1. mGlu2/3 receptor in the prelimbic cortex is implicated in stress resilience and vulnerability in mice.
- Author
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Jing XY, Wang Y, Zou HW, Li ZL, Liu YJ, and Li LF
- Subjects
- Amino Acids pharmacology, Amino Acids therapeutic use, Animals, Depression etiology, Depression prevention & control, Depression psychology, Disease Models, Animal, Humans, Male, Mice, Prefrontal Cortex drug effects, Prefrontal Cortex metabolism, Receptors, Metabotropic Glutamate antagonists & inhibitors, Resilience, Psychological drug effects, Social Defeat, Stress, Psychological drug therapy, Stress, Psychological etiology, Stress, Psychological psychology, Xanthenes pharmacology, Xanthenes therapeutic use, Depression pathology, Prefrontal Cortex pathology, Receptors, Metabotropic Glutamate metabolism, Stress, Psychological pathology
- Abstract
Resilience, referring to "achieving a positive outcome in the face of adversity", is a common phenomenon in daily life. Elucidating the mechanisms of stress resilience is instrumental to developing more effective treatments for stress-related psychiatric disorders such as depression. Metabotropic glutamate receptors (mGlu2/3 and mGlu5) within the medial prefrontal cortex (mPFC) have been recently recognized as promising therapeutic targets for rapid-acting antidepressant treatment. In this study, we assessed the functional roles of the mGlu2/3 and mGlu5 within different subregions of the mPFC in modulating stress resilience and vulnerability by using chronic social defeat stress (CSDS) paradigms in mice. Our results showed that approximately 51.6% of the subjects exhibited depression- or anxiety-like behaviors after exposure to CSDS. When a susceptible mouse was confronted with an attacker, c-Fos expression in the prelimbic cortex (PrL) subregion of the mPFC substantially increased. Compared with the resilient and control groups, the expression of mGlu2/3 was elevated in the PrL of the susceptible group. The expression of mGlu5 showed no significant difference among the three groups in the whole mPFC. Finally, we found that the social avoidance symptoms of the susceptible mice were rapidly relieved by intra-PrL administration of LY341495-an mGluR2/3 antagonists. The above results indicate that mGluR2/3 within the PrL may play an important regulatory role in stress-related psychiatric disorders. Our results are meaningful, as they expand our understanding of stress resilience and vulnerability which may open an avenue to develop novel, personalized approaches to mitigate depression and promote stress resilience., (Copyright © 2021 Elsevier B.V. All rights reserved.)
- Published
- 2021
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