Archives of Biological Sciences (Jan 2019)

The role of potassium channels and calcium in the relaxation mechanism of magnesium sulfate on the isolated rat uterus

  • Sokolović Dragana,
  • Drakul Dragana,
  • Oreščanin-Dušić Zorana,
  • Tatalović Nikola,
  • Pecelj Milica,
  • Milovanović Slobodan,
  • Blagojević Duško

DOI
https://doi.org/10.2298/ABS180615031S
Journal volume & issue
Vol. 71, no. 1
pp. 5 – 11

Abstract

Read online

MgSO4 is used as a tocolytic agent. It is considered to be a calcium channel antagonist, but a different mechanism of its action might be involved. The aim of this study was to examine the contribution of calcium concentrations and potassium channels in the mechanism of MgSO4-mediated uterine relaxation. Isolated uteri from female Wister rats were treated with increasing MgSO4 concentrations (0.1-30 mM). MgSO4 induced dose-dependent inhibition of spontaneous activity. Addition of Ca2+ (6 mM and 12 mM) stimulated uterine contractile activity and attenuated the inhibitory activity of MgSO4. In order to analyze the role of different subtypes of potassium channels, Ca2+-stimulated uteri were pretreated with glibenclamide (Glib), a selective ATP-sensitive potassium channel inhibitor (KATP), tetraethylammonium (TEA), a non-specific inhibitor of large conductance calcium-activated potassium channels (BKCa), and 4-aminopyridine (4-AP), a voltage-sensitive potassium channel inhibitor (Kv), at concentrations that had no effect per se. Pretreatment with 4-AP had no effect on MgSO4-mediated relaxation of Ca2+-stimulated uteri. The relaxing effect of MgSO4 was potentiated by pretreatment with glibenclamide. Pretreatment with TEA attenuated the MgSO4-mediated decrease in frequency. Our results suggest that MgSO4 acts as a general calcium antagonist that influences Ca2+-mediated potassium channels. Furthermore, it seems that MgSO4 uterine relaxation activity is partially mediated by selective ATP-sensitive potassium channels, suggesting an ATP-dependent role. [Project of the Serbian Ministry of Education, Science and Technological Development, Grant no. 173014: Molecular Mechanisms of Redox Signaling in Homeostasis: Adaptation and Pathology]

Keywords