Back to Search
Start Over
AngiotensinII preconditioning promotes angiogenesis in vitro via ERKs phosphorylation.
- Source :
-
Journal of biomedicine & biotechnology [J Biomed Biotechnol] 2012; Vol. 2012, pp. 737134. Date of Electronic Publication: 2012 Feb 28. - Publication Year :
- 2012
-
Abstract
- AngiotensinII (AngII) is involved in not only the formation of cardiac hypertrophy but also the development of cardiac remodeling both of which are associated with myocardial angiogenesis. This study was therefore performed to clarify the effects of AngII on the formation of vasculatures by cultured cardiac microvascular endothelial cells (CMVECs) after a long-period stimulation with or without the AngII preconditioning. Incubation with AngII for 18 hrs significantly impaired the formation of capillary-like tubes comparing to that without AngII. CMVECs with AngII pretreatment for 5 and 10 min formed more capillary-like tubes than those without AngII pretreatment, suggesting that preconditioning with AngII at a lower dose for a short period could prevent the further damage of CMVECs by a higher concentration of AngII. Moreover, AngII (10(-7) M) stimulation for 5 and 10 min significantly induced the increase in extracellular signal-regulated protein kinases (ERKs) phosphorylation, and an ERKs inhibitor, PD98059, abrogated the increase in the formation of capillary-like tubes induced by the AngII-pretreatment. In conclusion, preconditioning with a lower concentration of AngII for a short period prevents the subsequent impairment of CMVECs by a higher dose of AngII, at least in part, through the increase in ERKs phosphorylation.
- Subjects :
- Analysis of Variance
Angiogenesis Inducing Agents pharmacology
Animals
Cells, Cultured
Endothelial Cells drug effects
Extracellular Signal-Regulated MAP Kinases antagonists & inhibitors
Flavonoids pharmacology
Male
Myocardium cytology
Phosphorylation
Protective Agents pharmacology
Rats
Rats, Wistar
Angiotensin II pharmacology
Endothelial Cells metabolism
Extracellular Signal-Regulated MAP Kinases metabolism
Neovascularization, Physiologic drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1110-7251
- Volume :
- 2012
- Database :
- MEDLINE
- Journal :
- Journal of biomedicine & biotechnology
- Publication Type :
- Academic Journal
- Accession number :
- 22500105
- Full Text :
- https://doi.org/10.1155/2012/737134