
suckling a neuromuscular precursor to chewing, or are
suckling and chewing independent systems? Electromyograms
(EMGs) were recorded in rat pups of ages 6, 9, 12, 15, 18,
and 21 days from the superficial masseter, anterior
digastric, sternohyoideus, and genioglossus muscles during
suckling and chewing. The EMG patterns of the 3 components
of suckling behavior (nipple attachment, rhythmic sucking
and the stretch response) are distinctive from one another
and reflect the musculoskeletal biomechanics of suckling.
Chewing EMGs are present by 12 days of age and attain the
adult pattern by 18-21 days of age. During nipple
attachment, pups exhibit a motor pattern that is similar to
that of adult chewing, but other aspects of suckling differ
from chewing in some EMG features. Comparison of EMGs
between behaviors and between ages allowed interpretation of
the degree of contunity of muscular activity across the
suckling-to-chewing transition.},
Doi = {10.1037//0735-7044.106.3.539},
Key = {fds251822}
}
@article{fds251820,
Author = {Swithers-Mulvey, SE and Mishu, KR and Hall, WG},
Title = {Oral habituation in rat pups is in the brainstem.},
Journal = {Physiology & behavior},
Volume = {51},
Number = {3},
Pages = {639-642},
Year = {1992},
Month = {March},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1523239},
Abstract = {We have previously demonstrated a decremental, oral,
experienced-based control of ingestion in rat pups that is
potent, diet-specific, and long lasting. This control of
ingestion is revealed in the decreases in mouthing responses
of rat pups to repeated oral stimulation, a phenomenon that
is well described as oral habituation. The present study
examined the neural basis for oral habituation by examining
the responses of decerebrate 10-day-old rat pups to
repeated, brief infusions of a sucrose solution. Like
neurologically intact pups, decerebrate pups showed distinct
decreases in mouthing responses following a series of oral
infusions. Thus, oral habituation is present in the
hindbrain. Although intact pups demonstrated sensitization
by showing increased responding to the first few stimulus
presentations, decerebrates failed to show a sensitization
to the stimulation. These results suggest that while the
brainstem alone is sufficient for the expression of oral
habituation, the forebrain also influences oral responsivity
in intact animals.},
Doi = {10.1016/0031-9384(92)90189-9},
Key = {fds251820}
}
@article{fds251819,
Author = {Hall, WG and Swithers-Mulvey, SE},
Title = {Developmental strategies in the analysis of ingestive
behavior.},
Journal = {Annals of the New York Academy of Sciences},
Volume = {662},
Pages = {1-15},
Year = {1992},
Month = {January},
ISSN = {0077-8923},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1456634},
Doi = {10.1111/j.1749-6632.1992.tb22851.x},
Key = {fds251819}
}
@article{fds251821,
Author = {Phifer, CB and Denzinger, A and Hall, WG},
Title = {The early presence of food-oriented appetitive behavior in
developing rats.},
Journal = {Developmental psychobiology},
Volume = {24},
Number = {7},
Pages = {453-461},
Year = {1991},
Month = {November},
ISSN = {0012-1630},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1797591},
Abstract = {The appetitive behavior of 3- to 6-day-old rat pups was
studied by testing their ability to direct their ingestive
behavior to a restricted food source. We found that, from 3
days of age, pups were able to feed efficiently from such a
source. More specifically, pups that were deprived of
nutrition but not of maternal care as well as pups that were
dehydrated ingested significantly more than nondeprived
animals, and did so whether liquid diet was spread over the
entire floor surface beneath them or restricted to a
fraction of the floor surface. However, pups that had been
nutritionally and maternally deprived were not able to
direct their feeding. The general locomotor activation of
pups in this latter group appeared to interfere with their
ability to direct their behavior to the restricted source.
These results indicate that from early ages, developing rats
possess the appetitive competence to guide their behavior
and suggest that previous findings of poorly directed
behavior were a confound of the behavioral activation shown
by pups tested in a state of maternal deprivation.},
Doi = {10.1002/dev.420240702},
Key = {fds251821}
}
@article{fds251824,
Author = {Swithers-Mulvey, SE and Miller, GL and Hall, WG},
Title = {Habituation of oromotor responding to oral infusions in rat
pups.},
Journal = {Appetite},
Volume = {17},
Number = {1},
Pages = {55-67},
Year = {1991},
Month = {August},
ISSN = {0195-6663},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1952916},
Abstract = {The influence of oromotor experience on the pattern of
ingestion in rat pups and the relation of this influence to
age and pups' physiological state were investigated using a
procedure designed to mimic the sham-feeding preparation in
adult rats. Six-, 12-, and 18-day-old pups received brief
intra-oral infusions of sucrose solutions once every minute.
Small infusion volumes minimized postoral effects. Pups'
oromotor responsiveness was assessed by recording the
pattern of mouthing behavior continuously during the test.
Pups were tested after 24, 6 or 0 h deprivation. During
testing, the mouthing behavior of all pups except 24-hr
deprived 6-day olds showed a marked decline. The specificity
of this decrement was demonstrated in a second experiment in
which the decremented response was restored by a switch in
solution flavor. Finally, the influence of postoral signals
on the decline in responsiveness was evaluated by comparing
the oral responsiveness of 18-day-old pups following
intragastric, oral, or no infusions. Oral infusions
suppressed subsequent oral responding, but intragastric
infusions did not. These results provide evidence for a
habituation-like role of oromotor experience in determining
patterns of ingestive behavior within a feeding test. Here,
major determinants of the pattern of decline were pups'
physiological state and developmental age.},
Doi = {10.1016/0195-6663(91)90084-6},
Key = {fds251824}
}
@article{fds251825,
Author = {Hall, WG and Swithers-Mulvey, SE and Agrawal, CM and Burka, NR and Horner, J and Menacherry, S},
Title = {Analysis of 2-DG autoradiograms using image-averaging and
image-differencing procedures for systems-level description
of neurobehavioral function.},
Journal = {Physiology & behavior},
Volume = {50},
Number = {1},
Pages = {109-119},
Year = {1991},
Month = {July},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/1946702},
Abstract = {Computer assisted 2-deoxyglucose (2-DG) autoradiography has
been used to provide functional maps of areas of altered
neural activity related to changes in an animal's behavior
or state. The standard procedure for comparison of
autoradiograms between different treatment groups has been
to take measurement samples from predefined neuroanatomical
regions and to average these across brains to attain
statistical sensitivity for detecting treatment effects.
