The daily caloric restriction and alternate-day fasting ameliorated lipid dysregulation in type 2 diabetic mice by downregulating hepatic pescadillo 1

• Published in: European journal of nutrition 2022-08, Vol.61 (5), p.2775-2797
• Main Authors: Zhou, Jielin, Jiang, Zhengxuan, Lin, Yan, Li, Chengcheng, Liu, Juan, Tian, Mengjun, Liu, Yong, Chen, Keyang
• Format: Article
• Language: English
• Subjects: Carnitine palmitoyltransferase; Chemistry; Chemistry and Materials Science; Diabetes; Diabetes mellitus (non-insulin dependent); Dietary restrictions; Fasting; Hepatocytes; Lipid metabolism; Lipids; Liver; Nutrition; Original Contribution; Palmitoyltransferase; Peroxisome proliferator-activated receptors; Rodents; siRNA; Triglycerides; Ubiquitination
• ISSN: 1436-6207; 1436-6215
• DOI: 10.1007/s00394-022-02850-x

Purpose A possible link between pescadillo 1 (PES1) and lipid metabolism has been reported. However, whether PES1 is involved in the effects of daily caloric restriction (CR) and alternate-day fasting (ADF) interventions on diabetes-related lipid dysregulation is not elucidated. The current study aims are to explore the role of PES1 in effects of CR and ADF on diabetic mice and related mechanism. Methods Eight-week-old male db/db mice with type 2 diabetes mellitus (T2DM) were randomly divided into untreated T2DM, CR and ADF groups. McArdle hepatocytes were treated with 48 h high glucose (HG), 48 h normal glucose (NG) and 24 h HG plus 24 h NG, respectively. Pes1 siRNA and overexpression plasmid were, respectively, transfected into liver cells, and AAV 9 - Pes1 -shRNA was injected into db/db mice. Results After 12-week interventions, the peroxisome proliferator-activated receptor alpha (PPAR-α) and carnitine palmitoyltransferase 1A (CPT1A) levels in livers of T2DM mice were enhanced by CR and ADF interventions with reductions of hepatic and plasma triglycerides. Unexpectedly, hepatic PES1 levels were downregulated by two interventions, consistent with the results of 48 h NG and 24 h HG plus 24 h NG-treated cells. Moreover, CPT1A level was upregulated in Pes1 -siRNA-treated cells and AAV 9 - Pes1 -shRNA injected murine livers, in contrast to Pes1 overexpression in cultured cells. Mechanistically, 48 h NG or 24 h HG plus 24 h NG treatment increased PPAR-α binding to Pes1 promoter, suppressing the PES1 expression, thereby lowering the PES1-mediated ubiquitination of CPT1A. Conclusion The present study suggests that CR and ADF may improve lipid dysregulation in diabetic mice by downregulating hepatic PES1.