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γ-氨基丁酸(GABA)受体的共激活通过脑缺血再灌注中谷氨酸受体6(GluR6)-突触后密度蛋白95(PSD95)-混合谱系激酶3(MLK3)信号模块的解体来抑制JNK3凋亡途径。

Co-activation of GABA receptors inhibits the JNK3 apoptotic pathway via the disassembly of the GluR6-PSD95-MLK3 signaling module in cerebral ischemic-reperfusion.

作者信息

Han Dong, Zhang Quan-Guang, Li Chong, Zong Yan-Yan, Yu Chang-Zhou, Wang Wei, Yan Jing-Zhi, Zhang Guang-Yi

机构信息

Research Center for Biochemistry and Molecular Biology, Xuzhou Medical College, Xuzhou, Jiangsu 221002, People's Republic of China.

出版信息

FEBS Lett. 2008 Apr 16;582(9):1298-306. doi: 10.1016/j.febslet.2008.02.044. Epub 2008 Feb 26.

Abstract

In this study, we investigated whether the increase of inhibitory gamma-amino butyric acid (GABA) signal suppresses the excitatory glutamate signal induced by cerebral ischemia and the underlying mechanisms. In global cerebral ischemia, focal cerebral ischemia and oxygen-glucose deprivation, application of muscimol and baclofen, agonists of GABA(A) receptor and GABA(B) receptor, exerted neuroprotection. The agonists inhibited the increased assembly of the GluR6-PSD-95-MLK3 module induced by cerebral ischemia and the activation of the MLK3-MKK4/7-JNK3 cascade. Our results suggest that stimulation of the inhibitory GABA receptors can attenuate the excitatory JNK3 apoptotic signaling pathway via inhibiting the increased assembly of the GluR6-PSD-95-MLK3 signaling module in cerebral ischemia.

摘要

在本研究中,我们探究了抑制性γ-氨基丁酸(GABA)信号增强是否会抑制脑缺血诱导的兴奋性谷氨酸信号及其潜在机制。在全脑缺血、局灶性脑缺血和氧-葡萄糖剥夺模型中,应用GABA(A)受体激动剂蝇蕈醇和GABA(B)受体激动剂巴氯芬可发挥神经保护作用。这些激动剂抑制了脑缺血诱导的GluR6-PSD-95-MLK3模块组装增加以及MLK3-MKK4/7-JNK3级联反应的激活。我们的结果表明,刺激抑制性GABA受体可通过抑制脑缺血时GluR6-PSD-95-MLK3信号模块组装增加来减弱兴奋性JNK3凋亡信号通路。

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