Effects of PKA inhibitors, H-compounds, on epithelial Na+ channels via PKA-independent mechanisms

被引:14
|
作者
Niisato, N
Ito, Y
Marunaka, Y
机构
[1] Hosp Sick Children, Res Inst, Dept Pediat, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Fac Med, Inst Med Sci, Toronto, ON M5G 1X8, Canada
关键词
amiloride; beta agonist; H8; H85; H89; H7; KT5720; myristoylated PKA inhibitory peptide [14-22; amide;
D O I
10.1016/S0024-3205(99)00341-0
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The Na+ transport in alveolar type II epithelial cells of rat fetal lung was stimulated by cAMP, which is generally thought to act through activation of protein kinase A (PKA). PKA inhibitors (H8, H89 and H7) stimulated amiloride-sensitive Naf transport in the alveolar type II epithelial cells. H85, an inactive form of H89 as a PKA inhibitor, had also mimicked the stimulatory action of H89 on the Na+ transport. On the other hand, another type of PKA inhibitor, KT5720 or myristoylated PKA inhibitory peptide [14-22] amide, did not stimulate the Na+ transport, but inhibited the Na+ transport unlike H-compounds. These observations suggest that H-compounds act on the Na+ transport depending on the structure. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:PL109 / PL114
页数:6
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