TY - JOUR T1 - In Vitro Metabolism of Isoline, a Pyrrolizidine Alkaloid from <em>Ligularia duciformis</em>, by Rodent Liver Microsomal Esterase and Enhanced Hepatotoxicity by Esterase Inhibitors JF - Drug Metabolism and Disposition JO - Drug Metab Dispos SP - 1832 LP - 1839 DO - 10.1124/dmd.107.016311 VL - 35 IS - 10 AU - Jun Tang AU - Teruaki Akao AU - Norio Nakamura AU - Zheng-Tao Wang AU - Kiyoshi Takagawa AU - Masakiyo Sasahara AU - Masao Hattori Y1 - 2007/10/01 UR - http://dmd.aspetjournals.org/content/35/10/1832.abstract N2 - Isoline, a major retronecine-type pyrrolizidine alkaloid (PA) from the Chinese medicinal herb Ligularia duciformis, was suggested to be the most toxic known PA. Its in vitro metabolism was thus examined in rat and mouse liver microsomes, and its toxicity was compared with that of clivorine and monocrotaline after i.p. injection in mice. Isoline was more rapidly metabolized by both microsomes than clivorine and monocrotaline and converted to two polar metabolites M1 and M2, which were spectroscopically determined to be bisline (a deacetylated metabolite of isoline) and bisline lactone, respectively. Both metabolites were formed in the presence or absence of an NADPH-generating system with liver microsomes but not cytosol. Their formation was completely inhibited by the esterase inhibitors, triorthocresyl phosphate (TOCP) and phenylmethylsulfonyl fluoride, but not at all or partially by cytochrome P450 (P450) inhibitors, α-naphthoflavone and proadifen (SKF 525A), respectively. These results demonstrated that both metabolites were produced by microsomal esterase(s) but not P450 isozymes. The esterase(s) involved showed not only quite different activities but also responses to different inhibitors in rat and mouse liver microsomes, suggesting that different key isozyme(s) or combinations might be responsible for the deacetylation of isoline. Isoline injected i.p. into mice induced liver-specific toxicity that was much greater than that with either clivorine or monocrotaline, as judged by histopathology as well as serum alanine aminotransferase and aspartate aminotransferase levels. Isoline-induced hepatotoxicity was remarkably enhanced by the esterase inhibitor TOCP but was reduced by the P450 inhibitor SKF 525A, indicating that rodent hepatic esterase(s) played a principal role in the detoxification of isoline via rapid deacetylation in vivo. The American Society for Pharmacology and Experimental Therapeutics ER -