[1]
|
J. Owczarek, M. Jasińska and D. Orszulak-Michalak, “Drug-Induced Myopathies. An Overview of the Possible Mechanisms,” Pharmacology, Vol. 57, No. 1, 2005, pp. 23-34.
|
[2]
|
T. Khazaeinia, A. A. Ramsey and Y. K. Tam, “The Effects of Exercise on the Pharmacokinetics of Drugs,” Journal of Pharmacy and Pharmaceutical Sciences, Vol. 3, No. 3, 2000, pp. 292-302.
|
[3]
|
J. R. Herman, “Drug Interaction and Statins,” Canadian Medical Association Journal, Vol. 161, 1999, pp. 2811286.
|
[4]
|
J. Warren, P. Blumbergs and P. Thompson, “Rhabdomyolysis: A Review,” Muscle & Nerve, Vol. 25, No. 3, 2002, pp. 332-347. doi:10.1002/mus.10053
|
[5]
|
Z. Argov, “Drug-Induced Myopathies,” Current Opinion in Neurology, Vol. 13, No. 5, 2000, pp. 541-545.
doi:10.1097/00019052-200010000-00006
|
[6]
|
D. Nebert and T. Dalton, “The Role of Cytochrome P450 Enzymes in Endogenous Signalling Pathways and Envi ronmental Carcinogenesis,” Nature Reviews Cancer, Vol. 6, 2006, pp. 947-960. doi:10.1038/nrc2015
|
[7]
|
B. Park, M. Pirmohamed and N. Kitteringham, “The Role of Cytochrome P450 Enzymes in Hepatic and Extrahepatic Human Drug Toxicity,” Pharmacology & Therapeutics, Vol. 68, No. 3, 1995, pp. 385-424.
doi:10.1016/0163-7258(95)02013-6
|
[8]
|
I. Biéche, C. Narjoz, T. Asselah, S. Vacher, P. Marcellin, R. Lidereau, P. Beaune and E. de Waziers, “Reverse Transcriptase-PCR Quantification of mRNA Levels from Cytochrome (CYP)1, CYP2 and CYP3 Families in 22 Different Human Tissues,” Pharmacogenetics & Genomics, Vol. 17, No. 9, 2007, pp. 731-742.
doi:10.1097/FPC.0b013e32810f2e58
|
[9]
|
P. Pavek and Z. Dvora, “Xenobiotic-Induced Transcriptional Regulation of Xenobiotic Metabolizing Enzymes of the Cytochrome P450 Superfamily in Human Extrahepatic Tissues,” Current Drug Metabolism, Vol. 9, No. 2, 2008, pp. 129-143. doi:10.2174/138920008783571774
|
[10]
|
S. Ellero, G. Chakhtoura, C. Barreau, S. Langoue, C. H. Benelli, L. Penicaud, P. Beaune and I. de Waziers, “Xenobiotic-Metabolizing Cytochromes P450 in Human White Adipose Tissue: Expression and Induction,” Drug Metabolism and Disposition, Vol. 38, No. 4, 2010, pp. 679-686. doi:10.1124/dmd.109.029249
|
[11]
|
S. C. Dogra, M. L. Whitelaw and B. K. May, “Transcriptional Activation of Cytochrome P450 Genes by Different Classes of Chemical Inducers,” Clinical and Experimental Pharmacology and Physiology, Vol. 25, No. 1, 1998, pp. 1-9. doi:10.1111/j.1440-1681.1998.tb02135.x
|
[12]
|
I. Bergheim, C. Bode and A. Parlesak, “Distribution of Cytochrome P450 2C, 2E1, 3A4, and 3A5 in Human Colon Mucosa,” BMC Clinical Pharmacology, Vol. 5, 2005, p. 4.
