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Details

Autor(en) / Beteiligte
Titel
Treatment of cardiovascular dysfunction associated with the metabolic syndrome and type 2 diabetes
Ist Teil von
  • Vascular pharmacology, 2008-01, Vol.48 (1), p.47-53
Ort / Verlag
United States: Elsevier Inc
Erscheinungsjahr
2008
Quelle
Elsevier ScienceDirect Journals
Beschreibungen/Notizen
  • Abstract Our previous studies have shown vascular dysfunction in small coronary and mesenteric arteries in Zucker obese rats, a model of the metabolic syndrome, and Zucker Diabetic Fatty (ZDF) rats, a model of type 2 diabetes. Because of their lipid lowering action and antioxidant activity, we predicted that treatment with Rosuvastatin, an HMG-CoA reductase inhibitor (statin) or Enalapril, an angiotensin converting enzyme (ACE) inhibitor would improve vascular dysfunction associated with the metabolic syndrome and type 2 diabetes. Methods 20-week-old Zucker obese and 16-week-old ZDF rats were treated with Rosuvastatin (25 mg/kg/day) or Enalapril (20 mg/kg/day) for 12 weeks. We examined metabolic parameters, indices of oxidative stress and vascular dysfunction in ventricular and mesenteric small arteries (75–175 µm intraluminal diameter) from lean, Zucker obese and ZDF rats (untreated and treated). Results Endothelial dependent responses were attenuated in coronary vessels from Zucker obese and ZDF rats compared to responses from lean rats. Both drugs improved metabolic parameters, oxidative stress, and vascular dysfunction in Zucker obese rats, however, only partial improvement was observed in ZDF rats, suggesting more aggressive treatment is needed when hyperglycemia is involved. Conclusion Vascular dysfunction is improved when Zucker obese and, to a lesser degree, when ZDF rats were treated with Rosuvastatin or Enalapril.
Sprache
Englisch
Identifikatoren
ISSN: 1537-1891
eISSN: 1879-3649
DOI: 10.1016/j.vph.2007.11.005
Titel-ID: cdi_proquest_miscellaneous_70220812
Format
Schlagworte
ACE inhibitors, Acetylcholine, Age Factors, Angiotensin-Converting Enzyme Inhibitors - pharmacology, Angiotensin-Converting Enzyme Inhibitors - therapeutic use, Animals, Blood Glucose - metabolism, Blood Pressure - drug effects, Body Weight - drug effects, Cardiovascular, Cardiovascular Diseases - complications, Cardiovascular Diseases - drug therapy, Cardiovascular Diseases - physiopathology, Cholesterol - blood, Coronary circulation, Coronary Vessels - drug effects, Coronary Vessels - metabolism, Coronary Vessels - physiopathology, Diabetes, Diabetes Mellitus, Type 2 - complications, Diabetes Mellitus, Type 2 - drug therapy, Diabetes Mellitus, Type 2 - physiopathology, Enalapril - pharmacology, Enalapril - therapeutic use, Endothelial function, Endothelium, Vascular - drug effects, Endothelium, Vascular - metabolism, Endothelium, Vascular - physiopathology, Fatty Acids - blood, Fluorobenzenes - pharmacology, Fluorobenzenes - therapeutic use, Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacology, Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use, Male, Mesenteric Arteries - drug effects, Mesenteric Arteries - physiopathology, Metabolic Syndrome - complications, Metabolic Syndrome - drug therapy, Metabolic Syndrome - physiopathology, Oxidative Stress - drug effects, Pyrimidines - pharmacology, Pyrimidines - therapeutic use, Rats, Rats, Zucker, Rosuvastatin Calcium, Statins, Sulfonamides - pharmacology, Sulfonamides - therapeutic use, Triglycerides - blood

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