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不同年龄雄性大鼠肝脏微粒体中苯并硝唑和硝呋替莫的硝基还原酶活性

Liver microsomal benznidazole and nifurtimox nitroreductase activity in male rats of different age.

作者信息

Aguilar E, de Arranz C K, de Toranzo E G, Castro J A

机构信息

Centro de Investigaciones Toxicológicas, (CEITOX)-CITEFA/CONICET, Pcia. de Buenos Aires, Argentina.

出版信息

Arch Int Pharmacodyn Ther. 1987 Sep;289(1):11-7.

PMID:3435199
Abstract

Nifurtimox (Nfx) and Benznidazole (Bz) are 2 drugs used in the chemotherapy of Chagas' disease, a sickness afflicting millions of Latin Americans. Their toxicity is related to nitroreductive activation. Nfx and Bz nitroreductase activity in liver microsomes from male rats is already present at low levels in the newborn and reaches full adult activity in 28 days. This suggests a better therapeutic approach by starting the treatment of transplacentally acquired Chagas' disease immediately after birth.

摘要

硝呋替莫(Nfx)和苯硝唑(Bz)是用于治疗恰加斯病化疗的两种药物,这种疾病折磨着数百万拉丁美洲人。它们的毒性与硝基还原激活有关。雄性大鼠肝微粒体中的Nfx和Bz硝基还原酶活性在新生大鼠中就已处于低水平,并在28天达到成年大鼠的完全活性。这表明通过在出生后立即开始治疗经胎盘感染的恰加斯病可能会有更好的治疗方法。

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