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Niflumic acid hyperpolarizes smooth muscle cells via calcium-activated potassium channel in spiral modiolar artery of guinea pigs

  
@article{APS4455,
	author = {Li Li and Ke-tao Ma and Lei Zhao and Jun-qiang Si and Zhong-shuang Zhang and He Zhu and Jing Li},
	title = {Niflumic acid hyperpolarizes smooth muscle cells via calcium-activated potassium channel in spiral modiolar artery of guinea pigs},
	journal = {Acta Pharmacologica Sinica},
	volume = {29},
	number = {7},
	year = {2016},
	keywords = {},
	abstract = {Aim: The influence of niflumic acid (NFA), a Cl- channel antagonist, on the membrane potentials in smooth muscle cells (SMC) of the cochlear spiral modiolar artery (SMA) in guinea pigs was examined.
Methods: The intracellular recording and whole-cell recording technique were used to record the NFA-induced response on the acutely-isolated SMA preparation.
Results: The SMC had 2 stable but mutually convertible levels of resting potentials (RP), that is, one was near −45 mV and the other was approximately −75 mV, termed as low and high RP, respectively. The bath application of NFA could cause a hyperpolarization in all the low RP cells, but had little effect on high RP cells. The induced responses were concentration-dependent. Large concentrations of NFA (≥100 μmol/L) often induced a shift of a low RP to high RP in cells with an initial RP at low level, and NFA (up to 100 μmol/L) had little effect on the membrane potentials of the high RP cells. However, when the high RP cells were depolarized to a level beyond −45 mV by barium and ouabain, NFA hyperpolarized these cells with the similar effect on those cells initially being the low RP. The NFA-induced response was almost completely blocked by charybdotoxin, iberiotoxin, tetraethylammonium, 1,2-bis(2-aminophenoxy) ethane-N,N,N′,N′-tetraacetic acid tetrakis acetoxymethyl ester, but not by 4-aminopyridine, barium, glipizide, apamin, ouabain, and CdCl2.
Conclusion: NFA induces a concentration-dependent reversible hyperpolarization in SMC in the cochlear SMA via activation of the Ca2+-activated potassium channels.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/4455}
}