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氨基糖苷类抗生素链霉素和新霉素对神经肌肉传递的影响。II. 突触后因素。

Effects of the aminoglycoside antibiotics, streptomycin and neomycin, on neuromuscular transmission. II. Postsynaptic considerations.

作者信息

Fiekers J F

出版信息

J Pharmacol Exp Ther. 1983 Jun;225(3):496-502.

PMID:6306208
Abstract

The postsynaptic effects of two aminoglycoside antibiotics, streptomycin and neomycin, were studied on miniature end-plate currents (mepcs) and acetylcholine-induced end-plate current fluctuations in voltage-clamped costocutaneous muscles of the garter snake (species Thamnophis). Neomycin decreased the amplitude of mepcs and accelerated the time constants of mepc decay in a concentration-dependent manner without altering the single exponential nature of mepc decay. Neomycin also produced a voltage- and concentration-dependent nonlinearity in the current/voltage relationship. The relationship between the time constants of mepc decay and membrane potential was progressively reduced with increasing concentrations of neomycin. A concentration-dependent reduction in single channel conductance and channel lifetime was also obtained with neomycin. In contrast, streptomycin, in concentrations up to 5 X 10(-5) M, did not significantly alter either mepc amplitude, the time constant of mepc decay, the relationship between the mepc decay time constant and membrane potential or the lifetime and conductance of single end-plate channels. In very high concentrations (greater than 1 mM) streptomycin decreased mepc amplitude and prolonged mepc decay at hyperpolarized membrane potentials. The results suggest that neomycin interacts with the ionic channels of the acetylcholine receptor in their open configuration, whereas streptomycin acts primarily by blocking the receptor. The significant differences in the molecular actions of these two antibiotics may provide an explanation for the observed differences in the character and reversal of the neuromuscular block produced by these antibiotics.

摘要

在束带蛇(美洲束带蛇属)电压钳制的肋皮肌中,研究了两种氨基糖苷类抗生素——链霉素和新霉素对微小终板电流(mepcs)以及乙酰胆碱诱导的终板电流波动的突触后效应。新霉素以浓度依赖性方式降低了mepcs的幅度,并加速了mepc衰减的时间常数,而未改变mepc衰减的单指数性质。新霉素还在电流/电压关系中产生了电压和浓度依赖性的非线性。随着新霉素浓度的增加,mepc衰减时间常数与膜电位之间的关系逐渐减弱。新霉素还导致单通道电导和通道寿命呈浓度依赖性降低。相比之下,浓度高达5×10⁻⁵ M的链霉素对mepc幅度、mepc衰减时间常数、mepc衰减时间常数与膜电位之间的关系或单个终板通道的寿命和电导均无显著影响。在非常高的浓度(大于1 mM)下,链霉素在超极化膜电位时降低了mepc幅度并延长了mepc衰减时间。结果表明,新霉素在乙酰胆碱受体的离子通道处于开放构象时与之相互作用,而链霉素主要通过阻断受体起作用。这两种抗生素分子作用的显著差异可能为观察到的这两种抗生素产生的神经肌肉阻滞的特征和逆转差异提供了解释。

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