首页> 美国卫生研究院文献>The Korean Journal of Physiology Pharmacology : Official Journal of the Korean Physiological Society and the Korean Society of Pharmacology >Inhibition of K+ outward currents by linopirdine in the cochlear outer hair cells of circling mice within the first postnatal week
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Inhibition of K+ outward currents by linopirdine in the cochlear outer hair cells of circling mice within the first postnatal week

机译:产后第一个星期内利尼平在循环小鼠耳蜗外毛细胞中抑制K +外向电流

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摘要

Inhibition of K+ outward currents by linopirdine in the outer hair cells (OHCs) of circling mice (homozygous (cir/cir) mice), an animal model for human deafness (DFNB6 type), was investigated using a whole cell patch clamp technique. Littermate heterozygous (+/cir) and ICR mice of the same age (postnatal day (P) 0 –P6) were used as controls. Voltage steps from –100 mV to 40 mV elicited small inward currents (–100 mV~–70 mV) and slow rising K+ outward currents (–60 mV ~40 mV) which activated near –50 mV in all OHCs tested. Linopirdine, a known blocker of K+ currents activated at negative potentials (IK,n), did cause inhibition at varying degree (severe, moderate, mild) in K+ outward currents of heterozygous (+/cir) or homozygous (cir/cir) mice OHCs in the concentration range between 1 and 100 µM, while it was apparent only in one ICR mice OHC out of nine OHCs at 100 µM. Although the half inhibition concentrations in heterozygous (+/cir) or homozygous (cir/cir) mice OHCs were close to those reported in IK,n, biophysical and pharmacological properties of K+ outward currents, such as the activation close to –50 mV, small inward currents evoked by hyperpolarizing steps and TEA sensitivity, were not in line with IK,n reported in other tissues. Our results show that the delayed rectifier type K+ outward currents, which are not similar to IK,n with respect to biophysical and pharmacological properties, are inhibited by linopirdine in the developing (P0~P6) homozygous (cir/cir) or heterozygous (+/cir) mice OHCs.
机译:研究了利尼平在循环小鼠(纯合子(cir / cir)小鼠)(人聋的动物模型)(DFNB6型)的外毛细胞(OHCs)中对K + 外向电流的抑制作用。全细胞膜片钳技术。相同年龄(产后天数(P)0 –P6)的同伴杂合子(+ / cir)和ICR小鼠用作对照。从–100 mV到40 mV的电压阶跃会引起较小的内向电流(–100 mV〜–70 mV)和缓慢上升的K + 外向电流(–60 mV〜40 mV),该电流在–50 mV附近激活在所有测试的OHC中。 Linopirdine是已知的负电势(IK,n)激活的K + 电流的阻滞剂,确实在不同程度上(严重,中度,轻度)引起了K + 向外的抑制作用杂合(+ / cir)或纯合(cir / cir)小鼠OHC的电流范围为1至100 µM,而在100 µM的9种OHC中,只有一只ICR小鼠OHC明显。尽管杂合子(+ / cir)或纯合子(cir / cir)小鼠OHC的半数抑制浓度与IK,n中报道的浓度接近,但K + 外向电流的生物物理和药理特性,例如接近–50 mV的激活,超极化步骤和TEA敏感性引起的小内向电流与其他组织中报道的IK,n不符。我们的研究结果表明,在发育中的(P0〜P6)纯合子中,利尼平抑制了在生物物理和药理特性方面与IK,n不相似的延迟整流器K + 的向外电流( cir / cir)或杂合(+ / cir)小鼠OHC。

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