Skip to content Skip to navigation
University of Warwick
  • Study
  • |
  • Research
  • |
  • Business
  • |
  • Alumni
  • |
  • News
  • |
  • About

University of Warwick
Publications service & WRAP

Highlight your research

  • WRAP
    • Home
    • Search WRAP
    • Browse by Warwick Author
    • Browse WRAP by Year
    • Browse WRAP by Subject
    • Browse WRAP by Department
    • Browse WRAP by Funder
    • Browse Theses by Department
  • Publications Service
    • Home
    • Search Publications Service
    • Browse by Warwick Author
    • Browse Publications service by Year
    • Browse Publications service by Subject
    • Browse Publications service by Department
    • Browse Publications service by Funder
  • Statistics
  • Help & Advice
University of Warwick

The Library

  • Login

The endogenous production of hydrogen sulphide in intrauterine tissues

Tools
- Tools
+ Tools

Patel, Pushpa, Vatish, Manu, Heptinstall, John, Wang, Rui and Carson, Ray J.. (2009) The endogenous production of hydrogen sulphide in intrauterine tissues. Reproductive Biology and Endocrinology, Vol.7 (No.10). ISSN 1477-7827

[img]
Preview
PDF
WRAP_Heptinstall_Endogenous_production_1477-7827-7-10.pdf - Requires a PDF viewer such as GSview, Xpdf or Adobe Acrobat Reader

Download (365Kb)
Official URL: http://dx.doi.org/10.1186/1477-7827-7-10

Abstract

Background: 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. Methods: 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. Results: 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. Conclusion: 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.

