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Resveratrol shows vasoprotective effect reducing oxidative stress without affecting metabolic disturbances in insulin-dependent diabetes of rabbits.

机译:白藜芦醇显示出血管保护作用,可降低氧化应激而不影响家兔胰岛素依赖性糖尿病的代谢紊乱。

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PURPOSE: 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. METHODS: 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. RESULTS: 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 nitriteitrate 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. CONCLUSION: 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.
机译:目的:白藜芦醇已显示出通过在各种病理生理条件下上调氧化防御机制而具有血管保护作用。但是,白藜芦醇对糖尿病的氧化应激以及血管和代谢异常的影响尚不完全清楚。因此,本研究旨在评估长期补充白藜芦醇是否对胰岛素依赖型糖尿病患者的代谢指标和氧化应激相关,对血管功能和完整性具有保护作用。方法:用四氧嘧啶诱导家兔糖尿病并维持8周。我们在兔子的饮用水中使用了5 mg / L(10周,从四氧嘧啶注射前开始的10天开始)和50 mg / L(8或10周,同时或四氧嘧啶注射之前的14天)的白藜芦醇剂量。结果:主动脉中对乙酰胆碱的松弛受到损害(对照组为75.6 +/- 3.59%,而糖尿病为42.23 +/- 2.53%),对去氧肾上腺素的收缩增加(对照组为136.89 +/- 2.27%,而糖尿病为159.37 +/- 6.27%)。来自糖尿病动物。这些变化与增加的基础或NAD(P)H诱导的超氧化物产生以及主动脉样品中的脂质过氧化物和超氧化物歧化酶(SOD)水平有关。用白藜芦醇治疗的糖尿病兔子对乙酰胆碱的最大舒张改善了75.74 +/- 9.04%。白藜芦醇治疗后对苯肾上腺素的收缩增加并未恢复至控制值,但对收缩的敏感性趋于下降。白藜芦醇增加亚硝酸盐/硝酸盐水平,并抑制主动脉中基础或NAD(P)H诱导的超氧化物生成和脂质过氧化物水平。重要的是,白藜芦醇可以增加血清胰岛素水平,而不会影响糖尿病兔子的血糖和血脂水平。通过电子显微镜检查,发现白藜芦醇可明显保护糖尿病患者的内皮完整性。结论:总的来说,白藜芦醇治疗组之间的糖尿病恢复没有显着差异。我们的结果表明,白藜芦醇通过减少血管氧化应激从而增加一氧化氮的生物利用度而不会改变代谢异常,从而减轻了1型糖尿病诱导的血管病变。

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