Abstract
The role of RAS in the development of hypertension and cardiovascular and renal diseases has been extensively studied and is well established. The impact of oxidative stress in vascular homeostasis has also been clearly defined. Many of the cellular effects of Ang II appear to be mediated by ROS generated by NAD(P)H oxidase. Here we provide an overview of ROS physiology in human vessels and in particular the interaction with RAS, as well as a discussion on mechanisms by which therapeutic interventions on RAS affect redox signaling in the vascular wall at a clinical level.
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Abbreviations
- ACE:
-
Angiotensin-converting enzyme
- ACEIs:
-
Angiotensin-converting enzyme inhibitors
- ADMA:
-
Asymmetric dimethylarginine
- AGT:
-
Angiotensinogen
- Ang:
-
Angiotensin
- ARBs:
-
AT1 receptor blockers
- AT1R:
-
Angiotensin type 1 receptors
- AT2R:
-
Angiotensin type 2 receptors
- BB:
-
β-blocker
- BH4 :
-
Tetrahydrobiopterin
- BP:
-
Blood pressure
- DDAH:
-
Dimethylarginine dimethylaminohydrolase
- DRI:
-
Direct renin inhibitors
- EGFR:
-
Epidermal growth factor receptor
- eNOS:
-
Endothelial nitric oxide synthase
- JAK:
-
Janus kinase
- MRAs:
-
Mineralocorticoid receptor antagonists
- NADPH:
-
Nicotinamide adenine dinucleotide phosphate
- PAI-1:
-
Plasminogen activator inhibitor-1
- PRA:
-
Plasma renin activity
- PKC:
-
Protein kinase C
- RAS:
-
Renin–angiotensin system
- ROS:
-
Reactive oxygen species
- TNF:
-
Tissue necrosis factor
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Koumallos, N., Sepehripour, A., Dimarakis, I., Paschalis, A., Nasir, A., Yonan, N. (2014). Reactive Oxygen Species Biology and Angiotensin Regulation of Human Vascular Tone – the Role of Angiotensin-Converting Enzyme (ACE) Inhibitors and AT1 Receptor Blockers (ARBs). In: Laher, I. (eds) Systems Biology of Free Radicals and Antioxidants. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-30018-9_67
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