Item Type: Journal Article
Subjects: Q Science > QL Zoology
R Medicine > RG Gynecology and obstetrics
Divisions: Faculty of Medicine > Warwick Medical School > Clinical Sciences Research Institute (CSRI)
Faculty of Medicine > Warwick Medical School > Reproductive Health
Faculty of Medicine > Warwick Medical School
Library of Congress Subject Headings (LCSH): Hydrogen sulfide -- Synthesis, Uterus, Cystathionine gamma-lyase
Journal or Publication Title: Reproductive Biology and Endocrinology
Publisher: BioMed Central Ltd.
ISSN: 1477-7827
Date: 6 February 2009
Volume: Vol.7
Number: No.10
Identification Number: 10.1186/1477-7827-7-10
Status: Peer Reviewed
Publication Status: Published
Access rights to Published version: Open Access
References: 1. Buhimschi I, Yallampalli C, Dong YL, Garfield RE: Involvement of a nitric oxide-cyclic guanosine monophosphate pathway in control of human uterine contractility during pregnancy. Am J Obstet & Gynecol 1995, 172:1577-1584. 2. Yallampalli C, Dong Y, Gangula PR, Fang L: Role and regulation of nitric oxide in uterus during pregnancy and parturition. J Soc Gynecol Invest 1998, 5(2):58-67. 3. Acevedo CH, Ahmed A: Hemeoxygenase-1 inhibits human myometrial contractility via carbon monoxide and is upregulated by progesterone during pregnancy. J Clin Invest 1998, 101(5):949-955. 4. Wang R: Two's company, three's a crowd – can H2S be the third endogenous gaseous transmitter? J Fed Am Soc Expl Biol 2002, 16:1792-1798. 5. Stipanuk MH, Beck PW: Charcaterization of the enzymic capacity for cysteine desulphhydration in liver and kidney of the rat. J Biochem 1982, 206:267-277. 6. Erickson PF, Maxwell IH, Su LJ, Baumann M, Glode LM: Sequence of cDNA for rat cystathionine gamma-lyase and comparison of deduced amino acid sequence with related Escherichia coli enzymes. Biochem J 1990, 269(2):335-340. 7. Swaroop M, Bradley K, Ohura T, Tahara T, Roper MD, Rosenberg LE, Kraus JP: Rat cystathionine beta-synthase. Gene organization and alternative splicing. J Biol Chem 1992, 267(16):11455-11461. 8. Abe K, Kimura H: The possible role of hydrogen sulphide as an endogenous neuromodulator. J. Neurosci 1996, 16(3):1066-1071. 9. Cheng Y, Ndisang JF, Tang G, Cao K, Wang R: Hydrogen sulphideinduced relaxation of resistance mesenteric artery beds of rats. Am J Physiol 2004, 287(5):H2316-H2323. 10. Smythe CV: The utilization of cysteine and cystine by rat liver with the production of hydrogen sulphide. J Biol Chem 1942, 142:387-400. 11. Hosoki R, Matsuki N, Kimura H: The possible role of hydrogen sulphide as an endogenous smooth muscle relaxant in synergy with nitric oxide. Biochem Biophys Res Comm 1997, 237(3):527-531. 12. Zhao W, Ndisang JF, Wang R: Modulation of endogenous production of H2S in rat tissues. Can J Physiol Pharmacol 2003, 81:848-853. 13. Zhao W, Zhang J, Lu Y, Wang R: The vasorelaxant effect of HS as a novel endogenous gaseous KATP channel opener. EMBO J 2001, 20:6008-6016. 14. Bhatia M, Wong FL, Fu D, Lau HY, Moochhala SM, Moore PK: Role of hydrogen sulphide in acute pancreatitis and associated lung injury. J Fed Am Soc Exp Biol 2005, 19(6):623-625. 15. Mok YY, Atan MS, Yoke Ping C, Zhong Jing W, Bhatia M, Moochhala S, Moore PK: Role of hydrogen sulphide in haemorrhagic shock in the rat: protective effect of inhibitors of hydrogen sulphide biosynthesis. Br J Pharmacol 2004, 143(7):881-889. 16. Collin M, Anuar FB, Murch O, Bhatia M, Moore PK, Thiemermann C: Inhibition of endogenous hydrogen sulphide formation reduces the organ injury caused by endotoxemia. Br J Pharmacol 2005, 146:498-505. 17. Teague B, Asiedu S, Moore PK: The smooth muscle relaxant effect of hydrogen sulphide in vitro:evidence for a physiological role to control intestinal contractility. Br J Pharmacol 2002, 137:139-145. 18. Sidhu R, Singh M, Samir G, Carson RJ: L-cysteine and sodium hydrosulphide inhibit spontaneous contractility in isolated pregnant uterine strips in vitro. Pharmacol Toxicol 2001, 88(4):198-203. 19. Liao L, Xu X, Wargovich MJ: Direct reprobing with anti-b-actin as an internal control for western blot analysis. Biotechniques 2000, 28:216-218. 20. Roper MD, Kraus JP: Rat cystathionine beta-synthase: expression of four alternatively spliced isoforms in transfected cultured cells. Arch Biochem Biophys 1992, 298(2):514-521. 21. Agarwal A, Gupta S, Sharma R: Role of oxidative stress in female reproduction. Reprod Biol Endocrinol 2005, 14(3):28. 22. Chappell LC, Seed PT, Kelly FJ, Briley A, Mallet AI, Hunt BJ, Charnock- Jones DS, Poston L: Vitamin E and C supplementation in women at risk of pre-eclampsia is associated with changes in indices of oxidative stress and placental function. Am J Obstet Gynecol 2002, 187:777-784. 23. Soleymanlou N, Jurisica I, Nevo O, Ietta F, Zhang X, Zamudio S, Post M, Caniggia I: Molecular Evidence of Placental Hypoxia in Preeeclampsia. J Clin Endocrinol Metabol 2005, 90(7):4299-4308. 24. Skovby F, Kraus JP, Rosenberg LE: Biosynthesis and proteolytic activation of cystathionine beta-synthase in rat liver. J Biol Chem 1984, 259(1):588-593. 25. Kraus JP, Packman S, Fowler B, Rosenberg LE: Purification and properties of cystathionine β-synthase from human liver. J Biol Chem 1978, 253:6523-6528. 26. Kraus JP, Rosenberg LE: Cystathionine β-synthase from human liver: Improved purification scheme and additional charac terization of the enzyme in crude and pure form. Arch Biochem Biophys 1983, 222:44-52. 27. Kraus JP: Cystathionine beta-synthase (human). Methods Enzymol 1987, 143:388-394. 28. Nagasawa T, Kanzaki H, Yamada H: Cystathionine gamma-lyase of Streptomyces phaeochromogenes. The occurrence of cystathionine gamma-lyase in filamentous bacteria and its purification and characterization. J Biol Chem 1984, 259(16):10393-10403. 29. Matsuo Y, Greenberg DM: A crystalline enzyme that cleaves homoserine and cystathionine I. Isolation procedure and some physiochemical properties. J Biol Chem 1958, 230:545-560. 30. Delavier-Klutchko C, Flavin M: Enzymatic synthesis and cleavage of cystathionine in fungi and bacteria. J Biol Chem 1965, 240:2537-2549. 31. Clausen T, Huber R, Prade L, Wahl MC, Messerschmidt A: Crystal structure of Escherichia coli cystathionine gamma-synthase at 1.5 A resolution. EMBO J 1998, 17(23):6827-6838. 32. Ratnam S, Maclean KN, Jacobs RL, Brosnan ME, Kraus JP, Brosnan JT: Hormonal regulation of cystathionine beta-synthase expression in liver. J Biol Chem 2002, 277(45):42912-42918.
URI: http://wrap.warwick.ac.uk/id/eprint/522

Data sourced from Thomson Reuters' Web of Knowledge

Request changes to a record

Actions (login required)

View Item View Item

Document Downloads

More statistics for this item...
twitter

Email us: publications@warwick.ac.uk
Contact Details
About Us