Unfortunately, when sampling is restricted to predefined
areas, important topographic information is lost along with
the ability to reveal an unexpected change in neural
activity. To preserve the rich topographical detail of
metabolic information and to enhance the capacity to uncover
novel areas of altered metabolic activity, we have developed
a system for averaging entire images from 2-DG
autoradiograms and for comparing the average images from two
experimental groups by creating an image of differences.
This procedure does not rely on sampling only preselected
regions, but still allows statistical comparisons between
experimental groups. The procedures we describe can be
readily and inexpensively adapted for use in individual
laboratories and are based on modifications of preexisting
image analysis software. We show that, when average and
difference images are created using standardized protocols
for sectioning brain tissue and editing section images, they
are impressively resolved and realistic and can serve as
effective topographic descriptions of group differences in
neural activity of functional and behavioral
relevance.},
Doi = {10.1016/0031-9384(91)90506-j},
Key = {fds251825}
}
@article{fds251826,
Author = {Phifer, CB and Ladd, MD and Hall, WG},
Title = {Effects of hydrational state on ingestion in infant rats: is
dehydration the only ingestive stimulus?},
Journal = {Physiology & behavior},
Volume = {49},
Number = {4},
Pages = {695-699},
Year = {1991},
Month = {April},
ISSN = {0031-9384},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1991FL39200007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {The physiological stimulus for deprivation-enhanced
ingestion was studied in developing rats. During an
overnight deprivation period, continuous gastric infusions
of isotonic saline or milk were made to 6- and 15-day-old
rat pups in order to preferentially maintain hydrational or
hydrational and nutritional status, respectively. Pups'
ingestion was then studied in oral-infusion tests. In
6-day-old pups that received either milk or saline
infusions, ingestion was depressed relative to intake in
pups that were simply deprived. But in 15-day-old pups, only
milk infusions reduced intake. These findings suggest that
the increased ingestion stimulated by deprivation in pups
less than a week of age results primarily from dehydration,
and thus that nutrient-related feeding does not emerge until
later in development.},
Doi = {10.1016/0031-9384(91)90304-7},
Key = {fds251826}
}
@article{fds251823,
Author = {Hall, WG and Swithers Mulvey and SE},
Title = {On Rowland's "When is a (sham) drink a (sham) feed?" and
Midkiff's response},
Journal = {SSIBlings},
Volume = {4},
Pages = {6},
Year = {1991},
Key = {fds251823}
}
@article{fds251827,
Author = {King, C and Hall, WG},
Title = {Developmental change in unilateral olfactory habituation is
mediated by anterior commissure maturation.},
Journal = {Behavioral neuroscience},
Volume = {104},
Number = {5},
Pages = {796-807},
Year = {1990},
Month = {October},
ISSN = {0735-7044},
url = {http://www.ncbi.nlm.nih.gov/pubmed/2244986},
Abstract = {Habituation of an orienting response in rat pups was used to
study the development of the anterior commissure (AC) and
its role in olfactory memory. Six- and 12-day-old pups
received odor presentations to one side of their olfactory
system and were tested later for habituation to additional
presentations made to either the trained or untrained side.
Six-day-old pups remembered only on the trained side.
Twelve-day-old pups remembered when tested on either side.
Transection of the AC in 12-day-old pups before, but not
after, training prevented the transfer of memory. Thus,
between 6 and 12 days of age, olfactory cross-projections
carried in the AC mature and provide a functional substrate
for transfer, at the time of training, of a form of
olfactory learning.},
Doi = {10.1037//0735-7044.104.5.796},
Key = {fds251827}
}
@article{fds251828,
Author = {Kucharski, D and Burka, N and Hall, WG},
Title = {The anterior limb of the anterior commissure is an access
route to contralateral stored olfactory preference
memories},
Journal = {Psychobiology},
Volume = {18},
Number = {2},
Pages = {195-204},
Year = {1990},
Month = {January},
ISSN = {0889-6313},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1990DJ94700003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Young rats learn to prefer novel odors that have been paired
with reinforcers. Memories for such preference learning can
be confined to one side of the olfactory system by blocking
the contralateral naris during odor-reinforcer training.
These memories can be accessed only from the trained naris
in 6-day-old pups. But in pups 12 days of age and older,
these memories, which are still stored only on one side, can
be accessed from either the trained or the untrained naris.
The ability of 12-day-olds to access unilaterally stored
memories from the untrained side of the olfactory system
permitted us to further explore the locations of olfactory
memories and the routes of access to these memories. We
report here that when preference memories were tested from
the untrained side after selective fiber-tract transections
on the trained side: (1) transection of the anterior limb of
the anterior commissure at various rostral-caudal levels
prevented retrieval of odor memories; (2) transection of the
posterior limb did not disrupt memory access; and (3)
transection of the olfactory peduncle on the trained side,
thereby removing the contribution of the trained olfactory
bulb, did not eliminate access to odor-preference memories.
