Role of Metabolism in Drug-Induced Idiosyncratic Hepatotoxicity
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[1] B. K. Park,et al. An investigation into the formation of stable, protein-reactive and cytotoxic metabolites from tacrine in vitro. Studies with human and rat liver microsomes. , 1993, Biochemical pharmacology.
[2] E. Eger,et al. Biotransformation of Halothane, Enflurane, Isoflurane, and Desflurane to Trifluoroacetylated Liver Proteins: Association Between Protein Acylation and Hepatic Injury , 1997, Anesthesia and analgesia.
[3] P. Beaune,et al. Anti-liver endoplasmic reticulum autoantibodies are directed against human cytochrome P-450IA2. A specific marker of dihydralazine-induced hepatitis. , 1990, The Journal of clinical investigation.
[4] D. Hill,et al. Microsomal metabolism of triazenylimidazoles. , 1975, Cancer research.
[5] M. D. Faiman,et al. In vitro and in vivo inhibition of rat liver aldehyde dehydrogenase by S-methyl N,N-diethylthiolcarbamate sulfoxide, a new metabolite of disulfiram. , 1992, Biochemical pharmacology.
[6] M. D. Faiman,et al. Identification of the human P-450 enzymes responsible for the sulfoxidation and thiono-oxidation of diethyldithiocarbamate methyl ester: role of P-450 enzymes in disulfiram bioactivation. , 1998, Alcoholism, clinical and experimental research.
[7] E. Coccaro,et al. An open trial of sertraline in personality disordered patients with impulsive aggression. , 1994, The Journal of clinical psychiatry.
[8] N. Abuaf,et al. A new antimitochondria antibody (anti-M6) in iproniazid-induced hepatitis. , 1982, Clinical and experimental immunology.
[9] F. Ballet,et al. Hepatotoxicity in drug development: detection, significance and solutions. , 1997, Journal of hepatology.
[10] S. Spielberg,et al. Anticonvulsant hypersensitivity syndrome. In vitro assessment of risk. , 1988, The Journal of clinical investigation.
[11] J. Uetrecht,et al. Prediction of a new drug's potential to cause idiosyncratic reactions. , 2001, Current opinion in drug discovery & development.
[12] J Leclaire,et al. In vitro metabolism of isaxonine phosphate: formation of two metabolites, 5-hydroxyisaxonine and 2-aminopyrimidine, and covalent binding to microsomal proteins. , 1992, European journal of pharmacology.
[13] G. Ellestad,et al. Calicheamicin gamma 1I: an antitumor antibiotic that cleaves double-stranded DNA site specifically. , 1988, Science.
[14] M. Cuthbert. Section 4 Adverse reactions to non-steroidal antirheumatic drugs , 1974 .
[15] D. Pessayre,et al. Inhibition of mitochondrial beta-oxidation as a mechanism of hepatotoxicity. , 1995, Pharmacology & therapeutics.
[16] D. Kupfer,et al. Cytochrome P-450-mediated activation and irreversible binding of the antiestrogen tamoxifen to proteins in rat and human liver: possible involvement of flavin-containing monooxygenases in tamoxifen activation. , 1991, Cancer research.
[17] M. Braun,et al. Characterization of rat and human UDP-glucuronosyltransferases responsible for the in vitro glucuronidation of diclofenac. , 2001, Toxicological sciences : an official journal of the Society of Toxicology.
[18] U. Boelsterli. Xenobiotic acyl glucuronides and acyl CoA thioesters as protein-reactive metabolites with the potential to cause idiosyncratic drug reactions. , 2002, Current drug metabolism.
[19] J. Uetrecht,et al. Detection of 2-hydroxyiminostilbene in the urine of patients taking carbamazepine and its oxidation to a reactive iminoquinone intermediate. , 1999, The Journal of pharmacology and experimental therapeutics.
[20] S. Lytton,et al. Expression of autoantibodies to specific cytochromes P450 in a case of disulfiram hepatitis. , 1998, Journal of hepatology.
[21] M Pirmohamed,et al. Role of drug disposition in drug hypersensitivity: a chemical, molecular, and clinical perspective. , 1998, Chemical research in toxicology.
[22] H. Bolt,et al. Implication of rifampicin-quinone in the irreversible binding of rifampicin to macromolecules. , 1976, Xenobiotica; the fate of foreign compounds in biological systems.
[23] J. Timbrell,et al. Isoniazid and iproniazid: activation of metabolites to toxic intermediates in man and rat. , 1976, Science.
[24] D. Pessayre,et al. Toxicity of alpidem, a peripheral benzodiazepine receptor ligand, but not zolpidem, in rat hepatocytes: role of mitochondrial permeability transition and metabolic activation. , 2001, The Journal of pharmacology and experimental therapeutics.
[25] Y. Masubuchi,et al. Differential selectivity in carbamazepine-induced inactivation of cytochrome P450 enzymes in rat and human liver , 2001, Archives of Toxicology.
[26] M. Horning,et al. Metabolism of carbamazepine. , 1982, Drug metabolism and disposition: the biological fate of chemicals.
[27] T. Tada,et al. High Incidence of Peliosis Hepatis in Autopsy Cases of Aplastic Anemia With Special Reference to Anabolic Steroid Therapy , 1984, Acta pathologica japonica.
[28] E. Levine,et al. Fialuridine and its metabolites inhibit DNA polymerase gamma at sites of multiple adjacent analog incorporation, decrease mtDNA abundance, and cause mitochondrial structural defects in cultured hepatoblasts. , 1996, Proceedings of the National Academy of Sciences of the United States of America.
