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格列齐特对新诊断 2 型糖尿病患者内皮功能的影响。

Effects of gliclazide on endothelial function in patients with newly diagnosed type 2 diabetes.

机构信息

Department of Endocrinology, Union Hospital, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Eur J Pharmacol. 2011 Jun 1;659(2-3):296-301. doi: 10.1016/j.ejphar.2011.02.044. Epub 2011 Mar 29.

Abstract

Endothelial dysfunction is thought to be a critical event in the pathogenesis of vasculopathy in type 2 diabetes and oxidant stress is a major etiological factor. Gliclazide, a second generation sulfonylurea, contains an azabicyclo-octyl ring, which has been described to have antioxidant properties. However, the effect of gliclazide on endothelial function is unknown. Therefore, in this study, we examined the effect of gliclazide on endothelial function in patients with newly diagnosed type 2 diabetes (diabetic group; n=33). A control group of non-diabetic subjects was also enrolled (n=25). All of the diabetic patients were treated with gliclazide for 12 weeks. Endothelial function was evaluated by flow-mediated vasodilation (FMD) before and after treatment. We also determined the number of circulating endothelial progenitor cells (EPCs), which were defined by CD45(low)/CD34(+)/VEGFR2(+) and quantified by flow cytometry, because these cells may offer a new biomarker for circulatory diseases. Oxidative stress was evaluated in terms of the serum levels of malondialdehyde, superoxide dismutase and nitric oxide. FMD, circulating EPC count and superoxide dismutase activity were significantly lower in the diabetic group than in the control group at baseline (P<0.05), and improved significantly following gliclazide treatment (P<0.05). Malondialdehyde and nitric oxide levels were higher in the diabetic group than in the control group at baseline (P<0.05), and decreased following gliclazide treatment. These results suggest that gliclazide could improve endothelial function in diabetes, which may be related to its antioxidant properties.

摘要

内皮功能障碍被认为是 2 型糖尿病血管病变发病机制中的一个关键事件,而氧化应激是一个主要的病因。格列齐特是第二代磺酰脲类药物,含有一个氮杂双环辛基环,据描述具有抗氧化特性。然而,格列齐特对内皮功能的影响尚不清楚。因此,在这项研究中,我们研究了格列齐特对新诊断的 2 型糖尿病患者(糖尿病组;n=33)内皮功能的影响。还招募了一组非糖尿病患者作为对照组(n=25)。所有糖尿病患者均接受格列齐特治疗 12 周。治疗前后通过血流介导的血管扩张(FMD)评估内皮功能。我们还测定了循环内皮祖细胞(EPC)的数量,这些细胞通过 CD45(low)/CD34(+)/VEGFR2(+)来定义,并通过流式细胞术进行定量,因为这些细胞可能为循环疾病提供新的生物标志物。用血清丙二醛、超氧化物歧化酶和一氧化氮水平来评估氧化应激。与对照组相比,糖尿病组患者在基线时的 FMD、循环 EPC 计数和超氧化物歧化酶活性显著降低(P<0.05),并在格列齐特治疗后显著改善(P<0.05)。与对照组相比,糖尿病组患者在基线时的丙二醛和一氧化氮水平较高(P<0.05),并在格列齐特治疗后降低。这些结果表明,格列齐特可改善糖尿病患者的内皮功能,这可能与其抗氧化特性有关。

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