These findings suggest that access to contralateral
olfactory memories is subserved by the anterior limb of the
anterior commissure, probably through access to its most
distal projections to the anterior olfactory nucleus and the
anterior piriform cortex, and that retrieval of preference
memories does not require access to the trained olfactory
bulb. © 1990, Psychonomic Society, Inc.. All rights
reserved.},
Doi = {10.3758/BF03327227},
Key = {fds251828}
}
@article{fds251829,
Author = {Swithers, SE and Hall, WG},
Title = {A nutritive control of independent ingestion in rat pups
emerges by nine days of age.},
Journal = {Physiology & behavior},
Volume = {46},
Number = {5},
Pages = {873-879},
Year = {1989},
Month = {November},
ISSN = {0031-9384},
url = {http://www.ncbi.nlm.nih.gov/pubmed/2516909},
Abstract = {The emergence of controls of independent ingestion in rat
pups was studied using nutritive (0.6 M glucose in saline or
water) and vehicle gastric preloads. Two hours after
preloading, ingestive responses were assessed in a 30-minute
test of feeding from the floor. In 6-day-olds, all preloads
had similar effects on consumption of a milk diet. In
9-day-olds, however, glucose-water preloads inhibited intake
compared to water preloads. This inhibition was secondary to
an effect on gastric emptying. Glucose preloads also
inhibited intake in 12- and 15-day-olds. Behavioral
observations indicated that feeding patterns were altered in
response to glucose preloads in 9-day-olds. These results
provide evidence for the emergence of a nutritive,
postgastric control of independent ingestion between 6 and 9
days of age.},
Doi = {10.1016/0031-9384(89)90051-6},
Key = {fds251829}
}
@article{fds251831,
Author = {Hall, WG},
Title = {Neural systems for early independent ingestion: regional
metabolic changes during ingestive responding and
dehydration.},
Journal = {Behavioral neuroscience},
Volume = {103},
Number = {2},
Pages = {386-411},
Year = {1989},
Month = {April},
ISSN = {0735-7044},
url = {http://www.ncbi.nlm.nih.gov/pubmed/2706082},
Abstract = {The ingestive behavior of young rodents, studied
independently of the mother and suckling, provides a system
for the developmental analysis of the neurobiology of
feeding and drinking. In these experiments regional neural
metabolic activity, as assessed by semiquantitative
deoxyglucose (DG) autoradiography, was related to
dehydration and ingestive behavior in 6-day-old rat pups.
During simple ingestive responding, changes in relative DG
uptake, representative of changes in neural metabolic
activity, occurred primarily in hindbrain sensory and motor
nuclei. Producing cellular dehydration resulted in activity
changes primarily in the basal forebrain. When pups were
dehydrated and allowed to ingest during the DG-uptake
period, activity changes were seen in both the hindbrain and
forebrain areas that responded to ingestion or dehydration
alone as well as in regions that were not affected by either
manipulation alone. These latter changes, which result from
an interaction of behavioral and physiological stimuli, call
attention to areas that may subserve motivational aspects of
behavior. Extracellular dehydration was found to produce
fewer and different forebrain responses in neural metabolic
activity. During ingestion, the only effects of
extracellular dehydration that overlapped with those of
cellular dehydration appeared in circumventricular
hypothalamic regions and brain stem motor nuclei. Thus,
there appeared to be only a limited final common pathway for
these two types of dehydration-induced drinking. Taken
together, these findings in infant rats depict distributed
neural systems subserving ingestion and responding to state
change. They provide a starting point early in ontogeny for
the developmental analysis of neural substrates of ingestive
systems.},
Doi = {10.1037//0735-7044.103.2.386},
Key = {fds251831}
}
@article{fds251830,
Author = {Saperstein, LA and Kucharski, D and Stanton, ME and Hall,
WG},
Title = {Developmental change in reversal learning of an olfactory
discrimination},
Journal = {Psychobiology},
Volume = {17},
Number = {3},
Pages = {293-299},
Publisher = {Springer Nature},
Year = {1989},
Month = {January},
ISSN = {0889-6313},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1989AQ58800013&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {We examined developmental changes in the reversal of a
learned discrimination in an olfactory conditioning paradigm
in three experiments. Preweanling rats were exposed to an
odor (CS+) paired with footshock and a different odor
(CS−) that was explicitly unpaired with footshock. The
rats were then immediately tested for their preference
between the CS+ and CS− odors. In Experiment 1, animals
trained at 12 or 18 days of age showed equivalent
conditioned aversions to the CS+. When the significance of
the cues was reversed, the younger animals showed rapid
reversal learning; that is, their aversion to the original
CS-I- was displaced by an aversion to the original CS−.
However, the 18-day-old animals were slower to acquire
discrimination reversal. In Experiment 2, a similar pattern
of results emerged when animals were given separate
preference tests involving the CS+ versus a novel odor, or
the CS− versus a novel odor. In Experiment 3, intact
18-day-old rats and 18-day-olds with damage to the septum
and fornix showed equivalent conditioned aversions to the
CS+. In contrast to the intact animals, however, the
lesioned rats showed rapid reversal of the discrimination,
which resembled that of intact 12-day-olds. Thus, there
appears to be a dramatic change in reversal learning of
conditioned odor aversions in rats after the second week of
postnatal life. These data are discussed with reference to
the role of septo-hippocampal maturation in the ontogeny of
olfactory learning. © 1989, Psychonomic Society, Inc.. All
rights reserved.},
Doi = {10.1007/BF03337783},
Key = {fds251830}
}
@article{fds251834,
Author = {Phifer, CB and Hall, WG},
Title = {Ingestive behavior in preweanling rats: emergence of
postgastric controls.},
Journal = {The American journal of physiology},
Volume = {255},
Number = {2 Pt 2},
Pages = {R191-R199},
Year = {1988},
Month = {August},
ISSN = {0002-9513},
url = {http://www.ncbi.nlm.nih.gov/pubmed/3407798},
Abstract = {Previous studies have indicated that the termination of
intake in very young rat pups is controlled almost
exclusively by the level of gastric fill; nutritive cues
from diet have no effect on intake. In the present series of
experiments, we investigated the ontogeny of postgastric
nutritive controls of intake in rat pups ingesting
independent of their dam. In 6-day-old pups, the level of
gastric fill required to terminate ingestion was not
affected by the presence or absence of post-gastric
nutritive cues, but by 15 days of age a greater level of
gastric fill was required to stop ingestion when postgastric
cues were eliminated by a closed pyloric noose. This
emergent post-gastric contribution to the inhibition of
intake in 15-day-old pups does not depend on preexisting
gastric fill signals, as sham-feeding pups (open gastric
fistula) with nutrients in their intestines ingested less
than pups without intestinal nutrients. These results
provide evidence that postgastric controls of ingestive
behavior mature during the postnatal period and just shortly
before they are required at weaning.},
Doi = {10.1152/ajpregu.1988.255.2.r191},
Key = {fds251834}
}
@article{fds251833,
Author = {Kucharski, D and Hall, WG},
Title = {Developmental change in the access to olfactory
memories.},
Journal = {Behavioral neuroscience},
Volume = {102},
Number = {3},
Pages = {340-348},
Year = {1988},
Month = {June},
ISSN = {0735-7044},
url = {http://www.ncbi.nlm.nih.gov/pubmed/3395445},
Abstract = {Memory for a learned odor preference can be functionally
confined to one side of the brain in 6-day-old rat pups by
preferentially stimulating a single naris and corresponding
olfactory bulb during training. We report here that this
