Aerobic exercise improves non-alcoholic fatty liver disease by down-regulating the protein expression of the CNPY2-PERK pathway
Non-alcoholic fatty liver disease (NAFLD) is highly prevalent, and physical exercise represents one of the most effective methods to attenuate NAFLD. However, the mechanism of aerobic exercise improving NAFLD remains unclear. This study aims to investigate the effect of aerobic exercise on CNPY2-PER...
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Published in | Biochemical and biophysical research communications Vol. 603; pp. 35 - 40 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Inc
07.05.2022
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Subjects | |
Online Access | Get full text |
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Summary: | Non-alcoholic fatty liver disease (NAFLD) is highly prevalent, and physical exercise represents one of the most effective methods to attenuate NAFLD. However, the mechanism of aerobic exercise improving NAFLD remains unclear. This study aims to investigate the effect of aerobic exercise on CNPY2-PERK pathway in mice with NAFLD. Our study found that a high-fat diet induced NAFLD, causing an abnormal lipid metabolism and liver function injury, and increased the expressions of CNPY2, CNPY2 mRNA, PERK, PERK mRNA, p-eIF2a and CHOP. However, aerobic exercise reversesd all these parameters. These data suggest that CNPY2-PERK pathway is involved in the formation of NAFLD, and aerobic exercise can effectively improve NAFLD, which may be related to down-regulate the protein expressions of the CNPY2-PERK pathway.
•The CNPY2-PERK signaling pathway is involved in the formation of non-alcoholic fatty liver disease (NAFLD) induced by a high fat diet in mice.•The aerobic exercise can effectively improve NAFLD.•The aerobic exercise down-regulats the protein expression of the CNPY2-PERK signaling pathway in mice with NAFLD.•The aerobic exercise can effectively improve NAFLD by down-regulating the expression of components of the CNPY2-PERK pathway. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0006-291X 1090-2104 1090-2104 |
DOI: | 10.1016/j.bbrc.2022.03.008 |