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胡芦巴对细胞色素P450 2D6和细胞色素P450 3A4代谢活性的影响。

Effect of Trigonella foenum-graecum L. on Metabolic Activity of CYP2D6 and CYP3A4.

作者信息

Al-Jenoobi Fahad I, Al-Thukair Areej A, Alam Mohd Aftab, Abbas Fawkeya A, Al-Mohizea Abdullah M, Alkharfy Khalid M, Al-Suwayeh Saleh A

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, Riyadh, Saudi Arabia.

出版信息

Forsch Komplementmed. 2015;22(3):180-4. doi: 10.1159/000432412. Epub 2015 Jun 22.

Abstract

BACKGROUND

The present study investigated the effect of fenugreek seeds powder and its alcoholic extract on metabolic activity of drug-metabolizing enzymes CYP2D6 and CYP3A4.

MATERIALS AND METHODS

Dextromethorphan (DEX) was used as a probe for measuring metabolic activity, based on its CYP2D6- and CYP3A4-mediated metabolism to dextrorphan (DOR) and 3-methoxymorphinan (3-MM), respectively. For the in vitro investigations, DEX (25µM) was incubated with human liver microsomes and NADPH and tested with and without the fenugreek extract. For the in vivo study, phase I, 6 subjects received a single dose of DEX (30 mg); in phase II, after washout period, the fenugreek seeds powder was administered for 1 week and DEX was administered with its last dose.

RESULTS

In vitro, fenugreek extract inhibits CYP2D6-mediated O-demethylation of DEX. Higher concentrations (50 and 100µg/ml) of extract inhibit CYP2D6 and CYP3A4 activity. In vivo results indicated that fenugreek does not significantly inhibit CYP2D6 and CYP3A4 metabolic activity. There was no significant change in the levels of DEX metabolites (DOR 12% and 3-MM 9%) excreted in urine and their urine metabolic ratios (P values: 0.257 and 0.333 DEX/DOR and DEX/3-MM, respectively).

CONCLUSION

In vitro and in vivo observations suggested that fenugreek may not have substantial effect on the metabolic activity of CYP2D6 and CYP3A4.

摘要

背景

本研究调查了胡芦巴种子粉及其乙醇提取物对药物代谢酶CYP2D6和CYP3A4代谢活性的影响。

材料与方法

右美沙芬(DEX)分别基于其由CYP2D6和CYP3A4介导代谢为右啡烷(DOR)和3-甲氧基吗啡喃(3-MM),用作测量代谢活性的探针。对于体外研究,将DEX(25µM)与人肝微粒体和NADPH一起孵育,并在有和没有胡芦巴提取物的情况下进行测试。对于体内研究,第一阶段,6名受试者接受单剂量DEX(30mg);在第二阶段,在洗脱期后,给予胡芦巴种子粉1周,并在最后一剂时给予DEX。

结果

在体外,胡芦巴提取物抑制DEX的CYP2D6介导的O-去甲基化。较高浓度(50和100µg/ml)的提取物抑制CYP2D6和CYP3A4活性。体内结果表明,胡芦巴不会显著抑制CYP2D6和CYP3A4的代谢活性。尿液中排泄的DEX代谢物(DOR为12%,3-MM为9%)水平及其尿液代谢比率没有显著变化(P值:DEX/DOR和DEX/3-MM分别为0.257和0.333)。

结论

体外和体内观察结果表明,胡芦巴可能对CYP2D6和CYP3A4的代谢活性没有实质性影响。

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