Menon M K, Kodama C K
Neuropharmacology. 1985 Sep;24(9):927-30. doi: 10.1016/0028-3908(85)90048-6.
A lipid soluble alpha 1-adrenoceptor agonist 2-(2-chloro-5-trifluoromethylphenylimino) imidazolidine (St 587) antagonized the hypnotic effect of ethanol in C57Bl/6 and CD-1 mice. In Swiss-Webster mice the effect of St 587 was weak and in BALB/c mice this drug potentiated ethanol hypnosis. St 587 did not enhance the elimination of ethanol. Cirazoline, an alpha 1-adrenoceptor agonist which is more potent than St 587, was relatively more effective in antagonizing the ethanol-induced hypnosis. Though it appears that St 587 exerted its ethanol antagonism by virtue of its alpha 1-adrenoceptor agonistic effect, other contributing factors may also have to be considered. St 587 may prove to be of value in understanding the mechanism of action of ethanol and in the treatment of acute ethanol intoxication.
一种脂溶性α1 - 肾上腺素能受体激动剂2 - (2 - 氯 - 5 - 三氟甲基苯基亚氨基)咪唑烷(St 587)可拮抗乙醇对C57Bl/6和CD - 1小鼠的催眠作用。在瑞士韦伯斯特小鼠中,St 587的作用较弱,而在BALB/c小鼠中,这种药物增强了乙醇的催眠作用。St 587并未增强乙醇的消除。可乐唑啉是一种比St 587更有效的α1 - 肾上腺素能受体激动剂,在拮抗乙醇诱导的催眠作用方面相对更有效。虽然似乎St 587凭借其α1 - 肾上腺素能受体激动作用发挥其对乙醇的拮抗作用,但也可能必须考虑其他促成因素。St 587可能在理解乙醇的作用机制和治疗急性乙醇中毒方面具有价值。