ArticlePublisher preview available

Context-Specificity of Target Versus Feature Inhibition in a Feature-Negative Discrimination

Authors:
To read the full-text of this research, you can request a copy directly from the authors.

Abstract

Four experiments with rats examined the effects of a context switch on inhibition that was acquired during a feature-negative discrimination. A target conditioned stimulus was paired with food when it was presented alone but occurred without food when it was combined with a feature stimulus. A context switch following training did not disrupt inhibition conditioned to the feature. However, responding to the target was more difficult to inhibit when it was tested in a different context. It is suggested that both the target and the feature acquired inhibition and that the target's inhibition was especially sensitive to the context. The feature may inhibit responding to the target (a) by directly suppressing the representation of the food and (b) by activating the target's own inhibitory association with food, which is at least partly context-specific. Implications for theories of inhibition and negative occasion-setting are discussed.
Journal
of
Experimental
Psychology:
Animal
Behavior
Processes
1994, Vol.
20, No. 1,
51-65
Copyright
1994
by the
American
Psychological
Association,
Inc.
0097-7403/94/S3.00
Context-Specificity
of
Target
Versus
Feature
Inhibition
in a
Feature-Negative
Discrimination
Mark
E.
Bouton
and
James
B.
Nelson
Four experiments with
rats
examined
the
effects
of a
context switch
on
inhibition that
was
acquired
during
a
feature-negative discrimination.
A
target conditioned stimulus
was
paired
with food when
it was
presented alone
but
occurred without food when
it was
combined with
&
feature stimulus.
A
context switch following training
did not
disrupt inhibition conditioned
to the
feature. However,
responding
to the
target
was
more
difficult
to
inhibit when
it was
tested
in a
different context.
It
is
suggested that both
the
target
and the
feature acquired inhibition
and
that
the
target's
inhibition
was
especially
sensitive
to the
context.
The
feature
may
inhibit responding
to the
target
(a) by
directly suppressing
the
representation
of the
food
and (b) by
activating
the
target's
own
inhibitory
association with food, which
is at
least partly context-specific. Implications
for
theories
of
inhi-
bition
and
negative
occasion-setting
are
discussed.
The
results
of a
number
of
experiments suggest that
ex-
tinction
performance
is
relatively specific
to the
context
in
which
it is
learned.
For
example,
if
conditioned
stimulus
(CS)-unconditioned stimulus (US) pairings
are
given
in one
context
and
then
CS-alone
training (extinction)
is
given
in
another context,
a
return
of the CS to the
original condi-
tioning context
can
renew extinguished performance
to the
CS
(e.g., Bouton
&
Holies,
1979; Bouton
&
King,
1983;
Bouton
&
Peck, 1989). Although extinction performance
is
specific
to its
context, conditioning performance
is
much less
so.
When
the
context
is
switched
after
conditioning, there
is
often
relatively little diminution
of the
conditioned response
(CR)
(e.g.,
Bouton
&
King, 1983; Bouton
&
Peck, 1989;
Bouton
&
Swartzentruber,
1986; Hall
&
Honey, 1989; Kaye
&
Mackintosh, 1990; Kaye, Preston, Szabo,
Druiff,
&
Mackintosh, 1987).
It
may be
reasonable
to
suppose that
the CS
acquires
a
second association during extinction
and
that this association
is
especially sensitive
to the
context (Bouton, 1993).
One
possibility
is
that
the
animal learns
a new
inhibitory asso-
ciation with
the CS
(e.g.,
CS-no
US) in
extinction. Such
learning
has
been proposed
by
several conditioning models
(e.g.,
Konorski,
1967;
Pearce,
1987;
Pearce
&
Hall, 1980;
Wagner,
1981;
see
also Pavlov, 1927) that assume that non-
reinforcement
of the CS in
extinction will cause
acquisition
of
a
second inhibitory association instead
of the
unlearning
of
the
original
CS-US
association (e.g., Rescorla
&
Wagner,
1972). According
to
these models,
at the end of
extinction,
the
CS has
both excitatory
and
inhibitory values.
On
this
Mark
E.
