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巴比妥类药物可阻断受刺激和钾离子去极化的大鼠交感神经节对钙的摄取。

Barbiturates block calcium uptake by stimulated and potassium-depolarized rat sympathetic ganglia.

作者信息

Blaustein M P

出版信息

J Pharmacol Exp Ther. 1976 Jan;196(1):80-6.

PMID:1519
Abstract

The effects of two barbiturates on calcium uptake by sympathetic ganglia have been examined. Sodium pentobarbital (0.4-0.75 mM) and sodium thiopental (0.3 mM) block the preganglionic stimulation-induced uptake of 45Ca by rat superior cervical ganglia but not action potential conduction in the presynaptic axons. The ganglionic-blocking agent, tetraethylammonium, does not inhibit stimulation-induced Ca uptake and does not prevent the blocking effect of thiopental. This effect is therefore probably presynaptic. Postassium-rich media also stimulate Ca uptake by the ganglia, and this effect is markedly inhibited by pentobarbital. Since the K stimulation effect is also observed in deafferented ganglia but not in guanethidine-denervated ganglia, this effect is probably associated primarily with postsynaptic elements. In sum, the data suggest that the barbiturates inhibit Ca permeability changes in both pre- and postsynaptic neurons.

摘要

研究了两种巴比妥类药物对交感神经节摄取钙的影响。戊巴比妥钠(0.4 - 0.75 mM)和硫喷妥钠(0.3 mM)可阻断节前刺激诱导的大鼠颈上神经节对45Ca的摄取,但不影响突触前轴突的动作电位传导。神经节阻断剂四乙铵不抑制刺激诱导的钙摄取,也不能阻止硫喷妥钠的阻断作用。因此,这种作用可能是突触前的。富含钾的培养基也能刺激神经节摄取钙,而这种作用被戊巴比妥显著抑制。由于在去传入神经节中也观察到钾刺激作用,但在胍乙啶去神经节中未观察到,这种作用可能主要与突触后成分有关。总之,数据表明巴比妥类药物抑制突触前和突触后神经元的钙通透性变化。

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