[29] W. Tang,et al. Fluorinated analogues as mechanistic probes in valproic acid hepatotoxicity: hepatic microvesicular steatosis and glutathione status. , 1995, Chemical research in toxicology.
[30] A. Israeli,et al. Cholestatic jaundice, an unusual side effect of etretinate. , 1985, Journal of the American Academy of Dermatology.
[31] W. Trager,et al. Bioactivation and irreversible binding of the cognition activator tacrine using human and rat liver microsomal preparations. Species difference. , 1993, Drug metabolism and disposition: the biological fate of chemicals.
[32] S. Dehal,et al. Evidence that the catechol 3,4-Dihydroxytamoxifen is a proximate intermediate to the reactive species binding covalently to proteins. , 1996, Cancer research.
[33] K. Tolman,et al. Hepatotoxicity of non-narcotic analgesics. , 1998, The American journal of medicine.
[34] F. Dreifuss,et al. Valproic acid hepatic fatalities , 1987, Neurology.
[35] J. Castillo,et al. Liver injury caused by ebrotidine: a new example of the utility of the postmarketing surveillance , 2000, European Journal of Clinical Pharmacology.
[36] T. Baillie,et al. Roles of human hepatic cytochrome P450s 2C9 and 3A4 in the metabolic activation of diclofenac. , 1999, Chemical research in toxicology.
[37] R. Schulick,et al. Immunochemical evidence of trifluoroacetylated cytochrome P-450 in the liver of halothane-treated rats. , 1985, Molecular pharmacology.
[38] M I Lucena,et al. Trovafloxacin-induced acute hepatitis. , 2000, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[39] R. Schinazi,et al. Cellular and molecular events leading to mitochondrial toxicity of 1-(2-deoxy-2-fluoro-1-beta-D-arabinofuranosyl)-5-iodouracil in human liver cells. , 1995, The Journal of clinical investigation.
[40] L. Teodori,et al. Report of a Case and Review of the Literature , 1981 .
[41] D. Greenblatt,et al. Nefazodone, meta-chlorophenylpiperazine, and their metabolites in vitro: cytochromes mediating transformation, and P450-3A4 inhibitory actions , 1999, Psychopharmacology.
[42] T. Baillie,et al. Studies on the metabolism of troglitazone to reactive intermediates in vitro and in vivo. Evidence for novel biotransformation pathways involving quinone methide formation and thiazolidinedione ring scission. , 2001, Chemical research in toxicology.
[43] Dominic P. Williams,et al. The metabolic formation of reactive intermediates from clozapine, a drug associated with agranulocytosis in man. , 1995, The Journal of pharmacology and experimental therapeutics.
[44] A. Breckenridge,et al. Drug-protein conjugates--XVIII. Detection of antibodies towards the antimalarial amodiaquine and its quinone imine metabolite in man and the rat. , 1989, Biochemical pharmacology.
[45] W. Pichler,et al. Direct, MHC-dependent presentation of the drug sulfamethoxazole to human alphabeta T cell clones. , 1997, The Journal of clinical investigation.
[46] J. Woodcock,et al. The safety of newly approved medicines: do recent market removals mean there is a problem? , 1999, JAMA.
[47] G. Danan,et al. [Iproniazid-induced hepatitis. The diagnostic value of a new antimitochondrial antibody anti-M6]. , 1983, Gastroenterologie clinique et biologique.
[48] R. Talaat,et al. Troglitazone quinone formation catalyzed by human and rat CYP3A: an atypical CYP oxidation reaction. , 2001, Biochemical pharmacology.
[49] C. D. Thompson,et al. Mechanisms of idiosyncratic drug reactions: the case of felbamate. , 2002, Chemico-biological interactions.
[50] G. Labbe,et al. Metabolic activation of the antidepressant tianeptine. II. In vivo covalent binding and toxicological studies at sublethal doses. , 1989, Biochemical Pharmacology.
[51] P L Morselli,et al. Comparative pharmacokinetic profile of two imidazopyridine drugs: zolpidem and alpidem. , 1992, Drug metabolism reviews.
[52] T. Baillie,et al. Drug-protein adducts: an industry perspective on minimizing the potential for drug bioactivation in drug discovery and development. , 2004, Chemical research in toxicology.
[53] M. Bonacini,et al. Jaundice and hepatocellular damage associated with nevirapine therapy , 2001, American Journal of Gastroenterology.
[54] J. Uetrecht,et al. Mechanism of idiosyncratic drug reactions: reactive metabolite formation, protein binding and the regulation of the immune system. , 2002, Current drug metabolism.
[55] M Pirmohamed,et al. Genetic susceptibility to adverse drug reactions. , 2001, Trends in pharmacological sciences.
[56] A. Li,et al. Reactivity of atropaldehyde, a felbamate metabolite in human liver tissue in vitro. , 2002, Chemico-biological interactions.
[57] K. Penttilä,et al. Effects of entacapone and tolcapone on mitochondrial membrane potential. , 2002, European journal of pharmacology.
[58] W. Palmer,et al. CINCHOPHEN—IS THERE A SAFE METHOD OF ADMINISTRATION? , 1936 .
[59] J. Karliner,et al. Metabolism of pirprofen in man, monkey, rat, and mouse. , 1982, Drug metabolism and disposition: the biological fate of chemicals.
[60] S. Strom,et al. Troglitazone increases cytochrome P-450 3A protein and activity in primary cultures of human hepatocytes. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[61] J. F. Lang,et al. Proceedings: The absorption, excretion and metabolism of perhexiline maleate by the human. , 1973, Postgraduate medical journal.