Bouton
and
James
B.
Nelson,
Department
of
Psychol-
ogy,
University
of
Vermont.
This
research
was
supported
by
Grants
BNS
89-08535
and
IBN
92-09454
from
the
National
Science
Foundation.
Correspondence
concerning
this
article
should
be
addressed
to
Mark
E.
Bouton,
Department
of
Psychology,
University
of
Vermont,
Burlington,
Vermont
05405.
view,
the
context-specificity
of
extinction could come about
if
inhibition
is
relatively specific
to the
context
in
which
it
is
learned.
The
present experiments were therefore designed
to
test
whether conditioned inhibition
is
reduced with
a
change
of
context.
To
produce inhibition,
we
used
a
feature-negative
discrimination procedure.
In
this sort
of
procedure,
a
target
CS,
such
as a
tone,
is
paired with
a US
when
it is
presented
alone
(T+)
but is
presented
without
a US
when
it is
combined
with
a
"feature" stimulus, such
as a
light
(LT-).
The
feature-
negative procedure
is
widely known
to
produce inhibition
to
the
feature (L). Indeed,
it is
sometimes taken
as the
basic
means
of
producing conditioned inhibition (e.g., Rescorla
&
Wagner,
1972).
If
conditioned inhibition
is
specific
to its
context, then
a
context switch
after
feature-negative training
might
cause
a
loss
of
inhibition
to the
feature
CS.
Recent theories
of
conditioning, however, suggest that
the
target stimulus might also acquire some inhibition
in the
feature-negative
discrimination.
As is
expected when
a CS is
nonreinforced
in
extinction,
the
target itself might acquire
an
inhibitory
association when
it is
nonreinforced
in
compound
with
the
feature
in
this paradigm (e.g., Pearce
&
Hall, 1980;
Wagner,
1981). Thus, both feature
and
target
may
acquire
some inhibition when
the
compound
is
nonreinforced
in the
feature-negative
paradigm.
We
designed
the
present experiments
to
investigate
the
effects
of
switching
the
context
after
feature-negative dis-
crimination training.
We
used
an
appetitive conditioning
preparation
in
which
we
monitored
the
number
of
times
the
rat
entered
the
food
cup or
magazine (magazine
en-
tries) during
the CS
(e.g.,
Hall
&
Channell,
1985; Hall
&
Honey,
1990; Kaye
&
Mackintosh, 1990; Wilson
&
Pearce, 1990).
The
results suggest that inhibition
is
indeed
attenuated
when
the
context
is
switched
after
feature-
negative training. However,
in the
present experiments,
the
context switch reduced inhibition
to the
target
CS but not
inhibition
to the
feature.
The
results have implications
for
the
issue
of
what
is
learned
in
feature-negative discrimina-
tion learning.
51
This document is copyrighted by the American Psychological Association or one of its allied publishers.
This article is intended solely for the personal use of the individual user and is not to be disseminated broadly.
... Various attempts at modeling and explaining the mechanism of occasion setting (i.e., modulation) have been proposed (Bonardi et al., 2017;Delamater, 2012;Schmajuk et al., 1998). The most parsimonious is that of Bouton and Nelson (1994), which can be described most accurately as inhibition of inhibition, or simply, disinhibition. Historically, disinhibition has been described as the removal of an inhibitory process (Pavlov, 1927). ...
... However, none of the typical tests of occasion setting were conducted, and no tests compared the pattern of behavior in this patterning task to a feature-positive discrimination, so it is not currently known whether dual-response procedures recruit true occasion setting mechanisms. Bouton and Nelson's (1994) mechanism could be extended to a scenario in which one response is correct on XA trials and a different response on A-alone trials (see Figure 1b). In a dual-response operant procedure (XA[R1+, R2−]/A[R1−, R2+]), X could come to disinhibit a particular response (R1) to A. Initially, both responses (R1 and R2) would be partially reinforced in the presence of A, making it excitatory op the ability to disinhibit Avelop its own excitation of R1, but that would be independent of its ability to disinhibit A. If X is disinhibiting A (i.e., occasion setting), then extinction of X should have little effect on responding during XA trials, but disrupt responding during test trials of X-alone. ...