form of unilateral learning is present only during the first
postnatal week; older pups show bilateral recall of
unilateral olfactory experience. The maturation of bilateral
learning probably depends on the postnatal growth and
development of olfactory commissural fibers, because
infantlike unilateral learning and memory is reinstated when
these commissural fibers are sectioned before training in
older pups. Section of commissural fibers after training
also resulted in unilateral preferences. This latter finding
indicates that the learned odor preference of older pups
tested with the untrained naris open depends on access to
unilaterally stored memories on the contralateral side,
access provided by the newly developed commissural
projections.},
Doi = {10.1037//0735-7044.102.3.340},
Key = {fds251833}
}
@article{fds251832,
Author = {Sullivan, RM and Hall, WG},
Title = {Reinforcers in infancy: classical conditioning using
stroking or intra-oral infusions of milk as
UCS.},
Journal = {Developmental psychobiology},
Volume = {21},
Number = {3},
Pages = {215-223},
Year = {1988},
Month = {April},
ISSN = {0012-1630},
url = {http://www.ncbi.nlm.nih.gov/pubmed/3371554},
Abstract = {Six-day-old rats received 20 forward pairings of an
odor-conditioned stimulus (CS) with one of two unconditioned
stimuli (UCS); 1) intra-oral milk infusions or 2) stroking
with a sable-hair brush. These UCS's produce a common
general response of increased behavioral activity, but
different specific behaviors. For each UCS, additional pups
received backward pairings of the CS and UCS, random
pairings of the CS and UCS, CS only, UCS only, or no
stimuli. Four hours later, pups received a two-odor choice
test to assess the development of an odor preference and a
CS-only test to assess the acquisition of conditioned
responding (CR). The results of the two-odor choice test
indicated that for both UCS's only forward pairings of the
CS and UCS resulted in an odor preference. Similarly, the
CS-only test showed that only forward pairings of the CS and
either UCS were effective in producing CR's; pups that
received forward pairings exhibited increased behavioral
activity during presentations of the CS, which is an
unconditioned response (UCR) to both UCS's. Only the forward
paired CS-milk UCS group exhibited increased mouthing and
probing during the CS only test; these are UCR's that occur
to milk infusions but infrequently to the stroking UCS.
These results demonstrate the development of similar
conditioned odor preferences using behaviorally activating
UCS's, but CR's which are specific to the form of the
UCR.},
Doi = {10.1002/dev.420210303},
Key = {fds251832}
}
@article{fds251835,
Author = {Hall, WG and Hudson, R and Brake, SC},
Title = {Terminology for use in investigations of nursing and
suckling.},
Journal = {Developmental psychobiology},
Volume = {21},
Number = {1},
Pages = {89-91},
Year = {1988},
Month = {January},
ISSN = {0012-1630},
url = {http://www.ncbi.nlm.nih.gov/pubmed/3338629},
Doi = {10.1002/dev.420210107},
Key = {fds251835}
}
@article{fds251836,
Author = {Kucharski, D and Hall, WG},
Title = {New routes to early memories.},
Journal = {Science (New York, N.Y.)},
Volume = {238},
Number = {4828},
Pages = {786-788},
Year = {1987},
Month = {November},
ISSN = {0036-8075},
url = {http://www.ncbi.nlm.nih.gov/pubmed/3672125},
Abstract = {Stimulation of one side of the olfactory system during
training with odor-milk pairings in neonatal rats results in
their ability to recall an odor memory by using the trained
but not the untrained side of the brain. In 12-day-old rats,
olfactory learning can be recalled by stimulation of either
the trained or untrained side. The development of bilateral
recall reflects the maturation of olfactory commissural
pathways that provide access to the olfactory memory stored
on the contralateral side. Furthermore, the commissural
pathways need not be present at the time of memory formation
but can establish new and specific access to already
existing olfactory memories.},
Doi = {10.1126/science.3672125},
Key = {fds251836}
}
@article{fds251837,
Author = {Hall, WG and Oppenheim, RW},
Title = {Developmental psychobiology: prenatal, perinatal, and early
postnatal aspects of behavioral development.},
Journal = {Annual review of psychology},
Volume = {38},
Pages = {91-128},
Year = {1987},
Month = {January},
ISSN = {0066-4308},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1987F872200005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Doi = {10.1146/annurev.ps.38.020187.000515},
Key = {fds251837}
}
@article{fds251838,
Author = {Bornstein, and H, B and Terry, and M, L and Browde, and A, J and Jr, and Assimon, and A, S and Hall, and G, W},
Title = {Sensory and nutritional contributions to rat pup's early
activational responses to ingestion},
Journal = {Dev. Psychobiol.},
Volume = {20},
Pages = {147-163},
Year = {1987},
Key = {fds251838}
}
@article{fds251839,
Author = {Kucharski, D and Johanson, IB and Hall, WG},
Title = {Unilateral olfactory conditioning in 6-day-old rat
pups.},
Journal = {Behavioral and neural biology},
Volume = {46},
Number = {3},
Pages = {472-490},
Year = {1986},
Month = {November},
ISSN = {0163-1047},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986F562200017&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {The potential that early olfactory learning might be
laterally organized in the brain was investigated in
6-day-old rats. This hypothesis is based on the finding that
the commissural systems that subserve bilateral olfactory
communication do not mature until the second week of
postnatal life. Pups were trained with pairings of cedar
odor and intraoral infusions of milk while one nostril was
occluded. Animals expressed a conditioned orientation
towards cedar if tested with the trained nostril open. No
such conditioning was observed if the untrained nostril was
open during testing. Further, when individual pups received
cedar odor/milk pairings with one nostril open and orange
odor/milk pairings with the other open, they expressed a
conditioned preference for orange when tested with the
orange-trained nostril open, and a preference for cedar when
tested with the cedar-trained nostril open. Classically
conditioned oral responses (mouthing) also appeared to be
lateralized. However, no such unilateral conditioning
occurred with respect to behavioral activation, which is
also conditioned in this paradigm. Increases in activity to
the odor CS were observed regardless of whether the trained
or untrained nostril was open during testing. These results
suggest that in developing rodents, olfactory memories may
be partly represented in structures that can be unilaterally
accessed during training and testing. They provide a
starting point for isolation of neural substrates of the
olfactory conditioning process.},
Doi = {10.1016/s0163-1047(86)90506-6},
Key = {fds251839}
}
@article{fds251840,
Author = {Phifer, CB and Browde, JA and Hall, WG},
Title = {Ontogeny of glucose inhibition of independent ingestion in
preweanling rats.},
Journal = {Brain research bulletin},
Volume = {17},
Number = {5},
Pages = {673-679},
Year = {1986},
Month = {November},
ISSN = {0361-9230},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986F071900009&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Rat pups that have been maternally and nutritionally
deprived will vigorously ingest diet infused directly into
the mouth. The development of nutritive controls in this
form of ingestion was examined by administering nutritive
and non-nutritive gastric preloads to 6- and 15-day-old
pups. In 6 day-old pups, nutritive gastric preloads (0.6 M
glucose in distilled H2O or saline) and vehicle preloads
were followed by similar intakes; only the change in
hydrational state caused by distilled H2O loads appeared to
affect intake. By 15 days of age, intake following nutritive
preloads was less than intake following non-nutritive
preloads. Also, at 15 days, stomach volume at the
termination of intake was less following nutritive preloads.
