[A long chain fatty acid receptor signaling as a new therapeutic target for stress-induced chronic pain].

Nihon Yakurigaku Zasshi

Department of Clinical Pharmacy, School of Pharmaceutical Sciences, Kobe Gakuin University.

Published: November 2024

AI Article Synopsis

  • Psychological and social stresses contribute to psychiatric disorders like depression and anxiety, and can also lead to prolonged pain; however, the mechanisms behind stress-induced chronic pain remain complex and poorly understood.
  • Research on the GPR40/FFAR1 receptor, which influences insulin secretion in the pancreas, has also revealed its role in regulating pain and emotions in the central nervous system.
  • Current investigations are focusing on the signaling pathways of fatty acid receptors in relation to stress-related chronic pain, presenting them as potential new therapeutic targets based on findings from a mouse model that simulates psychosocial stress.

Article Abstract

Psychological and social stresses are known to be risk factors for psychiatric disorders, including depression and anxiety. On the other hand, exposure to these stresses can also cause prolonged and severe pain. However, the pathological mechanism for stress-induced chronic pain is complex, and there are many unresolved aspects, and no effective therapeutic drugs have been established. Since the discovery of the long-chain fatty acid receptor GPR40/FFAR1 about 20 years ago, research on the mechanism that promotes insulin secretion in the pancreas has progressed. Previously, we have worked to elucidate the physiological effects of GPR40/FFAR1 in the central nervous system and has found that it is involved in the regulation of pain and emotion. Based on these findings, they are now investigating the involvement of fatty acid receptors signaling in the development of stress-related chronic pain. In this review, we discuss the status of psychological stress-related chronic pain and the GPR40/FFAR1-mediated and -striking regulatory mechanisms of stress-induced chronic pain, based on our findings using a mouse model of chronic pain created by loading postoperative pain to a social defeat stress model mouse that mimics psychosocial stress. We summarized about the involvement of fatty acid receptor signaling as a new therapeutic candidate for chronic pain in this review.

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Source
http://dx.doi.org/10.1254/fpj.24047DOI Listing

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