Mood disorders and their treatment: Alterations in the regulation of receptor-G protein coupling

被引:2
作者
Schreiber, G [1 ]
Avissar, S
机构
[1] Ben Gurion Univ Negev, Fac Hlth Sci, Dept Psychiat, IL-84105 Beer Sheva, Israel
[2] Ben Gurion Univ Negev, Dept Clin Pharmacol, IL-84105 Beer Sheva, Israel
关键词
mood disorders; depression; antidepressant; bipolar disorder; mood stabilizer; lithium; pathogenesis; pathophysiology; diagnosis; pharma cocentric; genomics; proteomics; G protein; beta-arrestin; GRK; receptor desensitization;
D O I
10.1002/ddr.20018
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Biochemical research in mood disorders has focused, along the cascade of events involved in signal transduction, from studies at the level monoamine neurotransmitters and their receptors to mechanisms beyond receptors. Growing evidence suggests that G proteins may be involved in the pathophysiology and treatment of mood disorders: (1) lithium, other antibipolar and antidepressant treatments affect G protein levels, function, and mRNA levels; (2) differential alterations exist in G proteins measures in peripheral blood elements of patients with mood disorders; (3) alterations in G proteins levels exist in postmortem tissues of patients with mood disorders; and (4) candidate G protein-encoding genes as susceptibility loci for bipolar mood disorder and depression were detected. G protein signal transcluction is regulated at a proximal point: following phosphorylation by G protein-coupled receptor kinases, receptors bind to arrestins, uncoupling the receptors from G proteins; at a distal regulatory point, regulators of G protein signaling proteins act primarily as GTPase-activating proteins. Both regulatory points have been recently found to be involved in the pathophysiology and treatment of mental disorders. It is to be hoped that an admixture of genomics, proteomics, multi-marker, large-scale automated measures, together with the "old" biochemical approaches, will enable the development of an objective biological differential diagnostic system for major mental disorders that will also enable monitoring and predicting response to treatments. Drug Dev. Res. 65:147-155, 2005. (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:147 / 155
页数:9
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