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大鼠产前暴露于阿昔洛韦后胸腺发育异常及免疫系统功能受损。

Abnormal thymus development and impaired function of the immune system in rats after prenatal exposure to aciclovir.

作者信息

Stahlmann R, Korte M, Van Loveren H, Vos J G, Thiel R, Neubert D

机构信息

Institut für Toxikologie und Embryopharmakologie, Freie Universität Berlin, Federal Republic of Germany.

出版信息

Arch Toxicol. 1992;66(8):551-9. doi: 10.1007/BF01973385.

Abstract

Aciclovir (synonym: acyclovir) causes abnormal thymus development in rats. After treatment on day 10 of gestation a weight reduction of the organ is obvious in 21-day-old fetuses which persists postnatally. Adult male rats exposed in utero to one or three injections of 100 mg aciclovir/kg body wt given to the dam on day 10 of pregnancy showed a reduction of the thymus weight to 333 +/- 158 mg and 276 +/- 61 mg (control: 428 +/- 92 mg; n = 10). Corresponding alterations were detectable in female offspring. Liver weight was also decreased and spleen weight (in relation to body wt) was significantly increased in the offspring after the three exposures. In a host resistance model with Trichinella spiralis the function of the immune system of rats prenatally exposed to aciclovir was examined. Six weeks postnatally 10-12 randomly selected male rat offspring of one control and two treatment groups (1 or 3 injections of 100 mg aciclovir/kg body wt on day 10 of gestation) were infected orally with 500 Trichinella spiralis muscle larvae. Before and several times after the infection blood was taken from a tail vein or obtained by decapitation for examination of the antibody titers (IgM, IgG, IgA, IgE) to antigens of T. spiralis. Six weeks after the infection the weight of relevant organs was determined and tongue preparations were used for T. spiralis muscle larvae counting. Aciclovir exposed animals showed a different immune response than control rats. IgM titers in both treatment groups were higher than in controls two weeks after the infection but not different by the end of the experiment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

阿昔洛韦(同义词:无环鸟苷)可导致大鼠胸腺发育异常。在妊娠第10天进行治疗后,21日龄胎儿的该器官重量明显减轻,且出生后仍持续存在。孕期第10天给孕鼠腹腔注射1次或3次100mg/kg体重的阿昔洛韦,成年雄性子代大鼠的胸腺重量降至333±158mg和276±61mg(对照组:428±92mg;n = 10)。雌性子代也可检测到相应变化。三次暴露后,子代的肝脏重量也降低,脾脏重量(相对于体重)显著增加。在旋毛虫宿主抵抗模型中,检测了产前暴露于阿昔洛韦的大鼠的免疫系统功能。产后6周,从一个对照组和两个治疗组(孕期第10天注射1次或3次100mg/kg体重的阿昔洛韦)中随机选取10 - 12只雄性大鼠子代,经口感染500条旋毛虫肌幼虫。感染前及感染后多次从尾静脉取血或断头取血,检测针对旋毛虫抗原的抗体滴度(IgM、IgG、IgA、IgE)。感染6周后,测定相关器官重量,并用舌组织切片计数旋毛虫肌幼虫。暴露于阿昔洛韦的动物表现出与对照大鼠不同的免疫反应。感染后两周,两个治疗组的IgM滴度均高于对照组,但实验结束时无差异。(摘要截断于250字)

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