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地昔帕明对大鼠行为的影响可通过同时给予乙醇来预防。

Effects of desipramine on rat behavior are prevented by concomitant treatment with ethanol.

作者信息

Rommelspacher H, Wolffgramm J, Widjaja S

机构信息

Department of Neuropsychopharmacology, Free University, Berlin, F.R. Germany.

出版信息

Pharmacol Biochem Behav. 1989 Feb;32(2):533-42. doi: 10.1016/0091-3057(89)90193-7.

Abstract

Ethanol prevents the decrease of the number of beta-adrenoceptors in the cerebral cortex induced by chronic treatment of rats with desipramine. The activation of the adenylate cyclase, the second messenger, by beta-adrenergic agonists is reduced somewhat less than after treatment with desipramine alone. The present paper examined the hypothesis that ethanol inhibits the neuronal adaptation to desipramine chronic treatment at the functional level as well. Desipramine reduced exploratory behavior (crossings, rearings) as did ethanol. Combined treatment attenuated the effect of desipramine. Cognitive performance was investigated using an active avoidance paradigm. Desipramine-treated rats did not learn the task in contrast to control animals. Again, combination treatment with ethanol improved the ability of the rats to perform the task. The activity of cerebral beta-adrenergic mechanisms was assessed by injection of salbutamol, a beta-adrenoceptor agonist in rats pretreated with 5-hydroxytryptophan (5-HTP). The augmentation of the 5-HTP-induced wet dog shake behavior by salbutamol was observed in all animals independent of the chronic treatment. However, rats treated with desipramine were less active than those treated with tap water or ethanol. The effect of desipramine in the presence of a high concentration of salbutamol was attenuated by ethanol. The observed increase of the number of wet dog shakes correlates with the function of these receptors. In two paradigms, spontaneous motility and apomorphine-induced hypothermia, ethanol did not affect the action of desipramine. It is noteworthy that desipramine acted in both situations within a short time period (minutes to hours). The findings strongly suggest that ethanol can prevent adaptive changes in the brain induced by chronic treatment with the antidepressant desipramine. This is of special interest since the adaptation of beta-adrenoceptors is thought to be critical for the antidepressant efficacy of various therapeutic interventions applied in psychiatric practice.

摘要

乙醇可防止因用去甲丙咪嗪长期治疗大鼠而导致的大脑皮质中β-肾上腺素能受体数量减少。β-肾上腺素能激动剂对第二信使腺苷酸环化酶的激活作用,其降低程度略小于单独用去甲丙咪嗪治疗后。本文检验了这样一种假说,即乙醇在功能水平上也抑制神经元对去甲丙咪嗪长期治疗的适应性。去甲丙咪嗪和乙醇一样,都会降低探索行为(穿越、直立)。联合治疗减弱了去甲丙咪嗪的作用。使用主动回避范式研究认知表现。与对照动物相比,用去甲丙咪嗪治疗的大鼠没有学会该任务。同样,乙醇联合治疗提高了大鼠执行该任务的能力。通过给用5-羟色氨酸(5-HTP)预处理的大鼠注射β-肾上腺素能受体激动剂沙丁胺醇,来评估大脑β-肾上腺素能机制的活性。在所有动物中,无论长期治疗情况如何,均观察到沙丁胺醇增强了5-HTP诱导的湿狗摇晃行为。然而,用去甲丙咪嗪治疗的大鼠比用自来水或乙醇治疗的大鼠活性更低。在高浓度沙丁胺醇存在的情况下,乙醇减弱了去甲丙咪嗪的作用。观察到的湿狗摇晃次数增加与这些受体的功能相关。在自发运动和阿扑吗啡诱导的体温过低这两种范式中,乙醇不影响去甲丙咪嗪的作用。值得注意的是,去甲丙咪嗪在这两种情况下均在短时间内(数分钟至数小时)起作用。这些发现有力地表明,乙醇可防止因用抗抑郁药去甲丙咪嗪长期治疗而在大脑中引起的适应性变化。这一点特别值得关注,因为β-肾上腺素能受体的适应性被认为对精神病学实践中应用的各种治疗干预措施的抗抑郁疗效至关重要。

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