Dichloroacetate, a metabolic modulator, prevents and reverses chronic hypoxic pulmonary hypertension in rats: role of increased expression and activity of voltage-gated potassium channels

Circulation. 2002 Jan 15;105(2):244-50. doi: 10.1161/hc0202.101974.

Abstract

Background: Chronic hypoxic pulmonary hypertension (CH-PHT) is associated with suppressed expression and function of voltage-gated K(+) channels (Kv) in pulmonary artery (PA) smooth muscle cells (SMCs) and a shift in cellular redox balance toward a reduced state. We hypothesized that dichloroacetate (DCA), a metabolic modulator that can shift redox balance toward an oxidized state and increase Kv current in myocardial cells, would reverse CH-PHT.

Methods and results: We studied 4 groups of rats: normoxic, normoxic+DCA (DCA 70 mg. kg(-1). d(-1) PO), chronically hypoxic (CH), and CH+DCA. CH and CH+DCA rats were kept in a hypoxic chamber (10% FiO(2)) for 2 to 3 weeks. DCA was given either at day 1 to prevent or at day 10 to reverse CH-PHT. We used micromanometer-tipped catheters and measured hemodynamics in closed-chest rats on days 14 to 18. CH+DCA rats had significantly reduced pulmonary vascular resistance, right ventricular hypertrophy, and PA remodeling compared with the CH rats. CH inhibited I(K), eliminated the acute hypoxia-sensitive I(K), and decreased Kv2.1 channel expression. In the short term, low-dose DCA (1 micromol/L) increased I(K) in CH-PASMCs. In a mammalian expression system, DCA activated Kv2.1 by a tyrosine kinase-dependent mechanism. When given long-term, DCA partially restored I(K) and Kv2.1 expression in PASMCs without altering right ventricular pyruvate dehydrogenase activity, suggesting that the beneficial effects of DCA occur by nonmetabolic mechanisms.

Conclusions: DCA both prevents and reverses CH-PHT by a mechanism involving restoration of expression and function of Kv channels. DCA has previously been used in humans and may potentially be a therapeutic agent for pulmonary hypertension.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cells, Cultured
  • Chronic Disease
  • Cricetinae
  • Delayed Rectifier Potassium Channels
  • Dichloroacetic Acid / pharmacology*
  • Electric Conductivity
  • Enzyme Inhibitors / pharmacology*
  • Hemodynamics / drug effects
  • Hypertension, Pulmonary / metabolism
  • Hypertension, Pulmonary / pathology
  • Hypertension, Pulmonary / physiopathology
  • Hypertension, Pulmonary / prevention & control*
  • Hypoxia / metabolism
  • Hypoxia / physiopathology
  • Hypoxia / prevention & control*
  • Immunoblotting
  • Male
  • Muscle, Smooth, Vascular / drug effects
  • Muscle, Smooth, Vascular / physiology
  • Potassium Channels / metabolism
  • Potassium Channels, Voltage-Gated / biosynthesis*
  • Potassium Channels, Voltage-Gated / metabolism
  • Potassium Channels, Voltage-Gated / physiology*
  • Protein Kinase Inhibitors
  • Protein Kinases*
  • Protein Serine-Threonine Kinases
  • Pulmonary Artery / drug effects
  • Pulmonary Artery / pathology
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Pyruvate Dehydrogenase Complex / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Shab Potassium Channels

Substances

  • Delayed Rectifier Potassium Channels
  • Enzyme Inhibitors
  • Kcnb1 protein, rat
  • Potassium Channels
  • Potassium Channels, Voltage-Gated
  • Protein Kinase Inhibitors
  • Pyruvate Dehydrogenase Acetyl-Transferring Kinase
  • Pyruvate Dehydrogenase Complex
  • Shab Potassium Channels
  • Dichloroacetic Acid
  • Protein Kinases
  • Protein Serine-Threonine Kinases