Synthetic Pyridoindole and Rutin Affect Upregulation of Endothelial Nitric Oxide Synthase and Heart Function in Rats Fed a High-Fat-Fructose Diet
Jazyk angličtina Země Česko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
34717058
PubMed Central
PMC8815465
DOI
10.33549/physiolres.934670
PII: 934670
Knihovny.cz E-zdroje
- MeSH
- biometrie MeSH
- fruktosa škodlivé účinky MeSH
- indoly farmakologie terapeutické užití MeSH
- krysa rodu Rattus MeSH
- metabolický syndrom farmakoterapie enzymologie etiologie MeSH
- myokard metabolismus MeSH
- NF-kappa B metabolismus MeSH
- potkani Wistar MeSH
- preklinické hodnocení léčiv MeSH
- pyridiny farmakologie terapeutické užití MeSH
- rutin farmakologie terapeutické užití MeSH
- srdce účinky léků MeSH
- synthasa oxidu dusnatého, typ III metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- fruktosa MeSH
- indoly MeSH
- NF-kappa B MeSH
- Nos3 protein, rat MeSH Prohlížeč
- pyridiny MeSH
- rutin MeSH
- SMe1EC2 MeSH Prohlížeč
- synthasa oxidu dusnatého, typ III MeSH
Metabolic syndrome (MetS) belongs to the serious health complications expanding in cardiovascular diseases, obesity, insulin resistance, and hyperglycemia. In this study, hypertriacylglycerolemic rats fed a high-fat-fructose diet (HFFD) were used as an experimental model of MetS to explore the effect of tested compounds. Effects of a new prospective pyridoindole derivative coded SMe1EC2 and the natural polyphenol rutin were tested. Endothelial nitric oxide synthase (NOS3) and nuclear factor kappa B (NF-?B) expression were assessed in the left ventricle immunohistochemically and left ventricle activity was monitored in isolated perfused rat hearts. NOS3 activity in the left ventricle decreased markedly as a result of a HFFD. NOS3 expression was upregulated by both substances. NF-?B expression was increased in the MetS group in comparison to control rats and the expression further increased in the SMe1EC2 treatment. This compound significantly improved the coronary flow in comparison to the control group during reperfusion of the heart followed after ischemia. Further, it tended to increase left ventricular systolic pressure, heart product, rate of maximal contraction and relaxation, and coronary flow during baseline assessment. Moreover, the compound SMe1EC2 decreased the sensitivity of hearts to electrically induced ventricular fibrillation. Contrary to this rutin decreased coronary flow in reperfusion. Present results suggest that despite upregulation of NOS3 by both substances tested, pyridoindole SMe1EC2 rather than rutin could be suitable in treatment strategies of cardiovascular disorders in MetS-like conditions.
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Metabolic Syndrome in Hypertriglyceridemic Rats: Effects of Antioxidants