P2X7 receptor: A receptor closely linked with sepsis-associated encephalopathy

被引:4
作者
Fan, Zhao [1 ]
Wang, Kaifang [1 ]
Zhao, Xiaoyong [1 ,2 ]
Sun, Xude [1 ,3 ]
机构
[1] Weifang Med Univ, Sch Anesthesiol, Shandong Prov Med & Hlth Key Lab Clin Anesthesia, Weifang 261053, Shandong, Peoples R China
[2] Weifang Med Univ, Affiliated Hosp, Weifang 261021, Shandong, Peoples R China
[3] Air Force Mil Med Univ, Tangdu Hosp, Dept Anesthesiol, Xian 710038, Shaanxi, Peoples R China
关键词
microglial cells; apoptosis; blood-brain barrier; sepsis-associated encephalopathy; INDUCED APOPTOSIS; BRAIN; ACTIVATION; EXPRESSION; NEUROINFLAMMATION; INFLAMMASOME; DYSFUNCTION; ASTROCYTES; PYROPTOSIS; CALCIUM;
D O I
10.1515/biol-2022-0775
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Sepsis is defined as a dysregulated host response to infection resulting in life-threatening organ dysfunction. Sepsis-associated encephalopathy (SAE) is the main manifestation of sepsis. Inflammation, peroxidation stress injury, and apoptosis are the main factors involved in the pathogenesis of SAE. A growing body of evidence has proved that P2X7 receptor (P2X7R), a cationic channel receptor that is widely distributed in the body, plays a major role in the occurrence and development of inflammatory injury. Therefore, this review mainly describes the activation of P2X7R in sepsis, which leads to the recruitment of inflammatory cells to the cerebral vasculature, the destruction of the blood-brain barrier, the activation of microglial cells in the brain, the apoptosis of brain cells, and other damage processes. This review also illustrates the potential therapeutic value of P2X7R inhibition in SAE.
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页数:8
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