In a separate experiment with 6-day-old pups, gastric
preloads of an alternative energy source, the ketone
beta-hydroxybutyrate, also failed to inhibit intake when
given at a dose that did not cause excessive gastric
distension. These results indicate that a nutritive control
of intake termination in rats is not present at 6 days of
age but develops by 15 days of age.},
Doi = {10.1016/0361-9230(86)90199-1},
Key = {fds251840}
}
@article{fds251841,
Author = {Phifer, CB and Sikes, CR and Hall, WG},
Title = {Control of ingestion in 6-day-old rat pups: termination of
intake by gastric fill alone?},
Journal = {The American journal of physiology},
Volume = {250},
Number = {5 Pt 2},
Pages = {R807-R814},
Year = {1986},
Month = {May},
ISSN = {0002-9513},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986C334900038&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Six-day-old rat pups, tested away from the dam, vigorously
ingested orally infused milk for up to 90 min when the
ingested milk was allowed to drain through a gastric
fistula. Total intake in pups with unplugged fistulas was
more than double that consumed by littermates with plugged
fistulas. This persistent feeding could not be due to the
absence of postgastric cues because blocking movement of the
milk into the intestine with a closed pyloric noose resulted
in less intake than when the noose was open. Furthermore, a
5% body weight gastric preload of milk or nonnutritive
saline suppressed intake in pups with either open or closed
pyloric nooses by an amount equal to the preload. Regardless
of noose or preload condition, ingestion stopped when
stomach content reached approximately 6.5% of body weight.
Thus level of gastric fill appeared critical for intake
control. When gastric fistulas were unplugged after pups had
ingested milk until they stopped, vigorous ingestion
followed, with total intakes of up to 20% body weight.
Intake termination in young rat pups thus appears to be
controlled exclusively by gastric fill level; pregastric
signals alone appear insufficient, and postgastric signals
appear unnecessary for termination of intake.},
Doi = {10.1152/ajpregu.1986.250.5.r807},
Key = {fds251841}
}
@article{fds251842,
Author = {Hall, WG and Browde, JA},
Title = {The ontogeny of independent ingestion in mice: or, why won't
infant mice feed?},
Journal = {Developmental psychobiology},
Volume = {19},
Number = {3},
Pages = {211-222},
Year = {1986},
Month = {May},
ISSN = {0012-1630},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1986C101800005&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Unlike infant rats, which show deprivation-related ingestion
in several different test situations, infant mice appeared
to be relatively unwilling to feed independently of suckling
until 12 days of age. We tested mouse pups that were
deprived (of food, water, suckling, and maternal care) for
1, 7, or 24 hr in ingestive tests in which a milk diet was
spread on the floor of their test container (Experiment 1).
Pups at 3, 6, and 9 days of age consumed small amounts of
the diet and showed little increase in intake when
deprivation was increased. In contrast (and like rat pups of
all ages), mouse pups 12 and 15 days of age actively
ingested the diet and increased their intake with increased
deprivation. Six-day-old mouse pups were similarly unwilling
to ingest a 5% sucrose solution, though 12-day-old pups
showed deprivation-related intake (Experiment 2). Cellular
dehydration (produced by hypertonic saline injection), a
potent stimulus for ingestion in infant rats, did not
stimulate ingestion in mice younger than 12 days of age
(Experiment 3). Finally, when ingestion was tested with diet
infusions made through oral cannulas, mouse pups at 6 and 9
days of age showed only a slight increase in intake with
increased deprivation. However, by 12 days of age, pups'
ingestion increased markedly with deprivation (Experiment
4). Thus, mouse pups seem to be very different from rat pups
with respect to the early existence of ingestive systems.
