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Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats
Pavlovian conditioned stimuli (CSs) play an important role in the reinforcement and motivation of instrumental active avoidance (AA). Conditioned threats can also invigorate ongoing AA responding [aversive Pavlovian–instrumental transfer (PIT)]. The neural circuits mediating AA are poorly understood...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2014
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166994/ https://www.ncbi.nlm.nih.gov/pubmed/25278858 http://dx.doi.org/10.3389/fnbeh.2014.00329 |
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author | McCue, Margaret G. LeDoux, Joseph E. Cain, Christopher K. |
author_facet | McCue, Margaret G. LeDoux, Joseph E. Cain, Christopher K. |
author_sort | McCue, Margaret G. |
collection | PubMed |
description | Pavlovian conditioned stimuli (CSs) play an important role in the reinforcement and motivation of instrumental active avoidance (AA). Conditioned threats can also invigorate ongoing AA responding [aversive Pavlovian–instrumental transfer (PIT)]. The neural circuits mediating AA are poorly understood, although lesion studies suggest that lateral, basal, and central amygdala nuclei, as well as infralimbic prefrontal cortex, make key, and sometimes opposing, contributions. We recently completed an extensive analysis of brain c-Fos expression in good vs. poor avoiders following an AA test (Martinez et al., 2013, Learning and Memory). This analysis identified medial amygdala (MeA) as a potentially important region for Pavlovian motivation of instrumental actions. MeA is known to mediate defensive responding to innate threats as well as social behaviors, but its role in mediating aversive Pavlovian–instrumental interactions is unknown. We evaluated the effect of MeA lesions on Pavlovian conditioning, Sidman two-way AA conditioning (shuttling) and aversive PIT in rats. Mild footshocks served as the unconditioned stimulus in all conditioning phases. MeA lesions had no effect on AA but blocked the expression of aversive PIT and 22 kHz ultrasonic vocalizations in the AA context. Interestingly, MeA lesions failed to affect Pavlovian freezing to discrete threats but reduced freezing to contextual threats when assessed outside of the AA chamber. These findings differentiate MeA from lateral and central amygdala, as lesions of these nuclei disrupt Pavlovian freezing and aversive PIT, but have opposite effects on AA performance. Taken together, these results suggest that MeA plays a selective role in the motivation of instrumental avoidance by general or uncertain Pavlovian threats. |
format | Online Article Text |
id | pubmed-4166994 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-41669942014-10-02 Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats McCue, Margaret G. LeDoux, Joseph E. Cain, Christopher K. Front Behav Neurosci Neuroscience Pavlovian conditioned stimuli (CSs) play an important role in the reinforcement and motivation of instrumental active avoidance (AA). Conditioned threats can also invigorate ongoing AA responding [aversive Pavlovian–instrumental transfer (PIT)]. The neural circuits mediating AA are poorly understood, although lesion studies suggest that lateral, basal, and central amygdala nuclei, as well as infralimbic prefrontal cortex, make key, and sometimes opposing, contributions. We recently completed an extensive analysis of brain c-Fos expression in good vs. poor avoiders following an AA test (Martinez et al., 2013, Learning and Memory). This analysis identified medial amygdala (MeA) as a potentially important region for Pavlovian motivation of instrumental actions. MeA is known to mediate defensive responding to innate threats as well as social behaviors, but its role in mediating aversive Pavlovian–instrumental interactions is unknown. We evaluated the effect of MeA lesions on Pavlovian conditioning, Sidman two-way AA conditioning (shuttling) and aversive PIT in rats. Mild footshocks served as the unconditioned stimulus in all conditioning phases. MeA lesions had no effect on AA but blocked the expression of aversive PIT and 22 kHz ultrasonic vocalizations in the AA context. Interestingly, MeA lesions failed to affect Pavlovian freezing to discrete threats but reduced freezing to contextual threats when assessed outside of the AA chamber. These findings differentiate MeA from lateral and central amygdala, as lesions of these nuclei disrupt Pavlovian freezing and aversive PIT, but have opposite effects on AA performance. Taken together, these results suggest that MeA plays a selective role in the motivation of instrumental avoidance by general or uncertain Pavlovian threats. Frontiers Media S.A. 2014-09-18 /pmc/articles/PMC4166994/ /pubmed/25278858 http://dx.doi.org/10.3389/fnbeh.2014.00329 Text en Copyright © 2014 McCue, LeDoux and Cain. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience McCue, Margaret G. LeDoux, Joseph E. Cain, Christopher K. Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title | Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title_full | Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title_fullStr | Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title_full_unstemmed | Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title_short | Medial Amygdala Lesions Selectively Block Aversive Pavlovian–Instrumental Transfer in Rats |
title_sort | medial amygdala lesions selectively block aversive pavlovian–instrumental transfer in rats |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166994/ https://www.ncbi.nlm.nih.gov/pubmed/25278858 http://dx.doi.org/10.3389/fnbeh.2014.00329 |
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