A possible pivotal role of mitochondrial free calcium in neurotoxicity mediated by N-methyl-d-aspartate receptors in cultured rat hippocampal neurons

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• 作者：Yuki Kambe¹ ; ^a ; Noritaka Nakamichi² ; ^a ; Takeshi Takarada^a ; Ryo Fukumori^a ; Ryota Nakazato^a ; Eiichi Hinoi^a ; Yukio Yoneda ; ^a ; ^{yyoneda@p.kanazawa-u.ac.jp"" rel=""nofollow}
• 关键词：NMDA neurotoxicity ; Hippocampus ; mPTP ; UCP2 ; Calcium ; Mitochondria
• 刊名：Neurochemistry International
• 出版年：2011
• 出版时间：August 2011
• 年：2011
• 卷：59
• 期：1
• 页码：10-20
• 全文大小：1063 K

文摘

We have previously shown that mitochondrial membrane potential disruption is involved in mechanisms underlying differential vulnerabilities to the excitotoxicity mediated by N-methyl-d-aspartate (NMDA) receptors between primary cultured neurons prepared from rat cortex and hippocampus. To further elucidate the role of mitochondria in the excitotoxicity after activation of NMDA receptors, neurons were loaded with the fluorescent dye calcein diffusible in the cytoplasm and organelles for determination of the activity of mitochondrial permeability transition pore (mPTP) responsible for the leakage of different mitochondrial molecules. The addition of CoCl₂ similarly quenched the intracellular fluorescence except mitochondria in both cultured neurons, while further addition of NMDA led to a leakage of the dye into the cytoplasm in hippocampal neurons only. An mPTP inhibitor prevented the NMDA-induced loss of viability in hippocampal neurons, while an activator of mPTP induced a similarly potent loss of viability in cortical and hippocampal neurons. Although NMDA was more effective in increasing rhodamine-2 fluorescence as a mitochondrial calcium indicator in hippocampal than cortical neurons, a mitochondrial calcium uniporter inhibitor significantly prevented the NMDA-induced loss of viability in hippocampal neurons. Expression of mRNA was significantly higher for the putative uniporter uncoupling protein-2 in hippocampal than cortical neurons. These results suggest that mitochondrial calcium uniporter would be at least in part responsible for the NMDA neurotoxicity through a mechanism relevant to promotion of mPTP orchestration in hippocampal neurons.