Different Renal Chronotoxicity of Bromobenzene and Its Intermediate Metabolites in Mice
Author:
Affiliation:
1. College of Pharmacy, Kinjo Gakuin University
2. Center for Craniofacial Research, The University of Texas Health Science Center at Houston, School of Dentistry
3. Department of Health Science, Yokohoma University of Pharmacy
Publisher
Pharmaceutical Society of Japan
Subject
Pharmaceutical Science,Pharmacology,General Medicine
Link
https://www.jstage.jst.go.jp/article/bpb/44/1/44_b20-00694/_pdf
Reference14 articles.
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2. 2) Zhao H, Cheng N, He L, Peng G, Liu Q, Ma T, Cao W. Hepatoprotective Effects of the Honey of apis cerana fabricius on bromobenzene-induced liver damage in mice. J. Food Sci., 83, 509–516 (2018).
3. 3) Vedi M, Sabina EP. Assessment of hepatoprotective and nephroprotective potential of withaferin A on bromobenzene-induced injury in Swiss albino mice: possible involvement of mitochondrial dysfunction and inflammation. Cell Biol. Toxicol., 32, 373–390 (2016).
4. 4) Dankovic DA, Billings RE. The role of 4-bromophenol and 4-bromocatechol in bromobenzene covalent binding and toxicity in isolated rat hepatocytes. Toxicol. Appl. Pharmacol., 79, 323–331 (1985).
5. 5) Lau SS, Monks TJ, Gillette JR. Identification of 2-bromohydroquinone as a metabolite of bromobenzene and o-bromophenol: implications for bromobenzene-induced nephrotoxicity. J. Pharmacol. Exp. Ther., 230, 360–366 (1984).
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