Massensini André Ricardo, Romano-Silva Marco Aurélio, Gomez Marcus Vinícius
Núcleo de Neurociências, Departamento de Fisiologia e Biofisica, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Carlos 6627, Belo Horizonte-MG, Brazil.
Neurochem Res. 2003 Oct;28(10):1607-11. doi: 10.1023/a:1025643030044.
Voltage-dependent sodium channels (VDSC) are an important class of ion channels in excitable cells, where they are responsible for the generation and conduction of action potential. In addition, the release of neurotransmitters from nerve terminals is influenced by sodium channel activity. The function of VDSC is subject to modulation by various neurotoxins, such as scorpion toxins, which have long been used as tools in the investigation of neurotransmitter release. This opens an interesting perspective concerning modulation of neurotransmission via pharmacological manipulation of sodium channel properties, which can lead to a better understanding of their physiological and pathological roles. Here we briefly review the studies of neurotoxins acting on sodium channels, focusing primarily on the view of the mechanisms of neurotransmitter release.
电压依赖性钠通道(VDSC)是可兴奋细胞中一类重要的离子通道,它们负责动作电位的产生和传导。此外,神经递质从神经末梢的释放受钠通道活性的影响。VDSC的功能受到多种神经毒素的调节,如蝎毒素,长期以来这些毒素一直被用作研究神经递质释放的工具。这为通过药理学手段操纵钠通道特性来调节神经传递打开了一个有趣的视角,有助于更好地理解它们的生理和病理作用。在此,我们简要回顾作用于钠通道的神经毒素的研究,主要聚焦于神经递质释放机制的观点。