The neural substrates for the ingestive responses that
subserve independent ingestion are only minimally present in
infant mice or are somehow inhibited.},
Doi = {10.1002/dev.420190307},
Key = {fds251842}
}
@article{fds251843,
Author = {Hall, WG},
Title = {What we know and don't know about the development of
independent ingestion in rats},
Journal = {Appetite},
Volume = {6},
Pages = {323-356},
Year = {1985},
Key = {fds251843}
}
@article{fds251845,
Author = {Johanson, IB and Hall, WG and Polefrone, JM},
Title = {Appetitive conditioning in neonatal rats: conditioned
ingestive responding to stimuli paired with oral infusions
of milk.},
Journal = {Developmental psychobiology},
Volume = {17},
Number = {4},
Pages = {357-381},
Year = {1984},
Month = {July},
ISSN = {0012-1630},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984SX98600003&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {Components of rat pups' ingestive responses to orally
infused milk came to be elicited by a novel odor conditioned
stimulus (cedar) that had been repeatedly paired with milk
infusions (Experiment I). Pups responded specifically to one
odor, and they did not generalize their conditioned
responding to either another odor or an unscented airstream
(Experiment II). Ingestive responses could also be
conditioned to a vibrotactile CS paired with milk, although
levels of conditioned responding were lower than were
obtained with an odor CS (Experiment III). Pups' internal
state determined the effectiveness of training, in that pups
that were removed from their dam for 24 hr showed reliable
conditioned responding, while nondeprived pups and
dehydrated pups did not (Experiment IV). Finally, pups
showed retention of conditioned responding for at least
several days after training (Experiment V).},
Doi = {10.1002/dev.420170404},
Key = {fds251845}
}
@article{fds251844,
Author = {Hall, WG and Bruno, JP},
Title = {Inhibitory controls of ingestion in 6-day-old rat
pups.},
Journal = {Physiology & behavior},
Volume = {32},
Number = {5},
Pages = {831-841},
Year = {1984},
Month = {May},
ISSN = {0031-9384},
url = {http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:A1984TD27800023&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=47d3190e77e5a3a53558812f597b0b92},
Abstract = {The ability of gastric preloads of milk, water, and isotonic
saline to inhibit ingestion was studied in deprived
6-day-old rat pups being fed through oral cannulas. Preloads
were delivered through gastric cannulas or by gavage, and
both the volume of the load and the interval between the
preload and testing were varied in order to assess the
relative contributions of pre- and post-absorptive cues from
the loads. Pups' willingness to initiate ingestion in short
(10 min) tests (appetite) was unaffected by the degree of
gastric filling produced by a load but was depressed by
post-absorptive changes in hydrational state. On the other
hand, pups terminated ingestion in long (30 min) tests
(satiety) in response to gastric filling. Cessation of
intake in long tests was only slightly influenced by
post-absorptive factors. These results reveal two distinct
phases of ingestion in infant rats and show that each is
controlled in a different manner.},
Doi = {10.1016/0031-9384(84)90202-6},
Key = {fds251844}
}
@article{fds21971,
Author = {Hall, W.G. and Williams, C.L.},
Title = {Suckling isn't feeding or is it? A search for developmental
continuities},
Volume = {13},
Pages = {220-254},
Booktitle = {Advances in Animal Behavior},
Editor = {J.S. Rosenblatt et al.},
Year = {1983},
Key = {fds21971}
}
@article{fds251846,
Author = {Johanson, IB and Hall, WG},
Title = {Appetitive conditioning in neonatal rats: Conditioned
orientation to a novel odor},
Journal = {Dev. Psychobiol.},
Volume = {15},
Pages = {379-397},
Year = {1982},
Key = {fds251846}
}
@article{fds251847,
Author = {Bruno, JP and Hall, WG},
Title = {Olfactory contributions to dehydration-induced anorexia in
weanling rats},
Journal = {Dev. Psychobiol.},
Volume = {15},
Pages = {493-505},
Year = {1982},
Key = {fds251847}
}
@article{fds251848,
Author = {Johanson, IB and Hall, WG},
Title = {The ontogeny of feeding in rats: V. Influence of texture,
home odor, and sibling presense on ingestive
behavior},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {95},
Pages = {837-847},
Year = {1981},
Key = {fds251848}
}
@article{fds251849,
Author = {Hall, WG and Bryan, TE},
Title = {The ontogeny of feeding in rats: IV. Taste development as
measured by intake and behavioral responses to oral
infusions of sucrose and quinine},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {95},
Pages = {240-251},
Year = {1981},
Key = {fds251849}
}
@article{fds251850,
Author = {DiRocco, RJ and Hall, WG},
Title = {Metabolic neural mapping in neonatal rats},
Journal = {N. Neurosci. Res.},
Volume = {6},
Pages = {13-19},
Year = {1981},
Key = {fds251850}
}
@article{fds251851,
Author = {Williams, CL and Hall, WG and Rosenblatt, JS},
Title = {Changing oral cues in suckling of weaning-age rats: Possible
contributions to weaning},
Journal = {Journal of Comparative and Physiological
Psychology},
Volume = {94},
Number = {3},
Pages = {472-483},
Publisher = {American Psychological Association (APA)},
Year = {1980},
Month = {June},
ISSN = {0021-9940},
url = {http://dx.doi.org/10.1037/h0077682},
Abstract = {Four experiments assessed the relative contribution of oral
and nutritional stimuli in the control of suckling in 20-
and 25-day-old Sprague-Dawley CD rat pups. Oral factors were
critical to suckling satiety, since the initiation of a
suckling bout in weanling pups was not retarded by food
infused directly into the stomach. As late as 20 days of
age, suckling deprivation induced suckling largely through
its stimulus-deprivation effects (olfactory, gustatory,
somesthetic, and proprioceptive sensations) rather than
through its food-deprivation effects. By 25 days of age, the
type of oral stimulation that led to suckling satiety
expanded; oral stimulation provided by independent feeding
