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Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease
BACKGROUND: Diabetes is a risk factor for coronary atherosclerosis and coronary heart disease. Resveratrol (RESV) is a natural compound with anti-inflammatory effects. The objective of this study is to evaluate the cardio protective effects of RESV in a diabetic rat model with coronary heart disease...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Scientific Literature, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346847/ https://www.ncbi.nlm.nih.gov/pubmed/30658350 http://dx.doi.org/10.12659/MSM.910996 |
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author | Huo, Xiuyue Zhang, Tao Meng, Qingfeng Li, Chunxiao You, Beian |
author_facet | Huo, Xiuyue Zhang, Tao Meng, Qingfeng Li, Chunxiao You, Beian |
author_sort | Huo, Xiuyue |
collection | PubMed |
description | BACKGROUND: Diabetes is a risk factor for coronary atherosclerosis and coronary heart disease. Resveratrol (RESV) is a natural compound with anti-inflammatory effects. The objective of this study is to evaluate the cardio protective effects of RESV in a diabetic rat model with coronary heart disease. MATERIAL/METHODS: Diabetic rat model with coronary heart disease was constructed by feeding high-fat and high-calorie diet, followed by injection of streptozotocin. The diabetic rats received RESV or DMSO as treatment. Insulin, total cholesterol, and total triglyceride levels in serum were measured using enzyme-linked immunosorbent assay (ELISA) to evaluate the effect of RESV in alleviating diabetic symptoms. Inflammatory factors, including tumor necrotic factor α, interleukin-6, interleukin-8, intracellular adhesion molecule 1, vascular-cell adhesion molecule 1, and monocyte chemoattractant protein-1 were assayed using ELISA. Real-time polymerase chain reaction and western blot analysis were performed to evaluate the impact of RESV treatment on the TLR4/MyD88/NF-κB signaling pathway (toll-like receptor 4/myeloid differentiation factor 88/nuclear factor kappa B signaling pathway). Hematoxylin and eosin staining was used to document pathological changes in cardiovascular muscles. RESULTS: RESV preserved pancreatic tissue, which therefore reduced levels of glucose and triglycerides glyceride in serum. Inflammatory factors were also suppressed by RESV. TLR4/MyD88/NF-κB signaling pathway was downregulated after RESV treatment. CONCLUSIONS: RESV offers protective effects of cardiovascular tissues in the diabetic rat model with coronary heart disease. Those effects are mediated by downregulating the TLR4/MyD88/NF-κB signaling pathway. |
format | Online Article Text |
id | pubmed-6346847 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | International Scientific Literature, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63468472019-02-11 Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease Huo, Xiuyue Zhang, Tao Meng, Qingfeng Li, Chunxiao You, Beian Med Sci Monit Animal Study BACKGROUND: Diabetes is a risk factor for coronary atherosclerosis and coronary heart disease. Resveratrol (RESV) is a natural compound with anti-inflammatory effects. The objective of this study is to evaluate the cardio protective effects of RESV in a diabetic rat model with coronary heart disease. MATERIAL/METHODS: Diabetic rat model with coronary heart disease was constructed by feeding high-fat and high-calorie diet, followed by injection of streptozotocin. The diabetic rats received RESV or DMSO as treatment. Insulin, total cholesterol, and total triglyceride levels in serum were measured using enzyme-linked immunosorbent assay (ELISA) to evaluate the effect of RESV in alleviating diabetic symptoms. Inflammatory factors, including tumor necrotic factor α, interleukin-6, interleukin-8, intracellular adhesion molecule 1, vascular-cell adhesion molecule 1, and monocyte chemoattractant protein-1 were assayed using ELISA. Real-time polymerase chain reaction and western blot analysis were performed to evaluate the impact of RESV treatment on the TLR4/MyD88/NF-κB signaling pathway (toll-like receptor 4/myeloid differentiation factor 88/nuclear factor kappa B signaling pathway). Hematoxylin and eosin staining was used to document pathological changes in cardiovascular muscles. RESULTS: RESV preserved pancreatic tissue, which therefore reduced levels of glucose and triglycerides glyceride in serum. Inflammatory factors were also suppressed by RESV. TLR4/MyD88/NF-κB signaling pathway was downregulated after RESV treatment. CONCLUSIONS: RESV offers protective effects of cardiovascular tissues in the diabetic rat model with coronary heart disease. Those effects are mediated by downregulating the TLR4/MyD88/NF-κB signaling pathway. International Scientific Literature, Inc. 2019-01-18 /pmc/articles/PMC6346847/ /pubmed/30658350 http://dx.doi.org/10.12659/MSM.910996 Text en © Med Sci Monit, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) |
spellingShingle | Animal Study Huo, Xiuyue Zhang, Tao Meng, Qingfeng Li, Chunxiao You, Beian Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title | Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title_full | Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title_fullStr | Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title_full_unstemmed | Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title_short | Resveratrol Effects on a Diabetic Rat Model with Coronary Heart Disease |
title_sort | resveratrol effects on a diabetic rat model with coronary heart disease |
topic | Animal Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6346847/ https://www.ncbi.nlm.nih.gov/pubmed/30658350 http://dx.doi.org/10.12659/MSM.910996 |
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