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大鼠乙醇戒断症状对γ-氨基丁酸(GABA)模拟物的差异敏感性:对听源性惊厥有阻断作用,但对前肢震颤无阻断作用。

Differential sensitivity of ethanol withdrawal signs in the rat to gamma-aminobutyric acid (GABA)mimetics: blockade of audiogenic seizures but not forelimb tremors.

作者信息

Frye G D, McCown T J, Breese G R

出版信息

J Pharmacol Exp Ther. 1983 Sep;226(3):720-5.

PMID:6310080
Abstract

Intraperitoneal injection of ethanol (1-2 g/kg) and chlordiazepoxide (2-16 mg/kg) suppressed susceptibility to audiogenically induced, clonic-tonic seizures and antagonized forelimb tremor in rats undergoing ethanol withdrawal, 30 min after treatment. However, a smaller dose of ethanol (0.5 g/kg) actually increased clonic seizure frequency, suggesting that ethanol exerts a biphasic proconvulsant/anticonvulsant action. Direct activation of gamma-aminobutyric acid (GABA) receptors by intracisternal administration of GABA (100-1000 micrograms), muscimol (0.3-1.0 micrograms) or 4,5,6,7-tetrahydroisoxazolo[5,4-c]pyridin-3-ol (THIP) (0.3-3.0 micrograms) 5 to 10 min before testing also reduced susceptibility to audiogenic clonic-tonic seizures. In sharp contrast to these anticonvulsant actions, GABA, muscimol and THIP had no effect on withdrawal-induced forelimb tremors. Blockade of GABA uptake with 1-2,4-diaminobutyric acid (300 and 600 mg/kg i.p.) and inhibition of GABA transaminase with aminooxyacetic acid (12.5 and 25.0 mg/kg i.p.) both reduced susceptibility to seizures. However, anticonvulsant doses of these two drugs, unlike GABA, muscimol and THIP, also reduced forelimb tremor. Three other GABA transaminase inhibitors, gamma-vinyl GABA (450 and 900 mg/kg i.p.), gamma-acetylenic GABA (50-150 mg/kg i.p.) and ethanolamine-O-sulfate (250-750 mg/kg i.p.), were inactive against ethanol withdrawal audiogenic seizures and forelimb tremors. These results indicate that direct GABA receptor activation can selectively suppress one type of ethanol withdrawal response (i.e., audiogenic seizure susceptibility) while failing to influence another (forelimb tremors).

摘要

腹腔注射乙醇(1 - 2克/千克)和氯氮卓(2 - 16毫克/千克)可抑制大鼠对听源性诱发性阵挛 - 强直惊厥的易感性,并在治疗后30分钟拮抗乙醇戒断大鼠的前肢震颤。然而,较小剂量的乙醇(0.5克/千克)实际上增加了阵挛性惊厥的频率,这表明乙醇具有双相性的促惊厥/抗惊厥作用。在测试前5至10分钟,通过脑池内注射γ-氨基丁酸(GABA)(100 - 1000微克)、蝇蕈醇(0.3 - 1.0微克)或4,5,6,7 - 四氢异恶唑并[5,4 - c]吡啶 - 3 - 醇(THIP)(0.3 - 3.0微克)直接激活GABA受体,也降低了对听源性阵挛 - 强直惊厥的易感性。与这些抗惊厥作用形成鲜明对比的是,GABA、蝇蕈醇和THIP对戒断诱导的前肢震颤没有影响。用1 - 2,4 - 二氨基丁酸(300和600毫克/千克腹腔注射)阻断GABA摄取以及用氨氧基乙酸(12.5和25.0毫克/千克腹腔注射)抑制GABA转氨酶,均降低了惊厥的易感性。然而,与GABA、蝇蕈醇和THIP不同,这两种药物的抗惊厥剂量也减少了前肢震颤。另外三种GABA转氨酶抑制剂,γ-乙烯基GABA(450和900毫克/千克腹腔注射)、γ-乙炔基GABA(50 - 150毫克/千克腹腔注射)和乙醇胺 - O - 硫酸盐(250 - 750毫克/千克腹腔注射),对乙醇戒断听源性惊厥和前肢震颤无活性。这些结果表明,直接激活GABA受体可以选择性地抑制一种类型的乙醇戒断反应(即听源性惊厥易感性),而不影响另一种反应(前肢震颤)。

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