Cryopreservation, which is a vital method for efficient, economical, long-term storage of sperm, has an irreplaceable advantage in breeding excellent breeding stocks, protecting endangered species and international germplasm exchange, while gene banks and planning of artificial insemination (AI) centres are also using a large amount of frozen-thawed semen (Pezo et al., 2019). Yet, only 1% of AI worldwide used frozen-thawed boar semen because boar sperm is more susceptible to the stress caused by low temperature, osmotic shock, reactive oxygen species (ROS) production and the toxicity of the cryoprotectants (De Andrade et al., 2022).

Liraglutide, an analog of human glucagon‐like peptide‐1 (GLP‐1), has been found to improve hepatic steatosis in clinical practice. However, the underlying mechanism remains to be fully defined. Increasing evidence suggests that retinoic acid receptor‐related orphan receptor α (RORα) is involved in hepatic lipid accumulation. In the current study, we investigated whether the ameliorating impact of liraglutide on lipid‐induced hepatic steatosis is dependent on RORα activity and examined the underlying mechanisms. Cre‐loxP‐mediated, liver‐specific Rorα knockout (Rora LKO) mice, and littermate controls with a Roraloxp/loxp genotype were established. The effects of liraglutide on lipid accumulation were evaluated in mice challenged with a high‐fat diet (HFD) for 12 weeks. Moreover, mouse AML12 hepatocytes expressing small interfering RNA (siRNA) of Rora were exposed to palmitic acid to explore the pharmacological mechanism of liraglutide. The results showed that liraglutide treatment significantly alleviated HFD‐induced liver steatosis, marked by reduced liver weight and triglyceride accumulation, improved glucose tolerance and serum levels of lipid profiles and aminotransferase. Consistently, liraglutide also ameliorated lipid deposits in a steatotic hepatocyte model in vitro. In addition, liraglutide treatment reversed the HFD‐induced downregulation of Rora expression and autophagic activity in mouse liver tissues. However, the beneficial effect of liraglutide on hepatic steatosis was not observed in Rora LKO mice. Mechanistically, the ablation of Rorα in hepatocytes diminished liraglutide‐induced autophagosome formation and the fusion of autophagosomes and lysosomes, resulting in weakened autophagic flux activation. Thus, our findings suggest that RORα is essential for the beneficial impact of liraglutide on lipid deposition in hepatocytes and regulates autophagic activity in the underlying mechanism.