Cargando…
Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects
Metabolic syndrome belongs to the most important risk factors of cardiovascular diseases. The aim of this study was to investigate changes in cardiovascular system induced by high cholesterol and high fat diet (HCHF) in HTG rats and their influence by a pyridoindole antioxidant – SMe1EC2 (S). The ef...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Slovak Toxicology Society SETOX
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107648/ https://www.ncbi.nlm.nih.gov/pubmed/30174531 http://dx.doi.org/10.1515/intox-2017-0014 |
_version_ | 1783350000159293440 |
---|---|
author | Knezl, Vladimír Sotníková, Ružena Brnoliaková, Zuzana Stankovičová, Tatiana Bauer, Viktor Bezek, Štefan |
author_facet | Knezl, Vladimír Sotníková, Ružena Brnoliaková, Zuzana Stankovičová, Tatiana Bauer, Viktor Bezek, Štefan |
author_sort | Knezl, Vladimír |
collection | PubMed |
description | Metabolic syndrome belongs to the most important risk factors of cardiovascular diseases. The aim of this study was to investigate changes in cardiovascular system induced by high cholesterol and high fat diet (HCHF) in HTG rats and their influence by a pyridoindole antioxidant – SMe1EC2 (S). The effects of S were compared with those of atorvastatin (A). Male HTG rats were fed HCHF (1% cholesterol + 7.5% lard) for 4 weeks. S and A were administered p.o., 50 mg/kg b.w. Following experimental groups were used: Wistar rats (W), hypertriglyceridemic rats (HTG), HTG rats fed HCHF (CHOL), HTG+S (S-HTG), CHOL+S (S-CHOL), and CHOL+A (A-CHOL). Values of blood pressure (BP) and selected ECG parameters were monitored in conscious animals, functions of the isolated heart and aorta were analyzed ex vivo. At the end of the experiment, systolic (sBP) and diastolic (dBP) blood pressure was increased in HTG and CHOL. S and A decreased BP in all treated groups. Accordingly with BP changes, the aortic endothelial function of CHOL was damaged. Both S and A administration ameliorated the endothelium-dependent relaxation to values of W. PQ and QTc intervals were prolonged in CHOL, while the treatment with S or A improved ECG findings. Prodysrhythmogenic threshold was decreased significantly in CHOL and both treatments returned it to the control values. In conclusion, HCHF increased BP, impaired endothelial relaxation of the aorta and potentiated susceptibility of myocardium to dysrhythmias. The effect of S on the changes induced by HCHF diet was more pronounced than that of A. |
format | Online Article Text |
id | pubmed-6107648 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Slovak Toxicology Society SETOX |
record_format | MEDLINE/PubMed |
spelling | pubmed-61076482018-08-31 Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects Knezl, Vladimír Sotníková, Ružena Brnoliaková, Zuzana Stankovičová, Tatiana Bauer, Viktor Bezek, Štefan Interdiscip Toxicol Original Article Metabolic syndrome belongs to the most important risk factors of cardiovascular diseases. The aim of this study was to investigate changes in cardiovascular system induced by high cholesterol and high fat diet (HCHF) in HTG rats and their influence by a pyridoindole antioxidant – SMe1EC2 (S). The effects of S were compared with those of atorvastatin (A). Male HTG rats were fed HCHF (1% cholesterol + 7.5% lard) for 4 weeks. S and A were administered p.o., 50 mg/kg b.w. Following experimental groups were used: Wistar rats (W), hypertriglyceridemic rats (HTG), HTG rats fed HCHF (CHOL), HTG+S (S-HTG), CHOL+S (S-CHOL), and CHOL+A (A-CHOL). Values of blood pressure (BP) and selected ECG parameters were monitored in conscious animals, functions of the isolated heart and aorta were analyzed ex vivo. At the end of the experiment, systolic (sBP) and diastolic (dBP) blood pressure was increased in HTG and CHOL. S and A decreased BP in all treated groups. Accordingly with BP changes, the aortic endothelial function of CHOL was damaged. Both S and A administration ameliorated the endothelium-dependent relaxation to values of W. PQ and QTc intervals were prolonged in CHOL, while the treatment with S or A improved ECG findings. Prodysrhythmogenic threshold was decreased significantly in CHOL and both treatments returned it to the control values. In conclusion, HCHF increased BP, impaired endothelial relaxation of the aorta and potentiated susceptibility of myocardium to dysrhythmias. The effect of S on the changes induced by HCHF diet was more pronounced than that of A. Slovak Toxicology Society SETOX 2017-11 2018-02-14 /pmc/articles/PMC6107648/ /pubmed/30174531 http://dx.doi.org/10.1515/intox-2017-0014 Text en Copyright © 2017 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. https://creativecommons.org/licenses/by-nc-nd/4.0/ This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License. (CC BY-NC-ND 4.0) |
spellingShingle | Original Article Knezl, Vladimír Sotníková, Ružena Brnoliaková, Zuzana Stankovičová, Tatiana Bauer, Viktor Bezek, Štefan Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title | Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title_full | Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title_fullStr | Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title_full_unstemmed | Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title_short | Monotherapy of experimental metabolic syndrome: II. Study of cardiovascular effects |
title_sort | monotherapy of experimental metabolic syndrome: ii. study of cardiovascular effects |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6107648/ https://www.ncbi.nlm.nih.gov/pubmed/30174531 http://dx.doi.org/10.1515/intox-2017-0014 |
work_keys_str_mv | AT knezlvladimir monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects AT sotnikovaruzena monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects AT brnoliakovazuzana monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects AT stankovicovatatiana monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects AT bauerviktor monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects AT bezekstefan monotherapyofexperimentalmetabolicsyndromeiistudyofcardiovasculareffects |