Mohammad F K, Dawood K A, al-Dabbagh S G
Department of Physiology, Biochemistry and Pharmacology, College of Veterinary Medicine, University of Mosul, Iraq.
Pharmacol Res. 1993 Jan-Feb;27(1):81-8. doi: 10.1006/phrs.1993.1008.
The actions of the alpha 2-antagonist yohimbine and methylxanthines aminophylline and caffeine were evaluated in reversing ataxia, increase in landing foot splay (LFS), produced by the alpha 2-agonist medetomidine in male rats. Medetomidine at 0.1 and 0.15 mg/kg, i.p. increased LFS by 42.9 and 69.6%, respectively. The peripherally acting alpha 2-agonist ST91 (0.125 to 0.5 mg/kg, i.p.) did not significantly affect the LFS. Intraperitoneal injection of yohimbine at 0.5 and 1 mg/kg, aminophylline at 25, 50 and 100 mg/kg, and caffeine at 25 and 50 mg/kg significantly antagonized medetomidine (0.15 mg/kg, i.p.)-induced ataxia. Yohimbine was more effective (100 and 111%) than the methylxanthines (28 to 72%) in reversing medetomidine ataxia. Aminophylline and caffeine, but not yohimbine, significantly reduced LFS in non-medetomidine treated rats. The data suggested that medetomidine ataxia in rats could be specifically antagonized by yohimbine and to a lesser extent by aminophylline and caffeine.
在雄性大鼠中,评估了α2拮抗剂育亨宾、甲基黄嘌呤氨茶碱和咖啡因对由α2激动剂美托咪定引起的共济失调及着陆足展度(LFS)增加的逆转作用。腹腔注射0.1和0.15 mg/kg的美托咪定分别使LFS增加了42.9%和69.6%。外周作用的α2激动剂ST91(腹腔注射0.125至0.5 mg/kg)对LFS无显著影响。腹腔注射0.5和1 mg/kg的育亨宾、25、50和100 mg/kg的氨茶碱以及25和50 mg/kg的咖啡因可显著拮抗美托咪定(腹腔注射0.15 mg/kg)诱导的共济失调。在逆转美托咪定引起的共济失调方面,育亨宾(100%和111%)比甲基黄嘌呤(28%至72%)更有效。氨茶碱和咖啡因,但育亨宾不能,显著降低未用美托咪定处理大鼠的LFS。数据表明,育亨宾可特异性拮抗大鼠的美托咪定共济失调,氨茶碱和咖啡因的拮抗作用较弱。