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褪黑素对9,10-二甲基-1,2-苯并蒽诱导的大鼠乳腺肿瘤发生过程中代表性的I相和II相药物代谢酶的潜在调节作用。

A possible modulatory influence of melatonin on representative phase I and II drug metabolizing enzymes in 9,10-dimethyl-1,2-benzanthracene induced rat mammary tumorigenesis.

作者信息

Kothari L, Subramanian A

机构信息

Endocrinology Unit, Tata Memorial Centre, Parel, Bombay, India.

出版信息

Anticancer Drugs. 1992 Dec;3(6):623-8. doi: 10.1097/00001813-199212000-00010.

Abstract

The oncosuppressive effect of melatonin on 9,10-dimethyl-1,2-benzanthracene (DMBA) induced rat mammary tumorigenesis led us to assess its possible modulatory influence on representative hepatic and mammary drug metabolizing enzymes in DMBA treated female Holtzman rats, reared in short and long photoperiods. Melatonin treated rats in either photoperiod showed a significant induction in hepatic and mammary levels of glutathione (GSH) and cytosolic activities of glutathione S-transferase (GST) when compared with the corresponding controls, along with a significant drop in hepatic microsomal contents of cytochromes b5 and P450. This induction of GSH and GST, and depletion of cytochromes b5 and P450 by melatonin may possibly be related to its anticarcinogenic potential in this tumor model.

摘要

褪黑素对9,10-二甲基-1,2-苯并蒽(DMBA)诱导的大鼠乳腺肿瘤发生具有抑癌作用,这促使我们评估其对在短光照周期和长光照周期饲养的DMBA处理的雌性霍尔兹曼大鼠中代表性肝脏和乳腺药物代谢酶的可能调节影响。与相应对照组相比,无论在何种光照周期下,褪黑素处理的大鼠肝脏和乳腺中的谷胱甘肽(GSH)水平及谷胱甘肽S-转移酶(GST)的胞质活性均显著升高,同时肝脏微粒体细胞色素b5和P450含量显著下降。褪黑素对GSH和GST的这种诱导作用以及对细胞色素b5和P450的消耗可能与其在该肿瘤模型中的抗癌潜力有关。

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