Literature DB >> 11772823

The role of K(+) channels on the inhibitor effect of sevoflurane in pregnant rat myometrium.

Haluk Kafali1, Tijen Kaya, Sinan Gürsoy, Ihsan Bagcivan, Baris Karadas, Yusuf Sarioglu.   

Abstract

UNLABELLED: Volatile anesthetics and K(+) channel openers inhibit spontaneous contractions in myometrial smooth muscle. Volatile anesthetics modulate K(+) channel activity. We investigated the role of two K(+) channel blockers on the effect of sevoflurane in pregnant rat myometrium. Term pregnant rat uteri were excised, and cross-sectional myometrial strips were mounted for isometric force recording. Sevoflurane inhibited the amplitude and frequency of spontaneous myometrial contractions in a concentration-dependent manner. The maximal inhibition measured in amplitude and frequency of spontaneous myometrial contractions with sevoflurane (at 3 minimum alveolar anesthetic concentration) was 44.32% and 33.32% of control contractions, respectively. Tetraethylammonium (TEA) and glibenclamide, K(+) channel blockers, increased spontaneous myometrial contractions in a concentration-dependent manner. Sevoflurane responses were repeated at concentrations with no effect on spontaneous contractility of TEA, a Ca(2+)-activated K(+) channel blocker, and glibenclamide, an adenosine triphosphate-sensitive K(+) channel blocker, in myometrial strips. TEA (3.10(-4) M) caused a significant reduction in sevoflurane-induced inhibitor responses, but glibenclamide (10(-6) M) did not. Sevoflurane-induced maximal inhibition (at 3 minimum alveolar anesthetic concentration) on amplitude and frequency of spontaneous myometrial contractions in the presence of TEA (3.10(-4) M) was 31.85% and 22.33% of control contractions, respectively (P < 0.05). These results suggest that the in vitroapplication of sevoflurane inhibited the amplitude and frequency of spontaneous myometrial contractions in pregnant rats in a concentration-dependent manner. Such inhibition was reduced by TEA. The inhibition of myometrial smooth muscle induced by sevoflurane seems to be mediated, at least in part, via activation of Ca(2+)-activated K(+) channels, because inhibition was reduced by TEA. IMPLICATIONS: In this study, we found that sevoflurane causes significantly decreased myometrial contractile activity in pregnant rats. The inhibition of myometrial smooth muscle induced by sevoflurane seems to be mediated, at least in part, via activation of Ca(2+)-activated K(+) channels, because inhibition was reduced by tetraethylammonium.

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Year:  2002        PMID: 11772823     DOI: 10.1097/00000539-200201000-00033

Source DB:  PubMed          Journal:  Anesth Analg        ISSN: 0003-2999            Impact factor:   5.108


  4 in total

Review 1.  Potassium channels and uterine function.

Authors:  Adam M Brainard; Victoria P Korovkina; Sarah K England
Journal:  Semin Cell Dev Biol       Date:  2007-05-24       Impact factor: 7.727

2.  Anesthesia for in utero repair of myelomeningocele.

Authors:  Marla Ferschl; Robert Ball; Hanmin Lee; Mark D Rollins
Journal:  Anesthesiology       Date:  2013-05       Impact factor: 7.892

3.  Inhibitory effect of alprostadil against sevoflurane-induced myometrial relaxation in rats.

Authors:  Yayoi Ohashi; Hiroyuki Sumikura; Takeshi Tateda
Journal:  J Anesth       Date:  2007-08-01       Impact factor: 2.078

4.  Impact of anesthetic agents on the amount of bleeding during dilatation and evacuation: A systematic review and meta-analysis.

Authors:  Hyun Ah Lee; Hiromasa Kawakami; Takahiro Mihara; Hitoshi Sato; Takahisa Goto
Journal:  PLoS One       Date:  2021-12-22       Impact factor: 3.240

  4 in total

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