A ketogenic diet improves vascular hyperpermeability in type 2 diabetic mice by downregulating vascular pescadillo1 expression

• Published in: Journal of cellular and molecular medicine Vol. 27; no. 10; pp. 1410 - 1422
• Main Authors: Wang, Song, Zhou, Jielin, Lu, Jing, Lin, Yan, Liu, Shuaishuai, Chen, Keyang
• Format: Journal Article
• Language: English
• Published: England John Wiley & Sons, Inc 01.05.2023; John Wiley and Sons Inc
• Subjects: Abdomen; Animals; Antibodies; Bioengineering; Cadherins; Capillary Permeability - physiology; Cells, Cultured; Coronary vessels; Diabetes; Diabetes mellitus; Diabetes Mellitus, Type 2 - diet therapy; Diet, Ketogenic; Down-Regulation; Endothelial cells; Feeds; Gene Knockdown Techniques; Glucose; High fat diet; Hyperglycemia - prevention & control; Ketogenesis; Laboratory animals; Low carbohydrate diet; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Molecular modelling; Original; Permeability; PES1; Proteins; RNA-Binding Proteins - genetics; RNA-Binding Proteins - metabolism; siRNA; Ubiquitination; Vascular endothelial growth factor; vascular permeability; β‐HB; China; KD; β-HB; vascular permeability; diabetes; PES1
• ISSN: 1582-1838; 1582-4934
• DOI: 10.1111/jcmm.17744

The role of pescadillo1 (PES1) in regulating vascular permeability has been unknown. This study probes the role of PES1 and its mediated molecular mechanism in modulating vascular hyperpermeability in diabetic mice. Male C57BL/6J and db/db mice were fed a standard diet and a ketogenic diet (KD). Meanwhile, mouse vascular endothelial cells (MVECs) were treated with β‐hydroxybutyric acid (β‐HB), Pes1 siRNA or a Pes1 overexpression plasmid. Additionally, knockout (KO) of Pes1 in mice was applied. After 12 weeks of feedings, enhanced vascular PES1 expression in diabetic mice was inhibited by the KD. The suppression of PES1 was also observed in β‐HB‐treated MVECs. In mice with Pes1 KO, the levels of vascular VEGF and PES1 were attenuated, while the levels of vascular VE‐cadherin, Ang‐1 and Occludin were upregulated. Similar outcomes also occurred after the knockdown of Pes1 in cultured MVECs, which were opposite to the effects induced by PES1 overexpression in MVECs. In vitro and in vivo experiments showed that high glucose concentration‐induced increases in vascular paracellular permeability declined after MVECs were treated by β‐HB or by knockdown of Pes1. In contrast, increases in vascular permeability were induced by overexpression of Pes1, which were suppressed by coadministration of β‐HB in cultured endothelial cells. Similarly declines in vascular permeability were found by Pes1 knockdown in diabetic mice. Mechanistically, β‐HB decreased PES1‐facilitated ubiquitination of VE‐cadherin. The KD suppressed the diabetes‐induced increase in PES1, which may result in vascular hyperpermeability through ubiquitination of VE‐cadherin in type 2 diabetic mice.