Ren J, Zhang L, Benishin C G
Department of Physiology, University of Alberta, Edmonton, Canada.
Can J Physiol Pharmacol. 1999 Nov;77(11):860-5.
Parathyroid hypertensive factor (PHF) has been implicated in regulation of vascular smooth muscle tone and pathogenesis of several forms of hypertension. Earlier studies have suggested that PHF enhances the actions of other vasoconstrictors, while it has no in vitro vasoconstrictor property of its own. PHF was previously found to enhance the L-type Ca channel currents and intracellular Ca responses to depolarization in vascular smooth muscle cells (VSMCs). The present study examined whether PHF might act on K channels in the plasma membrane of VSMCs. Primary cultured VSMCs from rat tail artery were used. The whole-cell version of the patch-clamp technique was used under conditions in which there was no contribution of Ca-activated K channels to the outward current. Both purified and semipurified PHF inhibited the delayed rectifier type potassium current in a dose-dependent manner. The effect was time dependent and was first significantly different from the control current after 30 min. The inhibition of the delayed rectifier K channel was associated with a time-dependent decrease in the resting membrane potential. Therefore, PHF may alter VSMC cellular Ca responses by reducing the membrane potential to a level closer to the activation potential of Ca channels.
甲状旁腺高血压因子(PHF)与血管平滑肌张力的调节以及多种形式高血压的发病机制有关。早期研究表明,PHF可增强其他血管收缩剂的作用,而其自身并无体外血管收缩特性。此前发现PHF可增强血管平滑肌细胞(VSMC)中的L型钙通道电流以及对去极化的细胞内钙反应。本研究检测了PHF是否可能作用于VSMC质膜中的钾通道。使用了从大鼠尾动脉原代培养的VSMC。在钙激活钾通道对外向电流无贡献的条件下,采用膜片钳技术的全细胞版本。纯化和半纯化的PHF均以剂量依赖方式抑制延迟整流型钾电流。该效应具有时间依赖性,30分钟后首次与对照电流有显著差异。延迟整流钾通道的抑制与静息膜电位的时间依赖性降低有关。因此,PHF可能通过将膜电位降低至更接近钙通道激活电位的水平来改变VSMC细胞的钙反应。