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原小檗碱和别隐品碱的生物转化和组织分布及罂粟总生物碱对肝药物代谢酶的影响。

Biotransformation and tissue distribution of protopine and allocryptopine and effects of Plume Poppy Total Alkaloid on liver drug-metabolizing enzymes.

机构信息

National and Local Union Engineering Research Center for the Veterinary Herbal Medicine Resources and Initiative, Hunan Agricultural University, Changsha, 410128, China.

Hunan Engineering Research Center of Veterinary Drug, College of Veterinary Medicine, Hunan Agricultural University, Changsha, 410128, China.

出版信息

Sci Rep. 2018 Jan 11;8(1):537. doi: 10.1038/s41598-017-18816-7.

Abstract

In this study, the biotransformation in the plasma, urine and feces of rats following oral administration of protopine (PRO) and allocryptopine (ALL)were explored using HPLC-QqTOF MS. An HPLC-MS/MS method for the determination of tissues was developed and applied to the tissue distribution study in rats following intragastric administration of Plume Poppy Total Alkaloid for 3 weeks. A total of ten PRO metabolites and ten ALL metabolites were characterized in rats in vivo. Among these metabolites, six PRO metabolites and five ALL metabolites were reported for the first time. The predicated metabolic pathways including ring cleavage, demethylation following ring cleavage, and glucuronidation were proposed. The low-concentration residue of PRO and ALL in various tissues was detected at 24 h and 48 h after dosing, which indicated that both compounds could be widely distributed in tissues and exist as low levels of residue. The activities of erythromycin N-demethylase, aminopyrine N-demethylase and NAD (P)H quinone oxidoreductase in female rats can be induced post-dose, but these activities were inhibited in male rats. The proposed biotransformation and residues of PRO and ALL and their effects on enzymes may provide a basis for clarifying the metabolism and interpreting pharmacokinetics.

摘要

本研究采用 HPLC-QqTOF MS 研究了大鼠口服原阿片碱(PRO)和别隐品碱(ALL)后血浆、尿液和粪便中的生物转化。建立了一种测定组织中 PRO 和 ALL 的 HPLC-MS/MS 方法,并应用于灌胃给予罂粟总碱 3 周后大鼠的组织分布研究。在大鼠体内共鉴定出 10 种 PRO 代谢物和 10 种 ALL 代谢物。其中,有 6 种 PRO 代谢物和 5 种 ALL 代谢物为首次报道。预测的代谢途径包括环裂解、环裂解后的去甲基化和葡萄糖醛酸化。给药后 24 和 48 小时,在各种组织中检测到 PRO 和 ALL 的低浓度残留,表明这两种化合物可以广泛分布在组织中,并以低水平的残留存在。雌鼠给药后可诱导红霉素 N-去甲基酶、氨基比林 N-去甲基酶和 NAD(P)H 醌氧化还原酶的活性,但这些活性在雄鼠中受到抑制。PRO 和 ALL 的拟议生物转化和残留及其对酶的影响可能为阐明代谢和解释药代动力学提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/99c6/5765031/d652e8062563/41598_2017_18816_Fig1_HTML.jpg

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