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[糖皮质激素增强巴氯芬的肌肉松弛作用]

[Enhancement of the muscle relaxant action of baclofen by glucocorticoids].

作者信息

Wakayama K

出版信息

Nihon Yakurigaku Zasshi. 1987 Feb;89(2):81-90. doi: 10.1254/fpj.89.81.

Abstract

Effects of pretreatment with hydrocortisone or prednisolone on the pharmacological effects of baclofen, particularly on the muscle relaxant action, were studied in young adult rats. Muscle relaxation was determined using an inclined board (50 degrees). A single injection of hydrocortisone (10 mg/kg, s.c.) 15 min prior to the administration of baclofen (5 mg/kg, i.p.) increased significantly the muscle relaxant time by baclofen. Prednisolone pretreatment (2 mg/kg, s.c.) also prolonged baclofen-induced muscle relaxation. Muscle relaxation due to tolperisone (50 mg/kg, i.p.) and mephenesin (80 mg/kg, i.p.) administration was enhanced by the pretreatment of hydrocortisone. Hydrocortisone pretreatment enhanced the muscle relaxant time of diazepam (2 mg/kg, i.p.) but at a lesser extent and only in males. No synergistic effect of hydrocortisone on the muscle relaxation time by suxamethonium (0.01 mg/kg, i.p.) was observed. Seven daily injections of 2 mg/kg hydrocortisone as well as of 0.4 mg/kg prednisolone did not enhance the muscle relaxation by baclofen when tested 24 hr after the last injection of the two steroids. Fifteen min priming with hydrocortisone had no effect on the antinociceptive and hypothermic effects of baclofen. 3H-Baclofen was injected i.v. as a tracer of 1 mg/kg unlabeled baclofen. In hydrocortisone-treated rats, the uptake of 3H-baclofen into the hippocampus, medulla oblongata and cerebellum was significantly higher than that in the vehicle-treated rats, whereas the radioactivity in the cervical, thoracic and lumbar spinal cord tended to decrease. The results indicate that acute priming with hydrocortisone enhances rather selectively the muscle relaxant action of the centrally acting muscle relaxant drugs. It is suggested that the primary site of the synergistic action of hydrocortisone to baclofen could be at the supraspinal level of the CNS.

摘要

在成年幼鼠中研究了氢化可的松或泼尼松龙预处理对巴氯芬药理作用的影响,特别是对肌肉松弛作用的影响。使用倾斜板(50度)测定肌肉松弛情况。在腹腔注射巴氯芬(5mg/kg)前15分钟皮下注射一次氢化可的松(10mg/kg),可显著延长巴氯芬的肌肉松弛时间。泼尼松龙预处理(2mg/kg,皮下注射)也可延长巴氯芬诱导的肌肉松弛时间。氢化可的松预处理可增强托哌酮(50mg/kg,腹腔注射)和美芬新(80mg/kg,腹腔注射)所致的肌肉松弛。氢化可的松预处理可增强地西泮(2mg/kg,腹腔注射)的肌肉松弛时间,但程度较小,且仅在雄性中出现。未观察到氢化可的松对琥珀胆碱(0.01mg/kg,腹腔注射)所致肌肉松弛时间的协同作用。在最后一次注射两种类固醇24小时后进行测试时,连续7天每天注射2mg/kg氢化可的松以及0.4mg/kg泼尼松龙均未增强巴氯芬的肌肉松弛作用。用氢化可的松进行15分钟预激发对巴氯芬的镇痛和降温作用无影响。静脉注射3H-巴氯芬作为1mg/kg未标记巴氯芬的示踪剂。在氢化可的松处理的大鼠中,3H-巴氯芬在海马、延髓和小脑中的摄取明显高于溶剂处理的大鼠,而颈、胸和腰脊髓中的放射性则有降低趋势。结果表明,氢化可的松急性预激发可选择性增强中枢性肌肉松弛药物的肌肉松弛作用。提示氢化可的松与巴氯芬协同作用的主要部位可能在中枢神经系统的脊髓上水平。

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