Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure

The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypert...

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Veröffentlicht in:Pharmacology & therapeutics (Oxford) 2019-01, Vol.193, p.121-134
Hauptverfasser: Dee, Rachel A., Mangum, Kevin D., Bai, Xue, Mack, Christopher P., Taylor, Joan M.
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container_issue
container_start_page 121
container_title Pharmacology & therapeutics (Oxford)
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creator Dee, Rachel A.
Mangum, Kevin D.
Bai, Xue
Mack, Christopher P.
Taylor, Joan M.
description The prevalence of high blood pressure (also known as hypertension) has steadily increased over the last few decades. Known as a silent killer, hypertension increases the risk for cardiovascular disease and can lead to stroke, heart attack, kidney failure and associated sequela. While numerous hypertensive therapies are currently available, it is estimated that only half of medicated patients exhibit blood pressure control. This signifies the need for a better understanding of the underlying cause of disease and for more effective therapies. While blood pressure homeostasis is very complex and involves the integrated control of multiple body systems, smooth muscle contractility and arterial resistance are important contributors. Strong evidence from pre-clinical animal models and genome-wide association studies indicate that smooth muscle contraction and BP homeostasis are governed by the small GTPase RhoA and its downstream target, Rho kinase. In this review, we summarize the signaling pathways and regulators that impart tight spatial-temporal control of RhoA activity in smooth muscle cells and discuss current therapeutic strategies to target these RhoA pathway components. We also discuss known allelic variations in the RhoA pathway and consider how these polymorphisms may affect genetic risk for hypertension and its clinical manifestations.
doi_str_mv 10.1016/j.pharmthera.2018.09.001
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subjects Animals
Blood Pressure
GTPase activating protein (GAP)
GTPase-Activating Proteins - physiology
Guanine nucleotide exchange factor (GEF)
Humans
Rho Kinase (ROCK)
RhoA
rhoA GTP-Binding Protein - physiology
Signal Transduction
Smooth muscle
title Druggable targets in the Rho pathway and their promise for therapeutic control of blood pressure
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