Nucleotides maintain the activity of Cav1.2 channels in guinea-pig ventricular myocytes

被引:3
|
作者
Liu, Shu-yuan [1 ,2 ]
Xu, Jian-jun [2 ]
Minobe, Etsuko [2 ]
Gao, Qing-hua [1 ]
Feng, Rui [1 ,3 ]
Zhao, Mei-mi [1 ,3 ]
Guo, Feng [1 ,3 ]
Yang, Lei [2 ]
Hao, Li-ying [1 ,3 ]
Kameyama, Masaki [2 ]
机构
[1] China Med Univ, Sch Pharm, Dept Pharmaceut Toxicol, Shenyang 110122, Peoples R China
[2] Kagoshima Univ, Grad Sch Med & Dent Sci, Dept Physiol, Kagoshima 8908544, Japan
[3] China Med Univ, Cardiovasc Inst, Shenyang 110001, Peoples R China
关键词
ATP; Nucleotide; Ca2+ channel; Cav1.2; Binding site; CALMODULIN KINASE-II; CARDIAC MYOCYTES; CALCIUM-CHANNELS; CA2+ CHANNELS; ATP; MODULATION; TRANSPORTERS; BINDING;
D O I
10.1016/j.bbrc.2015.03.111
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The activity of Cav1.2 Ca2+ channels is maintained in the presence of calmodulin and ATP, even in cell-free patches, and thus a channel ATP-binding site has been suggested. In this study, we examined whether other nucleotides, such as GTP, UTP, CTP, ADP and AMP, could be substituted for ATP in guinea-pig ventricular myocytes. We found that all the nucleotides tested could re-prime the Ca2+ channels in the presence of 1 mu M calmodulin in the inside-out mode. The order of efficacy was ATP > GTP > UTP > ADP > CTP AMP. Thus, the presumed nucleotide-binding site in the channel seemed to favor a purine rather than pyrimidine base and a triphosphate rather than a di- or monophosphate group. Furthermore, a high concentration (10 mM) of GTP, UTP, CTP, ADP and AMP had inhibitory effects on the channel activity. These results provide information on the putative nucleotide-binding site(s) in Cav1.2 Ca2+ channels. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:813 / 818
页数:6
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