... (a) A typical feature-positive discrimination where trials of XA are paired with R1, and A develops both excitatory and inhibitory links with R1 and its associated outcome (A:R1-/XA:R1+). (b) Modified from Bouton and Nelson (1994) to include a conditioning procedure with trials of A-alone paired with reinforcement of R2, and other trials of X-alone and A-alone paired with reinforcement of R1 (A:R1-/R2+; XA:R1+/R2-). The target (A) develops both excitatory and inhibitory links to R1 and R2 and their associated outcomes, respectively. ...
Article
Full-text available
In a typical feature-positive discrimination, responding is reinforced (+) during the target stimulus (A) on trials with the feature stimulus (X), but not during target-alone trials (A−). When X and A are presented simultaneously, direct control by X is typically observed; however, when the stimuli are presented serially, X sets the occasion for responding to A. In the current dual-response procedures, one response (e.g., left lever press) was reinforced during feature-target trials (XA+) and a different response (e.g., right lever press) was reinforced during target-alone trials (A+). In Experiment 1, rats received either serial (X → A+) or simultaneous (X:A+) presentations of the feature-target compound along with target-alone trials (A+). Contrary to our predictions, the serial group failed to learn the discrimination and the simultaneous group demonstrated occasion setting. In Experiment 2, the salience of the feature was increased, which resulted in direct control by the feature in both groups. In Experiment 3, an additional serial group was included with a longer interval between the feature (X) and target (A). Despite the reduced temporal proximity of X to reinforcement, direct control was again observed in all groups. The current pattern of results in the simultaneous and serial groups is interpreted in relation to the enhanced salience of A relative to X, due to separate pairings of A-alone with reinforcement in the dual-response procedure. Consistent with previous findings, occasion setting was observed when A was most salient relative to X (Experiment 1, simultaneous group), but direct control was found when the salience of X was increased (Experiments 2–3).
... Disinhibition Account Bouton (1997); Bouton & Nelson (1994 The target has both inhibitory and excitatory associations. The feature can disinhibit the inhibitory target-US association. ...
... For example, we have shown in rats that prior stress impaired fear extinction to a much greater extent than conditioned inhibition within the same animal, indicating extinction learning and conditioned inhibition are not always congruent (Woon et al., 2020). It has also been well documented that the fear-reducing benefits of extinction training are limited to the context the extinction training occurred in (Garfinkel et al., 2014;Rougemont-Bücking et al., 2011;Shvil et al., 2014), while a conditioned inhibitor is able to inhibit responding to a target cue across different contexts, both in a fear task (Miguez et al., 2015) and an appetitive task (Bouton & Nelson, 1994). It is widely viewed that during fear extinction, a separate inhibitory memory representing a cue-no shock association is created that competes with the original excitatory cue-shock association, and the context becomes a powerful cue to guide behavior toward high or low fear expression (Bouton et al., 2006(Bouton et al., , 2021Maren et al., 2013). ...
Article
Full-text available
There is a growing number of studies investigating discriminatory fear conditioning and conditioned inhibition of fear to assess safety learning, in addition to extinction of cued fear. Despite all of these paradigms resulting in a reduction in fear expression, there are nuanced differences among them, which could be mediated through distinct behavioral and neural mechanisms. These differences could impact how we approach potential treatment options in clinical disorders with dysregulated fear responses. The objective of this review is to give an overview of the conditional discrimination and inhibition findings reported in both animal models and human neuropsychiatric disorders. Both behavioral and neural findings are reviewed among human and rodent studies that include conditional fear discrimination via conditional stimuli with and without reinforcement (CS+ vs. CS−, respectively) and/or conditional inhibition of fear through assessment of the fear response to a compound CS−/CS+ cue versus CS+. There are several parallels across species in behavioral fear expression as well as neural circuits promoting fear reduction in response to a CS− and/or CS−/CS+ compound cue. Continued and increased efforts to compare similar behavioral fear inhibition paradigms across species are needed to make breakthrough advances in our understanding and treatment approaches to individuals with fear disorders.
