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天然存在的酚酸对大鼠谷胱甘肽S-转移酶同工酶表达的影响。

Effect of naturally occurring phenolic acids on the expression of glutathione S-transferase isozymes in the rat.

作者信息

Krajka-Kuźniak Violetta, Kaczmarek Jolanta, Baer-Dubowska Wanda

机构信息

Department of Pharmaceutical Biochemistry, University of Medical Sciences, Poznań, Poland.

出版信息

Food Chem Toxicol. 2008 Mar;46(3):1097-102. doi: 10.1016/j.fct.2007.11.004. Epub 2007 Nov 19.

DOI:10.1016/j.fct.2007.11.004
PMID:18155342
Abstract

Naturally occurring plant phenols, protocatechuic and tannic acids, have been reported to be inhibitors of chemical mutagenesis and carcinogenesis in experimental models. Our previous studies, have shown that these compounds modulate the activity of phases 1 and 2 enzymes in rodents. The aim of the present study was to investigate whether these compounds affect protein levels of rat hepatic and renal glutathione S-transferase (GST) isozymes. Male Wistar rats were treated intraperitoneally with protocatechuic or tannic acid at 50 mg/kg body weight five times during 14 days. 3-Methylcholanthrene (MC) was administered at 20 mg/kg body weight on day 13 (the last treatment with phenolic compounds) and on day 14. Tissues were obtained from rats terminated 24 h after the last treatment. Western blot analysis with specific antibodies showed significant differences in the effect of the phenolic compounds in the liver and kidney. In the liver, protocatechuic acid significantly increased the constitutive GSTmicro, while tannic acid reduced the GSTalpha protein level by 60%. Both plant phenols decreased all classes of constitutive GST isozymes in the kidney including GSTpi, and also the MC-induced GSTalpha and/or pi protein levels. These results, as well as our previous reports, suggest that protocatechuic and tannic acids interfere with the pathways related to xenobiotic toxicities and carcinogenesis. This effect may be important for chemoprotective activity of these plant phenols.

摘要

据报道,天然存在的植物酚类,如原儿茶酸和单宁酸,在实验模型中是化学诱变和致癌作用的抑制剂。我们之前的研究表明,这些化合物可调节啮齿动物中1期和2期酶的活性。本研究的目的是调查这些化合物是否会影响大鼠肝脏和肾脏中谷胱甘肽S-转移酶(GST)同工酶的蛋白质水平。雄性Wistar大鼠在14天内以50 mg/kg体重腹腔注射原儿茶酸或单宁酸,共5次。在第13天(最后一次酚类化合物处理)和第14天,以20 mg/kg体重给予3-甲基胆蒽(MC)。在最后一次处理后24小时处死大鼠并获取组织。用特异性抗体进行的蛋白质免疫印迹分析表明,酚类化合物对肝脏和肾脏的影响存在显著差异。在肝脏中,原儿茶酸显著增加了组成型GSTμ,而单宁酸使GSTα蛋白水平降低了60%。两种植物酚都降低了肾脏中所有组成型GST同工酶的水平,包括GSTπ,以及MC诱导的GSTα和/或π蛋白水平。这些结果以及我们之前的报告表明,原儿茶酸和单宁酸会干扰与外源性毒性和致癌作用相关的途径。这种作用可能对这些植物酚的化学保护活性很重要。

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