Department of Pharmacology, School of Medicine, Universidad Complutense de Madrid, Ciber Enfermedades Respiratorias (CIBERES), 28040, Madrid, Spain.
Adv Exp Med Biol. 2010;661:391-401. doi: 10.1007/978-1-60761-500-2_25.
Serotonin (5-HT) and voltage-gated potassium (KV) channels have emerged as two major factors in the pathogenesis of pulmonary arterial hypertension (PAH). In pulmonary artery smooth muscle cells (PASMC), KV channels play a major role in the regulation of pulmonary arterial tone and proliferation. Thus, activation of KV channels leads to vasodilatation and enhances apoptosis, while their inhibition is associated with vasoconstriction and proliferation in PASMC. Moreover, these channels have a prominent role as a common target for pulmonary vasoconstrictors. Modulation of these channels by vasoconstrictors involves the activation of a variety of protein kinases. Here we review the role of localization and internalization as a novel mechanism for acute regulation of KV channels and pulmonary vascular tone by agonists such as serotonin.
血清素(5-HT)和电压门控钾(KV)通道已成为肺动脉高压(PAH)发病机制中的两个主要因素。在肺动脉平滑肌细胞(PASMC)中,KV 通道在调节肺动 脉张力和增殖方面起着主要作用。因此,KV 通道的激活导致血管舒张和增强凋亡,而其抑制与 PASMC 中的血管收缩和增殖有关。此外,这些通道作为肺血管收缩剂的共同靶标具有突出的作用。血管收缩剂对这些通道的调节涉及多种蛋白激酶的激活。在这里,我们回顾了定位和内化作为一种新的机制的作用,该机制通过激动剂(如血清素)对 KV 通道和肺血管张力进行急性调节。