Why the study?
Does Ginkgo biloba extract alter the pharmacokinetics and metabolism of clopidogrel in rats?
Does Ginkgo biloba extract alter the pharmacokinetics and metabolism of clopidogrel in rats?
Ginkgo biloba extract alters the pharmacokinetics of clopidogrel in rats, highlighting a potential herb-drug interaction that warrants clinical awareness.
GBE may enhance clopidogrel activation in rat microsomes; hypothesis-generating for herb-drug interactions, clinical studies needed.
Ginkgo biloba extract (GBE), a traditional herbal product used worldwide as both medicine and supplement, is often supplied with clopidogrel for the treatment of cerebrovascular diseases. The aim of the current study was to explore the effect of GBE on the metabolism and pharmacokinetics of clopidogrel. The in vitro study using rat liver microsomes revealed that GBE significantly induced the conversion of clopidogrel into its active metabolite. The effect of GBE on the pharmacokinetics of clopidogrel was also investigated in vivo . Compared to rats without GBE pretreatment, administration of 4 mg/kg, 20 mg/kg, and 100 mg/kg of GBE significantly decreased the C max and the AUC 0–∞ of clopidogrel in a dose‐dependent manner. As expected, pretreatment of high dose GBE significantly increased the C max and AUC 0–∞ of the clopidogrel active metabolite. However, no marked change was observed following medium and low dose of GBE, suggesting that the biotransformation of clopidogrel was altered differently by high dose of GBE. Our study suggested that the awareness of the potential herb–drug interactions between GBE and clopidogrel should be increased in clinical practice.
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Deng et al. (2016) studied this question.
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