[62] S. Iverson,et al. Identification of a reactive metabolite of terbinafine: insights into terbinafine-induced hepatotoxicity. , 2001, Chemical research in toxicology.
[63] Albert P. Li,et al. A review of the common properties of drugs with idiosyncratic hepatotoxicity and the "multiple determinant hypothesis" for the manifestation of idiosyncratic drug toxicity. , 2002, Chemico-biological interactions.
[64] P. R. Montellano. Cytochrome P-450 , 1986, Springer US.
[65] B. Denis,et al. [Hepatitis induced by alpidem (Ananxyl). Four cases, one of them fatal]. , 1994, Gastroenterologie clinique et biologique.
[66] T. Macgregor,et al. Disposition and biotransformation of the antiretroviral drug nevirapine in humans. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[67] Stephen Naylor,et al. S-methyl N,N-diethylthiocarbamate sulfone, a potential metabolite of disulfiram and potent inhibitor of low Km mitochondrial aldehyde dehydrogenase. , 1995, Biochemical pharmacology.
[68] J. Timbrell,et al. Hepatotoxicity and metabolism of iproniazid and isopropylhydrazine. , 1978, The Journal of pharmacology and experimental therapeutics.
[69] P. Beaune,et al. Combined glutathione‐S‐transferase M1 and T1 genetic polymorphism and tacrine hepatotoxicity , 2000, Clinical pharmacology and therapeutics.
[70] W. Santos,et al. The chemistry, toxicology, and identification in rat and human urine of 4-hydroxy-5-phenyl-1,3-oxazaperhydroin-2-one: a reactive metabolite in felbamate bioactivation. , 2001, Chemical research in toxicology.
[71] W. Fleischhacker,et al. Hepatotoxicity of clozapine. , 1997, Journal of clinical psychopharmacology.
[72] J. Uetrecht,et al. Carbamazepine metabolism to a reactive intermediate by the myeloperoxidase system of activated neutrophils. , 1993, Biochemical pharmacology.
[73] D. Mansuy,et al. Oxidation of tienilic acid by human yeast-expressed cytochromes P-450 2C8, 2C9, 2C18 and 2C19. Evidence that this drug is a mechanism-based inhibitor specific for cytochrome P-450 2C9. , 1996, European journal of biochemistry.
[74] A L Burlingame,et al. Mechanisms for covalent binding of benoxaprofen glucuronide to human serum albumin. Studies By tandem mass spectrometry. , 1998, Drug metabolism and disposition: the biological fate of chemicals.
[75] G. Williams,et al. Major difference in the hepatocarcinogenicity and DNA adduct forming ability between toremifene and tamoxifen in female Crl:CD(BR) rats. , 1993, Cancer research.
[76] Jürg Reichen,et al. The endothelin antagonist bosentan inhibits the canalicular bile salt export pump: A potential mechanism for hepatic adverse reactions , 2001, Clinical pharmacology and therapeutics.
[77] F. B. Padilla,et al. Terbinafine hepatotoxicity. A case report and review of literature. , 2003, Annals of hepatology.
[78] G. Hopfgartner,et al. Absorption, excretion, and metabolism of the endothelin receptor antagonist bosentan in healthy male subjects. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[79] R. Paschke,et al. Mechanisms of hepatotoxicity caused by dacarbazine in rats , 2005, Journal of Cancer Research and Clinical Oncology.
[80] H. Zimmerman,et al. Idiosyncratic liver toxicity of nonsteroidal antiinflammatory drugs: molecular mechanisms and pathology. , 1995, Critical reviews in toxicology.
[81] P. Paliard,et al. Perhexiline maleate-induced hepatitis. , 1978, Digestion.
[82] E. Kharasch,et al. Cytochrome P450 2E1 is the principal catalyst of human oxidative halothane metabolism in vitro. , 1997, The Journal of pharmacology and experimental therapeutics.
[83] M. Pirmohamed,et al. An investigation of the formation of cytotoxic, protein-reactive and stable metabolites from carbamazepine in vitro. , 1992, Biochemical pharmacology.
[84] C. D. Thompson,et al. Synthesis and in vitro reactivity of 3-carbamoyl-2-phenylpropionaldehyde and 2-phenylpropenal: putative reactive metabolites of felbamate. , 1996, Chemical research in toxicology.
[85] D. Evans,et al. Polymorphic hydroxylation of perhexiline maleate in man. , 1984, Journal of medical genetics.
[86] J. Reid,et al. Metabolic activation of dacarbazine by human cytochromes P450: the role of CYP1A1, CYP1A2, and CYP2E1. , 1999, Clinical cancer research : an official journal of the American Association for Cancer Research.
[87] G. Garas,et al. Ticlopidine‐associated cholestatic hepatitis , 2002, Internal medicine journal.
[88] Hueper Wc. Cinchophen (atophan) a critical review. , 1948 .
[89] S. Dehal,et al. Cytochrome P-450 3A and 2D6 catalyze ortho hydroxylation of 4-hydroxytamoxifen and 3-hydroxytamoxifen (droloxifene) yielding tamoxifen catechol: involvement of catechols in covalent binding to hepatic proteins. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[90] D. Scott,et al. Identification of 9-hydroxylamine-1,2,3,4-tetrahydroacridine as a hepatic microsomal metabolite of tacrine by high-performance liquid chromatography and electrochemistry. , 1989, Journal of chromatography.
[91] H. Pettit,et al. DPI-3290 [(+)-3-((α-R)-α-((2S,5R)-4-Allyl-2,5-dimethyl-1-piperazinyl)-3-hydroxybenzyl)-N-(3-fluorophenyl)-N-methylbenzamide]. II. A Mixed Opioid Agonist with Potent Antinociceptive Activity and Limited Effects on Respiratory Function , 2003, Journal of Pharmacology and Experimental Therapeutics.
