Impaired mitochondrial medium-chain fatty acid oxidation drives periportal macrovesicular steatosis in sirtuin-5 knockout mice

• Published in: Scientific reports Vol. 10; no. 1; p. 18367
• Main Authors: Goetzman, Eric S., Bharathi, Sivakama S., Zhang, Yuxun, Zhao, Xue-Jun, Dobrowolski, Steven F., Peasley, Kevin, Sims-Lucas, Sunder, Monga, Satdarshan P.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 27.10.2020; Nature Publishing Group
• Subjects: 631/443; 631/45; 692/4017; Acyl-CoA dehydrogenase; Acyl-CoA Dehydrogenase, Long-Chain - metabolism; Animals; Coconut oil; Coconut Oil - administration & dosage; Dietary Fats - administration & dosage; Endoplasmic reticulum; Fatty acids; Fatty Acids - metabolism; Fatty liver; Female; High fat diet; Humanities and Social Sciences; Liver; Liver diseases; Male; Mice; Mice, Knockout; Mitochondria; Mitochondria, Liver - metabolism; multidisciplinary; Non-alcoholic Fatty Liver Disease - genetics; Non-alcoholic Fatty Liver Disease - metabolism; Oxidation; Oxidation-Reduction; Pediatrics; Phenotypes; Science; Science (multidisciplinary); Sirtuins - genetics; Steatosis; Triglycerides; Triglycerides - metabolism
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-020-75615-3

Medium-chain triglycerides (MCT), containing C 8 –C 12 fatty acids, are used to treat several pediatric disorders and are widely consumed as a nutritional supplement. Here, we investigated the role of the sirtuin deacylase Sirt5 in MCT metabolism by feeding Sirt5 knockout mice (Sirt5KO) high-fat diets containing either C 8 /C 10 fatty acids or coconut oil, which is rich in C 12 , for five weeks. Coconut oil, but not C 8 /C 10 feeding, induced periportal macrovesicular steatosis in Sirt5KO mice. 14 C–C 12 degradation was significantly reduced in Sirt5KO liver. This decrease was localized to the mitochondrial β-oxidation pathway, as Sirt5KO mice exhibited no change in peroxisomal C 12 β-oxidation. Endoplasmic reticulum ω-oxidation, a minor fatty acid degradation pathway known to be stimulated by C 12 accumulation, was increased in Sirt5KO liver. Mice lacking another mitochondrial C 12 oxidation enzyme, long-chain acyl-CoA dehydrogenase (LCAD), also developed periportal macrovesicular steatosis when fed coconut oil, confirming that defective mitochondrial C 12 oxidation is sufficient to induce the steatosis phenotype. Sirt5KO liver exhibited normal LCAD activity but reduced mitochondrial acyl-CoA synthetase activity with C 12 . These studies reveal a role for Sirt5 in regulating the hepatic response to MCT and may shed light into the pathogenesis of periportal steatosis, a hallmark of human pediatric non-alcoholic fatty liver disease.