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氯胺酮对骨骼肌机电耦合作用的一些潜在机制。

Some mechanisms underlying actions of ketamine on electromechanical coupling in skeletal muscle.

作者信息

Marwaha J

出版信息

J Neurosci Res. 1980;5(1):43-50. doi: 10.1002/jnr.490050107.

Abstract

The effects on excitation contraction coupling (ECC) of ketamine (a dissociative general anesthetic) were investigated using the sartorius muscle of the frog. Extracellular studies revealed that ketamine depressed action potential production in a concentration-dependent manner. Ketamine decreased both the conduction velocity and the compound action potential while concomitantly increasing the threshold current. Intracellular studies showed that ketamine caused a slight non-significant decrease in the membrane potential and also decreased the threshold potential (mechanical threshold). Ketamine (1.5 X 10(-4) M and 3.0 X 10(-4) M) initially potentiated and then blocked the twitch response elicited by direct muscle stimulation. Both of these effects were statistically different from control values. These findings suggest that ketamine alters action potential production in frog skeletal muscle. This property of ketamine contributes in part to the disruption of ECC observed with this drug. The results suggest the ketamine probably interferes with calcium binding, its release and/or its fluxes which may contribute to the intial potentiation and subsequent depression of twitch tension.

摘要

利用青蛙的缝匠肌研究了氯胺酮(一种分离型全身麻醉剂)对兴奋-收缩偶联(ECC)的影响。细胞外研究表明,氯胺酮以浓度依赖的方式抑制动作电位的产生。氯胺酮降低了传导速度和复合动作电位,同时增加了阈电流。细胞内研究表明,氯胺酮使膜电位略有下降,但无统计学意义,同时也降低了阈电位(机械阈)。氯胺酮(1.5×10⁻⁴ M和3.0×10⁻⁴ M)最初增强然后阻断直接肌肉刺激引起的抽搐反应。这两种效应在统计学上均与对照值不同。这些发现表明氯胺酮改变了青蛙骨骼肌中动作电位的产生。氯胺酮的这一特性部分导致了该药物所观察到的ECC破坏。结果表明,氯胺酮可能干扰钙结合、钙释放和/或钙通量,这可能导致抽搐张力的最初增强和随后的降低。

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