[92] U. Boelsterli,et al. Selective protein adducts to membrane proteins in cultured rat hepatocytes exposed to diclofenac: radiochemical and immunochemical analysis. , 1994, Molecular pharmacology.
[93] J. Leeder,et al. A comparison of the covalent binding of clozapine and olanzapine to human neutrophils in vitro and in vivo. , 1998, Molecular pharmacology.
[94] J. Lieberman,et al. Agranulocytosis: incidence and risk factors. , 1994, The Journal of clinical psychiatry.
[95] R. Gasser,et al. Metabolism and excretion of tolcapone, a novel inhibitor of catechol-O-methyltransferase. , 1999, British journal of clinical pharmacology.
[96] T. Myers,et al. Immunochemical detection of liver protein adducts of the nonsteroidal antiinflammatory drug diclofenac. , 1993, Chemical research in toxicology.
[97] T G Myers,et al. Metabolic activation and immunochemical localization of liver protein adducts of the nonsteroidal anti-inflammatory drug diclofenac. , 1994, Chemical research in toxicology.
[98] D. Mansuy,et al. Opposite behaviors of reactive metabolites of tienilic acid and its isomer toward liver proteins: use of specific anti-tienilic acid-protein adduct antibodies and the possible relationship with different hepatotoxic effects of the two compounds. , 1999, Chemical research in toxicology.
[99] C. Lim,et al. Toremifene metabolism in rat, mouse and human liver microsomes: identification of alpha-hydroxytoremifene by LC-MS. , 2002, Biomedical chromatography : BMC.
[100] S. Wolfe,et al. Timing of new black box warnings and withdrawals for prescription medications. , 2002, JAMA.
[101] S. Shibutani,et al. Identification of tamoxifen-DNA adducts formed by alpha-sulfate tamoxifen and alpha-acetoxytamoxifen. , 1997, Chemical research in toxicology.
[102] D. Acosta,et al. Metabolism of ketoconazole and deacetylated ketoconazole by rat hepatic microsomes and flavin-containing monooxygenases. , 1997, Drug metabolism and disposition: the biological fate of chemicals.
[103] K. Ishak,et al. Isoniazid-associated hepatitis in 114 patients. , 1975, Gastroenterology.
[104] D. Wysowski,et al. Flutamide hepatotoxicity. , 1996, The Journal of urology.
[105] P C Smith,et al. Disposition and reactivity of ibuprofen and ibufenac acyl glucuronides in vivo in the rhesus monkey and in vitro with human serum albumin. , 1995, Drug metabolism and disposition: the biological fate of chemicals.
[106] Stephen Naylor,et al. Determination of in vivo adducts of disulfiram with mitochondrial aldehyde dehydrogenase. , 2001, Biochemical pharmacology.
[107] M. Lucena,et al. Hepatotoxicity associated with the new antidepressants. , 2002, The Journal of clinical psychiatry.
[108] A. Wood. The safety of new medicines: the importance of asking the right questions. , 1999, JAMA.
[109] K. Ishak,et al. Ticrynafen‐Associated Hepatic Injury: Analysis of 340 Cases , 1984, Hepatology.
[110] G. Khursigara,et al. Transformation of lupus-inducing drugs to cytotoxic products by activated neutrophils. , 1994, Science.
[111] J. Arseneau,et al. Hepatic veno‐occlusive disease due to DTIC , 1980, Cancer.
[112] A. Fauq,et al. Inhibition of recombinant human mitochondrial aldehyde dehydrogenase by two intermediate metabolites of disulfiram. , 1998, Biochemical pharmacology.
[113] R. Nilakantan,et al. Calicheamicin gamma 1I and DNA: molecular recognition process responsible for site-specificity. , 1989, Science.
[114] D. Vergani,et al. Antibodies to the surface of halothane-altered rabbit hepatocytes in patients with severe halothane-associated hepatitis. , 1980, The New England journal of medicine.
[115] A. J. Gandolfi,et al. The Involvement of Endotoxin in Halothane‐associated Liver Injury , 1984, Anesthesiology.
[116] D. Pessayre,et al. Metabolic activation of the tricyclic antidepressant amineptine--I. Cytochrome P-450-mediated in vitro covalent binding. , 1987, Biochemical pharmacology.
[117] J. Luyendyk,et al. Ranitidine Treatment during a Modest Inflammatory Response Precipitates Idiosyncrasy-Like Liver Injury in Rats , 2003, Journal of Pharmacology and Experimental Therapeutics.
[118] U. Boelsterli,et al. Diclofenac covalent protein binding is dependent on acyl glucuronide formation and is inversely related to P450-mediated acute cell injury in cultured rat hepatocytes. , 1993, Toxicology and applied pharmacology.
[119] Elizabeth M Joshi,et al. In vitro metabolism of 2-acetylbenzothiophene: relevance to zileuton hepatotoxicity. , 2004, Chemical research in toxicology.
[120] J N Weinstein,et al. Hydroxyurea as an inhibitor of human immunodeficiency virus-type 1 replication. , 1994, Science.
[121] D. Thompson,et al. Quinone methide formation from para isomers of methylphenol (cresol), ethylphenol, and isopropylphenol: relationship to toxicity. , 1995, Chemical research in toxicology.
[122] P. Neuvonen,et al. Isoniazid is a mechanism-based inhibitor of cytochrome P450 1A2, 2A6, 2C19 and 3A4 isoforms in human liver microsomes , 2001, European Journal of Clinical Pharmacology.
