Yuan Yukun, Otero-Montañez James K L, Yao Aizhen, Herden Christina J, Sirois Jay E, Atchison William D
Department of Pharmacology/Toxicology and Neuroscience Program, Michigan State University, East Lansing, MI 48824-1317, USA.
Neurotoxicology. 2005 Jun;26(3):439-54. doi: 10.1016/j.neuro.2005.03.005. Epub 2005 Apr 26.
The concentration- and time-dependence of effects of methylmercury (MeHg) on voltage-gated outward K(+) (Kv) channels, inwardly rectifying K(+) (Kir) channels, voltage-gated Ca(2+) channels and GABA(A) receptor activated channels were compared in cerebellar granule cells in culture using whole cell patch clamp recording techniques. The objective was to determine if MeHg equally affects different types of ion channels. Under similar experimental conditions, these four ion channel types displayed markedly different sensitivity to MeHg. At 0.1-1 microM, MeHg caused apparent inhibition of Ca(2+)-channel and GABA(A) receptor-mediated currents, but did not cause any significant effect on Kv or Kir channels. Among the four channel types examined, GABA(A) receptors appeared to be the most sensitive to MeHg. The Kv channels, particularly the delayed rectifiers (DRs), appeared to be relatively resistant to MeHg compared with GABA(A) receptors and Ca(2+) channels. Kir channels were virtually unaffected by MeHg in the concentration range of 10-100 microM. The differential sensitivity of GABA(A) receptors and Kv channels to MeHg was also observed in granule and Purkinje cells in freshly isolated cerebellar slices of rat. The insensitivity of Kir channel to MeHg was also seen in Xenopus laevis oocytes expressing cloned Kir7.1 channels. Thus, these appear to be general properties of these channels as opposed to distinct effects associated with granule cells in culture. These results suggest that MeHg does preferentially affect certain types of ion channels. Hence, the effects of MeHg on membrane ion channels are not due simply to nonspecific actions on the membrane. Furthermore, at least certain types of Kir channels appear to be the most resistant type of ion channel reported to date to effects of MeHg.
使用全细胞膜片钳记录技术,比较了甲基汞(MeHg)对培养的小脑颗粒细胞中电压门控外向钾离子(Kv)通道、内向整流钾离子(Kir)通道、电压门控钙离子通道和GABAA受体激活通道的作用的浓度和时间依赖性。目的是确定MeHg是否同等地影响不同类型的离子通道。在相似的实验条件下,这四种离子通道类型对MeHg表现出明显不同的敏感性。在0.1 - 1微摩尔浓度下,MeHg对钙离子通道和GABAA受体介导的电流有明显抑制作用,但对Kv或Kir通道没有显著影响。在所研究的四种通道类型中,GABAA受体似乎对MeHg最敏感。与GABAA受体和钙离子通道相比,Kv通道,特别是延迟整流器(DRs),似乎对MeHg相对耐药。在10 - 100微摩尔浓度范围内,Kir通道实际上不受MeHg影响。在新鲜分离的大鼠小脑切片中的颗粒细胞和浦肯野细胞中也观察到GABAA受体和Kv通道对MeHg的敏感性差异。在表达克隆的Kir7.1通道的非洲爪蟾卵母细胞中也发现Kir通道对MeHg不敏感。因此,这些似乎是这些通道的一般特性,而不是与培养的颗粒细胞相关的独特效应。这些结果表明,MeHg确实优先影响某些类型的离子通道。因此,MeHg对膜离子通道的作用并非仅仅由于对膜的非特异性作用。此外,至少某些类型的Kir通道似乎是迄今为止报道的对MeHg作用最具耐药性的离子通道类型。