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Comparative effect of vitamin D3 and carbenoxolone treatments in metabolic syndrome rats.

Abstract
Metabolic syndrome (MetS) is a cluster of cardiovascular risk factors including central obesity, hypertension, insulin resistance, dyslipidemia, and hyperglyemia. MetS is found to be a positive predictor of cardiovascular morbidity and mortality. The present study was planned to test the efficacy of vitamin D3 supplementation as compared with cortisol inhibition on MetS parameters. Wistar rats were allocated into four groups: control, untreated MetS, and MetS treated with either vitamin D3 (10 µg/kg) or carbenoxolone (50 mg/kg). MetS was induced by combination of high-fat diet and oral fructose. After the induction period (8 weeks), MetS was confirmed, and treatment modalities started for a further 4 weeks. Compared with untreated MetS, vitamin D3- and carbenoxolone-treated rats showed significant reduction in blood pressure, body mass index, Lee index, waist circumference, retroperitoneal fat, and improvement of dyslipidemia. Meanwhile, treatment with carbenoxolone significantly lowered the elevated liver enzymes, and vitamin D3 resulted in improved insulin sensitivity, enhanced glucose uptake by muscles, and replenished glycogen content in the liver and muscles near control levels. In conclusion, although treatment with vitamin D3 or carbenoxolone reduced the risk factors associated with MetS, vitamin D3 was effective in ameliorating insulin resistance which is the hallmark of MetS.
AuthorsNermine Saleh, Ansam Aly Seif, Ienass Bahaa, Enas A Abdel-Hady
JournalCanadian journal of physiology and pharmacology (Can J Physiol Pharmacol) Vol. 100 Issue 5 Pg. 412-421 (May 2022) ISSN: 1205-7541 [Electronic] Canada
PMID34855519 (Publication Type: Journal Article)
Chemical References
  • Blood Glucose
  • Cholecalciferol
  • Carbenoxolone
Topics
  • Animals
  • Blood Glucose (metabolism)
  • Carbenoxolone (pharmacology, therapeutic use)
  • Cholecalciferol (pharmacology, therapeutic use)
  • Insulin Resistance
  • Metabolic Syndrome (metabolism)
  • Rats
  • Rats, Wistar

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