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荨麻对对照及3-甲基胆蒽暴露大鼠体内CYP1A表达的影响

In vivo effects of Urtica urens (dwarf nettle) on the expression of CYP1A in control and 3-methylcholanthrene-exposed rats.

作者信息

Ozkarsli M, Sevim H, Sen A

机构信息

Biology, Kinikli Campus, Pamukkale University, Denizli, Turkey.

出版信息

Xenobiotica. 2008 Jan;38(1):48-61. doi: 10.1080/00498250701713968.

Abstract

The in vivo effects of the intraperitoneal administration of an Urtica urens L. (dwarf nettle) seed extract were examined on the hepatic, pulmonary, and renal cytochrome P450-dependent monooxygenase activities of rats co-administered with 3-methylcholanthrene (MC). Urtica extract was administered by intraperitoneal injection to male Wistar rats at 200 mgkg(-1)day(-1) for 4 days from which were also co-administered with intraperitoneal injection of 50mg of MC kg(-1) of body weight twice on days 1 and 3. MC treatment increased the 7-ethoxyresorufin O-deethylase (EROD) activity of the liver, lung, and kidney 54-, 21-, and 119-fold, respectively. Urtica treatment substantially reduced the 3MC induction of hepatic, lung, and renal EROD activity by 79, 42, and 50%, respectively. Similarly, compared with the control, MROD activities in liver and kidney were increased after MC administration, and these increases were significantly inhibited by Urtica. reverse transcriptase-polymerase chain reaction (RT-PCR) analysis clearly showed that the hepatic CYP1A1 and CYP1A2 mRNA levels substantially increased after treatment with MC, which was suppressed by Urtica supplementation. Western blotting studies also supported the alterations observed in the catalytic activities and mRNA levels. In conclusion, substantial reduction in CYP1A1 and CYP1A2 expression levels and related activities with Urtica are possibly associated with a potential chemoprotective ability of the Urtica due to the anticipated decrease in the activation of environmental chemical carcinogens through modulation of the CYP1A enzymes.

摘要

研究了腹腔注射荨麻(Urtica urens L.)种子提取物对与3-甲基胆蒽(MC)共同给药的大鼠肝脏、肺和肾脏中细胞色素P450依赖性单加氧酶活性的体内影响。将荨麻提取物以200mgkg(-1)day(-1)的剂量腹腔注射给雄性Wistar大鼠,持续4天,同时在第1天和第3天腹腔注射50mg MC kg(-1)体重。MC处理使肝脏、肺和肾脏的7-乙氧基异吩恶唑酮O-脱乙基酶(EROD)活性分别增加了54倍、21倍和119倍。荨麻处理分别使肝脏、肺和肾脏EROD活性的3MC诱导显著降低了79%、42%和50%。同样,与对照组相比,MC给药后肝脏和肾脏中的MROD活性增加,而荨麻显著抑制了这些增加。逆转录聚合酶链反应(RT-PCR)分析清楚地表明,MC处理后肝脏CYP1A1和CYP1A2 mRNA水平显著增加,而荨麻补充剂抑制了这种增加。蛋白质印迹研究也支持了在催化活性和mRNA水平上观察到的变化。总之,荨麻使CYP1A1和CYP1A2表达水平及相关活性大幅降低,这可能与荨麻潜在的化学保护能力有关,因为预计通过调节CYP1A酶可减少环境化学致癌物的活化。

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