[123] P. Beaune,et al. Covalent binding of carbamazepine reactive metabolites to P450 isoforms present in the skin. , 1998, Chemico-biological interactions.
[124] H. Satoh,et al. Metabolic basis for a drug hypersensitivity: antibodies in sera from patients with halothane hepatitis recognize liver neoantigens that contain the trifluoroacetyl group derived from halothane. , 1988, The Journal of pharmacology and experimental therapeutics.
[125] S. Davies,et al. Fatal acute fulminant liver failure due to clozapine: a case report and review of clozapine-induced hepatotoxicity. , 1997, Gastroenterology.
[126] S. Bursian,et al. Underlying endotoxemia augments toxic responses to chlorpromazine: is there a relationship to drug idiosyncrasy? , 2002, The Journal of pharmacology and experimental therapeutics.
[127] T. Macdonald,et al. A mechanistic approach to understanding species differences in felbamate bioactivation: relevance to drug-induced idiosyncratic reactions. , 2000, Drug metabolism and disposition: the biological fate of chemicals.
[128] Arnold Th,et al. Dantrolene sodium: urinary metabolites and hepatotoxicity. , 1983 .
[129] S. Aust,et al. Free radicals produced during the oxidation of hydrazines by hypochlorous acid. , 1996, Chemical research in toxicology.
[130] R. O. Oude Elferink,et al. Selective protein adduct formation of diclofenac glucuronide is critically dependent on the rat canalicular conjugate export pump (Mrp2). , 1998, Chemical research in toxicology.
[131] D J Graham,et al. Temafloxacin syndrome: review of 95 cases. , 1994, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[132] H. Yamazaki,et al. Oxidation of troglitazone to a quinone-type metabolite catalyzed by cytochrome P-450 2C8 and P-450 3A4 in human liver microsomes. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[133] J. Uetrecht,et al. New concepts in immunology relevant to idiosyncratic drug reactions: the "danger hypothesis" and innate immune system. , 1999, Chemical research in toxicology.
[134] T. Baillie,et al. Bioactivation of diclofenac via benzoquinone imine intermediates-identification of urinary mercapturic acid derivatives in rats and humans. , 2001, Drug metabolism and disposition: the biological fate of chemicals.
[135] G. Labbe,et al. Metabolic activation of the antidepressant tianeptine. I. Cytochrome P-450-mediated in vitro covalent binding. , 1989, Biochemical pharmacology.
[136] M. Pirmohamed,et al. Enzyme-induction dependent bioactivation of troglitazone and troglitazone quinone in vivo. , 2001, Chemical research in toxicology.
[137] N. Theodore,et al. Report of two cases and review of the literature , 2006 .
[138] J. Sinclair,et al. Multiple cytochrome P-450s involved in the metabolism of terbinafine suggest a limited potential for drug-drug interactions. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[139] B. Denis,et al. Hépatite imputable à l'alpidem (Ananxyl®) : quatre cas dont un mortel , 1994 .
[140] E. Gale. Lessons from the glitazones: a story of drug development , 2001, The Lancet.
[141] B. K. Park,et al. Species variation in the bioactivation of tacrine by hepatic microsomes. , 1995, Xenobiotica; the fate of foreign compounds in biological systems.
[142] K. Knights,et al. In vitro metabolism of acitretin by human liver microsomes: evidence of an acitretinoyl-coenzyme A thioester conjugate in the transesterification to etretinate. , 2000, Biochemical pharmacology.
[143] S. Gutman,et al. Methyldopa Hepatitis. A report of six cases and review of the literature. , 1976, The American journal of medicine.
[144] C. Ioannides,et al. Induction of the cytochrome P450 I and IV families and peroxisomal proliferation in the liver of rats treated with benoxaprofen. Possible implications in its hepatotoxicity. , 1991, Biochemical pharmacology.
[145] S. Sherlock,et al. Impaired oxidation of debrisoquine in patients with perhexiline liver injury. , 1984, Gut.
[146] H. Conjeevaram,et al. Hepatic failure and lactic acidosis due to fialuridine (FIAU), an investigational nucleoside analogue for chronic hepatitis B. , 1995, The New England journal of medicine.
[147] J. Bolton,et al. The influence of 4-alkyl substituents on the formation and reactivity of 2-methoxy-quinone methides: evidence that extended pi-conjugation dramatically stabilizes the quinone methide formed from eugenol. , 1995, Chemico-biological interactions.
[148] H. Stierlin,et al. Biotransformation of diclofenac sodium (Voltaren) in animals and in man. II. Quantitative determination of the unchanged drug and principal phenolic metabolites, in urine and bile. , 1979, Xenobiotica; the fate of foreign compounds in biological systems.
[149] J. Neuberger,et al. Antibody mediated hepatocyte injury in methyl dopa induced hepatotoxicity. , 1985, Gut.
[150] G. Bryan,et al. N-demethylation the antineoplastic agent4(5)-(3,3-dimethyl-1-triazeno)imidazole-5(4)-carboxamide by rats and man. , 1970, Cancer research.
[151] C. Karema,et al. Efficacy of amodiaquine alone and combined with sulfadoxine-pyrimethamine and of sulfadoxine pyrimethamine combined with artesunate. , 2003, The American journal of tropical medicine and hygiene.
[152] D. Pessayre,et al. Dihydralazine hepatitis: report of a case and review of the literature. , 1983, Digestion.
[153] J. Boitnott,et al. Dantrolene-associated hepatic injury. Incidence and character. , 1977, Gastroenterology.
