2026/6/5
Mohammad Parastesh

Mohammad Parastesh

Academic rank: Associate Professor
ORCID: https://orcid.org/0000-0002-0273-9955
Education: PhD.
H-Index:
Faculty: Sport Sciences
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E-mail: mohamad.parastesh [at] gmail.com
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Research

Title
High-intensity interval training prevents high-fat diet-induced hepatic steatosis by modulating miRNA-34a, miRNA-467b, and their primary target proteins in male rats
Type
JournalPaper
Keywords
Non-alcoholic fatty liver disease – High-intensity intermittent training – microRNA-34a – microRNA-467b – Obesity
Year
2025
Journal Archives of Physiology And Biochemistry
DOI
Researchers Amir Mohammad Mohammadi Hajivand ، Hasan Kordi ، reza Gharakhanlou ، Hamid Reza Khaluonejad ، Mohammad Parastesh

Abstract

Aims: High-fat diet (HFD) consumption contributes to obesity and liver damage, while exercise training may counteract these effects. Given the regulatory role of microRNAs in lipid metabolism, this study investigates the impact of high-intensity interval training (HIIT) and HFD on hepatic fat accumulation, as well as the expression of miRNA-34a, miRNA-467b, and their associated proteins. Main methods: Twenty-four male rats were randomly assigned to four groups: (1) CON, (2) HIIT, (3) HFD, and (4) HIIT+HFD. The HFD groups received a 60% fat diet, while the rats in the HIIT groups performed high-intensity interval training (3 sessions/week, 2.5minutes high-intensity running × 90% maximal running capacity (MRC) with 2.5minutes active rest × 50% MRC, for ten weeks). Forty-eight hours post-intervention, blood and liver samples were collected to assess histopathology, liver enzymes, and the expression of miRNA-34a, miRNA-467b, SIRT1, PPAR-ɑ, and LPL proteins. Key findings: The HFD group exhibited excessive hepatic lipid accumulation, whereas HIIT significantly prevented HFD-induced hepatic steatosis, as confirmed by histopathological examinations. Liver enzyme levels (AST, ALT, and ALP) were significantly higher in the HFD group and significantly lower in both the HIIT and HIIT+HFD groups. Additionally, HIIT significantly increased miRNA-467b, SIRT1, and PPAR-ɑ expression while significantly decreasing miRNA-34a and LPL expression, preventing the effects of HFD. Significance: Our findings identified a novel molecular mechanism confirming that HIIT is beneficial to prevent hepatic steatosis and hepatic damage induced by HFD, likely due to the modulation of miRNA-467b, miRNA-34a, and their main target proteins.