Abstract
Large conductance potassium channels (BK Ca channels) play a central role in maintaining myometrial tone, thus activation of these channels proved to have therapeutic potential in preterm labor. Present study aims to unravel the presence of BK Ca (maxi-K) channels in buffalo myometrium. Tension experiments, mRNA and protein expression studies were done to characterize BK Ca channels in buffalo myometrium. Isolated myometrial preparations exhibited rhythmic spontaneity with regular pattern of amplitude and frequency. Selective blockers of BK Ca channels iberiotoxin (IbTx; 100 nM) and tetraethylammonium (TEA; 1 mM) produced excitatory effects as evidenced by increase in amplitude and frequency of myogenic activity. 1,3-Dihydro-1-[2-hydroxy-5-(trifluoromethyl)phenyl]-5-(trifluoromethyl)-2H-benzimi-dazol-2-one (NS-1619; 10 −7–10 −4 M), a BK Ca channel opener, produced concentration-dependent relaxation of myometrium with pD 2 of 5.02 ± 0.19 and R max of 31.35 ± 3.5% ( n = 5). TEA significantly antagonized NS-1619-induced relaxation (pD 2 of 4.72 ± 0.12 and R max of 22.72 ± 1.78%; n = 5). IbTx also significantly shifted the dose response curve of NS-1619 towards right (pD 2 of 3.98 ± 0.16; n = 4) without significant change in the per cent maximal response. Further, RT-PCR study detected mRNA encoding BK Ca α-subunit and Western blot analysis detected its protein expression in myometrium. Based on the results of the present investigation, it is suggested that BK Ca channels are present in the buffalo myometrium and are open in the resting state. Thus, their activation by potassium channel opener/β 2-adrenoceptor agonist (tocolytic drug) may lead to uterine relaxation in preterm labor.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.