[154] G. Siest,et al. Induction of hepatic cytochrome P-450c-dependent monooxygenase activities by dantrolene in rat. , 1987, Biochemical pharmacology.
[155] P. Ganey,et al. Concurrent inflammation as a determinant of susceptibility to toxicity from xenobiotic agents. , 2001, Toxicology.
[156] S. Nelson,et al. Synthesis, decomposition kinetics, and preliminary toxicological studies of pure N-acetyl-p-benzoquinone imine, a proposed toxic metabolite of acetaminophen. , 1982, Journal of medicinal chemistry.
[157] D. Ac,et al. Fatal acute liver failure associated with pirprofen. Report of a case and a review of the literature. , 1990 .
[158] O. Jensen,et al. Disulfiram generates a stable N,N-diethylcarbamoyl adduct on Cys-125 of rat hemoglobin beta-chains in vivo. , 2000, Chemical research in toxicology.
[159] J. Uetrecht,et al. Clozapine is oxidized by activated human neutrophils to a reactive nitrenium ion that irreversibly binds to the cells. , 1995, The Journal of pharmacology and experimental therapeutics.
[160] T. Baillie,et al. Identification of novel glutathione conjugates of disulfiram and diethyldithiocarbamate in rat bile by liquid chromatography-tandem mass spectrometry. Evidence for metabolic activation of disulfiram in vivo. , 1994, Chemical research in toxicology.
[161] T. Baillie,et al. Metabolic activation of unsaturated derivatives of valproic acid. Identification of novel glutathione adducts formed through coenzyme A-dependent and -independent processes. , 1994, Chemico-biological interactions.
[162] P. Cadrobbi,et al. Severe hepatic failure related to nevirapine treatment. , 1999, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.
[163] D. Pessayre,et al. Toxicity of the antiandrogen flutamide in isolated rat hepatocytes. , 1994, The Journal of pharmacology and experimental therapeutics.
[164] P. Mummaneni,et al. Report of two cases and review of the literature , 2004 .
[165] A. Gasbarrini,et al. Acute liver injury related to the use of niperotidine. , 1997, Journal of hepatology.
[166] D. Mansuy,et al. Human anti-mitochondria autoantibodies appearing in iproniazid-induced immunoallergic hepatitis recognize human liver monoamine oxidase B. , 1996, Biochemical and biophysical research communications.
[167] Stuart Johnson,et al. Adverse effects associated with use of nevirapine in HIV postexposure prophylaxis for 2 health care workers. , 2000, JAMA.
[168] Tommy B Andersson,et al. Amodiaquine clearance and its metabolism to N-desethylamodiaquine is mediated by CYP2C8: a new high affinity and turnover enzyme-specific probe substrate. , 2002, The Journal of pharmacology and experimental therapeutics.
[169] P. Beaune,et al. Metabolic activation of the nitroaromatic antiandrogen flutamide by rat and human cytochromes P-450, including forms belonging to the 3A and 1A subfamilies. , 1993, The Journal of pharmacology and experimental therapeutics.
[170] M. Osman,et al. Metabolic Disposition of 14C‐Bromfenac in Healthy Male Volunteers , 1998, Journal of clinical pharmacology.
[171] B. Stricker,et al. Glafenine-associated hepatic injury. Analysis of 38 cases and review of the literature. , 2008, Liver.
[172] R. Tukey,et al. Human UDP-glucuronosyltransferases: metabolism, expression, and disease. , 2000, Annual review of pharmacology and toxicology.
[173] N. Abuaf,et al. A new anti-liver-kidney microsome antibody (anti-LKM2) in tienilic acid-induced hepatitis. , 1984, Clinical and experimental immunology.
[174] T. Baillie,et al. Metabolic activation of valproic acid and drug-mediated hepatotoxicity. Role of the terminal olefin, 2-n-propyl-4-pentenoic acid. , 1988, Chemical research in toxicology.
[175] D. Hatsukami,et al. High-dose naltrexone therapy and dietary counseling for obesity , 1987, Biological Psychiatry.
[176] D. Holaday,et al. Resistance of Isoflurane to Biotransformation in Man , 1975, Anesthesiology.
[177] N. Kerenyi,et al. Disulfiram-induced hepatitis , 1985, Digestive diseases and sciences.
[178] P. Matzinger. Tolerance, danger, and the extended family. , 1994, Annual review of immunology.
[179] F. Lombardo,et al. BIOACTIVATION OF THE NONTRICYCLIC ANTIDEPRESSANT NEFAZODONE TO A REACTIVE QUINONE-IMINE SPECIES IN HUMAN LIVER MICROSOMES AND RECOMBINANT CYTOCHROME P450 3A4 , 2005, Drug Metabolism and Disposition.
[180] C. D. Thompson,et al. Identification of modified atropaldehyde mercapturic acids in rat and human urine after felbamate administration. , 1997, Chemical research in toxicology.
[181] J. Goldstein,et al. Ticlopidine as a selective mechanism-based inhibitor of human cytochrome P450 2C19. , 2001, Biochemistry.
[182] D. Pessayre,et al. Metabolic activation of the tricyclic antidepressant amineptine by human liver cytochrome P-450. , 1987, Biochemical pharmacology.
[183] K. Hornbuckle,et al. Evaluation of the Characteristics of Safety Withdrawal of Prescription Drugs from Worldwide Pharmaceutical Markets-1960 to 1999 , 2001 .
[184] D. Thompson,et al. Studies on the mechanism of hepatotoxicity of 4-methylphenol (p-cresol): effects of deuterium labeling and ring substitution. , 1996, Chemico-biological interactions.
