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Vanillylmandelic acid protects against reperfusion injury in an experimental animal model of myocardial infarction
- Source :
- Pathophysiology. 26:343-347
- Publication Year :
- 2019
- Publisher :
- Elsevier BV, 2019.
-
Abstract
- Vanillylmandelic acid, a catecholamine end-metabolite, has been shown to have several biological properties in previous studies, despite considered biologically inactive. We examined the potential effects of vanillylmandelic acid on the ischemic heart following myocardial infarction and reperfusion on a rat model. Thirty-four female Wistar rats were randomized into two groups, control and experimental. They were anesthetized and subjected to myocardial infarction through left anterior descending artery ligation. A previously studied dose of vanillylmandelic acid (10 mg/kg) was administered and the following parameters were studied during ischemia and reperfusion: a) mortality b) severity of ventricular tachyarrhythmias c) premature ventricular contractions and d) heart rate. Administration of vanillymandelic acid significantly reduced the severity of ventricular tachyarrhythmias and mortality rate during reperfusion, while it did not affect any other of the parameters studied. In conclusion, reperfusion injury was blunted through vanillylmandelic acid administration, which seems to be mediated by parasympathetic activation.
- Subjects :
- 0301 basic medicine
medicine.medical_specialty
business.industry
Rat model
Ischemia
030204 cardiovascular system & hematology
medicine.disease
Pathology and Forensic Medicine
03 medical and health sciences
chemistry.chemical_compound
Experimental animal
030104 developmental biology
0302 clinical medicine
chemistry
Physiology (medical)
Internal medicine
Heart rate
medicine
Catecholamine
Cardiology
Vanillylmandelic acid
Myocardial infarction
business
Reperfusion injury
medicine.drug
Subjects
Details
- ISSN :
- 09284680
- Volume :
- 26
- Database :
- OpenAIRE
- Journal :
- Pathophysiology
- Accession number :
- edsair.doi.dedup.....b98e827d3b530cccfdf9a11816fa384f
- Full Text :
- https://doi.org/10.1016/j.pathophys.2019.09.001