Biswas S, Mukhopadhyay S, Poddar M K
Department of Biochemistry, University College of Science, University of Calcutta, India.
Methods Find Exp Clin Pharmacol. 1991 May;13(4):255-61.
Long-term diazepam (DZ) treatment (5 mg/kg, i.p. for 15-30 consecutive days) reduced GABAergic activity in hypothalamus and cerebellum with the alteration of GABA synthesis and its release process. This long-term DZ-induced inhibition in GABAergic activity in hypothalamus and cerebellum was not altered when DZ-treated rats were exposed (2 h/day) to lower environmental temperature (LET; 12 degrees C) for 7-30 consecutive days. Although repeated exposure to LET did not affect the GABA system in cerebellum and hypothalamus, striatal GABAergic activity was significantly enhanced under similar conditions. This LET-induced (repeated exposure) stimulation in striatal GABAergic activity was prevented when rats were treated with DZ along with repeated LET exposure (2 h/day) under long-term conditions.
长期给予地西泮(DZ)治疗(5毫克/千克,腹腔注射,连续15 - 30天)会降低下丘脑和小脑的γ-氨基丁酸(GABA)能活性,并改变GABA的合成及其释放过程。当接受DZ治疗的大鼠连续7 - 30天每天暴露(2小时)于较低环境温度(LET;12摄氏度)时,这种长期由DZ诱导的下丘脑和小脑GABA能活性抑制并未改变。尽管反复暴露于LET对小脑和下丘脑的GABA系统没有影响,但在类似条件下纹状体GABA能活性显著增强。当大鼠在长期条件下接受DZ治疗并同时反复暴露于LET(每天2小时)时,这种LET诱导的(反复暴露)纹状体GABA能活性刺激被阻止。