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Asymmetric dimethylarginine and angiogenesis: biological significance
- Source :
- International Angiology. 37
- Publication Year :
- 2018
- Publisher :
- Edizioni Minerva Medica, 2018.
-
Abstract
- Competitive inhibition of endothelial nitric oxide synthase (eNOS) is the main biological effect of asymmetric dimethylarginine (ADMA), i.e. the methylated derivative of L-arginine. The resulting low level of NO is becoming one of the elements of pathogenesis of numerous cardiovascular disorders, mainly related to atherosclerosis, but also other metabolic diseases including type 2 diabetes. It appears that a high level of ADMA is not only a marker of pathological conditions such as chronic kidney failure, but also a significant factor which damages the endothelium. Despite multiple studies, the mechanisms of reducing the level of ADMA, which would allow to inhibit the progression of cardiovascular diseases and effective treatment, e.g. by means of L-arginine supplementation or medicines which are lowering ADMA levels, are still unclear. Perhaps, linking ADMA with the processes of new blood cell formation (angiogenesis) will allow us to explain these multifactor mechanisms.
- Subjects :
- 0301 basic medicine
Endothelium
Angiogenesis
Neovascularization, Physiologic
Type 2 diabetes
030204 cardiovascular system & hematology
Pharmacology
Arginine
Neovascularization
Pathogenesis
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Downregulation and upregulation
Enos
Animals
Humans
Medicine
Neovascularization, Pathologic
biology
business.industry
Endothelial Cells
Atherosclerosis
biology.organism_classification
medicine.disease
Plaque, Atherosclerotic
Up-Regulation
030104 developmental biology
medicine.anatomical_structure
chemistry
Cardiovascular Diseases
medicine.symptom
Cardiology and Cardiovascular Medicine
business
Asymmetric dimethylarginine
Signal Transduction
Subjects
Details
- ISSN :
- 18271839 and 03929590
- Volume :
- 37
- Database :
- OpenAIRE
- Journal :
- International Angiology
- Accession number :
- edsair.doi.dedup.....6060356bdcfa6e5b18b27ebd9b50a0ab
- Full Text :
- https://doi.org/10.23736/s0392-9590.18.04017-8