acquired characteristics that allowed it also to inhibit
suckling. This developmental change in the stimuli that
modulated suckling did not appear to be critically dependent
on sensory changes in the dam or experiential events within
the litter. The behavioral change, therefore, may represent
a maturation of neural systems that facilitate the
transition from suckling to independent feeding. (38 ref)
(PsycINFO Database Record (c) 2006 APA, all rights
reserved). © 1980 American Psychological
Association.},
Doi = {10.1037/h0077682},
Key = {fds251851}
}
@article{fds251852,
Author = {Szechtman, H and Hall, WG},
Title = {Otongeny of oral behavior induced by tail pinch and
electrical stimulation of the tail in rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {94},
Pages = {436-445},
Year = {1980},
Key = {fds251852}
}
@article{fds251853,
Author = {Stoloff, ML and Kenny, JT and Blass, EM and Hall,
WG},
Title = {The role of experience in suckling maintenance in albino
rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {94},
Pages = {847-856},
Year = {1980},
Key = {fds251853}
}
@article{fds251854,
Author = {Johanson, IB and Hall, WG},
Title = {The ontogeny of feeding in rats: III. Thermal determinants
of early ingestive responding},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {94},
Pages = {977-992},
Year = {1980},
Key = {fds251854}
}
@article{fds251855,
Author = {Hall, WG and Bryan, TE},
Title = {The ontogeny of feeding in rats: II. Independent ingestive
behavior},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {94},
Pages = {746-756},
Year = {1980},
Key = {fds251855}
}
@article{fds251856,
Author = {Cramer, CP and Blass, EM and Hall, WG},
Title = {The ontogeny of nipple-shifting behavior in albino rats:
Mechanisms of control and possible significance},
Journal = {Dev. Psychobiol.},
Volume = {13},
Pages = {165-180},
Year = {1980},
Key = {fds251856}
}
@article{fds251857,
Author = {Williams, CL and Rosenblatt, JS and Hall, WG},
Title = {Inhibition of suckling in weaning-age rats: a possible
serotonergic mechanism.},
Journal = {Journal of comparative and physiological
psychology},
Volume = {93},
Number = {3},
Pages = {414-429},
Year = {1979},
Month = {June},
url = {http://dx.doi.org/10.1037/h0077592},
Abstract = {The nature, development, and specificity of serotonergic
involvement in the control of suckling behavior in rat pups
from 10 to 35 days of age were studied. During development,
suckling normally declines after 10 days and is abandoned
after 30 days. It was found that (a) methysergide, a
serotonin (5-HT) receptor blocker, reinstated suckling
behavior in pups 15 days of age and older but had no effect
on the suckling of 10-day old pups, (b) quipazine, a 5-HT
receptor agonist, inhibited suckling of pups 10 days of age
and older, (c) methysergide pretreatment blocked the
quipazine inhibition of suckling, and (d) metergoline,
another 5-HT blocker, also stimulated suckling, and
fenfluramine, a 5-HT releaser, blocked suckling in deprived
pups. Together, these data support the hypothesis that a
serotonergic inhibitory mechanism modulates the suckling of
weaning-age rats. These pharmacological manipulations of
5-HT appear to alter specific components of suckling
behavior involved in its initiation and maintenance but do
not appear to alter a general hunger system.},
Doi = {10.1037/h0077592},
Key = {fds251857}
}
@article{fds251858,
Author = {Kornblith, C and Hall, WG},
Title = {Brain transections selectively alter ingestion and
behavioral activation in neonatal rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {93},
Pages = {1109-1117},
Year = {1979},
Key = {fds251858}
}
@article{fds251859,
Author = {Johanson, IB and Hall, WG},
Title = {Appetitive learning in 1-day-old rat pups},
Journal = {Science},
Volume = {205},
Pages = {419-421},
Year = {1979},
Key = {fds251859}
}
@article{fds251860,
Author = {Hall, WG and Rosenblatt, JS},
Title = {Developmental changes in the suckling behavior of hamster
pups: A comparison with rat pups},
Journal = {Dev. Psychobiol.},
Volume = {12},
Pages = {553-560},
Year = {1979},
Key = {fds251860}
}
@article{fds251861,
Author = {Hall, WG},
Title = {The otongeny of feeding in rats: I. Ingestive and behavioral
responses to oral infusions},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {93},
Pages = {977-1000},
Year = {1979},
Key = {fds251861}
}
@article{fds251862,
Author = {Hall, WG},
Title = {Feeding and behavioral activation in infant
rats},
Journal = {Science},
Volume = {205},
Pages = {206-209},
Year = {1979},
Key = {fds251862}
}
@article{fds251863,
Author = {Balss, EM and Beardsley, W and Hall, WG},
Title = {Age-dependent inhibition of suckling by cholecystokinin},
Journal = {Am. J. Physiol.},
Volume = {236},
Pages = {E567-E570},
Year = {1979},
Key = {fds251863}
}
@article{fds251864,
Author = {Nock, B and Williams, CL and Hall, WG},
Title = {Suckling behavior of the infant rat: modulation by a
developing neurotransmitter system.},
Journal = {Pharmacology, biochemistry, and behavior},
Volume = {8},
Number = {3},
Pages = {277-280},
Year = {1978},
Month = {March},
ISSN = {0091-3057},
url = {http://dx.doi.org/10.1016/0091-3057(78)90316-7},
Abstract = {Drugs which alter serotonin receptor activity modified the
suckling behavior of 20-day-old rat pups. Suckling could be
reinstated in nondeprived pups, which normally do not
suckle, by blockade of serotonin receptors with
methysergide. Stimulation of serotonin receptors with
quipazine inhibited suckling in deprived pups, and this
effect was prevented by methysergide pretreatment. This
evidence suggests that suckling in weaning age pups is
controlled by a serotonergic inhibitory mechanism.},
Doi = {10.1016/0091-3057(78)90316-7},
Key = {fds251864}
}
@article{fds251865,
Author = {Hall, WG and Rosenblatt, JS},
Title = {Development of nutritional control of food intake in
suckling rat pups},
Journal = {Behav. Biol.},
Volume = {24},
Pages = {413-427},
Year = {1978},
Key = {fds251865}
}
@article{fds251866,
Author = {Hall, WG and Cramer, CP and Blass, EM},
