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Pulmonary arterial hypertension is incurable but animal model study suggests an experimental drug may be effective
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Pulmonary arterial hypertension is incurable but animal model study suggests an experimental drug may be effective

by Delthia Ricks, Medical Xpress TCS2 protein reduction in SMA-positive areas in small PAs from SM22-Tsc+/- mice. a: SM22-Cre mice were bred with Tsc2flox/flox mice to generate SM22-Tsc+/- mice. b: Immunohistochemical analysis of lung tissue sections of SM22-Tsc2+/- mice to detect TSC2 (red), smooth muscle α-actin (SMA) (green), and DAPI (blue). Representative images from n=5 WT and 7 SM22-Tsc2+/- mice...

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Antiarrhythmic drug identified as potential treatment for pulmonary arterial hypertension

Findings reported in The American Journal of Pathology suggest dofetilide may counteract pathological changes in potassium channels associated with pulmonary arterial hypertension in humans and rats Philadelphia, December 12, 2019 – High blood pressure in the lungs, known as pulmonary arterial hypertension (PAH), is a potentially fatal disease caused by obstruction of blood flow in...

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Researchers find beta blockers have positive effect in pulmonary arterial hypertension

A team of Cleveland Clinic researchers found that a common heart disease medication, beta blockers, may help treat pulmonary arterial hypertension (PAH), a debilitating lung disease. Caused by high blood pressure in the pulmonary arteries, PAH is a progressive disease which usually leads to right-sided heart failure and death within five to seven years of diagnosis. In fact,...