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首页> 外文期刊>Neurotoxicology >L-type voltage-dependent calcium channel is involved in the snake venom group IA secretory phospholipase A2-induced neuronal apoptosis.
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L-type voltage-dependent calcium channel is involved in the snake venom group IA secretory phospholipase A2-induced neuronal apoptosis.

机译:L型电压依赖性钙通道参与蛇毒组IA分泌磷脂酶A2诱导的神经元凋亡。

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摘要

Snake venom group IA secretory phospholipase A2 (sPLA2-IA) is known as a neurotoxin. Snake venom sPLA2s are neurotoxic in vivo and in vitro, causing synergistic neurotoxicity to cortical cultures when applied with toxic concentrations of glutamate. However, it has not yet been cleared sufficiently how sPLA2-IA exerts neurotoxicity. Here, we found sPLA2-IA induced neuronal cell death in a concentration-dependent manner. This death was a delayed response requiring a latent time for 6h. sPLA2-IA-induced neuronal cell death was accompanied with apoptotic blebbing, condensed chromatin, and fragmented DNA, exhibiting apoptotic features. NMDA receptor blockers suppressed the neurotoxicity of sPLA2-IA, but an AMPA receptor blocker did not. Interestingly, L-type voltage-dependent Ca(2+) channel (L-VDCC) blocker significantly protected neurons from the sPLA2-IA-induced apoptosis. On the other hand, neither N-VDCC blockers nor P/Q-VDCC blocker did. In conclusion, we demonstrated that sPLA2-IA induced neuronal cell death via apoptosis. Furthermore, the present study suggests that not only NMDA receptor but also L-VDCC contributed to the neurotoxicity of snake venom sPLA2-IA.
机译:蛇毒IA组分泌磷脂酶A2(sPLA2-IA)被称为神经毒素。蛇毒sPLA2s在体内和体外均具有神经毒性,当与毒性浓度的谷氨酸一起使用时,会对皮层培养物产生协同神经毒性。然而,尚未充分清楚sPLA2-IA如何发挥神经毒性。在这里,我们发现sPLA2-IA以浓度依赖性方式诱导神经元细胞死亡。此死亡是延迟反应,需要潜伏6小时。 sPLA2-IA诱导的神经元细胞死亡伴随细胞凋亡起泡,染色质浓缩和DNA片段化,表现出细胞凋亡特征。 NMDA受体阻滞剂抑制了sPLA2-IA的神经毒性,但AMPA受体阻滞剂没有。有趣的是,L型电压依赖性Ca(2+)通道(L-VDCC)阻滞剂显着保护神经元免受sPLA2-IA诱导的细胞凋亡。另一方面,N-VDCC阻止程序和P / Q-VDCC阻止程序都没有。总之,我们证明了sPLA2-IA通过凋亡诱导神经元细胞死亡。此外,本研究表明,不仅NMDA受体而且L-VDCC也对蛇毒sPLA2-IA的神经毒性有贡献。

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