Song M, Messing R O
Ernest Gallo Clinic and Research Center, Department of Neurology, Graduate Program in Neuroscience, University of California, San Francisco, 5858 Horton Street, Suite 200, Emeryville, California, 94608, USA.
Cell Mol Life Sci. 2005 Jan;62(2):119-27. doi: 10.1007/s00018-004-4339-x.
Pharmacological studies with drugs that activate or inhibit several protein kinase C (PKC) isozymes have identified the PKC family of serine-threonine kinases as important in the regulation of gamma-aminobutyric acid type A (GABA(A)) receptor function. PKC modulates GABA(A) receptor surface density, chloride conductance and receptor sensitivity to positive allosteric modulators such as neurosteroids, ethanol, benzodiazepines and barbiturates. Recent studies using PKC isozyme-selective reagents and gene-targeted mice have begun to identify critical roles for three isozymes, PKCbetaII, PKCvarepsilon and PKCgamma, in various aspects of GABA(A) receptor regulation. Progress in this field touches upon therapeutic areas that are of great clinical importance such as anxiety and addiction. Increased understanding of how PKC regulates GABA(A) receptors and which PKC isozymes are involved holds promise for development of new treatments for diverse neuropsychiatric disorders.
使用激活或抑制几种蛋白激酶C(PKC)同工酶的药物进行的药理学研究已确定,丝氨酸-苏氨酸激酶的PKC家族在调节γ-氨基丁酸A型(GABAA)受体功能方面很重要。PKC调节GABAA受体的表面密度、氯离子传导以及受体对诸如神经甾体、乙醇、苯二氮䓬和巴比妥类等正性变构调节剂的敏感性。最近使用PKC同工酶选择性试剂和基因靶向小鼠的研究已开始确定三种同工酶PKCβII、PKCε和PKCγ在GABAA受体调节的各个方面的关键作用。该领域的进展涉及焦虑和成瘾等具有重大临床意义的治疗领域。对PKC如何调节GABAA受体以及涉及哪些PKC同工酶的进一步了解为开发针对各种神经精神疾病的新疗法带来了希望。