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作 者:薛现中[1] 郭宏[1] 庞德水[1] 任忠法[1] 薛现霞[1] 王开芹[1] 陈玉萍[1]
机构地区:[1]山东省滕州市中心人民医院内分泌科,滕州277500
出 处:《中国实用医刊》2008年第20期4-6,共3页Chinese Journal of Practical Medicine
摘 要:目的观察吡格列酮对2型糖尿病患者氧化应激和抗氧化指标的影响并探讨其可能机制。方法选择符合WHO1999年诊断标准的2型糖尿病患者70例,随机分为治疗组(35例)和对照组(35例)。治疗组降糖药物选用胰岛素+吡格列酮,对照组仅用胰岛素控制血糖,其他常规治疗药物中不用血管紧张素转换酶抑制剂(ACEI)、他汀类、维生素C、维生素E等药物。疗程3个月。所有病人治疗前后均于清晨空腹抽血,留取标本,分别用于血清硝化酪氨酸(NT)、12(S)-羟基二十碳四烯酸[12(S)-HETE]、谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GSH—PX)等的测定。结果70例病人共有65例完成了本观察,两组病人治疗后氧化应激指标NT和12(S)-HETE水平均较治疗前有明显降低(P均〈0.01),治疗后两组相比治疗组NT和12(S)-HETE下降水平明显高于对照组(P分别〈0.01和〈0.05)。两组病人治疗后抗氧化指标GSH和GSH—PX水平均较治疗前有提高(P分别〈0.05和〈0.01),治疗后两组相比治疗组GSH和GSH—PX升高水平高于对照组(P分别〈0.01和〈0.05)。在治疗中无一例病人出现明显不良反应。结论吡格列酮具有独立于降血糖作用外的抗氧化作用,可以降低糖尿病患者血中氧化应激指标NT和12(S)-HETE水平,并升高GSH和GSH—PX抗氧化指标水平,改善2型糖尿病患者氧化应激状态提高其抗氧化能力。Objective To investigate the effect and mechanism of pioglitazone on oxidation stress and antioxidation conditions in patients of type 2 diabetes mellitus(T2DM). Methods Seventy patients of T2DM, diagnosed according to the standards of WHO, 1999, were divided randomly into treated group ( n = 35 ) and control group ( n = 35 ). Patients of the former group were treated with insulin and pioglitazone, while the latter were given insulin only to control blood glucose level. In other normal therapies,ACEI, statins, Vitamin C and Vitamin E were excluded. All patients were treated for 3 months. Fasting blood samples were got before and after treatment and reserved for measurement of NT, 12 ( S ) - HETE, GSH and GSH - PX. Results Sixty - five patients underwent the whole observation. The level of NT and 12(S) - HETE decreased markedly after treatment in both groups ( P 〈0.01 ),with more significant in treated group than in control group ( P 〈 0. 01 and P 〈 0.05). The levels of GSH and GSH - PX elevated markedly after treatment in both groups ( P 〈 0.01 and P 〈 0.05, respectively), with more significant in treated group than in control group ( P 〈0. 01 and P 〈 0.05 ). No adverse reactions were found during the treating process. Conclusion Pioglitazone shows antioxidant potency safely independent of glucose - lowering effect by decreasing of level of oxidation stress NT and 12(S) -HETE and increasing of level of antioxidant GSH and GSH -PX.
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