|
[13]
|
C. Tang, J. H. Lin and A. Y. Lu, “Metabolism-Based Drug-Drug Interactions: What Determines Individual Variability in Cytochrome P450 Induction?” Drug Metabolism and Disposition, Vol. 33, No. 5, 2005, pp. 603613. doi:10.1124/dmd.104.003236
|
[14]
|
X. Ding and L. Kaqminski, “Human Extrahepatic Cytochrome P450: Function in Xenobiotic Metabolism and Tissue-Selective Chemical Toxicity in the Respiratory and Gastrointestinal Tracts,” Annual Review of Pharmacology and Toxicology, Vol. 43, 2003, pp. 149-173.
doi:10.1146/annurev.pharmtox.43.100901.140251
|
[15]
|
P. Rickham, “Human Experimentation. Code of Ethics of the World Medical Association,” British Medical Journal, Vol. 2, 1964, p. 177. doi:10.1136/bmj.2.5402.177
|
[16]
|
O. Lowry, N. Rosebrough, A. Farr and R. Randall, “Protein Measurement with the Folin Phonol Reagent,” The Journal of Biological Chemistry, Vol. 193, No. 1, 1951, pp. 265-275.
|
[17]
|
K. Livack and T. Schmittgen, “Analysis of Relative Gene Expression Data Using Real-Time Quantitative PCR and the 2 Delta Delta C (T),” Methods, Vol. 25, 2001, pp. 402-408.
|
[18]
|
G. L. Kearns, S. M. Abdel-Rahman, S. W. Alander, D. L. Blowey, J. S. Leeder, et al., “Developmental Pharmacology—Drug Disposition, Action, and Therapy in Infants and Children,” The New England Journal of Medicine, Vol. 349, 2003, pp. 1157-1167.
doi:10.1056/NEJMra035092
|
[19]
|
D. Nebert, T. Dalton, A. Okey and F. Gonzalez, “Role of Aryl Hydrocarbon Receptor-Mediated Induction of the CYP1 Enzymes in Environmental Toxicity and Cancer,” The Journal of Biological Chemistry, Vol. 279, 2004, pp. 23847-23850. doi:10.1074/jbc.R400004200
|
[20]
|
D. Nebert and C. Karp, “Endogenous Functions of the Aryl Hydrocarbon Receptor (AHR): Intersection of Cytochrome P450 1 (CYP1)-Metabolized Eicosanoids and AHR Biology,” The Journal of Biological Chemistry, Vol. 283, 2008, pp. 36061-36065.
doi:10.1074/jbc.R800053200
|
[21]
|
L. Nguyen and C. Bradfield, “The Search for Endogenous Activators of the Aryl Hydrocarbon Receptor,” Chemical Research in Toxicology, Vol. 21, No. 1, 2008, pp. 102116. doi:10.1021/tx7001965
|
[22]
|
T. Shimada, “Arylhydrocarbon Receptor-Dependent Induction of Liver and Lung Cytochromes P450 1A1, 1A2, and 1B1 by Polycyclic Aromatic Hydrocarbons and Polychlorinated Biphenyls in Genetically Engineered C57BL/6J Mice,” Carcinogenesis, Vol. 23, No. 7, 2002, pp. 1199-1207. doi:10.1093/carcin/23.7.1199
|
[23]
|
C. Martucci and J. Fishman, “P450 Enzymes of Estrogen Metabolism,” Pharmacology & Therapeutics, Vol. 57, No. 2-3, 1993, pp. 237-257.
doi:10.1016/0163-7258(93)90057-K
|
[24]
|
K. Aizawa, M. Iemitsu, T. Otsuki, S. Maeda, T. Miyauchi and N. Mesaki, “Sex Differences in Steroidogenesis in Skeletal Muscle Following a Single Bout of Exercise in Rats,” Journal of Applied Physiology, Vol. 104, No. 1, 2008, pp. 67-74. doi:10.1152/japplphysiol.00558.2007
|
[25]
|
C. Patten, P. Thomas, R. Guy, M. Lee, F. Gonzalez, F. Guengerich, et al., “Cytochrome P450 Enzymes Involved in Acetaminophen Activation by Rat and Human Liver Microsomes and Their Kinetics,” Chemical Research in Toxicology, Vol. 6, No. 4, 1993, pp. 511-518.
