Why the study?
Is PI3Kγ a suitable therapeutic target for lowering blood pressure and preventing target organ damage in hypertension?
Is PI3Kγ a suitable therapeutic target for lowering blood pressure and preventing target organ damage in hypertension?
This review highlights PI3Kγ as a novel therapeutic target for hypertension that may lower blood pressure and independently protect against target organ damage.
Answers are grounded in this paper and cite their sources.
May warrant PI3Kγ inhibitor trials in hypertension; leaves open clinical efficacy and target-organ protection in humans.
In the past decade, several studies have characterized a number of cellular and molecular mechanisms that contribute to the regulation of the vascular myogenic response, thus affecting blood pressure regulation. Recently, phosphoinositide 3-kinase γ (PI3Kγ) has been identified as a main regulator of vascular myogenic tone and blood pressure, a result further strengthened by a highly significant genome-wide association of a single nucleotide polymorphism flanking this gene with blood pressure regulation, in a large human population. The goal of this review is to summarize the available information regarding the mechanism whereby PI3Kγ exerts blood pressure control, regulating myogenic tone at the level of L-type calcium channel in smooth muscle cells. Moreover, an overview of the pharmacological approaches available for targeting this signalling pathway shows that PI3Kγ is a suitable candidate for antihypertensive therapy, capable of lowering blood pressure. Finally, a survey of the studies dissecting the role of PI3Kγ in pathological conditions that are typically induced by hypertension in its target organs provides a more complete picture of the high potential of this novel therapeutic approach for fighting hypertension and, at the same time, its target organ damage, independently of blood pressure-lowering effects.
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Carnevale et al. (2012) studied this question.
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