Title = {Ontogeny of suckling in rats: Transitions toward adult
ingestion},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {91},
Pages = {1141-1155},
Year = {1977},
Key = {fds251866}
}
@article{fds251867,
Author = {Hall, WG and Rosenblatt, JS},
Title = {Suckling behavior and intake control in the developing rat
pup},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {91},
Pages = {1232-1247},
Year = {1977},
Key = {fds251867}
}
@article{fds251868,
Author = {Hall, WG and Blass, EM},
Title = {Orogastric determinants of drinking in rats: Interaction
between absorptive and peripheral controls},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {91},
Pages = {365-373},
Year = {1977},
Key = {fds251868}
}
@article{fds251869,
Author = {Blass, EM and Teicher, MH and Cramer, CP and Bruno, JP and Hall,
WG},
Title = {Olfactory, thermal, and tactile controls of suckling in
preauditory and previsual rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {91},
Pages = {1248-1260},
Year = {1977},
Key = {fds251869}
}
@article{fds251870,
Author = {Blass, EM and Jobaris, R and Hall, WG},
Title = {Oropharyngeal control of drinking in rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {90},
Pages = {909-916},
Year = {1976},
Key = {fds251870}
}
@article{fds251871,
Author = {Blass, EM and Hall, WG},
Title = {Drinking termination: Interactions among hydrational,
orograstric, and behavioral controls in rats},
Journal = {Psych. Rev.},
Volume = {83},
Pages = {356-374},
Year = {1976},
Key = {fds251871}
}
@article{fds251872,
Author = {Hall, WG and Cramer, CP and Blass, EM},
Title = {Developmental changes in suckling of rat
pups},
Journal = {Nature},
Volume = {258},
Pages = {318-320},
Year = {1975},
Key = {fds251872}
}
@article{fds251873,
Author = {Hall, WG and Blass, EM},
Title = {Orogastric, hydrational, and behavioral controls of drinking
following water deprivation in rats},
Journal = {J. Comp. Physiol. Psychol.},
Volume = {89},
Pages = {939-954},
Year = {1975},
Key = {fds251873}
}
@article{fds251874,
Author = {Hall, WG},
Title = {Weaning and growth of artificially reared
rats},
Journal = {Science},
Volume = {190},
Pages = {1313-1315},
Year = {1975},
Key = {fds251874}
}
@article{fds251875,
Author = {Blass, EM and Hall, WG},
Title = {Behavioral and physiological bases of drinking inhibition in
water deprived rats},
Journal = {Nature},
Volume = {249},
Pages = {485-486},
Year = {1974},
Key = {fds251875}
}
@article{fds251876,
Author = {Hall, WG},
Title = {A remote stomach clamp to evaluate oral and gastric controls
of drinking in the rat},
Journal = {Physiological Behavior},
Volume = {11},
Pages = {897-901},
Year = {1973},
Key = {fds251876}
}
%% Chapters in Books
@misc{fds22007,
Author = {W.G. Hall},
Title = {Experiential Contributions of the Development of Olfactory
Cross Projection Systems},
Volume = {3},
Pages = {69-76},
Booktitle = {Development, Growth and Senescence in the Chemical
Senses},
Publisher = {NIH},
Editor = {Getchell, T.V. and Pearl, J. and Beauchamp, G.K. and Mistretta,
C.M.},
Year = {1993},
Key = {fds22007}
}
@misc{fds22009,
Author = {Hall, W.G. and Heimer, H.},
Title = {Components of the feeding sequence, their development and
control},
Pages = {63-81},
Booktitle = {Ontogeny and Social Transmission of Food Preferences in
Mammals: Basic and Applied Research},
Editor = {Galef, B.G., Jr. and Mainardi, M.},
Year = {1993},
Key = {fds22009}
}
@misc{fds21996,
Author = {W.G. Hall},
Title = {The ontogeny of drinking},
Pages = {35-52},
Booktitle = {Thirst: Physiological and Psychological Aspects},
Publisher = {(Int. Life Sci. Inst.), Springer-Verlag, New
York},
Editor = {D. Ramsay and D. Booth},
Year = {1991},
Key = {fds21996}
}
@misc{fds21994,
Author = {W.G. Hall},
Title = {The ontogeny of ingestive behavior: Changing control of
components in the feeding sequence},
Pages = {77-123},
Booktitle = {Handbook of Behavioral Neurobiology: Food and Water
Intake},
Publisher = {Plenum Press, New York},
Editor = {E.M. Stricker},
Year = {1990},
Key = {fds21994}
}
@misc{fds21982,
Author = {W.G. Hall},
Title = {Early Motivation, reward, learning and their neural bases:
Developmental revelations and simplifications},
Booktitle = {Psychobiological Aspects of Behavioral Development},
Publisher = {New York: Academic},
Editor = {N.A. Krasnegor et al.},
Year = {1987},
Key = {fds21982}
}
@misc{fds21985,
Author = {Phifer, C.B. and Hall, W.G.},
Title = {The development of feeding behavior},
Pages = {189-229},
Booktitle = {Methods and Techniques to Study Feeding and Drinking
Behavior},
Publisher = {Amsterdam: Elsevier},
Editor = {N.E. Rowland and F. Toates},
Year = {1987},
Key = {fds21985}
}
@misc{fds21973,
Author = {Johanson, I.B. and Hall, W.G.},
Title = {Ontogeny of appetitive learning: Independent ingestion as a
model motivational system},
Pages = {135-157},
Booktitle = {Comparative Perspectives on the Development of
Memory},
Publisher = {Hillsdale, N.J.: Earlbaum},
Editor = {R. Kail and N.E. Spear},
Year = {1984},
Key = {fds21973}
}
@misc{fds21962,
Author = {W.G. Hall},
Title = {Feeding, food reward, and learning: An appetitive system for
ingestive behavior in infant rats},
Booktitle = {Symposium neuroontogeneticium},
Publisher = {Prague: Charles University Press},
Editor = {S. Trojan and J. Mourek},
Year = {1982},
Key = {fds21962}
}
@misc{fds21944,
Author = {Blass, E.M. and Hall, W.G. and Teicher, M.H.},
Title = {The ontogeny of suckling and ingestive behaviors},
Volume = {8},
Booktitle = {Progress in psychobiology and physiological
psychology},
Publisher = {New York: Academic Press},
Editor = {J.M. Sprague and A.N. Epstein},
Year = {1979},
Key = {fds21944}
}
@misc{fds21945,
Author = {Blass, E.M. and Kenny, S.T. and Stoloff, M. and Bruno, J.P. and Teicher, M.H. and Hall, W.G.},
Title = {Motivation, learning and memory in the ontogeny of suckling
in albino rats},
Booktitle = {The ontogeny of learning the memory},
Publisher = {Hillsdale, N.J.: Earlbaum},
Editor = {N.E. Spear and B.A. Campbell},
Year = {1979},
Key = {fds21945}
}
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