Study of long non-coding RNA and mitochondrial dysfunction in diabetic rats

Tissue Cell. 2021 Aug:71:101516. doi: 10.1016/j.tice.2021.101516. Epub 2021 Feb 26.

Abstract

Diabetes mellitus (DM) is a worldwide health problem. The Micro- and macro-vascular complications are the major causes of morbidity and mortality of DM. Molecular regulation of mitochondrial fission/fusion cycles is being studied, but the results were not conclusive. The aim of this study is to investigate the possible functional role of lncRNA H19 and its relation to mitofusin-2 (Mfn-2) gene expression in diabetic rats with cardiac and renal complications. Streptozotocin-induced diabetic male, albino rats and a matched control group were investigated. Cardiac weights, blood pressure and ECG were recorded. Biochemical evaluation of cardiac and renal functions was performed. Molecular determination of lncRNA H19 and Mfn-2 gene expression and histological examination by light and electron microscopy for cardiac and renal tissues were performed. Diabetic rats showed a significant increase of left ventricle weight/whole body weight ratio, R wave voltage, and a significant decrease of blood pressure, heart rate, and P wave voltage. At the molecular level, lncRNA H19 and Mfn-2 mRNA showed altered expression with a statistically significant downregulation of Mfn-2 mRNA expression in renal tissues. In conclusion, the changes in lncRNA H19 and Mfn-2 mRNA expression may help better understanding of the pathogenesis of cardiac and renal dysfunctions associated with type 1 DM.

Keywords: Diabetes mellitus; Gene expression; LncRNA H19; Mitofusin.

MeSH terms

  • Animals
  • Diabetes Mellitus, Experimental / metabolism*
  • Diabetes Mellitus, Experimental / pathology
  • Diabetes Mellitus, Type 1 / metabolism*
  • Diabetes Mellitus, Type 1 / pathology
  • GTP Phosphohydrolases / biosynthesis*
  • Gene Expression Regulation*
  • Kidney / metabolism
  • Kidney / pathology
  • Male
  • Mitochondria, Heart / metabolism*
  • Mitochondrial Proteins / biosynthesis*
  • Myocardium / metabolism
  • Myocardium / pathology
  • RNA, Long Noncoding / biosynthesis*
  • Rats

Substances

  • H19 long non-coding RNA
  • Mitochondrial Proteins
  • RNA, Long Noncoding
  • GTP Phosphohydrolases
  • Mfn2 protein, rat