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机构地区:[1]浙江大学医学院附属第一医院感染科
出 处:《中国新药杂志》2007年第4期293-295,共3页Chinese Journal of New Drugs
基 金:浙江省台州市科技计划基金(043235)
摘 要:目的:观察前列地尔对D-氨基半乳糖致急性肝损伤大鼠肝匀浆IL-18水平升高的抑制作用。方法:32只SD大鼠一次性腹腔注射D-氨基半乳糖(D-Gal)1.4 g.kg-1,建立急性肝损伤模型。造模后大鼠随机分为前列地尔注射液治疗组(L ipo PGE130μg.kg-1)和阴性对照组(灭菌生理氯化钠溶液),均为一次性腹腔注射。检测两组造模前和造模后6,12,24 h血清谷丙转氨酶(ALT)、谷草转氨酶(AST)和肝匀浆IL-18的水平。结果:D-氨基半乳糖造模后,两组大鼠血清ALT,AST和肝匀浆IL-18值呈动态升高(P<0.05)。在造模后6,12和24 h,前列地尔30μg.kg-1治疗组的血清ALT,AST和肝匀浆IL-18值均明显低于阴性对照组。结论:前列地尔对D-氨基半乳糖致急性肝损伤大鼠有肝脏保护作用,其机制可能与降低肝脏IL-18水平有关。Objective:To evaluate if and how alprostadil for injection inhibits IL-18 levels in rats with D-galactosamine (D-Gal)-induced acute hepatic injury. Methods:Thirty-two SD rats were abdominally administered with a single injection of D-Gal 1.4 g· kg^-1 to induce experimental hepatic injury. Subsequently, the rats were randomly abdominally injected with sterilized normal saline or alprostadil for injection 30 ug·kg^-1 In 0, 6, 12 and 24 h of the injection with alprostadil or normal saline, the levels ALT, AST and IL-18 in the liver homogenates were measured, respectively. Results: The D-Gal-treated rats significantly experienced a dynamic escalation of ALT, AST and IL-18 levels (P 〈 0.05 ). The alprostadil for injection significantly decreased the levels of serum AST, ALT and IL-18 compared with the rats treated with normal saline. Conclusion: Alprostadil prevented the rats from D-Gal-induced hepatic injury by inhibition of IL-18 levels.
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