... Another issue raised by our use of different contexts for each phase of training and testing concerns the context specificity of conditioned inhibition. Bouton and Nelson (1994) found that conditioned inhibition can be context specific. Specifically, in their experiments they found that the target of conditioned inhibition training loses its ability to be inhibited when tested in a context other than that in which it was trained (Experiments 3 and 4), while the feature (the inhibitor) readily transfers to other contexts (Experiments 2 and 4). ...
Article
Full-text available
Two experiments with rats investigated the temporal relationships under which conditioned inhibition will transfer to an independently conditioned excitor (CS) in a summation test. Experiment 1 trained 2 simultaneous inhibitors with either a trace or delay excitatory CS. Transfer of inhibitory behavioral control depended on the temporal relationship of the transfer CS to the unconditioned stimulus (US). Experiment 2 extended these findings by training 2 inhibitors (1 simultaneous and 1 serial) with a single delay excitatory CS. Again, testing with trace and delay transfer CSs found that transfer of inhibitor control depended on the temporal relationship of the transfer CS to the US. In both studies, maximal inhibition was observed when the inhibitor signaled US omission at the same time as the transfer excitor signaled US presentation. The results are discussed in terms of the temporal coding hypothesis.
... These include fear renewal, reinstatement, spontaneous recovery, and reacquisition (Bouton et al., 2020). During these phenomena, there is an assumption that the excitatory CS-US memory trace overrides the inhibitory CS-no US memory trace (Bouton, 1994;Bouton & Nelson, 1994). ...
Thesis
Full-text available
Fear-related psychopathologies, such as post-traumatic stress disorder, are strongly linked to aberrant neural circuits governing learning, memory, and emotion. Unexplored cells in the lateral hypothalamus (LH) and zona incerta (ZI) that express the relaxin-3 peptide receptor, RXFP3, are putatively involved in these processes. Anterograde tracing from this population revealed projections to the periaqueductal gray, lateral habenula, and lateral septum, which are implicated in associative learning, context discrimination, and control of defensive behaviours. Thus, it is plausible that these cells are involved in context-dependent Pavlovian fear conditioning and extinction. To interrogate this possibility, RXFP3-Cre mice were bilaterally injected with a Cre-dependent excitatory DREADD (hM3Dq) or mCherry control virus into the LH/ZI. Mice were subjected to a three-day context-dependent fear conditioning protocol involving tone-footshock (CS-US) conditioning (Day 1), fear extinction (Day 2), and recall test (Day 3). RXFP3+ LH/ZI neurons were activated by injection of CNO (3 mg/kg, i.p.) during fear extinction, which decreased freezing to the CS in extinction context B, but not extinction context A. Interestingly, activating these cells also enhanced general locomotion and caused escape-like jumping. Subsequent analysis revealed that jumping did not significantly drive attenuated freezing. However, it remains unclear if this result reflected changes in context-dependent fear expression or increased arousal. Additionally, activating RXFP3+ LH/ZI cells during extinction did not affect extinction memory retrieval or fear renewal. Though this suggests that these cells may not have been involved in extinction memory encoding, this result may have indicated issues with strainspecific contextual discrimination. Additionally, brain-wide Fos expression analysis revealed that activating RXFP3+ LH/ZI neurons increased coordinated activity in numerous stress, arousal, learning, and memory implicated regions. Overall, this study provided novel information regarding RXFP3+ LH/ZI cells’ involvement in Pavlovian fear conditioning and extinction, and highlighted the putative role of these cells in various aspects of stress, learning, and memory.
... Unlike inhibitors from FN discriminations, extinguished discriminative stimuli have a history of both reinforcement and nonreinforcement, and this sort of factor is known to play a role in inhibition learning. For example, Bouton and Nelson (1994) found that inhibition to a Pavlovian conditioned inhibitor (X) trained in an Aþ/AXÀ procedure transferred successfully across contexts, whereas inhibition to the inhibited A stimulus (that was both reinforced and nonreinforced) did not. And of course, extinction of a Pavlovian excitor is also widely known not to transfer across contexts (e.g., Bouton et al., 2021). ...
