首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >Neuroprotection by group I metabotropic glutamate receptor antagonists in forebrain ischemia of gerbil.
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Neuroprotection by group I metabotropic glutamate receptor antagonists in forebrain ischemia of gerbil.

机译:I组代谢型谷氨酸受体拮抗剂在沙土鼠前脑缺血中的神经保护作用。

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摘要

Stimulation of group I metabotropic glutamate receptors (mGluR 1 and 5) activates G-protein coupled-phospholipase C (PLC) to release 1,2-diacylglycerol (DAG) and arachidonic acid (ArAc). To elucidate the role of group I mGluR, we tested the effects of (S)-alpha-methyl-4-carboxy-phenylglycine (MCPG, mGluR 1 and 5 antagonist), 1-aminoindan-1,5-dicarboxylic acid (AIDA, mGluR 1a specific antagonist) and 2-methyl-6-(phenylethynyl) pyridine (MPEP, mGluR 5 antagonist) on ArAc release and neuronal survival after transient forebrain ischemia in gerbils. Ischemia resulted in (a) significant release of ArAc at 1-day reperfusion and (b) significant neuronal death in the hippocampal CA1 subfield after 6-day reperfusion. MCPG and MPEP decreased ArAc release and also significantly increased neuronal survival. AIDA was less effective in decreasing ArAc release and had no effect on neuronal death. These results suggest that activation of mGluR 5 may be an important pathway in ArAc release and neuronal death after transient ischemia.
机译:刺激I组代谢型谷氨酸受体(mGluR 1和5)激活G蛋白偶联磷脂酶C(PLC)释放1,2-二酰基甘油(DAG)和花生四烯酸(ArAc)。为了阐明I组mGluR的作用,我们测试了(S)-α-甲基-4-羧基-苯基甘氨酸(MCPG,mGluR 1和5拮抗剂),1-氨基茚满-1,5-二羧酸(AIDA, mGluR 1a特异性拮抗剂)和2-甲基-6-(苯基乙炔基)吡啶(MPEP,mGluR 5拮抗剂)对沙鼠短暂前脑缺血后ArAc释放和神经元存活的影响。缺血导致(a)1天再灌注后ArAc大量释放,以及(b)6天再灌注后海马CA1子区大量神经元死亡。 MCPG和MPEP减少ArAc释放,也显着增加神经元存活率。 AIDA在减少ArAc释放方面效果较差,对神经元死亡没有影响。这些结果表明,mGluR 5的激活可能是短暂缺血后ArAc释放和神经元死亡的重要途径。

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