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Suppression of channel conductance by diacetyl monoxime in guinea pig and embryonic chick cardiomyocytes

  
@article{APS6401,
	author = {Hideaki Sada and Takashi Ban and Nicholas Sperelakis},
	title = {Suppression of channel conductance by diacetyl monoxime in guinea pig and embryonic chick cardiomyocytes},
	journal = {Acta Pharmacologica Sinica},
	volume = {17},
	number = {3},
	year = {2016},
	keywords = {},
	abstract = {AIM: To examine the effects of diacetyl monoxime (DAM), and putative dephospohrylating agent, on conductance of the cardiac Ca, Na, and K channels.
METHODS: The Ca (ICa), Na (INa), and K (IK) currents were recorded in single ventricular myocytes from guinea pigs and chick embryos before and after addition of DAM using the whole-cell voltage-clamp technique.
RESULTS: DAM 10 mmol.L-1 reduced rapidly the amplitudes of ICa (by about 30%), INa (by about 25%), and IK (by 25%-50%) without alterations of the voltage-dependence.
CONCLUSION: DAM was a channel inhibitor of the unique type having nonselective phosphatase activities.},
	issn = {1745-7254},	url = {http://www.chinaphar.com/article/view/6401}
}