Effect of Garden Cress Seeds Powder and Its Alcoholic Extract on the Metabolic Activity of CYP2D6 and CYP3A4

被引:5
作者
Al-Jenoobi, Fahad I. [1 ]
Al-Thukair, Areej A. [1 ]
Alam, Mohd Aftab [1 ]
Abbas, Fawkeya A. [2 ]
Al-Mohizea, Abdullah M. [1 ]
Alkharfy, Khalid M. [3 ]
Al-Suwayeh, Saleh A. [1 ]
机构
[1] King Saud Univ, Dept Pharmaceut, Coll Pharm, Riyadh 11451, Saudi Arabia
[2] King Saud Univ, Dept Pharmacognosy, Coll Pharm, Riyadh 11451, Saudi Arabia
[3] King Saud Univ, Dept Clin Pharm, Coll Pharm, Riyadh 11451, Saudi Arabia
关键词
HERB-DRUG INTERACTIONS; LEPIDIUM-SATIVUM; IN-VIVO; CYTOCHROME-P450; 3A4; DEXTROMETHORPHAN; MEDICINES; PROBE; PHARMACOKINETICS; URINE; VITRO;
D O I
10.1155/2014/634592
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
The powder and alcoholic extract of dried seeds of garden cress were investigated for their effect on metabolic activity of CYP2D6 and CYP3A4 enzymes. In vitro and clinical studies were conducted on human liver microsomes and healthy human subjects, respectively. Dextromethorphan was used as a common marker for measuring metabolic activity of CYP2D6 and CYP3A4 enzymes. In in vitro studies, microsomes were incubated with NADPH in presence and absence of different concentrations of seeds extract. Clinical investigations were performed in two phases. In phase I, six healthy female volunteers were administered a single dose of dextromethorphan and in phase II volunteers were treated with seeds powder for seven days and dextromethorphan was administered with last dose. The O-demethylated and N-demethylated metabolites of dextromethorphan were measured as dextrorphan (DOR) and 3-methoxymorphinan (3-MM), respectively. Observations suggested that garden cress inhibits the formation of DOR and 3-MM metabolites. This inhibition of metabolite level was attributed to the inhibition of CYP2D6 and CYP3A4 activity. Garden cress decreases the level of DOR and 3-MM in urine and significantly increases the urinary metabolic ratio of DEX/DOR and DEX/3-MM. The findings suggested that garden cress seeds powder and ethanolic extract have the potential to interact with CYP2D6 and CYP3A4 substrates.
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页数:6
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