Melatonin Modulates the GABAergic Response in Cultured Rat Hippocampal Neurons
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概要
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In the present study, we investigated the effect of melatonin on the GABA-induced current (<I>I</I><SUB>GABA</SUB>) and GABAergic miniature inhibitory postsynaptic currents (mIPSCs) in cultured rat hippocampal neurons using the whole-cell patch-clamp technique. We found that melatonin rapidly and reversibly enhanced <I>I</I><SUB>GABA</SUB> in a dose-dependent manner, with an EC<SUB>50</SUB> of 949 <I>μ</I>M. Melatonin markedly enhanced the peak amplitude of a subsaturating <I>I</I><SUB>GABA</SUB> but not that of a saturating <I>I</I><SUB>GABA</SUB>. Interestingly, melatonin was effective only when GABA and melatonin were applied together. Furthermore, the effect of melatonin on <I>I</I><SUB>GABA</SUB> was voltage-independent and did not change the ion selectivity of the GABA<SUB>A</SUB> receptor. The melatonin enhancement on <I>I</I><SUB>GABA</SUB> can not be blocked by luzindole, a melatonin receptor antagonist, indicating that melatonin-induced <I>I</I><SUB>GABA</SUB> enhancement was not via activation of its own membrane receptors. However, this enhancement may be mediated via high-affinity benzodiazepine sites as it was inhibited by the classical benzodiazepine antagonist flumazenil, suggesting an allosteric modulation of melatonin by binding to the sites of GABA<SUB>A</SUB> receptors. In addition, melatonin increased both amplitude and frequency of GABAergic mIPSCs, indicating that melatonin enhances GABAergic inhibitory transmission. Hence, our observation that melatonin has an enhancing effect on the GABAergic system may implicate a potential pathway for the neuroprotective effects of melatonin.
- 2012-06-20
著者
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Zhou Jiang-ning
Cas Key Laboratory Of Brain Function And Disease And School Of Life Sciences University Of Science And Technology Of China
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CHENG Xin-Ping
CAS Key Laboratory of Brain Function and Disease, and School of Life Sciences, University of Science and Technology of China
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SUN Hao
CAS Key Laboratory of Brain Function and Disease, and School of Life Sciences, University of Science and Technology of China
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YE Zeng-You
CAS Key Laboratory of Brain Function and Disease, and School of Life Sciences, University of Science and Technology of China
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Cheng Xin-ping
Cas Key Laboratory Of Brain Function And Disease And School Of Life Sciences University Of Science And Technology Of China
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Sun Hao
Cas Key Laboratory Of Brain Function And Disease And School Of Life Sciences University Of Science And Technology Of China
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Ye Zeng-you
Cas Key Laboratory Of Brain Function And Disease And School Of Life Sciences University Of Science And Technology Of China