Your browser doesn't support javascript.
loading
Melatonin/nicotinamide mononucleotide/ubiquinol: a cocktail providing superior cardioprotection against ischemia/reperfusion injury in a common co-morbidities modelled rat.
Mokhtari, Behnaz; Høilund-Carlsen, Poul Flemming; Chodari, Leila; Yasami, Masoud; Badalzadeh, Reza; Ghaffari, Samad.
Afiliación
  • Mokhtari B; Alavi Aging Research Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Høilund-Carlsen PF; Department of Physiology, Faculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
  • Chodari L; Department of Nuclear Medicine, Odense University Hospital, Odense, Denmark.
  • Yasami M; Department of Clinical Research, University of Southern Denmark, Odense, Denmark.
  • Badalzadeh R; Neurophysiology Research Center, Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences, Urmia, Iran.
  • Ghaffari S; Department of Physiology, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.
Mol Biol Rep ; 50(4): 3525-3537, 2023 Apr.
Article en En | MEDLINE | ID: mdl-36787055
ABSTRACT

BACKGROUND:

The metabolic and intracellular abnormalities in aging and diabetes cause loss of cardioprotection by routine interventions against myocardial ischemia/reperfusion (I/R) injury. We aimed to evaluate the possible interaction of aging and type-2 diabetes mellitus with cardioprotection and the potential protective effect of a mitochondrial cocktail (melatonin/nicotinamide mononucleotide (NMN)/ubiquinol) on myocardial I/R injury in aged diabetic rats.

METHODS:

Male Wistar rats (n = 108, 22-24 months old, 400-450 g) received high-fat diet/low dose of streptozotocin to induce type-2 diabetes, then were randomized into 9 groups of 12 rats each with/without I/R and/or melatonin, NMN, and ubiquinol, alone or in dual or triple combinations. Myocardial I/R was induced by LAD occlusion for 30 min followed by 24 h reperfusion. NMN (100 mg/kg/48 h, intraperitoneally) was administered for 28 days before I/R operation. Melatonin (10 mg/kg, intraperitoneally) and/or ubiquinol (30 mg/kg, intravenously) were administered at early reperfusion. Finally, hemodynamic index changes, infarct size, CK-MB levels, mitochondrial functional endpoints, and expression of mitochondrial biogenesis genes (SIRT-1/PGC-1α/NRF-2/TFAM) were assessed.

RESULTS:

The solo and dual applications of melatonin, NMN, and ubiquinol did not exert remarkable cardioprotective impacts. However, the triple combination improved myocardial function and decreased infarct size and CK-MB levels following myocardial I/R (P < .05 to P < .01). It also improved mitochondrial function and restored mitochondrial biogenesis genes (P < .01).

CONCLUSIONS:

Combination therapy with melatonin, NMN, and ubiquinol exerted significant cardioprotection and improved mitochondrial function and biogenesis via upregulation of SIRT-1/PGC-1α/NRF-2/TFAM profiles in aged diabetic rats and, thus, offers a promising strategy for providing noticeable cardioprotection against I/R injury also in aged diabetic patients.
Asunto(s)
Palabras clave

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Daño por Reperfusión Miocárdica / Isquemia Miocárdica / Diabetes Mellitus Experimental / Diabetes Mellitus Tipo 2 / Melatonina Tipo de estudio: Clinical_trials Límite: Animals Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Daño por Reperfusión Miocárdica / Isquemia Miocárdica / Diabetes Mellitus Experimental / Diabetes Mellitus Tipo 2 / Melatonina Tipo de estudio: Clinical_trials Límite: Animals Idioma: En Año: 2023 Tipo del documento: Article