Hypercholesterolemia induces up-regulation of K ACh cardiac currents via a mechanism independent of phosphatidylinositol 4,5-bisphosphate and Gβγ
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Hypercholesterolemia is a well-known risk factor for cardiovascular disease. In the heart, activation of K ACh mediates the vagal (parasympathetic) negative chronotropic effect on heart rate. Yet, the effect of cholesterol on K ACh is unknown. Here we show that cholesterol plays a critical role in modulating K AChcurrents (I K,ACh) in atrial cardiomyocytes. Specifically, cholesterol enrichment of rabbit atrial cardiomyocytes led to enhanced channel activity while cholesterol depletion suppressed I K,ACh. Moreover, a high-cholesterol diet resulted in up to 3-fold increase in I K,ACh in rodents. In accordance, elevated currents were observed in Xenopus oocytes expressing the Kir3.1/Kir3.4 heteromer that underlies I K,ACh. Furthermore, our data suggest that cholesterol affects I K,ACh via a mechanism which is independent of both PI(4,5)P 2 and Gβγ. Interestingly, the effect of cholesterol on I K,ACh is opposite to its effect on I K1 in atrial myocytes. The latter are suppressed by cholesterol enrichment and by high-cholesterol diet, and facilitated following cholesterol depletion. These findings establish that cholesterol plays a critical role in modulating I K,ACh in atrial cardiomyocytes via a mechanism independent of the channel%27s major modulators. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.
Hypercholesterolemia is a well-known risk factor for cardiovascular disease. In the heart, activation of K ACh mediates the vagal (parasympathetic) negative chronotropic effect on heart rate. Yet, the effect of cholesterol on K ACh is unknown. Here we show that cholesterol plays a critical role in modulating K AChcurrents (I K,ACh) in atrial cardiomyocytes. Specifically, cholesterol enrichment of rabbit atrial cardiomyocytes led to enhanced channel activity while cholesterol depletion suppressed I K,ACh. Moreover, a high-cholesterol diet resulted in up to 3-fold increase in I K,ACh in rodents. In accordance, elevated currents were observed in Xenopus oocytes expressing the Kir3.1/Kir3.4 heteromer that underlies I K,ACh. Furthermore, our data suggest that cholesterol affects I K,ACh via a mechanism which is independent of both PI(4,5)P 2 and Gβγ. Interestingly, the effect of cholesterol on I K,ACh is opposite to its effect on I K1 in atrial myocytes. The latter are suppressed by cholesterol enrichment and by high-cholesterol diet, and facilitated following cholesterol depletion. These findings establish that cholesterol plays a critical role in modulating I K,ACh in atrial cardiomyocytes via a mechanism independent of the channel's major modulators. © 2012 by The American Society for Biochemistry and Molecular Biology, Inc.
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Cardio-vascular disease; Cardiomyocytes; Channel activity; Cholesterol depletion; Chronotropic effect; Heart rates; Hypercholesterolemia; Myocytes; Phosphatidylinositol 4 ,5-Bisphosphate; Risk factors; Up-regulation; Xenopus oocyte; Mammals; Nutrition; Cholesterol; cholesterol; guanine nucleotide binding protein beta subunit; guanine nucleotide binding protein gamma subunit; membrane protein; phosphatidylinositol 4,5 bisphosphate; protein Kir3.1; protein Kir3.4; unclassified drug; animal cell; animal experiment; animal model; article; cholesterol diet; controlled study; depletion; female; heart atrium; heart muscle cell; hypercholesterolemia; male; metabolic regulation; nonhuman; oocyte; potassium current; priority journal; protein expression; rabbit; rat; signal transduction; upregulation; Xenopus; Animals; Cholesterol; Dietary Fats; G Protein-Coupled Inwardly-Rectifying Potassium Channels; Heart Atria; Hyperhomocysteinemia; Myocytes, Cardiac; Phosphatidylinositol 4,5-Diphosphate; Rabbits; Up-Regulation; Xenopus laevis; Oryctolagus cuniculus; Rodentia
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