Comparison of the effects of methanethiol and sodium sulphide on uterine contractile activity.

Published

Journal Article

BACKGROUND: Our aim was to investigate the effect of methanethiol (CH3SH) on contractility of rat uterus and activities of redox-active enzymes, and to compare them with the effect of sodium sulphide (Na2S), a hydrogen sulphide (H2S/HS(-)) donor. METHODS: Uteri were isolated from virgin Wistar rats, divided into six groups, controls (untreated uteri allowed to contract spontaneously and in the presence of Ca(2+)(6mM)), CH3SH treated (spontaneously active and Ca(2+) induced) and Na2S treated (spontaneously active and Ca(2+) induced). Underlying antioxidative enzyme activities (superoxide dismutase--SOD, glutathione peroxidase--GSHPx, glutathione reductase--GR) in CH3SH- or Na2S-treated uteri were compared to controls. RESULTS: Our experiments showed that CH3SH and Na2S provoked reversible relaxation of both spontaneous and Ca(2+)-induced uterine contractions. The dose-response curves differed in shape, and CH3SH curve was shifted to higher concentration compared to H2S/HS(-). The effects of Na2S fitted sigmoid curve, whereas those of CH3SH fitted linearly. CH3SH provoked increased SOD activity and decreased GR activity. However, Na2S (H2S/HS(-)) provoked an increase in SOD activity exclusively in Ca(2+)-stimulated uteri, while the activity of GSHPx was increased in both types of active uteri. CONCLUSION: Our results imply that CH3SH may have a constructive role in the control of muscle function and metabolism. Observed differences between CH3SH and H2S/HS(-) could be attributed to a larger moiety that is present in CH3SH compared to H2S, but they are more likely to be a consequence of the specific actions of HS(-), in relation to its negative charge.

Full Text

Cited Authors

  • Mijušković, A; Oreščanin-Dušić, Z; Nikolić-Kokić, A; Slavić, M; Spasić, MB; Spasojević, I; Blagojević, D

Published Date

  • June 2014

Published In

Volume / Issue

  • 66 / 3

Start / End Page

  • 373 - 379

PubMed ID

  • 24905511

Pubmed Central ID

  • 24905511

International Standard Serial Number (ISSN)

  • 1734-1140

Digital Object Identifier (DOI)

  • 10.1016/j.pharep.2013.12.012

Language

  • eng