[通过胆碱能受体调节虎耳蟾毒无毒部分对骨骼肌收缩的影响]。

A Cheikh, C Cognard, D Potreau, J Bescond, G Raymond, M El Ayeb, R Benkhalifa
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引用次数: 0

摘要

胆碱能受体在中枢神经系统中具有重要的生理作用,因为它们通过激活烟碱受体(nAChRs)或毒蕈碱受体(mAChRs)参与大脑神经肌肉连接处的高级功能和周围神经系统。此外,胆碱能受体可以被从蛇毒中分离出来的动物毒素或动物或植物来源的生物碱识别。在这种情况下,我们的目标是在Buthus occitanus tunetanus scorpion, M1的无毒毒液部分中发现这些分子,因此可能构成有前途的医疗工具。我们在这里提出了一项骨骼肌细胞的生理研究,该研究重新组合了最近发表的数据,并提出了一些新的结果,加强了最后的结果。首次在离体神经-肌肉制备中研究了M1的整体效应。在培养的肌管中,我们发现当ryanodine或肌醇1,4,5-三磷酸受体受到抑制时,M1诱导的细胞内钙增加被阻断。此外,我们已经表明,M1应用于肌管,诱导膜去极化与乙酰胆碱所见。甲鼠毒素治疗肌管后,其去极化振幅大部分被阻断。因此,这些结果证实了在nachr中至少存在一种M1活性成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Modulation of skeletal muscle contraction by the non-toxic fraction of Buthus occitanus tunetanus venom via the cholinergic receptors].

Cholinergic receptors have an essential physiological role in the central nervous system because of their implication in higher functions in the neuromuscular junction within the brain and also in the peripheral nervous system by activating nicotinic (nAChRs) or muscarinic (mAChRs) receptors. Moreover, cholinergic receptors could be recognized by animal toxins isolated from snake venoms or alkaloids having animal or vegetal origin. In this context, we aim to find such molecules in a non toxic venom fraction of Buthus occitanus tunetanus scorpion, M1, which could therefore constitute promising medical tool. We present here a physiological study in skeletal muscle cells that regroups data that have been recently published and some new results reinforcing the last ones. The global effect of M1, was firstly studied on isolated nerve-muscle preparation. In cultured myotubes, we have found that the intracellular calcium increase, induced by M1 was blocked when ryanodine or inositol 1,4,5-triphosphate receptors are inhibited. Moreover, we have shown that M1 application on myotubes, induced a membrane depolarization as seen with acetylcholine. The treatment of myotubes with alpha-bungarotoxin blocked in most parts the depolarization amplitude. Thus, these results confirm the presence of at least one component in M1 active in nAChRs.

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