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Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes
Chronic hyperglycemia contributes to vascular complications in diabetes. Resveratrol exerts anti-diabetic and anti-platelet action. This study aimed to evaluate the effects of resveratrol on metabolism and the function of blood platelets under static and in in vitro flow conditions in patients with...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026466/ https://www.ncbi.nlm.nih.gov/pubmed/35458194 http://dx.doi.org/10.3390/nu14081633 |
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author | Michno, Anna Grużewska, Katarzyna Ronowska, Anna Gul-Hinc, Sylwia Zyśk, Marlena Jankowska-Kulawy, Agnieszka |
author_facet | Michno, Anna Grużewska, Katarzyna Ronowska, Anna Gul-Hinc, Sylwia Zyśk, Marlena Jankowska-Kulawy, Agnieszka |
author_sort | Michno, Anna |
collection | PubMed |
description | Chronic hyperglycemia contributes to vascular complications in diabetes. Resveratrol exerts anti-diabetic and anti-platelet action. This study aimed to evaluate the effects of resveratrol on metabolism and the function of blood platelets under static and in in vitro flow conditions in patients with type 2 diabetes. Blood obtained from 8 healthy volunteers and 10 patients with type 2 diabetes was incubated with resveratrol and perfused over collagen-coated capillaries. Isolated blood platelets were incubated with resveratrol and activated by collagen to assess platelet function, metabolism, ATP release, TXA(2) production, lipid peroxidation, and gluthatione content. In the type 2 diabetes group, plasma glucose and fructosamine concentrations were significantly higher than in the healthy group. In in vitro studies, collagen-induced thrombi formation in the blood of diabetic patients was 33% higher than in the healthy group. Resveratrol reduced thrombi by over 50% in the blood of healthy and diabetic patients. TXA(2) production was 47% higher in diabetic platelets than in the healthy group. Resveratrol reduced TXA(2) release by 38% in healthy platelets and by 79% in diabetic platelets. Resveratrol also reduced the activities of enzymes responsible for glycolysis and oxidative metabolism in the platelets of both groups. These data indicate that the resveratrol-induced inhibition of platelet metabolism and TXA(2) release may lead to a reduction of platelet function and thrombus formation in patients with type 2 diabetes. Therefore, resveratrol may be beneficial to prevent vascular complications as a future complementary treatment in aspirin-resistant diabetic patients. |
format | Online Article Text |
id | pubmed-9026466 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-90264662022-04-23 Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes Michno, Anna Grużewska, Katarzyna Ronowska, Anna Gul-Hinc, Sylwia Zyśk, Marlena Jankowska-Kulawy, Agnieszka Nutrients Article Chronic hyperglycemia contributes to vascular complications in diabetes. Resveratrol exerts anti-diabetic and anti-platelet action. This study aimed to evaluate the effects of resveratrol on metabolism and the function of blood platelets under static and in in vitro flow conditions in patients with type 2 diabetes. Blood obtained from 8 healthy volunteers and 10 patients with type 2 diabetes was incubated with resveratrol and perfused over collagen-coated capillaries. Isolated blood platelets were incubated with resveratrol and activated by collagen to assess platelet function, metabolism, ATP release, TXA(2) production, lipid peroxidation, and gluthatione content. In the type 2 diabetes group, plasma glucose and fructosamine concentrations were significantly higher than in the healthy group. In in vitro studies, collagen-induced thrombi formation in the blood of diabetic patients was 33% higher than in the healthy group. Resveratrol reduced thrombi by over 50% in the blood of healthy and diabetic patients. TXA(2) production was 47% higher in diabetic platelets than in the healthy group. Resveratrol reduced TXA(2) release by 38% in healthy platelets and by 79% in diabetic platelets. Resveratrol also reduced the activities of enzymes responsible for glycolysis and oxidative metabolism in the platelets of both groups. These data indicate that the resveratrol-induced inhibition of platelet metabolism and TXA(2) release may lead to a reduction of platelet function and thrombus formation in patients with type 2 diabetes. Therefore, resveratrol may be beneficial to prevent vascular complications as a future complementary treatment in aspirin-resistant diabetic patients. MDPI 2022-04-14 /pmc/articles/PMC9026466/ /pubmed/35458194 http://dx.doi.org/10.3390/nu14081633 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Michno, Anna Grużewska, Katarzyna Ronowska, Anna Gul-Hinc, Sylwia Zyśk, Marlena Jankowska-Kulawy, Agnieszka Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title | Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title_full | Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title_fullStr | Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title_full_unstemmed | Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title_short | Resveratrol Inhibits Metabolism and Affects Blood Platelet Function in Type 2 Diabetes |
title_sort | resveratrol inhibits metabolism and affects blood platelet function in type 2 diabetes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9026466/ https://www.ncbi.nlm.nih.gov/pubmed/35458194 http://dx.doi.org/10.3390/nu14081633 |
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