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巴比妥类药物对去极化诱导的钙离子流入大鼠突触体的急性和慢性影响。

Acute and chronic effects of barbituartes on depolarization-induced calcium influx into rat synaptosomes.

作者信息

Leslie S W, Friedman M B, Wilcox R E, Elrod S V

出版信息

Brain Res. 1980 Mar 10;185(2):409-17. doi: 10.1016/0006-8993(80)91078-1.

Abstract

Depolarization-induced 45Ca2+ influx into synaptosomes isolated from nontreated control and acutely treated rats (given 60 mg/kg phenobarbital i.p.) was significantly depressed (54 and 37%, respectively) by an in vitro challenge with pentobarbital, 0.3 mM (final concentration). However, depolarization-induced 45Ca2+ influx into synaptosomes isolated from tolerant rats (received dietary phenobarbital, 2.5 mg/g of diet, for 13 days) was not significantly altered when the synaptosomes were challenged with 0.3 mM pentobarbital. This suggests that synaptosomal membranes adapt during chronic exposure to barbiturates to allow for an enhanced Ca2+ influx subsequent to depolarization. Our data suggest that sedation may, at least in part, occur as a result of depressed stimulus-secretion coupling and that behavioral tolerance to sedation may occur because of the development of membrane tolerance to allow enhanced calcium influx.

摘要

用0.3 mM(终浓度)戊巴比妥进行体外刺激时,去极化诱导的45Ca2+流入从未经处理的对照大鼠和急性处理大鼠(腹腔注射60 mg/kg苯巴比妥)分离的突触体中显著降低(分别为54%和37%)。然而,当用0.3 mM戊巴比妥刺激从耐受大鼠(接受含2.5 mg/g苯巴比妥的饮食13天)分离的突触体时,去极化诱导的45Ca2+流入没有显著改变。这表明突触体膜在长期暴露于巴比妥类药物期间会发生适应性变化,以便在去极化后增强Ca2+流入。我们的数据表明,镇静作用可能至少部分是由于刺激-分泌偶联的抑制,而对镇静的行为耐受性可能是由于膜耐受性的发展以允许增强的钙流入。

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