Moodley I, Grouhel A, Lelièvre V, Junien J L
Institut de Recherche Jouveinal, Fresnes, France.
J Lipid Mediat. 1991 Jan-Feb;3(1):51-70.
Tixocortol 17-butyrate,21-propionate (JO 1222) is a novel, locally acting, C-21 thioester-linked corticosteroid with significant activity in a number of models of inflammation. In models of acute inflammation, JO 1222 had an ED30 of 3 micrograms in carrageenan-induced oedema, an ED50 of 5 ng in croton oil-induced inflammation, and 4 micrograms and 2 micrograms/pleural cavity in carrageenin-induced pleurisy in the rat and mouse respectively. In a model of subchronic inflammation JO 1222 had an ED50 of 39 micrograms/pellet (cotton pellet-induced granuloma) and an ED50 of 13 ng in oxazolone-induced hypersensitivity. The overall relative potency was found to be beclomethasone DP greater than betamethasone DP = JO 1222 greater than hydrocortisone 17-butyrate,21-propionate greater than hydrocortisone acetate. In contrast to any of the other corticosteroids, including beclomethasone DP, JO 1222 did not have any marked systemic effects in any of the above models following oral or local administration. Furthermore, in contrast to other locally acting corticosteroids such as beclomethasone DP, JO 1222 had little or no effect on the thymus or body weight. These findings suggest that JO 1222 is a novel, potent, locally acting corticosteroid with little or no systemic effects and thus has therapeutical potential in diseases such as asthma, arthritis, ulcerative colitis and rhinitis.
曲安西龙 17 - 丁酸酯,21 - 丙酸酯(JO 1222)是一种新型的、具有局部作用的、C - 21硫酯连接的皮质类固醇,在多种炎症模型中具有显著活性。在急性炎症模型中,JO 1222对角叉菜胶诱导的水肿的半数有效剂量(ED30)为3微克,对巴豆油诱导的炎症的半数有效剂量(ED50)为5纳克,对角叉菜胶诱导的大鼠和小鼠胸膜炎分别为4微克和2微克/胸腔。在亚慢性炎症模型中,JO 1222对棉球诱导的肉芽肿的半数有效剂量(ED50)为39微克/丸,对恶唑酮诱导的超敏反应的半数有效剂量(ED50)为13纳克。发现总体相对效价为倍氯米松双丙酸酯大于倍他米松双丙酸酯 = JO 1222大于氢化可的松17 - 丁酸酯,21 - 丙酸酯大于醋酸氢化可的松。与包括倍氯米松双丙酸酯在内的任何其他皮质类固醇不同,JO 1222在口服或局部给药后,在上述任何模型中均未产生任何明显的全身作用。此外,与其他局部作用的皮质类固醇如倍氯米松双丙酸酯不同,JO 1222对胸腺或体重几乎没有影响。这些发现表明,JO 1222是一种新型的、强效的、具有局部作用且几乎没有全身作用的皮质类固醇,因此在哮喘、关节炎、溃疡性结肠炎和鼻炎等疾病中具有治疗潜力。