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Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses

BACKGROUND: Microvascular anastomosis patency is adversely affected by local and systemic factors. Impaired intimal recovery and endothelial mechanisms promoting thrombus formation at the anastomotic site are common etiological factors of reduced anastomosis patency. Epigallocatechin gallate (EGCG)...

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Autores principales: İğde, Murat, Onur Öztürk, Mehmet, Yaşar, Burak, Hakan Bulam, Mehmet, Ergani, Hasan Murat, Ünlü, Ramazan Erkin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Plastic and Reconstructive Surgeons 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536869/
https://www.ncbi.nlm.nih.gov/pubmed/31113184
http://dx.doi.org/10.5999/aps.2018.00157
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author İğde, Murat
Onur Öztürk, Mehmet
Yaşar, Burak
Hakan Bulam, Mehmet
Ergani, Hasan Murat
Ünlü, Ramazan Erkin
author_facet İğde, Murat
Onur Öztürk, Mehmet
Yaşar, Burak
Hakan Bulam, Mehmet
Ergani, Hasan Murat
Ünlü, Ramazan Erkin
author_sort İğde, Murat
collection PubMed
description BACKGROUND: Microvascular anastomosis patency is adversely affected by local and systemic factors. Impaired intimal recovery and endothelial mechanisms promoting thrombus formation at the anastomotic site are common etiological factors of reduced anastomosis patency. Epigallocatechin gallate (EGCG) is a catechin derivative belonging to the flavonoid subgroup and is present in green tea (Camellia sinensis). This study investigated the effects of EGCG on the structure of vessel tips used in microvascular anastomoses and evaluated its effects on thrombus formation at an anastomotic site. METHODS: Thirty-six adult male Wistar albino rats were used in the study. The right femoral artery was cut and reanastomosed. The rats were divided into two groups (18 per group) and were systemically administered either EGCG or saline. Each group were then subdivided into three groups, each with six rats. Axial histological sections were taken from segments 1 cm proximal and 1 cm distal to the microvascular anastomosis site on days 5, 10, and 14. RESULTS: Thrombus formation was significantly different between the EGCG and control groups on day 5 (P=0.015) but not on days 10 or 14. The mean luminal diameter was significantly greater in the EGCG group on days 5 (P=0.002), 10 (P=0.026), and 14 (P=0.002). Intimal thickening was significantly higher on days 5 (P=0.041) and 10 (P=0.02). CONCLUSIONS: EGCG showed vasodilatory effects and led to reduced early thrombus formation after microvascular repair. Similar studies on venous anastomoses and random or axial pedunculated skin flaps would also contribute valuable findings relevant to this topic.
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spelling pubmed-65368692019-06-03 Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses İğde, Murat Onur Öztürk, Mehmet Yaşar, Burak Hakan Bulam, Mehmet Ergani, Hasan Murat Ünlü, Ramazan Erkin Arch Plast Surg Original Article BACKGROUND: Microvascular anastomosis patency is adversely affected by local and systemic factors. Impaired intimal recovery and endothelial mechanisms promoting thrombus formation at the anastomotic site are common etiological factors of reduced anastomosis patency. Epigallocatechin gallate (EGCG) is a catechin derivative belonging to the flavonoid subgroup and is present in green tea (Camellia sinensis). This study investigated the effects of EGCG on the structure of vessel tips used in microvascular anastomoses and evaluated its effects on thrombus formation at an anastomotic site. METHODS: Thirty-six adult male Wistar albino rats were used in the study. The right femoral artery was cut and reanastomosed. The rats were divided into two groups (18 per group) and were systemically administered either EGCG or saline. Each group were then subdivided into three groups, each with six rats. Axial histological sections were taken from segments 1 cm proximal and 1 cm distal to the microvascular anastomosis site on days 5, 10, and 14. RESULTS: Thrombus formation was significantly different between the EGCG and control groups on day 5 (P=0.015) but not on days 10 or 14. The mean luminal diameter was significantly greater in the EGCG group on days 5 (P=0.002), 10 (P=0.026), and 14 (P=0.002). Intimal thickening was significantly higher on days 5 (P=0.041) and 10 (P=0.02). CONCLUSIONS: EGCG showed vasodilatory effects and led to reduced early thrombus formation after microvascular repair. Similar studies on venous anastomoses and random or axial pedunculated skin flaps would also contribute valuable findings relevant to this topic. Korean Society of Plastic and Reconstructive Surgeons 2019-05 2019-05-15 /pmc/articles/PMC6536869/ /pubmed/31113184 http://dx.doi.org/10.5999/aps.2018.00157 Text en Copyright © 2019 The Korean Society of Plastic and Reconstructive Surgeons This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
İğde, Murat
Onur Öztürk, Mehmet
Yaşar, Burak
Hakan Bulam, Mehmet
Ergani, Hasan Murat
Ünlü, Ramazan Erkin
Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title_full Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title_fullStr Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title_full_unstemmed Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title_short Antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
title_sort antithrombotic effect of epigallocatechin gallate on the patency of arterial microvascular anastomoses
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536869/
https://www.ncbi.nlm.nih.gov/pubmed/31113184
http://dx.doi.org/10.5999/aps.2018.00157
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