The anti-inflammation pharmacodynamics of lithium: Therapy of bipolar disorder

被引:0
|
作者
Zhou, Yuyang [1 ]
Zheng, Weizhi [1 ]
Guo, Feichang [1 ]
Wu, Shijin [1 ]
Zhong, Congjie [2 ]
机构
[1] Guangdong Pharmaceut Univ, Sch Pharm, 280 Waihuan East Rd Higher Educ Mega Ctr, Guangzhou 510006, Guangdong, Peoples R China
[2] Guangdong Pharmaceut Univ, Sch Publ Hlth, Guangzhou, Peoples R China
关键词
Bipolar disorder; lithium; inflammation; pharmacodynamics; target; mechanism; GLYCOGEN-SYNTHASE KINASE-3-BETA; NITRIC-OXIDE SYNTHASE; NF-KAPPA-B; HPA AXIS; OXIDATIVE STRESS; MAJOR DEPRESSION; DOUBLE-BLIND; BRAIN; SCHIZOPHRENIA; PATHOPHYSIOLOGY;
D O I
10.1177/02698811251326942
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Bipolar disorder is a severe mental disorder that necessitates effective long-term treatment strategies. Clinically, lithium has demonstrated favorable outcomes in managing this condition. The inflammatory theory posits that bipolar disorder is influenced by an inflammatory response, and lithium is thought to mitigate this disorder by inhibiting such responses. In terms of the pharmacodynamics of blocking inflammatory mediators, lithium mainly acts on GSK-3 beta. Upon interaction with GSK-3 beta, lithium can suppress the gene expression of inflammatory mediators, subsequently reducing their secretion. This mechanism influences multiple downstream pathways, ultimately contributing to the therapeutic effects observed in bipolar disorder. Specifically, these pathways include the arachidonic acid pathway, nitric oxide synthase pathway, neurotransmitter pathway, and so on. This article reviews the pharmacodynamic targets and mechanisms of lithium, offering insights into the appropriate clinical application of lithium and the advancement of lithium pharmacotherapies.
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页数:12
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