Isoform-specific regulation of the sodium pump by alpha- and beta-adrenergic agonists in the guinea-pig ventricle.
Isoform-specific regulation of the sodium pump by alpha- and beta-adrenergic agonists in the guinea-pig ventricle.
复制标题
豚鼠心室中α-和β-肾上腺素能激动剂对钠泵的亚型特异性调节。
DOI:
10.1111/j.1469-7793.1999.0377v.x
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发表时间:
1999
期刊:
影响因子:
--
通讯作者:
Baldo,GJ
中科院分区:
文献类型:
--
作者:
Gao,J;Wymore,R;Wymore,RT;Wang,Y;McKinnon,D;Dixon,JE;Mathias,RT;Cohen,IS;Baldo,GJ
Guinea-pig ventricle was used in the RNase protection assays to determine which α-isoforms of the Na+-K+ pumps are present, and ventricular myocytes were used in whole cell patch clamp studies to investigate the actions of α- and β-adrenergic agonists on Na+-K+ pump current. RNase protection assays showed that two isoforms of the α-subunit of the Na+-K+-ATPase are present in guinea-pig ventricle. The mRNA for the α1-isoform comprises 82 % of the total pump message, the rest being the α2-isoform. We have previously shown that β-adrenergic agonists affect Na+-K+ pump current (Ip) through a protein kinase A (PKA)-dependent pathway. We now show that these β-effects are targeted to the α1-isoform of the Na+-K+ pumps. We have also previously shown that α-adrenergic agonists increase Ip through a protein kinase C (PKC)-dependent pathway. We now show that these α-isoform effects are targeted to the α2-isoform of the Na+-K+ pumps. These results suggest the effects of adrenergic activation on Na+-K+ pump activity in the heart can be regionally specific, depending on which α-isoform of the Na+-K+ pump is expressed.