共 83 条
Purinergic P2X7 receptor as a potential therapeutic target in depression
被引:7
作者:

Qi, Wang
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机构:
First Peoples Hosp Yancheng, Dept Pharmacol, Yancheng 224000, Jiangsu, Peoples R China Nantong Univ, Pharm Coll, Dept Pharmacol, Nantong 226001, Jiangsu, Peoples R China

Jin, Xiang
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机构:
Second Peoples Hosp Nantong, Dept Pharm, Nantong 226002, Jiangsu, Peoples R China Nantong Univ, Pharm Coll, Dept Pharmacol, Nantong 226001, Jiangsu, Peoples R China

Guan, Wei
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h-index: 0
机构:
Nantong Univ, Pharm Coll, Dept Pharmacol, Nantong 226001, Jiangsu, Peoples R China
Nantong Univ, Pharm Coll, Dept Pharmacol, 19 QiXiu Rd, Nantong 226001, Jiangsu, Peoples R China Nantong Univ, Pharm Coll, Dept Pharmacol, Nantong 226001, Jiangsu, Peoples R China
机构:
[1] Nantong Univ, Pharm Coll, Dept Pharmacol, Nantong 226001, Jiangsu, Peoples R China
[2] First Peoples Hosp Yancheng, Dept Pharmacol, Yancheng 224000, Jiangsu, Peoples R China
[3] Second Peoples Hosp Nantong, Dept Pharm, Nantong 226002, Jiangsu, Peoples R China
[4] Nantong Univ, Pharm Coll, Dept Pharmacol, 19 QiXiu Rd, Nantong 226001, Jiangsu, Peoples R China
关键词:
Depression;
Expression levels;
Targets;
Antidepressant;
NLRP3 INFLAMMASOME ACTIVATION;
MICE LACKING;
CELLS;
RELEASE;
STRESS;
INVOLVEMENT;
ANTAGONIST;
PLASTICITY;
BEHAVIORS;
PATHWAY;
D O I:
10.1016/j.bcp.2023.115959
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
The elaborate mechanisms of depression have always been a research hotspot in recent years, and the pace of research has never ceased. The P2X7 receptor (P2X7R) belongs to one of the adenosine triphosphates (ATP)gated cation channels that exist widely in brain tissues and play a prominent role in the regulation of depressionrelated pathology. To date, the role of purinergic P2X7R in the mechanisms underlying depression is not fully understood. In this review, we conclude that the purinergic receptor P2X7 is a potential therapeutic target for depression based on research results published over the past 5 years in Google Scholar and the National Library of Medicine (PubMed). Additionally, we introduced the functional characteristics of P2X7R and confirmed that excessive activation of P2X7R led to increased release of inflammatory cytokines, which eventually contributed to depression. Furthermore, the inhibition of P2X7R produced antidepressant-like effects in animal models of depression, further proving that P2X7R signalling mediates depression-like behaviours. Finally, we summarised related studies on drugs that exert antidepressant effects by regulating the expression of P2X7R. We hope that the conclusions of this review will provide information on the role of P2X7R in the neuropathophysiology of depression and novel therapeutic targets for the treatment of depression.
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