Resveratrol Shows Vasoprotective Effect Reducing Oxidative Stress Without Affecting Metabolic Disturbances in Insulin-dependent Diabetes of Rabbits

被引:36
作者
Akar, Fatma [1 ,2 ]
Pektas, M. Bilgehan [2 ]
Tufan, Can [2 ]
Soylemez, Selen [2 ]
Sepici, Aylin [3 ]
Ulus, A. Tulga [4 ]
Gokalp, Burcu [2 ]
Ozturk, Kamile [5 ]
Surucu, H. Selcuk [6 ]
机构
[1] Gazi Univ, Farmakol Anabilim Dali, Eczacilik Fak, TR-06330 Ankara, Turkey
[2] Gazi Univ, Dept Pharmacol, Fac Pharm, TR-06330 Ankara, Turkey
[3] Gazi Univ, Fac Med, TR-06330 Ankara, Turkey
[4] Turkiye Yuksek Ihtisas Hosp Cardiovasc Surg Clin, Dept Cardiovasc Surg, Ankara, Turkey
[5] Aksaray Univ, Dept Mol Biol, Fac Sci, Aksaray, Turkey
[6] Hacettepe Univ, Fac Med, Dept Anat, Ankara, Turkey
关键词
Resveratrol; Endothelial and vascular function; Superoxide; Nitric oxide; Insulin; Alloxan; Diabetic rabbits; ENDOTHELIAL DYSFUNCTION; TRANS-RESVERATROL; NITRIC-OXIDE; FEMALE RATS; CELLS; SUPEROXIDE; RELAXATION; AORTA; SIRT1; ANTIOXIDANT;
D O I
10.1007/s10557-010-6255-7
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Resveratrol has been shown to have vasoprotective effects by upregulating oxidative defense mechanisms in a variety of pathophysiological conditions. However, the effect of resveratrol on diabetic oxidative stress and vascular and metabolic abnormalities is not completely understood. Therefore, this study was designed to evaluate whether long-term resveratrol supplementation has a protective effect on vascular function and integrity in association with metabolic parameters and oxidative stress in insulin-dependent diabetes. Diabetes was induced in rabbits with alloxan and maintained for 8 weeks. We used a resveratrol dose of 5 mg/L (10 weeks, starting 14 days before alloxan injection) and 50 mg/L (8 or 10 weeks, starting concomitantly or 14 days before alloxan injection) in the drinking water of rabbits. Relaxation to acetylcholine was impaired (control 75.6 +/- 3.59%, versus diabetic 42.23 +/- 2.53%) and contractions to phenylephrine increased (control 136.89 +/- 2.27%, versus diabetic 159.37 +/- 6.27%) in aortas from diabetic animals. These changes were associated with increased basal or NAD(P)H-induced superoxide production, as well as lipid peroxide and superoxide dismutase (SOD) levels in the aortic samples. The maximal relaxation to acetylcholine improved by 75.74 +/- 9.04% in diabetic rabbits treated with resveratrol. The increased contractions to phenylephrine were not restored to control values after resveratrol treatments, but sensitivity to the contractions tended to decrease. Resveratrol increased nitrite/nitrate levels and suppressed basal or NAD(P)H-induced superoxide production and lipid peroxide levels in the aortas. Importantly, resveratrol increased serum insulin levels without affecting blood glucose and the lipid profile in diabetic rabbits. Using electron microscopic examinations, resveratrol was found to markedly protect the endothelial integrity from diabetes. Overall, there was no noticeable difference between resveratrol treatment groups on the recovery from diabetes. Our results indicate that resveratrol alleviates type 1 diabetes-induced vasculopathy by decreasing vascular oxidative stress and thereby increasing the bioavailability of nitric oxide without changing metabolic abnormalities.
引用
收藏
页码:119 / 131
页数:13
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