Albert P. Li

Transporters and Drug-Metabolizing Enzymes in Drug Toxicity


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contribution to drug toxicity. The intent of this chapter is to emphasize the importance of the incorporation of mechanistic studies, at least starting with understanding the role of metabolism and transport in drug toxicity, to hopefully enhance the accuracy of human drug safety evaluation before the exposure of a new drug to the patient population.

      3.2.1 Drug Metabolism and Toxicity

      APAP represents a prototypical protoxicant in which metabolic activation is a key mechanism of its hepatotoxicity. Its metabolic activation pathways have been extensively evaluated in both human in vitro systems as well as in vivo in laboratory animals. The generally accepted metabolic activation scheme is that APAP undergoes oxidative metabolism by P450 to N‐acetyl‐p‐benzoquinone imine (NAPQI) which is a highly reactive metabolite that is either detoxified via glutathione (GSH) conjugation or undergoes covalent binding with cellular macromolecules, leading to hepatocellular necrosis. Inflammatory response elicited by cellular injuries and the subsequent Increased oxygen/nitrogen stress mediated by Kupffer cell activation [23] and recruitment of neutrophils [24] may also be involved in APAP hepatotoxicity.

      In vitro studies using recombinant human P450 isoforms show that, in comparison to the other human P450 isoforms (CYP1A2, CYP2E1, and CYP2D6), CYP3A4 is the most effective in the metabolism of APAP to NAPQI, with Km equal to plasma drug concentration at therapeutic doses [25]. The association of alcohol consumption with APAP hepatotoxicity has led to the postulation that alcohol enhancement of CYP2E1 activity via increased gene expression [26] and/or enzyme stabilization [27], may be responsible for the increased toxicity [28, 29]. An alternative explanation is that APAP is metabolically activated by CYP3A4 while alcohol consumption depletion of cellular GSH [30–32], leading to compromised detoxification of NAPQI and thereby enhanced toxicity.

      3.2.2 Transporters and Toxicity

      3.2.3 Risk Factors

      As APAP is metabolically activated by the inducible P450 isoforms, especially CYP1A2 and CYP3A4, to NAPQI which in turn is detoxified by GSH conjugation, genetic or environmental factors leading to increased CYP3A4 activity and depletion of hepatocellular GSH concentration are likely risk factors of its hepatotoxicity [38]. Omeprazole induction of CYP1A2 in CYP2C19 poor metabolizers have been postulated to be a risk factor of APAP toxicity [39]. Induction of CYP3A4 as a risk factor has been substantiated in a clinical study where a patient coadministered with phenytoin, a CYP3A4 inducer, experienced APAP hepatotoxicity at therapeutic doses [40, 41]. There is also evidence that concurrent inflammatory events may enhance APAP toxicity, suggesting that bacterial or viral infection may be risk factors [23, 42, 43]. As efflux transporters may have protective roles toward APAP toxicity, environmental and genetic factors leading to compromised efflux transporter activities may also be risk factors.

      Life style risk factors for APAP toxicity include obesity [44] and chronic alcohol consumption [18, 45, 46]. It is interesting to note that alcohol consumption has been reported to lead to GSH depletion in human subjects [47], thereby supporting GSH as a key risk factor for APAP toxicity.

      Cerivastatin belongs to a class of 3‐hydroxy‐3‐methylglutaryl coenzyme A (HMG‐CoA) reductase inhibitors commonly known as statins. Statins are one of the most prescribed drugs indicated for the lowering of plasma cholesterol. Cerivastatin was introduced by Bayer into the U.S. market in June 1997 and was withdrawn in August 2001 due to 31 deaths due to rhabdomyolysis [48–53]. Cerivastatin was introduced to compete with an existing statin, atorvastatin. Statins are commonly coadministered with fibrates for the treatment of patients with mixed hyperlipidemia [54]. Pharmacokinetic drug interactions between cerivastatin and fibrates, leading to elevated plasma levels of cerivastatin, is believed to be the major cause of rhabdomyolysis.

      3.3.1 Drug Metabolism and Toxicity

      Rhabdomyolysis is also observed in patients administered cerivastatin alone. Association of CYP2C8 genetic polymorphism and cerivastatin toxicity, however, is not as definitive as that observed with fibrate inhibition of CYP2C8 activity [61]. Patients with rhabdomyolysis administered only cerivastatin and not coadministered with fibrate have been found to have a higher frequency of CYP2C8 polymorphic genes [62], leading to CYP2C8 activity both higher and lower than that for wildtype. Genetic polymorphism leading to lower CYP2C8 activity would lead to slower hepatic clearance, resulting in higher cerivastatin activity, thereby enhancing the likelihood of rhabdomyolysis. Higher CYP2C8 activity should lead to lower plasma cerivastatin concentrations and therefore would not lead to toxicity. It is possible that for these patients, the role of uptake transporter plays a greater role in hepatic clearance than CYP2C8 (see below).

      3.3.2 Transporter and Toxicity

      Cerivastatin is one of the drugs where toxicity can be a function of both drug metabolism and transport. Besides being a CYP2C8 inhibitor, Gemfibrozil and its glucuronide are inhibitors of cerivastatin uptake by the organic anion transporting polypeptide 2 (OATP2/OATP1B1:SLC21A6) [58, 63]. Inhibition of transporter‐mediated uptake of cerivastatin into hepatocytes leads to lower hepatic metabolic clearance. Physiologically based pharmacokinetic (PBPK) models have been developed to evaluate the complex interaction between cerivastatin and gemfibrozil, taking into account the inhibitory effects of gemfibrozil on cerivastatin