Reduction of Cytotoxic p-Quinone Metabolites of tert-Butylhydroquinone by Human Aldo-keto Reductase (AKR) 1B10-Reference-Cited by-同舟云学术

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Reduction of Cytotoxic p-Quinone Metabolites of tert-Butylhydroquinone by Human Aldo-keto Reductase (AKR) 1B10

Published:2012 Issue:5 Volume:27 Page:553-558
ISSN:1347-4367
Container-title:Drug Metabolism and Pharmacokinetics
language:en
Short-container-title:Drug Metabolism and Pharmacokinetics

Author:

Matsunaga Toshiyuki,Endo Satoshi,Takemura Mayuko,Soda Midori,Yamamura Keiko,Tajima Kazuo,Miura Takeshi,Terada Tomoyuki,El-Kabbani Ossama,Hara Akira

Publisher

Japanese Society for the Study of Xenobiotics

Subject

Pharmacology (medical),Pharmaceutical Science,Pharmacology

Reference37 articles.

1. 1) Verhagen, H., Schilderman, P. A. and Kleinjans, J. C.: Butylated hydroxyanisole in perspective. Chem. Biol. Interact., 80: 109–134 (1991).

2. 2) Gharavi, N., Haggarty, S. and El-Kadi, A. O.: Chemoprotective and carcinogenic effects of tert-butylhydroquinone and its metabolites. Curr. Drug Metab., 8: 1–7 (2007).

3. 3) Schilderman, P. A., van Maanen, J. M., Smeets, E. J., ten Hoor, F. and Kleinjans, J. C.: Oxygen radical formation during prostaglandin H synthase-mediated biotransformation of butylated hydroxyanisole. Carcinogenesis, 14: 347–353 (1993).

4. 4) Li, Y., Seacat, A., Kuppusamy, P., Zweier, J. L., Yager, J. D. and Trush, M. A.: Copper redox-dependent activation of 2-tert-butyl(1,4)hydroquinone: formation of reactive oxygen species and induction of oxidative DNA damage in isolated DNA and cultured rat hepatocytes. Mutat. Res., 518: 123–133 (2002).

5. 5) Nakamura, Y., Kumagai, T., Yoshida, C., Naito, Y., Miyamoto, M., Ohigashi, H., Osawa, T. and Uchida, K.: Pivotal role of electrophilicity in glutathione S-transferase induction by tert-butylhydroquinone. Biochemistry, 42: 4300–4309 (2003).

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