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Prevention of Vascular Apoptosis in Myocardial Infarction by Losartan
- Source :
- Journal of cardiovascular pharmacology and therapeutics. 4(2)
- Publication Year :
- 2000
-
Abstract
- Background: Previous studies have demonstrated the occurrence of apoptosis in cardiomyo cytes in different types of cardiovascular diseases. This report provides the first evidence for the presence of vascular apoptosis in myocardial infarction induced in rats by occluding the coronary artery for 7 weeks. Methods and Results: Apoptosis was characterized by DNA fragmentation, upregulation of caspase-3, downregulation of poly (ADP-ribose) polymerase (PARP), increased c-fos mRNA expression and caspase-3/PARP ratio in aortic vascular smooth muscle cells. The results show apoptotic changes in 10-25% of the aortic vascular cells after myocardial in farction ; these alterations were prevented after treating the 3-week operated animals with an angiotensin II receptor antagonist, losartan (25 mg/kg/day; intraperitoneal) for 4 weeks. Cultured rat aortic smooth muscle cells exposed to 10 nmol/L angiotensin II for 48 hours also exhibited apoptotic changes, which were inhibited by 10 nmol/L losartan. Conclusions: These results suggest that vascular apoptosis occurs in myocardial infarction, and this may be due to an increase in the circulating levels of angiotensin II.
- Subjects :
- Pharmacology
medicine.medical_specialty
Vascular smooth muscle
business.industry
Angiotensin II receptor antagonist
030204 cardiovascular system & hematology
medicine.disease
Angiotensin II
03 medical and health sciences
0302 clinical medicine
medicine.anatomical_structure
Endocrinology
Losartan
Downregulation and upregulation
Apoptosis
Internal medicine
medicine
Pharmacology (medical)
030212 general & internal medicine
Myocardial infarction
Cardiology and Cardiovascular Medicine
business
Artery
medicine.drug
Subjects
Details
- ISSN :
- 19404034
- Volume :
- 4
- Issue :
- 2
- Database :
- OpenAIRE
- Journal :
- Journal of cardiovascular pharmacology and therapeutics
- Accession number :
- edsair.doi.dedup.....6d3f3301c0120927278166b9ce6a0ba1