Coordination between midcingulate cortex and retrosplenial cortex in pain regulation

The cingulate cortex, with its subregions ACC, MCC, and RSC, is key in pain processing. However, the detailed interactions among these regions in modulating pain sensation have remained unclear. In this study, chemogenetic tools were employed to selectively activate or inhibit neuronal activity in t...

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Published inFrontiers in molecular neuroscience Vol. 17; p. 1405532
Main Authors Qiu, Yunya, Lian, Yan-Na, Wu, Cheng, Liu, Li, Zhang, Chen, Li, Xiang-Yao
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 06.08.2024
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Summary:The cingulate cortex, with its subregions ACC, MCC, and RSC, is key in pain processing. However, the detailed interactions among these regions in modulating pain sensation have remained unclear. In this study, chemogenetic tools were employed to selectively activate or inhibit neuronal activity in the MCC and RSC of rodents to elucidate their roles in pain regulation.Results: Our results showed that chemogenetic activation in both the RSC and MCC heightened pain sensitivity. Suppression of MCC activity disrupted the RSC's regulation of both mechanical and thermal pain, while RSC inhibition specifically affected the MCC's regulation of thermal pain. The findings indicate a complex interplay between the MCC and RSC, with the MCC potentially governing the RSC's pain regulatory mechanisms. The RSC, in turn, is crucial for the MCC's control over thermal sensation, revealing a collaborative mechanism in pain processing. This study provides evidence for the MCC and RSC's collaborative roles in pain regulation, highlighting the importance of their interactions for thermal and mechanical pain sensitivity. Understanding these mechanisms could aid in developing targeted therapies for pain disorders.
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Meritxell Llorca-Torralba, University of Cádiz, Spain
Edited by: Robert John Vandenberg, The University of Sydney, Australia
Reviewed by: Akiya Watakabe, RIKEN Center for Brain Science (CBS), Japan
ISSN:1662-5099
1662-5099
DOI:10.3389/fnmol.2024.1405532