Article
Full-text available
Six experiments with rats examined the nature of inhibition learned in an operant feature-negative (FN) discrimination. The results of prior experiments that examined instrumental extinction rather than FN learning suggest that inhibition can be very specific to the inhibited response. In Experiment 1, we trained lever-press and chain-pull responses in separate but parallel FN discriminations (AR1+, ABR1-, CR2+, and CDR2-) and then tested both inhibitors (B and D) with both responses. Of primary interest was the extent to which the inhibitors suppressed the response they were trained with (same-response inhibition) versus the other response (cross-response inhibition). We found that cross-response inhibition was robust and essentially equal to same-response inhibition. Experiment 2 replicated this result and confirmed stronger inhibition after FN learning than after a differential inhibition procedure (AR1+, BR1-, CR2+, and DR2-). There was also little evidence that cross-response inhibition was due to a demonstrable competing response. Experiment 3 found that cross-response inhibition did not depend on having the two responses reinforced by a common outcome. Experiments 4 and 5 then found that cross-response inhibition depended substantially (though not completely) on the transfer target response having been trained in its own FN discrimination. However, Experiment 6 found that inhibition after instrumental extinction (as opposed to FN learning) was still highly response-specific when the transferred-to response had been trained in an FN discrimination. The overall results suggest that the characteristics of inhibition in instrumental extinction and FN learning differ and that transfer of FN inhibition across responses depends at least partly on previous "inhibitability" of the target response. (PsycInfo Database Record (c) 2022 APA, all rights reserved).
Article
Full-text available
Recent theories suggest that reduced serotonin transporter (5‐HTT) function, which increases serotonin (5‐HT) levels at the synapse, enhances neural plasticity and affects sensitivity to environmental cues. This may promote learning about emotionally relevant events. However, the boundaries that define such emotional learning remain to be established. This was investigated using 5‐HTT knockout (5‐HTTKO) mice which provide a model of long‐term elevated 5‐HT transmission and are associated with increased anxiety. Compared to wild‐type controls, 5‐HTTKO mice were faster to discriminate between an auditory cue that predicted footshock (CS+) and a cue predicting no footshock (CS−). Notably, this enhanced discrimination performance was driven not by faster learning that the CS+ predicted footshock, but rather by faster learning that the CS− cue signals the absence of footshock and thus provides temporary relief from fear/anxiety. Similarly, 5‐HTTKO mice were also faster to reduce their fear of the CS+ cue during subsequent extinction. These findings are consistent with facilitated inhibitory learning that predicts the absence of potential threats in 5‐HTTKO mice. However, 5‐HTTKO mice also exhibited increased generalisation of fear learning about ambiguous aversive cues in a novel context, different from the training context. Thus, 5‐HTTKO mice can exhibit both more and less fear compared to wild‐type controls. Taken together, our results support the idea that loss of 5‐HTT function, and corresponding increases in synaptic 5‐HT availability, may facilitate learning by priming of aversive memories. This both facilitates inhibitory learning for fear memories but also enhances generalisation of fear.
Article
Learning to stop responding is an important process that allows behavior to adapt to a changing and variable environment. This article reviews recent research in this laboratory and others that has studied how animals learn to stop responding in operant extinction, punishment, and feature-negative learning. Extinction and punishment are shown to be similar in two fundamental ways. First, the response-suppressing effects of both are highly context-specific. Second, the response-suppressing effects of both can be remarkably response-specific: Inhibition of one response transfers little to other responses. Learning to inhibit the response so specifically may result from the correction of "response error," the difference between the level of responding and what the current reinforcer supports. In contrast, the inhibition of responding that develops in feature-negative learning, where the response is reinforced during one discriminative stimulus (A) but not in a compound of A and stimulus B, is less response-specific: The inhibition of responding by stimulus B transfers and inhibits a second response, especially if the second response has itself been inhibited before. The results thus indicate both response-specific and response-general forms of behavioral inhibition. One possibility is that response-specific inhibition is learned when the circumstances encourage the organism to pay attention to the response-to what it is actually doing-as behavioral suppression is learned.
