Infralimbic cortex controls fear memory generalization and susceptibility to extinction during consolidation

被引:25
|
作者
Bayer, Hugo [1 ]
Bertoglio, Leandro Jose [1 ]
机构
[1] Univ Fed Santa Catarina UFSC, Dept Farmacol, CCB, Campus Univ S-N, BR-88049900 Florianopolis, SC, Brazil
关键词
MEDIAL PREFRONTAL CORTEX; PROTEIN-SYNTHESIS; PRELIMBIC CORTEX; EXCITABILITY; SUPPRESSION; MODULATION; ACTIVATION; RETRIEVAL; NEURONS; MODEL;
D O I
10.1038/s41598-020-72856-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lesioning or inactivating the infralimbic (IL) subregion of the medial prefrontal cortex before acquisition produces more generalized and extinction-resistant fear memories. However, whether and how it modulates memory specificity and extinction susceptibility while consolidation takes place is still unknown. The present study aims to investigate these questions using muscimol-induced temporary inactivation and anisomycin-induced protein synthesis inhibition in the rat IL following contextual fear conditioning. Results indicate that the IL activity immediately after acquisition, but not six hours later, controls memory generalization over a week, regardless of its strength. Such IL function depends on the context-shock pairing since muscimol induced no changes in animals exposed to immediate shocks or the conditioning context only. Animals in which the IL was inactivated during consolidation extinguished similarly to controls within the session but were unable to recall the extinction memory the following day. Noteworthy, these post-acquisition IL inactivation-induced effects were not associated with changes in anxiety, as assessed in the elevated plus-maze test. Anisomycin results indicate that the IL protein synthesis during consolidation contributes more to producing extinction-sensitive fear memories than memory specificity. Collectively, present results provide evidence for the IL's role in controlling generalization and susceptibility to extinction during fear memory consolidation.
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页数:13
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