Related resources
Search for item elsewhere
University researcher(s)
Academic department(s)
Modulation of the molecular composition of large conductance, Ca(2+) activated K(+) channels in vascular smooth muscle during hypertension.
Amberg G, Bonev A, Rossow C, Nelson MT, Santana L
Journal of Clinical Investigation. 2003;112( 5):717-24.
Access to files
Full-text and supplementary files are not available from Manchester eScholar. Use our list of Related resources to find this item elsewhere. Alternatively, request a copy from the Library's Document supply service.
Abstract
Hypertension is a clinical syndrome characterized by increased vascular tone. However, the molecular mechanisms underlying vascular dysfunction during acquired hypertension remain unresolved. Localized intracellular Ca2+ release events through ryanodine receptors (Ca2+ sparks) in the sarcoplasmic reticulum are tightly coupled to the activation of large-conductance, Ca2+-activated K+ (BK) channels to provide a hyperpolarizing influence that opposes vasoconstriction. In this study we tested the hypothesis that a reduction in Ca2+ spark-BK channel coupling underlies vascular smooth muscle dysfunction during acquired hypertension. We found that in hypertension, expression of the beta1 subunit was decreased relative to the pore-forming alpha subunit of the BK channel. Consequently, the BK channels were functionally uncoupled from Ca2+ sparks. Consistent with this, the contribution of BK channels to vascular tone was reduced during hypertension. We conclude that downregulation of the beta1 subunit of the BK channel contributes to vascular dysfunction in hypertension. These results support the novel concept that changes in BK channel subunit composition regulate arterial smooth muscle function.
Keyword(s)
Animals; Down-Regulation; Gene Expression Regulation; Male; Protein Subunits; Rats; Rats, Sprague-Dawley; analysis: RNA, Messenger; chemistry: Potassium Channels, Calcium-Activated; drug effects: Vasoconstriction; etiology: Hypertension; metabolism: Calcium; pharmacology: Peptides; physiology: Muscle, Smooth, Vascular