Exercise-promoted adiponectin secretion activates autolysosomes to protect the liver of ApoE mice from a high-fat diet

• Published in: Food & function Vol. 15; no. 19; pp. 9796 - 9812
• Main Authors: Wu, Weijia, Jian, Ye, Yuan, Shunling, Li, Xuan, Tang, Yingzhe, Zeng, Fanqi, Liu, Wenjing, Zhao, Zhe, Wang, Yirong, Wang, Yiyang, Liu, Wenfeng
• Format: Journal Article
• Language: English
• Published: England Royal Society of Chemistry 30.09.2024
• Subjects: Adiponectin; Adiponectin - metabolism; Animals; Apolipoprotein E; Apolipoproteins E - genetics; Apolipoproteins E - metabolism; Arteriosclerosis; Atherosclerosis; CD36 antigen; Deposition; Diet; Diet, High-Fat - adverse effects; Fat metabolism; Food intake; Gluconeogenesis; High fat diet; Hyperlipidemia; Lipid metabolism; Lipids; Liver; Liver - metabolism; Liver diseases; Lysosomes - metabolism; Male; Metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Nuclear transport; Physical Conditioning, Animal; Scavenging; Side effects; Signal transduction; Translocation
• ISSN: 2042-6496; 2042-650X; 2042-650X
• DOI: 10.1039/d4fo02984d

Fat is a "double-edged sword": while it is a necessary substance for the body, the long-term intake of excessive fat will cause obesity, with the liver subjected to lipotoxicity as it accumulates. It will then continue to deteriorate, eventually leading to liver failure, which is a negative impact of high-fat food intake. Research has shown that exercise can reverse the side effects of a chronic high-fat diet and help the body to mitigate the harmful effects of lipotoxicity. In our study, it was found that moderate-intensity cardio-training (MICT) and high-intensity interval exercise (HIIT) effectively protected the livers of high-fat diet (HFD) ApoE −/− mice against lipotoxicity. Previous results demonstrated that 12 weeks of HFD resulted in a significant elevation of CD36 in the livers of C57BL/6J mice, while knockdown of CD36 did not reduce the accumulation of fat in the liver. Therefore, we used ApoE −/− mice as experimental subjects. Although HFD caused the development of hyperlipidemia and atherosclerosis, it is interesting to note that, due to the knockdown of ApoE, the livers of ApoE −/− mice in the non-exercise group did not show significant lipid deposition; however, after 12 weeks of MICT and HIIT, the livers of ApoE −/− mice showed significant lipid deposition. After we analyzed the lipid metabolism in their livers, we found that this was caused by the promotion of transport of peripheral fat into the liver due to exercise. Moreover, 12 weeks of exercise effectively reduced atherosclerosis, and the livers of ApoE −/− mice in the exercise group were not damaged by lipotoxicity. The results showed that a 12-week exercise treatment activated AMPK in the livers of HFD ApoE −/− mice through the APN-AdipoR1 signaling pathway, improved hepatic lipid metabolism disorders, and promoted the nuclear translocation of TFEB to enhance autophagic-lysosomal lipid scavenging. After the peripheral lipid is input into the liver due to exercise, the energy generated through gluconeogenesis can be used to replenish the energy consumed by exercise and maintain the normal operation of various functions in the liver, based on which the high autophagic flux in the liver can be maintained and the lipid clearance rate can be enhanced to protect the liver from lipotoxicity. Treadmill exercise promotes liver fat uptake, activates lipolysis and inhibits DNL, and activates autolysosomes through APN-AdipoR1 to accelerate lipolysis and protect hepatocytes from lipotoxicity.