Cibulsky S M, Sather W A
Department of Pharmacology and Neuroscience Center, University of Colorado Health Sciences Center, Denver, Colorado, USA.
J Pharmacol Exp Ther. 1999 Jun;289(3):1447-53.
The dye ruthenium red (RuR) has diverse experimental uses, including block of ion channels. RuR is a well described antagonist of one class of intracellular Ca2+ release channels, the ryanodine receptors, but recently this compound has also been identified as a putative blocker of voltage-gated calcium channels of the surface membrane involved in neurotransmitter release. Using electrophysiological methods, we have studied the action of RuR upon pure populations of neuronal voltage-gated ion channels heterologously expressed in Xenopus laevis oocytes. All four channel types studied, including class A (P/Q-type), class B (N-type), class C (L-type), and class E channels, are sensitive to RuR, with IC50 values ranging from 0.7 to 67.1 microM. Block of class C and class E channels most likely results from 1:1 binding of ruthenium red at a site in the extracellular entrance to the pore, resulting in obstruction of permeant ion flux through these channels. The mechanism of block of class A and class B channels is more complex, requiring binding of more than one molecule of RuR per channel.
钌红(RuR)染料有多种实验用途,包括阻断离子通道。RuR是一类细胞内Ca2+释放通道即兰尼碱受体的一种广为人知的拮抗剂,但最近该化合物也被确定为参与神经递质释放的表面膜电压门控钙通道的一种假定阻滞剂。我们使用电生理方法,研究了RuR对非洲爪蟾卵母细胞中异源表达的纯神经元电压门控离子通道群体的作用。所研究的所有四种通道类型,包括A类(P/Q型)、B类(N型)、C类(L型)和E类通道,都对RuR敏感,IC50值范围为0.7至67.1微摩尔。C类和E类通道的阻断很可能是由于钌红在孔的细胞外入口处的一个位点以1:1的比例结合,导致通透离子通过这些通道的通量受阻。A类和B类通道的阻断机制更为复杂,每个通道需要结合不止一个RuR分子。