Zoheir A Damanhouri
King Abdulaziz University, KSA
Title: Herbal drug interaction and its implication: inhibitory effect of Nigella sativa on human CYP3A4, CYP3A5, CYP2C9 and CYP3A7
Biography
Biography: Zoheir A Damanhouri
Abstract
Nigella sativa (N. sativa) (Family Ranunculaceae) is a widely used medicinal plant throughout the world especially in Asia, Africa and many Middle Eastern countries. It is considered as one of the greatest forms of healing medicine. Extensive studies on N.sativa seeds have shown its potential pharmacological and therapeutic effects including antidiabetic, antihypertensive, diuretic, digestive, anticancer, antioxidant, analgesic, immunomodulator, antimicrobial, anti-inflammatory, spasmolytic, gastroprotective, hepatoprotective effects etc. However, there has been much concerned about herbal-drug interactions due to the increasingly reported adverse drug effects and poisoning associated with the use of herbal medicine. The effect of N. sativa extract on hepatic drug metabolism in the rat was investigated in our laboratory. Both in vivo and in vitro experiments were employed to investigate the possibility of induction and inhibition effects on drug metabolism. Acute dosing (0.56g/Kg) with N. sativa extract to rats caused a significant increase in plasma level of dicoumarol. In vitro studies assessed in 10,000 xg liver homogenates from treated animals showed a significant decrease in benzphetamine N-demythelation, dicoumarol oxidation and ethoxycoumarin O-deethylation activities compared to liver homogenates from control animals. In addition, N. sativa extracts was tested in vitro for its possible inhibitory effect on cDNA-expressed human cytochrome P450 3A4, 3A5, 2C9 and 3A7-mediated metabolism of marker substrates. The present study investigates and throws light on the possible interactions of N. sativa with conventional drugs.