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荷叶生物碱组分能强烈抑制CYP2D6同工酶活性。

Lotus leaf alkaloid fraction can strongly inhibit CYP2D6 isoenzyme activity.

作者信息

Ye Lin-Hu, Kong Ling-Ti, Yan Ming-Zhu, Cao Fang-Rui, Wang Li-Sha, Liao Yong-Hong, Pan Rui-Le, Chang Qi

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100193, China; Department of Pharmacy, The First People's Hospital of Bijie, Bijie 551700, China.

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100193, China.

出版信息

J Ethnopharmacol. 2016 Dec 24;194:913-917. doi: 10.1016/j.jep.2016.10.055. Epub 2016 Oct 19.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

The Chinese herbal medicine He-Ye, the leaves of the lotus (Nelumbo nucifera) plant, is traditionally used in China for the treatment of sunstroke, thirst, diarrhea, and fever. Currently, the leaf is used not only as an herbal tea to reduce lipid level and control body weight, but also as a major ingredient in some lipid-lowering Chinese patented medicines. Our previous study demonstrated that the alkaloid fraction (AF) of the herb has a strong inhibitory effect on CYP2D6 isoenzyme activity in vitro. The present study aims to further verify this activity using the in vivo rat model and to explore the inhibitory mechanism on CYP2D6 using human liver microsomes (HLMs).

MATERIALS AND METHODS

After a continuous 7-d oral dose of AF (50mg/kg) or a vehicle, Sprague Dawley rats received a single intravenous dose of dextromethorphan or metoprolol. Blood samples were collected at various time points, and the plasma concentrations of the relevant metabolites dextrorphan and hydroxymetoprolol were assayed by LC-MS/MS for evaluating the effect of AF on their pharmacokinetics and CYP2D6 activity. Dextromethorphan as a probe at different concentrations was incubated with HLMs in an incubation buffer system, in the presence or absence of AF at different concentrations. After incubation, the produced metabolite was assayed.

RESULTS

After being pretreated with AF in rats, the plasma concentrations of dextrorphan and hydroxymetoprolol significantly decreased, with C going from 79.44 to 29.96 and 151.18 to 83.39hng/mL (P<0.05), AUC from 167.27 to 62.25 and 347.68 to 223.24hng/mL (P<0.05), and AUC from 183.39 to 84.76 and 350.59 to 234.57hng/mL (P<0.05), respectively, in comparison with those of untreated rats. The t of hydroxymetoprolol significantly increased from 1.14 to 1.99h (P<0.05). The in vitro incubation test showed that AF competitively inhibited the CYP2D6, with apparent K value of 0.64µg/mL.

CONCLUSIONS

AF can strongly inhibit the activity of CYP2D6 enzyme, as confirmed by in vivo and in vitro models. Possible drug interactions may occur between AF and other medications metabolized by CYP2D6. Thus, caution should be paid when the lotus leaf and its preparations are concurrently administered with conventional medicines.

摘要

民族药理学相关性

中药荷叶,即莲(Nelumbo nucifera)的叶子,在中国传统上用于治疗中暑、口渴、腹泻和发热。目前,荷叶不仅用作草药茶以降低血脂水平和控制体重,还作为一些降脂中成药的主要成分。我们之前的研究表明,该草药的生物碱组分(AF)在体外对CYP2D6同工酶活性具有强烈抑制作用。本研究旨在使用体内大鼠模型进一步验证该活性,并使用人肝微粒体(HLM)探索对CYP2D6的抑制机制。

材料与方法

连续7天口服AF(50mg/kg)或赋形剂后,Sprague Dawley大鼠接受单次静脉注射右美沙芬或美托洛尔。在不同时间点采集血样,通过LC-MS/MS测定相关代谢物右啡烷和羟基美托洛尔的血浆浓度,以评估AF对其药代动力学和CYP2D6活性的影响。在孵育缓冲系统中,将不同浓度的右美沙芬作为探针与HLM一起孵育,存在或不存在不同浓度的AF。孵育后,测定产生的代谢物。

结果

大鼠经AF预处理后,右啡烷和羟基美托洛尔的血浆浓度显著降低,C分别从79.44降至29.96以及从151.18降至83.39hng/mL(P<0.05),AUC分别从167.27降至62.25以及从347.68降至223.24hng/mL(P<0.05),以及从183.39降至84.76以及从350.59降至234.57hng/mL(P<0.05),与未处理的大鼠相比。羟基美托洛尔的t从1.14显著增加至1.99h(P<0.05)。体外孵育试验表明,AF竞争性抑制CYP2D6,表观K值为0.64µg/mL。

结论

体内和体外模型均证实,AF可强烈抑制CYP2D6酶的活性。AF与其他经CYP2D6代谢的药物之间可能发生药物相互作用。因此,当荷叶及其制剂与传统药物同时给药时应谨慎。

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