Holsapple M P, Malave A, Lowy M T, Yim G K
J Pharmacol Exp Ther. 1984 May;229(2):399-403.
Systemic (i.p. and p.o.) administration of clonidine significantly reduced the acute inflammatory swelling of the rat paw produced by carrageenin, histamine and serotonin. Clonidine did not reduce carrageenin swelling when given i.c.v. Intraperitoneal administration of a structural analog of clonidine, 2-(2-methyl-4- chlorophenylamine ) -2-imidazoline (CDMI), was only effective against carrageenin swelling. CDMI was 10 times more effective when given centrally (i.c.v.) than when given systemically (i.p. or p.o.). The slopes of the individual dose-response curves were not significantly different which suggested a common mechanism of action. However, although adrenalectomy did not reduce the anti-inflammatory activity of i.p. CDMI, i.c.v. CDMI was ineffective in adrenalectomized rats. These results indicate that imidazolines represent a unique class of anti-inflammatory agents with actions mediated both peripherally and centrally.
可乐定经全身(腹腔注射和口服)给药可显著减轻角叉菜胶、组胺和血清素所致的大鼠足急性炎性肿胀。脑室内注射可乐定时,对角叉菜胶所致肿胀无减轻作用。可乐定的结构类似物2-(2-甲基-4-氯苯胺)-2-咪唑啉(CDMI)腹腔注射仅对角叉菜胶所致肿胀有效。CDMI经中枢(脑室内)给药时的效果比经全身(腹腔注射或口服)给药强10倍。各剂量反应曲线的斜率无显著差异,提示其作用机制相同。然而,虽然肾上腺切除并未降低腹腔注射CDMI的抗炎活性,但脑室内注射CDMI对肾上腺切除大鼠无效。这些结果表明,咪唑啉类代表一类独特的抗炎药,其作用在外周和中枢均有介导。