[185] A. J. Gandolfi,et al. Hepatotoxicological evaluation of dantrolene sodium. , 1984, Drug and chemical toxicology.
[186] W. Santos,et al. Interaction between human serum albumin and the felbamate metabolites 4-Hydroxy-5-phenyl-[1,3]oxazinan-2-one and 2-phenylpropenal. , 2002, Chemical research in toxicology.
[187] M. Nalesnik,et al. Severe cholestatic hepatitis in a patient taking acitretin , 2002, American Journal of Gastroenterology.
[188] D. Stewart,et al. Hepatic Adverse Reactions Associated with Nefazodone , 2002, Canadian journal of psychiatry. Revue canadienne de psychiatrie.
[189] S. Roy,et al. Interaction of dantrolene with the hepatic mixed function oxidase system. , 1980, Research communications in chemical pathology and pharmacology.
[190] N. Pumford,et al. Covalent binding of xenobiotics to specific proteins in the liver. , 1997, Drug metabolism reviews.
[191] M. D. Faiman,et al. Disulfiram metabolism as a requirement for the inhibition of rat liver mitochondrial low Km aldehyde dehydrogenase. , 1991, Biochemical pharmacology.
[192] P. Corey,et al. Incidence of Adverse Drug Reactions in Hospitalized Patients , 2012 .
[193] H. Askmark,et al. Epidemiology of adverse reactions to carbamazepine as seen in a spontaneous reporting system , 1990, Acta neurologica Scandinavica.
[194] P. Kaheinen,et al. Entacapone, a novel catechol-O-methyltransferase inhibitor for Parkinson's disease, does not impair mitochondrial energy production. , 1997, European journal of pharmacology.
[195] I. White. Tamoxifen: is it safe? Comparison of activation and detoxication mechanisms in rodents and in humans. , 2003, Current drug metabolism.
[196] P. Beaune,et al. Interactions of dihydralazine with cytochromes P4501A: a possible explanation for the appearance of anti-cytochrome P4501A2 autoantibodies. , 1994, Molecular pharmacology.
[197] D. Mansuy,et al. Thiophene derivatives as new mechanism-based inhibitors of cytochromes P-450: inactivation of yeast-expressed human liver cytochrome P-450 2C9 by tienilic acid. , 1994, Biochemistry.
[198] J. Luyendyk,et al. Inflammation and Drug Idiosyncrasy—Is There a Connection? , 2003, Journal of Pharmacology and Experimental Therapeutics.
[199] A. J. Gandolfi,et al. Bioactivation and covalent binding of halothane in vitro: studies with [3H]- and [14C]halothane. , 1980, The Journal of pharmacology and experimental therapeutics.
[200] E. Dybing,et al. Oxidation of alpha-methyldopa and other catechols by cytochrome P-450-generated superoxide anion: possible mechanism of methyldopa hepatitis. , 1976, Molecular pharmacology.
[201] T. Macdonald,et al. In vitro metabolism of tolcapone to reactive intermediates: relevance to tolcapone liver toxicity. , 2003, Chemical research in toxicology.
[202] Stephen Naylor,et al. Overview--in vitro inhibition of aldehyde dehydrogenase by disulfiram and metabolites. , 2001, Chemico-biological interactions.
[203] N. Kitteringham,et al. Structural requirements for bioactivation of anticonvulsants to cytotoxic metabolites in vitro. , 1989, British journal of clinical pharmacology.
[204] N. Hewitt,et al. Differential in vitro hepatotoxicity of troglitazone and rosiglitazone among cryopreserved human hepatocytes from 37 donors. , 2002, Chemico-biological interactions.
[205] I. Lindén,et al. Comparative toxicological study on the hepatic safety of entacapone and tolcapone in the rat , 2001, Journal of Neural Transmission.
[206] H. Zimmerman,et al. Hepatocellular jaundice as a complication of iproniazid therapy. , 1960, Archives of internal medicine.
[207] D. Acosta,et al. Comparison of ketoconazole- and fluconazole-induced hepatotoxicity in a primary culture system of rat hepatocytes. , 1995, Toxicology.
[208] W. Pichler,et al. Involvement of T cells in drug-induced allergies. , 1998, Trends in pharmacological sciences.
[209] S. Bird,et al. Severe Cholestatic Hepatitis Caused by Thiazolidinediones: Risks Associated with Substituting Rosiglitazone for Troglitazone , 2002, Digestive Diseases and Sciences.
[210] A. Tsuchida,et al. Toxic effect of troglitazone on cultured rat hepatocytes. , 2001, Life sciences.
[211] B. Martin,et al. Human anti-endoplasmic reticulum antibodies in sera of patients with halothane-induced hepatitis are directed against a trifluoroacetylated carboxylesterase. , 1989, Proceedings of the National Academy of Sciences of the United States of America.
[212] D. Pessayre,et al. Antigenic targets in tienilic acid hepatitis. Both cytochrome P450 2C11 and 2C11-tienilic acid adducts are transported to the plasma membrane of rat hepatocytes and recognized by human sera. , 1996, The Journal of clinical investigation.
[213] N. Kitteringham,et al. The mechanism of bioactivation and antigen formation of amodiaquine in the rat. , 1992, Biochemical pharmacology.
[214] J. Timbrell,et al. Isoniazid hepatoxicity: the relationship between covalent binding and metabolism in vivo. , 1980, The Journal of pharmacology and experimental therapeutics.
[215] D. Acosta,et al. N-deacetyl ketoconazole-induced hepatotoxicity in a primary culture system of rat hepatocytes. , 1997, Toxicology.
