scispace - formally typeset
Open AccessJournal ArticleDOI

Angiotensin II, NADPH oxidase, and redox signaling in the vasculature.

Reads0
Chats0
TLDR
There is still a paucity of information on how Ang II exerts cell-specific effects through ROS and how Nox isoforms are differentially regulated by Ang II, and exact mechanisms whereby ROS induce oxidative modifications of signaling molecules mediating Ang II actions remain elusive.
Abstract
Significance: Angiotensin II (Ang II) influences the function of many cell types and regulates many organ systems, in large part through redox-sensitive processes. In the vascular system, Ang II is a potent vasoconstrictor and also promotes inflammation, hypertrophy, and fibrosis, which are important in vascular damage and remodeling in cardiovascular diseases. The diverse actions of Ang II are mediated via Ang II type 1 and Ang II type 2 receptors, which couple to various signaling molecules, including NADPH oxidase (Nox), which generates reactive oxygen species (ROS). ROS are now recognized as signaling molecules, critically placed in pathways activated by Ang II. Mechanisms linking Nox and Ang II are complex and not fully understood. Recent Advances: Ang II regulates vascular cell production of ROS through various recently characterized Noxs, including Nox1, Nox2, Nox4, and Nox5. Activation of these Noxs leads to ROS generation, which in turn influences many downstream signaling targets of Ang II, including MAP kinases, RhoA/Rho kinase, transcription factors, protein tyrosine phosphatases, and tyrosine kinases. Activation of these redox-sensitive pathways regulates vascular cell growth, inflammation, contraction, and senescence. Critical Issues: Although there is much evidence indicating a role for Nox/ROS in Ang II function, there is still a paucity of information on how Ang II exerts cell-specific effects through ROS and how Nox isoforms are differentially regulated by Ang II. Moreover, exact mechanisms whereby ROS induce oxidative modifications of signaling molecules mediating Ang II actions remain elusive. Future Directions: Future research should elucidate these issues to better understand the significance of Ang II and ROS in vascular (patho) biology. Antioxid. Redox Signal. 19, 1110–1120.

read more

Citations
More filters
Journal ArticleDOI

Reperfusion injury and reactive oxygen species: The evolution of a concept.

TL;DR: The possibility that multiple ROS sources contribute to reperfusion injury in most tissues is supported by evidence demonstrating that redox-signaling enables ROS produced by one enzymatic source to activate and enhance ROS production by a second source.
Journal ArticleDOI

Angiotensin II Signal Transduction: An Update on Mechanisms of Physiology and Pathophysiology.

TL;DR: It is expected that rigorous translational research of the ANG II signaling pathways including those in large animals and humans will contribute to establishing effective new therapies against various diseases.
Journal ArticleDOI

Strategies to increase nitric oxide signalling in cardiovascular disease

TL;DR: This Review discusses the identification of new pathways for enhancing NO synthase activity; ways to amplify the nitrate–nitrite–NO pathway; novel classes of NO-donating drugs; drugs that limit NO metabolism through effects on reactive oxygen species; and ways to modulate downstream phosphodiesterases and soluble guanylyl cyclases.
Journal ArticleDOI

Oxidative Stress, Inflammation, and Vascular Aging in Hypertension.

TL;DR: Oxidative stress and inflammation, key mechanisms of endothelial dysfunction and arterial damage, link these risk factors to vascular disease, arterial stiffness, and aging.
Journal ArticleDOI

Oxidative Stress in Cardiovascular Diseases: Still a Therapeutic Target?

TL;DR: This review aims at giving an introduction into oxidative stress in CVD, with special focus on endothelial dysfunction, and then examining in detail the role of oxidative Stress in the most prevalent of these diseases.
References
More filters
Journal ArticleDOI

SOD Isoforms and Signaling in Blood Vessels: Evidence for the Importance of ROS Compartmentalization

TL;DR: Superoxide is the most likely ROS to have distinct effects depending on its subcelullar localization, because of its short half life, its low diffusivity through lipid membranes, and its ability to quickly react with NO to produce perxinitrite.
Journal ArticleDOI

α2-Adrenoceptors Enhance Angiotensin II–Induced Renal Vasoconstriction: Role for NADPH Oxidase and RhoA

TL;DR: It is concluded that NADPH oxidase/superoxide and RhoA/Rho kinase are involved in the interaction between α2-adrenoceptors and angiotensin II on renal vascular resistance by mediating signaling events downstream of the phospholipase C/protein kinases C/c-src pathway.
Journal ArticleDOI

Regulation of Angiotensin II receptor signaling by cysteine modification of NF-κB

TL;DR: In cardiac fibroblasts, stimulation with cytokines or bacterial toxins induces AT(1)R up-regulation through NADPH oxidase-dependent ROS production, and the spatial and temporal regulation of cysteine modification by ROS or RNS may underlie the resultant changes of AT( 1)R signaling induced by agonism.
Related Papers (5)