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褪黑素联合给药可逆转锡原卟啉(SnPP)诱导的大鼠体内细胞色素P450含量下降。

Co-administration of melatonin reverses the tin-protoporphyrin (SnPP) induced decline of cytochrome P450 content in vivo in rats.

作者信息

Chandra R, Upadhyaya G, Dass S K, Jain R

机构信息

Dr B. R. Ambedkar Center for Biomedical Research, University of Delhi, Delhi, India.

出版信息

Eur J Drug Metab Pharmacokinet. 2000 Jul-Dec;25(3-4):213-8. doi: 10.1007/BF03192316.

Abstract

Melatonin (N-acetyl-5 methoxytryptamine) is a low molecular weight antioxidant and is an endogeneous defense system against the deleterious actions of the extremely reactive hydroxyl radical. Among the enzymes that participate in the antioxidant functions is cytochrome P-450, a stalwart of the detoxification system in the body. Our results revealed that tin-protoporphyrin administration brought about a marked decline in cytochrome P-450 levels. This decline was, however, reversed by the coadministration of the antioxidant, melatonin. Thus, the enhanced antioxidant status in melatonin-treated rats may act as a protective mediator of various pharmacological functions altered during tin-protoporphyrin (an antihyperbilirubemenic agent) administration to Wistar rats.

摘要

褪黑素(N-乙酰-5-甲氧基色胺)是一种低分子量抗氧化剂,是抵御极具反应性的羟基自由基有害作用的内源性防御系统。参与抗氧化功能的酶包括细胞色素P-450,它是体内解毒系统的中流砥柱。我们的研究结果显示,给予锡原卟啉会导致细胞色素P-450水平显著下降。然而,同时给予抗氧化剂褪黑素可逆转这种下降。因此,在对Wistar大鼠给予锡原卟啉(一种抗高胆红素血症药物)期间,褪黑素处理的大鼠体内增强的抗氧化状态可能作为各种改变的药理功能的保护介质。

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