Keyword search (4,163 papers available)

"Sciascia JM" Authored Publications:

Title Authors PubMed ID
1 Comparing ABA, AAB, and ABC Renewal of Appetitive Pavlovian Conditioned Responding in Alcohol- and Sucrose-Trained Male Rats. Khoo SY, Sciascia JM, Brown A, Chaudhri N 32116588
PSYCHOLOGY
2 The medial prefrontal cortex is required for responding to alcohol-predictive cues but only in the absence of alcohol delivery. Khoo SY, Sciascia JM, Pettorelli A, Maddux JN, Chaudhri N 31070082
PSYCHOLOGY
3 Vendor differences in alcohol consumption and the contribution of dopamine receptors to Pavlovian-conditioned alcohol-seeking in Long-Evans rats. Sparks LM, Sciascia JM, Ayorech Z, Chaudhri N 24096535
PSYCHOLOGY
4 Alcohol-Seeking Triggered by Discrete Pavlovian Cues is Invigorated by Alcohol Contexts and Mediated by Glutamate Signaling in the Basolateral Amygdala. Sciascia JM, Reese RM, Janak PH, Chaudhri N 25953360
PSYCHOLOGY

 

Title:Comparing ABA, AAB, and ABC Renewal of Appetitive Pavlovian Conditioned Responding in Alcohol- and Sucrose-Trained Male Rats.
Authors:Khoo SYSciascia JMBrown AChaudhri N
Link:https://www.ncbi.nlm.nih.gov/pubmed/32116588?dopt=Abstract
DOI:10.3389/fnbeh.2020.00005
Publication:Frontiers in behavioral neuroscience
Keywords:Pavlovian conditioningalcoholcontextreinstatementrelapserenewalrewardsucrose
PMID:32116588 Category:Front Behav Neurosci Date Added:2020-03-03
Dept Affiliation: PSYCHOLOGY
1 Center for Studies in Behavioural Neurobiology, Department of Psychology, Concordia University, Montreal, QC, Canada.

Description:

Comparing ABA, AAB, and ABC Renewal of Appetitive Pavlovian Conditioned Responding in Alcohol- and Sucrose-Trained Male Rats.

Front Behav Neurosci. 2020;14:5

Authors: Khoo SY, Sciascia JM, Brown A, Chaudhri N

Abstract

Conditioned responding can be renewed by re-exposure to the conditioning context following extinction in a different context (ABA renewal) or by removal from the extinction context (AAB or ABC renewal). ABA renewal is robust in Pavlovian and operant conditioning paradigms. However, fewer studies have investigated AAB and ABC renewal of appetitive conditioning, and those that did predominantly used operant conditioning tasks. Renewal has theoretical relevance for extinction and for exposure-based treatments for substance use disorders that aim to extinguish reactivity to drug-predictive cues. We therefore investigated ABA, AAB, and ABC renewal of Pavlovian conditioned responding to cues that predicted either alcohol or sucrose. Male, Long-Evans rats (Charles River) were exposed to either 15% ethanol (Study 1: "alcohol") or 10% sucrose (Study 2: "sucrose") in their home cages. Next, they were trained to discriminate between two auditory stimuli (white noise and clicker; 10 s) in conditioning chambers equipped with distinct olfactory, visual, and tactile contextual stimuli (context A). One conditioned stimulus (CS+) was paired with fluid delivery (0.2 ml/CS+; 3.2 ml/session; alcohol or sucrose in separate experiments), and the second CS (CS-) was not. In all sessions (conditioning, extinction, and test), each CS was presented 16 times/session on a variable-time 67-s schedule, and entries into the fluid port were recorded. CS+ port entries were then extinguished by withholding fluid delivery either in context A or in a second, different context (context B). Next, we assessed ABA, AAB, and ABC renewal in the absence of fluid delivery. During extinction, CS+ port entries were initially elevated in context A relative to context B. ABA renewal of CS+ port entries occurred in both alcohol- and sucrose-trained rats. ABC renewal approached statistical significance when data from both experiments were combined. No AAB renewal was observed, and, in fact, alcohol-trained rats showed AAB suppression. These results corroborate the reliability of ABA renewal and suggest that ABC renewal is a modest effect that may require greater statistical power to detect. From a treatment perspective, the lack of AAB renewal suggests that exposure-based treatments for substance use disorders might benefit from implementation in real-world, drug-use contexts.

PMID: 32116588 [PubMed]





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