Chronotoxicity of bromobenzene-induced hepatic injury in mice

• Published in: Journal of toxicological sciences Vol. 42; no. 2; pp. 251 - 258
• Main Authors: Yoshioka, Hiroki, Nonogaki, Tsunemasa, Fukuishi, Nobuyuki, Shinohara, Yasuro, Hwang, Gi-Wook, Ohtani, Katsumi, Miura, Nobuhiko
• Format: Journal Article
• Language: English
• Published: Japan The Japanese Society of Toxicology 2017; Japan Science and Technology Agency
• Subjects: Alanine; Alanine Transaminase - blood; Animals; Aspartate Aminotransferases - blood; Blood Urea Nitrogen; Bromobenzene; Bromobenzenes - toxicity; Chemical and Drug Induced Liver Injury - blood; Chemical and Drug Induced Liver Injury - pathology; Chronotoxicity; Circadian Rhythm; Circadian rhythms; Creatinine; Creatinine - blood; Diurnal variation; Injuries; Kidney - drug effects; Kidney - metabolism; Kidney - pathology; Lipids; Liver; Liver - drug effects; Liver - metabolism; Liver - pathology; Male; Malondialdehyde - metabolism; Markers; Mice, Inbred ICR; Mortality; Periodic variations; Solvents - toxicity; Toxicity; Zeitgeber
• ISSN: 0388-1350; 1880-3989
• DOI: 10.2131/jts.42.251

The aim of the present study is to investigate whether or not bromobenzene (BB) toxicity varies with circadian periodicity. Seven-week-old male ICR mice were injected with 900 mg/kg (5.73 mmol/kg) BB intraperitoneally at 4 different time points of a day (zeitgeber time [ZT]: ZT0, ZT6, ZT12, and ZT18). Mortality was then monitored for 7 days after injection. Interestingly, mice were sensitive to BB acute toxicity at ZT6 while tolerant at ZT18. Moreover, in mice that were given a non-lethal dose of BB (540 mg (3.44 mmol)/kg), levels of alanine aminotransferase and aspartate aminotransferase, used as markers of hepatic injury, markedly increased in response to injection at ZT6, but did not increase significantly in response to injection at ZT18. In contrast, the markers of renal injury (creatinine and blood urea nitrogen), showed no significant difference in response to the two injection times. To further investigate this extreme circadian variation, we examined hepatic and renal lipid peroxidation levels, and conducted histopathological studies. Similar to our observation with alanine aminotransferase and creatinine, hepatic lipid peroxidation and histopathological changes were more pronounced than renal changes, and showed circadian variation. Our present investigation demonstrated that BB-induced mortality had clear circadian variation, and suggested that hepatic injury was one of the important factors for determination of this variation.