The endogenous production of hydrogen sulphide in intrauterine tissues

<p>Abstract</p> <p>Background</p> <p>Hydrogen sulphide is a gas signalling molecule which is produced endogenously from L-cysteine via the enzymes cystathionine beta-synthase (CBS) and cystathionine gamma-lyase (CSE). The possible role of hydrogen sulphide in reproducti...

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Main Authors: Wang Rui, Heptinstall John, Vatish Manu, Patel Pushpa, Carson Ray J
Format: Article
Language:English
Published: BMC 2009-02-01
Series:Reproductive Biology and Endocrinology
Online Access:http://www.rbej.com/content/7/1/10
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author Wang Rui
Heptinstall John
Vatish Manu
Patel Pushpa
Carson Ray J
author_facet Wang Rui
Heptinstall John
Vatish Manu
Patel Pushpa
Carson Ray J
author_sort Wang Rui
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Hydrogen sulphide is a gas signalling molecule which is produced endogenously from L-cysteine via the enzymes cystathionine beta-synthase (CBS) and cystathionine gamma-lyase (CSE). The possible role of hydrogen sulphide in reproduction has not yet been fully investigated. It has been previously demonstrated that hydrogen sulphide relaxes uterine smooth muscle in vitro. The aim of the present study was to investigate the endogenous production of hydrogen sulphide in rat and human intrauterine tissues in vitro.</p> <p>Methods</p> <p>The production of hydrogen sulphide in rat and human intrauterine tissues was measured in vitro using a standard technique. The expression of CBS and CSE was also investigated in rat and human intrauterine tissues via Western blotting. Furthermore, the effects of nitric oxide (NO) and low oxygen conditions on the production rates of hydrogen sulphide were investigated.</p> <p>Results</p> <p>The order of hydrogen sulphide production rates (mean +/- SD, n = 4) for rat tissues were: liver (777 +/- 163 nM/min/g) > uterus (168 +/- 100 nM/min/g) > fetal membranes (22.3 +/- 15.0 nM/min/g) > placenta (11.1 +/- 4.7 nM/min/g), compared to human placenta (200 +/- 102 nM/min/g). NO significantly increased hydrogen sulphide production in rat fetal membranes (P < 0.05). Under low oxygen conditions the production of hydrogen sulphide was significantly elevated in human placenta, rat liver, uterus and fetal membranes (P < 0.05). Western blotting (n = 4) detected the expression of CBS and CSE in all rat intrauterine tissues, and in human placenta, myometrium, amnion and chorion.</p> <p>Conclusion</p> <p>Rat and human intrauterine tissues produce hydrogen sulphide in vitro possibly via CBS and CSE enzymes. NO increased the production of hydrogen sulphide in rat fetal membranes. The augmentation of hydrogen sulphide production in human intrauterine tissues in a low oxygen environment could have a role in pathophysiology of pregnancy.</p>
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spelling doaj.art-76fbf59248714450b8d21934b0b142aa2022-12-22T01:19:42ZengBMCReproductive Biology and Endocrinology1477-78272009-02-01711010.1186/1477-7827-7-10The endogenous production of hydrogen sulphide in intrauterine tissuesWang RuiHeptinstall JohnVatish ManuPatel PushpaCarson Ray J<p>Abstract</p> <p>Background</p> <p>Hydrogen sulphide is a gas signalling molecule which is produced endogenously from L-cysteine via the enzymes cystathionine beta-synthase (CBS) and cystathionine gamma-lyase (CSE). The possible role of hydrogen sulphide in reproduction has not yet been fully investigated. It has been previously demonstrated that hydrogen sulphide relaxes uterine smooth muscle in vitro. The aim of the present study was to investigate the endogenous production of hydrogen sulphide in rat and human intrauterine tissues in vitro.</p> <p>Methods</p> <p>The production of hydrogen sulphide in rat and human intrauterine tissues was measured in vitro using a standard technique. The expression of CBS and CSE was also investigated in rat and human intrauterine tissues via Western blotting. Furthermore, the effects of nitric oxide (NO) and low oxygen conditions on the production rates of hydrogen sulphide were investigated.</p> <p>Results</p> <p>The order of hydrogen sulphide production rates (mean +/- SD, n = 4) for rat tissues were: liver (777 +/- 163 nM/min/g) > uterus (168 +/- 100 nM/min/g) > fetal membranes (22.3 +/- 15.0 nM/min/g) > placenta (11.1 +/- 4.7 nM/min/g), compared to human placenta (200 +/- 102 nM/min/g). NO significantly increased hydrogen sulphide production in rat fetal membranes (P < 0.05). Under low oxygen conditions the production of hydrogen sulphide was significantly elevated in human placenta, rat liver, uterus and fetal membranes (P < 0.05). Western blotting (n = 4) detected the expression of CBS and CSE in all rat intrauterine tissues, and in human placenta, myometrium, amnion and chorion.</p> <p>Conclusion</p> <p>Rat and human intrauterine tissues produce hydrogen sulphide in vitro possibly via CBS and CSE enzymes. NO increased the production of hydrogen sulphide in rat fetal membranes. The augmentation of hydrogen sulphide production in human intrauterine tissues in a low oxygen environment could have a role in pathophysiology of pregnancy.</p>http://www.rbej.com/content/7/1/10
spellingShingle Wang Rui
Heptinstall John
Vatish Manu
Patel Pushpa
Carson Ray J
The endogenous production of hydrogen sulphide in intrauterine tissues
Reproductive Biology and Endocrinology
title The endogenous production of hydrogen sulphide in intrauterine tissues
title_full The endogenous production of hydrogen sulphide in intrauterine tissues
title_fullStr The endogenous production of hydrogen sulphide in intrauterine tissues
title_full_unstemmed The endogenous production of hydrogen sulphide in intrauterine tissues
title_short The endogenous production of hydrogen sulphide in intrauterine tissues
title_sort endogenous production of hydrogen sulphide in intrauterine tissues
url http://www.rbej.com/content/7/1/10
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