[216] C. Fichtenbaum,et al. Interactions Between Antiretroviral Drugs and Drugs Used for the Therapy of the Metabolic Complications Encountered During HIV Infection , 2002, Clinical pharmacokinetics.
[217] U. Boelsterli,et al. Mechanism of covalent adduct formation of diclofenac to rat hepatic microsomal proteins. Retention of the glucuronic acid moiety in the adduct. , 1994, Drug metabolism and disposition: the biological fate of chemicals.
[218] P. Beaune,et al. Tienilic acid-induced autoimmune hepatitis: anti-liver and-kidney microsomal type 2 autoantibodies recognize a three-site conformational epitope on cytochrome P4502C9. , 1996, Molecular pharmacology.
[219] W. Fleischhacker,et al. Hepatotoxicity of clozapine , 1996, Schizophrenia Research.
[220] M Pirmohamed,et al. Advances in molecular toxicology-towards understanding idiosyncratic drug toxicity. , 2000, Toxicology.
[221] L. Lesko,et al. Effect of troglitazone on cytochrome P450 enzymes in primary cultures of human and rat hepatocytes , 2000, Xenobiotica; the fate of foreign compounds in biological systems.
[222] K. Nill,et al. Carbonyl reduction of naltrexone and dolasetron by oxidoreductases isolated from human liver cytosol , 2004, The Journal of pharmacy and pharmacology.
[223] R. Chapman,et al. Diclofenac associated hepatitis. , 1990, Journal of hepatology.
[224] D. Knopman,et al. Naltrexone hydrochloride (Trexan): a review of serum transaminase elevations at high dosage. , 1986, NIDA research monograph.
[225] G. Labbe,et al. Inhibition of mitochondrial beta-oxidation of fatty acids by pirprofen. Role in microvesicular steatosis due to this nonsteroidal anti-inflammatory drug. , 1987, The Journal of pharmacology and experimental therapeutics.
[226] H. Yamazaki,et al. Formation of a novel quinone epoxide metabolite of troglitazone with cytotoxicity to HepG2 cells. , 2002, Drug metabolism and disposition: the biological fate of chemicals.
[227] W. Richter,et al. Biotransformation of diclofenac sodium (Voltaren) in animals and in man. I. Isolation and identification of principal metabolites. , 1979, Xenobiotica; the fate of foreign compounds in biological systems.
[228] M. Rowlands,et al. The deuterium isotope effect for the alpha-hydroxylation of tamoxifen by rat liver microsomes accounts for the reduced genotoxicity of [D5-ethyl]tamoxifen. , 1995, Carcinogenesis.
[229] A. Li,et al. Primary human hepatocytes as a tool for the evaluation of structure-activity relationship in cytochrome P450 induction potential of xenobiotics: evaluation of rifampin, rifapentine and rifabutin. , 1997, Chemico-biological interactions.
[230] S. Kirkman,et al. Isolation and identification of bromfenac glucoside from rat bile. , 1998, Drug metabolism and disposition: the biological fate of chemicals.
[231] R. Rowland,et al. Perhexiline Maleate Induced Cirrhosis , 1983, Pathology.
[232] A. Rettie,et al. Human CYP2C9 and CYP2A6 mediate formation of the hepatotoxin 4-ene-valproic acid. , 1997, The Journal of pharmacology and experimental therapeutics.
[233] K. Knights,et al. Benoxaprofen induced toxicity in isolated rat hepatocytes. , 1986, Toxicology.
[234] J. Rabkin,et al. Fatal Fulminant Hepatitis Associated with Bromfenac Use , 1999, The Annals of pharmacotherapy.
[235] F. V. van Pelt,et al. Formation of trifluoroacetylated protein antigens in cultured rat hepatocytes exposed to halothane in vitro. , 1994, Biochemical pharmacology.
[236] S. Sherlock,et al. Hepatic reactions associated with ketoconazole in the United Kingdom. , 1987, British medical journal.
[237] J. Trudell,et al. Urinary Metabolites of Halothane in Man , 1975, Anesthesiology.
[238] B. K. Park,et al. The effect of enzyme inhibition on the metabolism and activation of tacrine by human liver microsomes. , 1994, British journal of clinical pharmacology.
[239] Amineptine induced liver injury. Report of two cases and brief review of the literature. , 1996, Hepato-gastroenterology.
[240] G. Danan,et al. Mechanism for isaxonine hepatitis. I. Metabolic activation by mouse and human cytochrome P-450. , 1984, The Journal of pharmacology and experimental therapeutics.
[241] T. Baillie,et al. Studies on cytochrome P-450-mediated bioactivation of diclofenac in rats and in human hepatocytes: identification of glutathione conjugated metabolites. , 1999, Drug metabolism and disposition: the biological fate of chemicals.
[242] L. Saidman,et al. The Biotransformation of Ēthrane in Man , 1971, Anesthesiology.
[243] E. Estey,et al. Mylotarg™ (gemtuzumab ozogamicin) therapy is associated with hepatic venoocclusive disease in patients who have not received stem cell transplantation , 2001, Cancer.
[244] R. Andrade,et al. Acute liver injury associated with the use of ebrotidine, a new H2-receptor antagonist. , 1999, Journal of hepatology.
[245] W. Trager,et al. Electrospray ionization mass spectrometric analysis of intact cytochrome P450: identification of tienilic acid adducts to P450 2C9. , 1999, Biochemistry.
[246] Y. Masubuchi,et al. Mechanism-based inactivation of cytochrome P450s 1A2 and 3A4 by dihydralazine in human liver microsomes. , 1999, Chemical research in toxicology.