doi:10.1021/tx00034a019
|
[26]
|
J. Raucy, J. Lasker, C. Lieber and M. Black, “Acetaminophen Activation by Human Liver Cytochromes P450IIE1 and P450IA2,” Archives of Biochemistry and Biophysics, Vol. 271, No. 1, 1989, pp. 270-283.
doi:10.1016/0003-9861(89)90278-6
|
[27]
|
M. Iwanari, M. Nakajima, R. Kizu, K. Hayakawa and T. Yokoi, “Induction of CYP1A1, CYP1A2, and CYP1B1 mRNAs by Nitropolycyclic Aromatic Hydrocarbons in Various Human Tissue-Derived Cells: Chemical-, Cytochrome P450 Isoform-, and Cell-Specific Differences,” Archives of Toxicology, Vol. 76, No. 5-6, 2002, pp. 287-298. doi:10.1007/s00204-002-0340-z
|
[28]
|
A. Gomez, M. Karlgren, D. Edler, M. Bernal, S. Mkrtchian, et al., “Expression of CYP2W1 in Colon Tumors: Regulation by Gene Methylation,” Pharmacogenomics, Vol. 8, No. 10, 2007, pp. 1315-1325.
doi:10.2217/14622416.8.10.1315
|
[29]
|
J. Riggs, “Alcohol-Associated Rhabdomyolysis: Ethanol Induction of Cytochrome P450 May Potentiate Myotoxicity,” Clinical Neuropharmacology, Vol. 21, No. 6, 1998, pp. 363-364.
|
[30]
|
C. Lieber, “Cytochrome P-4502E1: Its Physiological and Pathological Role,” Physiological Reviews, Vol. 77, No. 2, 1997, pp. 517-544.
|
[31]
|
M. J. J. Ronis, K. O. Lindros and M. Ingelman-Sundberg, “The CYP2E Subfamily,” In: C. Ioannides and D. V. Parke, Eds., Cytochromes P450: Metabolic and Toxicological Aspects, CRC Press, Boca Raton, 1996, pp. 211239.
|
[32]
|
D. R. Nelson, “Cytochrome P450 and the Individuality of Species,” Archives of Biochemistry and Biophysics, Vol. 369, No. 1, 1999, pp. 1-10. doi:10.1006/abbi.1999.1352
|
[33]
|
V. Wacher, C. Wu and L. Benet, “Overlapping Substrate Specificities and Tissue Distribution of Cytochrome P450 3A and P-Glycoprotein: Implications for Drug Delivery and Activity in Cancer Chemotherapy,” Oncology & Radiotherapy, Vol. 13, No. 3, 1995, pp. 129-134.
doi:10.1002/mc.2940130302
|
[34]
|
P. Guengerich, “Cytochrome P450 3A4: Regulation and Role in Drug Metabolism,” Annual Review of Pharmacology and Toxicology, Vol. 39, 1999, pp. 1-17.
doi:10.1146/annurev.pharmtox.39.1.1
|
[35]
|
K. Thummel, D. Shen, T. Podoll, K. Kunze, W. Trager, et al., “Use of Midazolam as a Human Cytochrome P450 3A Probe: II. Characterization of Interand Intraindividual Hepatic CYP3A Variability after Liver Transplantation,” Journal of Pharmacology and Experimental Therapeutics, Vol. 271, No. 1, 1994, pp. 557-566.
|
[36]
|
L. M. Forrester, C. J. Henderson, M. J.Glancey, D. J. Back, B. K. Park, S. E. Ball, N. R. Kitteringham, A. W. McLaren, J. S. Miles, P. Skett, et al., “Relative Expression of Cytochrome P450 Isoenzymes in Human Liver and Association with the Metabolism of Drugs and Xenobiotics,” Biochemical Journal, Vol. 281, 1992, pp. 359-368.
|