Induction of mitochondrial biogenesis protects against acetaminophen hepatotoxicity
Document Type
Journal Article
Publication Date
10-1-2017
Journal
Food and Chemical Toxicology
Volume
108
DOI
10.1016/j.fct.2017.08.020
Keywords
Acetaminophen; Hepatotoxicity; Mitochondria biogenesis; PPARγ co-activator 1-α; Regeneration; SRT1720
Abstract
© 2017 Elsevier Ltd Mitochondrial biogenesis (MB) is an adaptive response to maintain metabolic homeostasis after mitochondrial dysfunction. Induction of MB during APAP hepatotoxicity has not been studied. To investigate this, mice were treated with toxic doses of APAP and euthanized between 0 and 96 h. At early time points, APAP caused both mitochondrial dysfunction and reduction of mitochondrial mass, indicated by reduced activity of electron transport chain (ETC) complexes I and IV and depletion of mitochondrial DNA (mtDNA), respectively. Both ETC activity and mtDNA gradually recovered after 12 h, suggesting that MB occurs at late time points after APAP overdose. Immunofluorescent staining of mitochondria with mitochondrial outer membrane protein Tom20 further demonstrated that MB occurs selectively in hepatocytes surrounding necrotic areas. MB signaling mediators including PPARγ co-activator 1-α (Pgc-1α), nuclear respiratory factor-1 (Nrf-1) and mitochondrial fission protein dynamin-related protein-1 (Drp-1) were induced. Pgc-1α was selectively increased in hepatocytes surrounding necrotic areas. In addition, the time course of MB induction coincides with increased liver regeneration. Post-treatment with the known MB inducer SRT1720 increased Pgc-1α expression and liver regeneration, resulting in protection against late liver injury after APAP overdose. Thus, induction of MB is an important feature during APAP hepatotoxicity and liver regeneration.
APA Citation
Du, K., Ramachandran, A., McGill, M., Mansouri, A., Asselah, T., Farhood, A., Woolbright, B., Ding, W., & Jaeschke, H. (2017). Induction of mitochondrial biogenesis protects against acetaminophen hepatotoxicity. Food and Chemical Toxicology, 108 (). http://dx.doi.org/10.1016/j.fct.2017.08.020