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作 者:程梅[1] 高海青[1] 许玲[1] 李保应[1] 李宪花[1]
机构地区:[1]山东大学齐鲁医院老年病科,山东济南250012
出 处:《山东大学学报(医学版)》2007年第4期404-406,411,共4页Journal of Shandong University:Health Sciences
摘 要:目的:观察葡萄子原花青素(grape seed proanthocyanidin extracts,GSPE)对链脲佐菌素(streptozoto-cin,STZ)糖尿病大鼠血浆糖基化终末产物(advanced glycation end products,AGEs)、心肌超微结构的影响;探讨GSPE对STZ糖尿病大鼠心肌的保护作用。方法:雄性Wistar大鼠尾静脉注射0.1%STZ以建立糖尿病模型,成模后随机分为2组,糖尿病对照组(DM1组,n=8)和糖尿病GSPE治疗组(GSPE250 mg/(kg.d),DM2组,n=12),另设2组,正常对照组(C1组,n=10)和正常GSPE治疗组(C2组,n=10)。24周后采血测血糖、糖化血红蛋白(glycosylated hemoglobin,HbA1c)、AGEs,电镜观察心肌超微结构变化。结果:DM2组AGEs较DM1组明显降低(t=2.792,P=0.02);DM1组肌原纤维和线粒体排列紊乱,经GSPE治疗后DM2组明显减轻。结论:GSPE能够抑制STZ糖尿病大鼠非酶糖基化反应,对其心脏超微结构有一定保护作用。Objective: To observe the effect of grape seed proanthocyanidin extracts (GSPE)on plasma advanced glycation end products (AGEs) and myocardial ultrastructures of streptozotocin (STZ) induced diabetic rats. Methods: Male Wistar rats were subjected to 0.1% STZ through the tail vein to induce diabetics. Then, they were randomly divided into two groups: the diabetic model (DM) group (DM1, n = 8)and the GSPE-treatment diabetic group (DM2, n = 12, 250 mg·kg^-1·d^-1). Non-diabetic Wistar rats were enrolled in an other two groups: the control group (C1, n = 10) and the GSPE -treatment group(C2 group, n = 10, 250 mg·kg^-1·d^-1 ). After 24 weeks, all rats were killed, and the fasting plasma glucose, glycosylated hemoglobin and AGEs were determined. Changes of myocardial ultrastructure were observed by an electronic microscope. Results: Plasma AGEs of DM2 group was lower than that of DM1 group ( t = 2.792, P = 0.02). The myofibrillaes and the chondriosomees were disordered in DM1 group, but changed after the GSPE treatment. Conclusion: GSPE can inhibit nonenzymatic reactions of glycosylation in STZ-induced diabetic rats and protect the myocardial ultra-structure.
关 键 词:葡萄子原花青素 糖尿病心肌病 糖基化终末产物 高级 超微结构 大鼠 Wistar
分 类 号:R542.2[医药卫生—心血管疾病]
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