Chapter
Originally published in 2007, this was the first textbook to focus specifically on disaster psychiatry. It brings together the views of international experts to provide a comprehensive review of the psychological, biological, and social responses to disaster, describing evidence-based clinical and service-led interventions to meet mental health needs and foster resilience and recovery. Chapters address the epidemiology of disaster response, the neurobiology of disaster exposure, socio-cultural issues, early intervention and consultation-liaison care, the role of non-governmental organizations, workplace policies, and implications for public health planning at the level of the individual and the community. This book is essential reading for all those involved in preparing for traumatic events and their clinical and social outcomes for public health planning.
Article
Full-text available
Two experiments using a conditioned suppression procedure with 64 Sprague-Dawley rats found that postconditioning reinforcement of an inhibitory feature stimulus (X) had substantially different effects depending on whether a serial or a simultaneous feature negative discrimination procedure was used to establish the inhibition. With the simultaneous procedure, acquisition of excitation to the previously inhibitory X was retarded when X was paired with shock. Subsequent summation tests showed no evidence of inhibition to X after reinforced X presentations. However, acquisition of excitation to X was unaffected by prior serial feature negative training, and X-shock pairings had relatively little effect on X's inhibitory power in summation tests. Data suggest that the nature of inhibition established in feature negative discriminations differs substantially depending on the temporal arrangement of stimuli. One possibility is that inhibitors established using simultaneous stimulus arrangements modulate behavior by acting on a representation of the UCS, but inhibitors established with serial procedures act on particular CS–UCS associations. (24 ref)
Article
Full-text available
In Exp I, using 20 female hooded Lister rats, the habituation of the orienting response (OR) shown by Ss to a discrete visual stimulus (a 10-sec light) in a given training context (A) was monitored. Dishabituation occurred, in that the OR returned to its initial level, when the light was presented in a different and novel context (B). In Exp II, 24 female rats received 2 sessions/day, one in each of the 2 contexts. For experimental Ss, the light was presented in Context A until the OR habituated. In the test phase, the light was presented in Context B, but the OR was not restored, suggesting that the dishabituation seen in Exp I depended on the absolute novelty of Context B. In Exp III, Ss from Exp II were required to form a light–food association in both contexts. Slow learning was observed in Ss trained with the familiar light in Context A, but learning proceeded normally with the familiar light in Context B. Thus, a context change that failed to produce dishabituation was enough to prevent the occurrence of a latent inhibition effect. (35 ref) (PsycINFO Database Record (c) 2012 APA, all rights reserved)
Article
Full-text available
Investigated rats' solutions of simultaneous feature positive discriminations (XA+, A–). When X was a visual cue and A was an auditory cue of moderate intensity, the rats solved the discrimination by associating X with the food unconditioned stimulus (UCS) and ignoring A. But when X was a visual cue and A was a loud auditory cue, the rats solved the discrimination by using X to set the occasion for responding that was based on associations between A and the UCS. The use of these two strategies was apparently determined by the perceptual (intensity) characteristics of A during learning of the discrimination: It was not affected by A's conditioning history prior to discrimination training, nor by A's intensity during a posttraining test. The results were discussed in terms of recent theories of occasion setting and generalization. (PsycINFO Database Record (c) 2012 APA, all rights reserved)
Article
Full-text available
Rats were used as subjects in four experiments to investigate the transfer of learning from one context to another. Subjects received two sessions of training each day, one in each of two different contexts. Experiment 1 showed that the habituation of the unconditioned response to a stimulus presented in one context was left intact when the stimulus was presented in another context, but that latent inhibition was attenuated when preexposure and conditioning phases occurred in different contexts. Experiments 2 and 3 demonstrated that a conditioned response made on the basis of an appetitive reinforcer was diminished when conditioning and testing occurred in different contexts, but that aversive conditioning was not influenced by the context in which testing occurred. In Experiment 4, the presence of an aversive reinforcer during training did not preclude the occurrence of context-specific conditioning on the basis of an appetitive reinforcer. Associative and retrieval-based interpretations of the results are explored. (PsycINFO Database Record (c) 2012 APA, all rights reserved)
Article
Four conditioned suppression experiments examined the influence of contextual stimuli on the rat's fear of an extinguished conditioned stimulus (CS). When rats received pairings of a CS with shock in one context and then extinction of the CS in another context, fear of the CS was renewed when the CS was returned to and tested in the original context (Experiments 1 and 3). No such renewal was obtained when the CS was tested in a second context after extinction had occurred in the conditioning context (Experiment 4). In Experiment 2, shocks presented following extinction reinstated fear of the CS, but only if they were presented in the context in which the CS was tested. In each experiment, the associative properties of the contexts were independently assessed. Contextual excitation was assessed primarily with context-preference tests in which the rats chose to sit in either the target context or an adjoining side compartment. Contextual inhibition was assessed with summation tests. Although reinstatement was correlated with demonstrable contextual excitation present during testing, the renewal effect was not. Moreover, there was no evidence that contextual inhibition developed during extinction. The results suggest that fear of an extinguished CS can be affected by the excitatory strength of the context but that independently demonstrable contextual excitation or inhibition is not necessary for contexts to control that fear.
