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用大麻二酚预处理成年雌性大鼠后对其肝脏微粒体药物代谢酶活性的抑制作用。

Suppression of liver microsomal drug-metabolizing enzyme activities in adult female rats pretreated with cannabidiol.

作者信息

Narimatsu S, Watanabe K, Matsunaga T, Yamamoto I, Imaoka S, Funae Y, Yoshimura H

机构信息

Department of Hygienic Chemistry, Faculty of Pharmaceutical Sciences, Hokuriku University, Kanazawa, Japan.

出版信息

Biol Pharm Bull. 1993 Apr;16(4):428-30. doi: 10.1248/bpb.16.428.

Abstract

The suppression by cannabidiol (CBD) of the liver microsomal drug-metabolizing enzyme activities in female rats was demonstrated and its mechanism was examined. Pretreatment of rats with CBD (10 mg/kg, i.p.) caused temporary decreases in contents of cytochrome P450 (P450) and b5 and NADPH-cytochrome c (P450) reductase activity compared with values from the vehicle control group. p-Nitroanisole O-demethylase, aniline hydroxylase, d-benzphetamine N-demethylase and delta 9-tetrahydrocannabinol 11-hydroxylase were also decreased by the CBD pretreatment. The latter two activities took a longer time to return to control levels than the former two. However, the CBD pretreatment, which reduced the protein level of P450 UT-2 (CYP2C11) in adult male rats, did not decrease the protein level of P450 F-1 (CYP2C6) or F-2 (CYP2C12) in liver microsomes from female rats. These results suggest that the mechanisms by which CBD suppresses liver microsomal drug-metabolizing enzyme activities are different in male and female rats.

摘要

已证实大麻二酚(CBD)对雌性大鼠肝脏微粒体药物代谢酶活性有抑制作用,并对其机制进行了研究。与溶剂对照组相比,用CBD(10mg/kg,腹腔注射)预处理大鼠会导致细胞色素P450(P450)、b5含量以及NADPH-细胞色素c(P450)还原酶活性暂时降低。对硝基苯甲醚O-脱甲基酶、苯胺羟化酶、d-苄非他明N-脱甲基酶和δ9-四氢大麻酚11-羟化酶也因CBD预处理而降低。后两种酶活性恢复到对照水平所需的时间比前两种酶更长。然而,降低成年雄性大鼠肝脏微粒体中P450 UT-2(CYP2C11)蛋白水平的CBD预处理,并未降低雌性大鼠肝脏微粒体中P450 F-1(CYP2C6)或F-2(CYP2C12)的蛋白水平。这些结果表明,CBD抑制肝脏微粒体药物代谢酶活性的机制在雄性和雌性大鼠中有所不同。

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