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[The role of subtypes of voltage-gated K+ channels in pulmonary vasoconstriction induced by 15-hydroeicosatetraenoic acid].

AbstractAIM:
To observe the effect of subtypes of Kv channels in rat pulmonary artery smooth muscle cells (PASMCs) on the process of pulmonary vasoconstriction induced by 15-HETE.
METHODS:
In the present study, ring of rabbit PA with specific Kv channel blockers were employed to functionally identify certain channel subtypes that took part in the process of 15-HETE induced pulmonary vasoconstriction; RT-PCR and Western blotting analysis were also used to measure the expression of subtypes of Kv in PASMCs exposed to 15-HETE,chronic hypoxia.
RESULTS:
Blocking of Kv1. 1, Kv1. 2, Kv1. 3 and Kv1. 6 channels did not affect 15-HETE induced vasoconstriction in normoxic rats; 15-HETE did not affect expression of Kv1. 1 and Kv1. 2 channels; 15-HETE significantly downregulated the expression of mRNA and protein of Kv1. 5 and Kv2. 1 in rat PASMCs.
CONCLUSION:
The results suggested that hypoxia may block Kv1. 5 and Kv2. 1 channels via 15-HETE mediated mechanism, leading to decrease numbers of functional Kv1. 5 and Kv2. 1 channels in PASMCs, leading to PA vasoconstriction.
AuthorsQian Li, Rong Zhang, Chang-Lian Lü, Yan Liu, Zhen Wang, Da-Ling Zhu
JournalYao xue xue bao = Acta pharmaceutica Sinica (Yao Xue Xue Bao) Vol. 41 Issue 5 Pg. 412-7 (May 2006) ISSN: 0513-4870 [Print] China
PMID16848316 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Hydroxyeicosatetraenoic Acids
  • Kv1.5 Potassium Channel
  • Potassium Channels, Voltage-Gated
  • RNA, Messenger
  • Shab Potassium Channels
  • 15-hydroxy-5,8,11,13-eicosatetraenoic acid
Topics
  • Animals
  • Cell Hypoxia
  • Cells, Cultured
  • Hydroxyeicosatetraenoic Acids (pharmacology)
  • Hypoxia (physiopathology)
  • Kv1.5 Potassium Channel (biosynthesis, genetics)
  • Male
  • Muscle, Smooth, Vascular (cytology)
  • Myocytes, Smooth Muscle (cytology, metabolism)
  • Potassium Channels, Voltage-Gated (antagonists & inhibitors)
  • Pulmonary Artery (physiopathology)
  • RNA, Messenger (biosynthesis, genetics)
  • Rats
  • Rats, Wistar
  • Shab Potassium Channels (biosynthesis, genetics)
  • Vasoconstriction (drug effects)

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