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Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery

The aim of this study is to reveal the regulatory role of cystathionine gamma-lyase (CSE), the main source of hydrogen sulphide (H(2)S) in perivascular adipose tissue (PVAT), of diabetic rats. Diabetes was induced in male rats by a single intraperitoneal injection of streptozotocin. Animals with glu...

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Autores principales: Emilova, Radoslava, Dimitrova, Daniela, Mladenov, Mitko, Daneva, Teodora, Schubert, Rudolf, Gagov, Hristo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433913/
https://www.ncbi.nlm.nih.gov/pubmed/26019628
http://dx.doi.org/10.1080/13102818.2014.991565
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author Emilova, Radoslava
Dimitrova, Daniela
Mladenov, Mitko
Daneva, Teodora
Schubert, Rudolf
Gagov, Hristo
author_facet Emilova, Radoslava
Dimitrova, Daniela
Mladenov, Mitko
Daneva, Teodora
Schubert, Rudolf
Gagov, Hristo
author_sort Emilova, Radoslava
collection PubMed
description The aim of this study is to reveal the regulatory role of cystathionine gamma-lyase (CSE), the main source of hydrogen sulphide (H(2)S) in perivascular adipose tissue (PVAT), of diabetic rats. Diabetes was induced in male rats by a single intraperitoneal injection of streptozotocin. Animals with glucose levels above 20 mmol/L were determined as diabetic. The rat gracilis arteries (a. gracilis) were dissected with or without PVAT. In all in vitro experiments endothelium-denuded preparations were used for isometric contraction measurements. Increasing concentrations of 5-hydroxytryptamine (5-HT) from 10(−10) to 10(−5) mol/L were applied to induce gradual increase in force of contractions of circular artery segments. The relaxing effect of CSE was inhibited by DL-propargyl glycine (PGG). The presence of PVAT decreases the contractile response to 5-HT of a. gracilis from control rats. This response is reversed in contraction studies in the same rat artery from diabetic rats. DL-PPG (1 mmol/L) induced significant increase of the force of contraction in artery preparations with PVAT from control rats in the whole range of 5-HT. In contrast, PGG had a relaxing effect in high concentrations of 5-HT (10(−6) and 10(−5) mol/L) in diabetic rat arteries with PVAT. It is concluded that in skeletal muscle artery from diabetic rats, a mediator related to H(2)S is released from PVAT. This paracrine mediator increases the maximal force of contraction of endothelium-denuded preparations at higher concentrations of 5-HT.
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spelling pubmed-44339132015-05-25 Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery Emilova, Radoslava Dimitrova, Daniela Mladenov, Mitko Daneva, Teodora Schubert, Rudolf Gagov, Hristo Biotechnol Biotechnol Equip Article; Medical Biotechnology The aim of this study is to reveal the regulatory role of cystathionine gamma-lyase (CSE), the main source of hydrogen sulphide (H(2)S) in perivascular adipose tissue (PVAT), of diabetic rats. Diabetes was induced in male rats by a single intraperitoneal injection of streptozotocin. Animals with glucose levels above 20 mmol/L were determined as diabetic. The rat gracilis arteries (a. gracilis) were dissected with or without PVAT. In all in vitro experiments endothelium-denuded preparations were used for isometric contraction measurements. Increasing concentrations of 5-hydroxytryptamine (5-HT) from 10(−10) to 10(−5) mol/L were applied to induce gradual increase in force of contractions of circular artery segments. The relaxing effect of CSE was inhibited by DL-propargyl glycine (PGG). The presence of PVAT decreases the contractile response to 5-HT of a. gracilis from control rats. This response is reversed in contraction studies in the same rat artery from diabetic rats. DL-PPG (1 mmol/L) induced significant increase of the force of contraction in artery preparations with PVAT from control rats in the whole range of 5-HT. In contrast, PGG had a relaxing effect in high concentrations of 5-HT (10(−6) and 10(−5) mol/L) in diabetic rat arteries with PVAT. It is concluded that in skeletal muscle artery from diabetic rats, a mediator related to H(2)S is released from PVAT. This paracrine mediator increases the maximal force of contraction of endothelium-denuded preparations at higher concentrations of 5-HT. Taylor & Francis 2015-01-02 2014-12-18 /pmc/articles/PMC4433913/ /pubmed/26019628 http://dx.doi.org/10.1080/13102818.2014.991565 Text en © 2014 The Author(s). Published by Taylor & Francis. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Article; Medical Biotechnology
Emilova, Radoslava
Dimitrova, Daniela
Mladenov, Mitko
Daneva, Teodora
Schubert, Rudolf
Gagov, Hristo
Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title_full Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title_fullStr Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title_full_unstemmed Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title_short Cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
title_sort cystathionine gamma-lyase of perivascular adipose tissue with reversed regulatory effect in diabetic rat artery
topic Article; Medical Biotechnology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4433913/
https://www.ncbi.nlm.nih.gov/pubmed/26019628
http://dx.doi.org/10.1080/13102818.2014.991565
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