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氨基糖苷类抗生素对钙动作电位和钙通道电流的影响。

Effects of aminoglycoside antibiotics on calcium action potentials and calcium channel currents.

作者信息

Suarez-Kurtz G

机构信息

Departamento de Farmacologia Básica e Clinica, Universidade Federal do Rio de Janeiro, Brasil.

出版信息

Acta Physiol Pharmacol Latinoam. 1989;39(4):407-18.

PMID:2520359
Abstract

The author reviews work from his laboratory on the effects of neomycin and streptomycin on the Ca(2+)-dependent electrogenesis of crustacean muscle fibers and on two distinct Ca2+ channel currents of pituitary cells. The data indicate that these aminoglycosides inhibit the graded electrogenesis and the action potentials of crustacean muscle; these effects are accompanied by inhibition of tension development upon membrane depolarization. Increasing the extracellular Ca2+ concentration reverses the aminoglycoside-induced blockade of the Ca(2+)-dependent electrogenesis of the muscle fibers. Neomycin blocked both the transient (T-type) and the slowly-inactivating (L-type) Ca2+ currents of clonal pituitary GH3 cells, studied with the whole cell modality of the patch clamp technique. The blockade of these currents was not modulated by activation or inactivation of the channels. Neomycin inhibited also the currents conveyed by Na+ through the slowly-inactivating Ca2+ in cells equilibrated with Ca(2+)-free media. Interpretation of these data led to the suggestion that the blockade of Ca2+ currents by neomycin (and other aminoglycosides) cannot be explained by competition with Ca2+ ions for binding to high affinity transition sites within the Ca2+ channel path.

摘要

作者回顾了其实验室关于新霉素和链霉素对甲壳类动物肌肉纤维钙(Ca2+)依赖性电发生以及垂体细胞两种不同钙通道电流影响的研究工作。数据表明,这些氨基糖苷类药物抑制甲壳类动物肌肉的分级电发生和动作电位;这些作用伴随着膜去极化时张力发展的抑制。增加细胞外钙浓度可逆转氨基糖苷类药物对肌肉纤维钙(Ca2+)依赖性电发生的阻断作用。采用膜片钳技术的全细胞模式研究发现,新霉素阻断了克隆垂体GH3细胞的瞬时(T型)和缓慢失活(L型)钙电流。这些电流的阻断不受通道激活或失活的调节。在无钙培养基中平衡的细胞中,新霉素还抑制了钠通过缓慢失活钙通道所传导的电流。对这些数据的解释表明,新霉素(和其他氨基糖苷类药物)对钙电流的阻断不能用与钙离子竞争结合钙通道路径内高亲和力转换位点来解释。

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