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首页> 外文期刊>Phytotherapy research: PTR >Biotransformation of Glucoaurantio-Obtusin Towards Aurantio-Obtusin Increases the Toxicity of Irinotecan Through Increased Inhibition Towards SN-38 Glucuronidation
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Biotransformation of Glucoaurantio-Obtusin Towards Aurantio-Obtusin Increases the Toxicity of Irinotecan Through Increased Inhibition Towards SN-38 Glucuronidation

机译:葡糖苷-奥布他汀向金葡菌素的生物转化通过对SN-38葡萄糖醛酸化的抑制作用增强而增加了伊立替康的毒性。

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The present study aims to investigate the influence of irinotecan's toxicity by the biotransformation of glucoaurantio-obtusin to aurantio-obtusin. Intraperitoneal administration (i.p.) of 100 mg/kg aurantio-obtusin significantly increased the toxicity of irinotecan, but the i.p. administration of 100 mg/kg glucoaurantio-obtusin showed negligible influence towards irinotecan's toxicity. Furthermore, the mechanism was explained through determining the inhibition potential of glucoaurantio-obtusin and aurantio-obtusin towards the glucuronidation metabolism of SN-38 that has been regarded to be the major active product responsible for the toxicity of irinotecan. The results showed that aurantio-obtusin exhibited strong competitive inhibition towards the glucuronidation of SN-38, but negligible inhibition potential of glucoaurantio-obtusin towards SN-38 glucuronidation was observed. These results showed that biotransformation of glucoaurantio-obtusin towards aurantio-obtusin increased the toxicity of irinotecan through increased inhibition of SN-38 glucuronidation.
机译:本研究旨在研究伊立替康的毒性通过葡萄糖金-ob素生物转化为金ur-ob素的影响。腹膜内(i.p.)100 mg / kg的aurantio-obtusin显着增加了伊立替康的毒性,但i.p.给予100 mg / kg的葡糖尿嘧啶-obtusin对伊立替康的毒性影响可忽略不计。此外,通过确定葡糖酸-金葡糖苷和金葡糖苷对SN-38的葡糖醛酸化代谢的抑制潜力来解释了该机理,SN-38被认为是造成伊立替康毒性的主要活性产物。结果表明,aurantio-obtusin对SN-38的葡萄糖醛酸化具有很强的竞争抑制作用,但对SN-38 lucuronidation的葡萄糖金-obtusin抑制作用却可以忽略不计。这些结果表明,通过增加对SN-38葡糖醛酸化的抑制作用,葡糖金--- in素向金ur-ob素的生物转化增加了伊立替康的毒性。

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