Potassium channels in vascular smooth muscle: a pathophysiological and pharmacological perspective.


Dogan M. F. , Yildiz O., Arslan S. O. , Ulusoy K. G.

Fundamental & clinical pharmacology, cilt.33, ss.504-523, 2019 (SCI Expanded İndekslerine Giren Dergi)

  • Cilt numarası: 33 Konu: 5
  • Basım Tarihi: 2019
  • Doi Numarası: 10.1111/fcp.12461
  • Dergi Adı: Fundamental & clinical pharmacology
  • Sayfa Sayısı: ss.504-523

Özet

Potassium (K+) ion channel activity is an important determinant of vascular tone by regulating cell membrane potential (MP). Activation of K+ channels leads to membrane hyperpolarization and subsequently vasodilatation, while inhibition of the channels causes membrane depolarization and then vasoconstriction. So far five distinct types of K+ channels have been identified in vascular smooth muscle cells (VSMCs): Ca+2-activated K+ channels (BKCa), voltage-dependent K+ channels (K-V), ATP-sensitive K+ channels (K-ATP), inward rectifier K+ channels (K-ir), and tandem two-pore K+ channels (K2P). The activity and expression of vascular K+ channels are changed during major vascular diseases such as hypertension, pulmonary hypertension, hypercholesterolemia, atherosclerosis, and diabetes mellitus. The defective function of K+ channels is commonly associated with impaired vascular responses and is likely to become as a result of changes in K+ channels during vascular diseases. Increased K+ channel function and expression may also help to compensate for increased abnormal vascular tone. There are many pharmacological and genotypic studies which were carried out on the subtypes of K+ channels expressed in variable amounts in different vascular beds. Modulation of K+ channel activity by molecular approaches and selective drug development may be a novel treatment modality for vascular dysfunction in the future. This review presents the basic properties, physiological functions, pathophysiological, and pharmacological roles of the five major classes of K+ channels that have been determined in VSMCs.