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PI3Kγ in hypertension: a novel therapeutic target controlling vascular myogenic tone and target organ damage
Daniela Carnevale1, Giuseppe Lembo
1Department of Angiocardioneurology, IRCCS Neuromed, Pozzilli, Italy.
Insights
Phosphoinositide 3-kinase gamma (PI3Kγ) regulates blood pressure by controlling vascular myogenic tone. Targeting PI3Kγ offers a promising therapeutic strategy for hypertension and associated organ damage.
Area of Science:
- Cardiovascular Physiology
- Molecular Biology
- Pharmacology
Background:
- Vascular myogenic response is crucial for blood pressure regulation.
- Phosphoinositide 3-kinase gamma (PI3Kγ) emerges as a key regulator of vascular tone.
- Genetic studies link PI3Kγ to blood pressure regulation in human populations.
Purpose of the Study:
- To review the mechanism of PI3Kγ in controlling blood pressure.
- To explore PI3Kγ's role in regulating myogenic tone via L-type calcium channels.
- To assess PI3Kγ as a therapeutic target for hypertension.
Main Methods:
- Literature review of cellular and molecular mechanisms.
- Analysis of genetic association studies.
- Survey of pharmacological approaches and target organ effects.
Main Results:
- PI3Kγ regulates vascular myogenic tone at the smooth muscle L-type calcium channel level.
- PI3Kγ is a viable target for antihypertensive therapy.
- PI3Kγ may mitigate hypertension-induced target organ damage independently of blood pressure reduction.
Conclusions:
- PI3Kγ is a significant regulator of blood pressure and vascular tone.
- Targeting PI3Kγ presents a dual therapeutic potential for hypertension and its complications.
- Further research into PI3Kγ modulation is warranted for novel antihypertensive strategies.
Abstract:
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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