Article
Conditioning may generalize from one context to another when latent inhibition (the effect on subsequent conditioning of prior unreinforced exposure to the stimulus) does not. Experiment 1 studied conditioned approach and licking by rats to a stimulus paired with the delivery of water and confirmed that latent inhibition could be abolished by a change of context, while prior aversive conditioning to the stimulus, produced by pairing it with mild shock, interfered with the acquisition of conditioned approach and licking regardless of this change of context. Thus even when conditioning and latent inhibition were measured in the same way, the former generalized across contexts, and the latter did not. Experiment 2 showed that the effects not only of unreinforced exposure to a stimulus but also of presentation of the stimulus uncorrelated with the delivery of water were confined to the context in which they occurred. Thus the generalization of conditioning from one context to another and the failure of latent inhibition to generalize cannot be attributed to the occurrence of rein-forcers during conditioning and their absence in latent inhibition. This conclusion was confirmed in Experiment 3, where animals received both aversive conditioning trials and unreinforced presentations of other stimuli in the treatment phase of the experiment, but were then conditioned to one of these stimuli paired with water. Once again, the effects of aversive conditioning transferred perfectly from one context to another, while those of unreinforced presentations did not. Latent inhibition, these results suggest, is not easily explained by supposing that animals associate an unreinforced stimulus with zero consequences and have to unlearn this association when the stimulus is then paired with a reinforcer.
Article
This chapter describes Pavlovian conditioning as the transfer of control of reflexes (unconditioned responses or URs) from stimuli that elicit them unconditionally (USs) to other stimuli that normally are incapable of eliciting them. Although auditory cues seldom elicit substantial salivation spontaneously, a tone provokes that response if it consistently predicts food delivery. This new-found control of salivation by the tone is typically attributed to the acquisition of some association or potentiated connection between the CS and US pathways: by virtue of that association, the CS becomes a substitute elicitor of activity along some portion of the US-UR pathway. This is often described as the CS's “activating a representation of the US”. Another behavioral control function occasionally ascribed to Pavlovian CSsis modulation. Rather than acquiring its own ability to elicit behavior usually controlled by another reflex system, a Pavlovian CS influences the efficacy of the normal elicitor of a response. The chapter is concerned with a particular modulatory function of CSs in rats solutions of elementary conditional discriminations, in which one CS modifies the efficacy of Pavlovian associations between other cues and the US. This function is called as occasion setting, which is readily distinguished from elicitation both conceptually and empirically, and perhaps anatomically as well. Furthermore, this occasion-setting function involves a hierarchical, multilayered organization of representations of events and relations and thus may aid the expansion of the domain of Pavlovian accounts of behavior.
Article
Instrumental learning involves three primary events: a stimulus (S), a response (R), and an outcome (O). Evidence is reviewed indicating the presence of binary associations among those events, as well as a hierarchical structure of the form S–(R–O). Experiments examining the conditions that produce learning, the content of the learning once it has occurred, and the way learning maps into performance all suggest the presence of such a hierarchical structure.