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通过用d-α-生育酚治疗预防糖尿病引起的视网膜血流异常。

Prevention of diabetes-induced abnormal retinal blood flow by treatment with d-alpha-tocopherol.

作者信息

Kunisaki M, Bursell S E, Umeda F, Nawata H, King G L

机构信息

Third Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Biofactors. 1998;7(1-2):55-67. doi: 10.1002/biof.5520070109.

Abstract

Hyperglycemia in diabetes mellitus has been shown to activate diacylglycerol (DAG)-protein kinase C (PKC) pathway in the vascular tissues, possibly altering vascular function. We have characterized the effects of vitamin E (d-alpha-tocopherol) on activation of PKC and DAG levels in retinal tissues of diabetic rats, and correlated its effects to retinal hemodynamics using video-based fluorescein angiography (VFA). Comparing streptozotocin-induced diabetic rats to controls, membranous PKC specific activities were increased by 71% (p < 0.05). Western blot analysis showed that the membranous PKC beta II isoform was significantly increased by 133 +/- 45% (p < 0.05). Intraperitoneal injection of d-alpha-tocopherol (40 mg/kg) every other day prevented the increases in membranous PKC specific activity and PKC beta II protein shown by immunoblots. Similar to PKC activities, total DAG levels were increased in the retina and were normalized by d-alpha-tocopherol treatment. Physiologically, abnormalities of retinal blood hemodynamics, as measured using VFA, which previously have been reported to be associated with increases of DAG and PKC levels in the diabetic rats, were prevented by d-alpha-tocopherol treatment in diabetic rats. The direct effect of d-alpha-tocopherol on total DAG and [3H]-palmitate incorporation into DAG were also examined using cultured bovine retinal endothelial cells (REC). Exposure of REC to 22 mM glucose for three days increased total DAG and [3H]-palmitate labeled DAG levels by 35 +/- 8% and 50 +/- 8%, respectively (p < 0.05). The presence of d-alpha-tocopherol (50 micrograms/ml) prevented the increase of both total DAG and [3H]-palmitate labeled DAG levels in cells exposed to 22 mM glucose. These findings suggested that the mechanism of the d-alpha-tocopherol's effect appears to be mediated by the normalization of the hyperglycemia-induced activation of the DAG-PKC pathway which leads to the normalization of abnormal retinal blood flow seen in diabetes mellitus.

摘要

糖尿病中的高血糖已被证明可激活血管组织中的二酰甘油(DAG)-蛋白激酶C(PKC)途径,这可能会改变血管功能。我们已经研究了维生素E(d-α-生育酚)对糖尿病大鼠视网膜组织中PKC激活和DAG水平的影响,并使用基于视频的荧光素血管造影(VFA)将其影响与视网膜血流动力学相关联。将链脲佐菌素诱导的糖尿病大鼠与对照组进行比较,膜性PKC的比活性增加了71%(p<0.05)。蛋白质印迹分析表明,膜性PKCβII亚型显著增加了133±45%(p<0.05)。每隔一天腹腔注射d-α-生育酚(40mg/kg)可防止免疫印迹显示的膜性PKC比活性和PKCβII蛋白增加。与PKC活性相似,视网膜中的总DAG水平增加,经d-α-生育酚治疗后恢复正常。从生理学角度来看,使用VFA测量的视网膜血液动力学异常,此前已报道与糖尿病大鼠中DAG和PKC水平的增加有关,而d-α-生育酚治疗可预防糖尿病大鼠的这种异常。还使用培养的牛视网膜内皮细胞(REC)研究了d-α-生育酚对总DAG和[3H]-棕榈酸掺入DAG的直接影响。将REC暴露于22mM葡萄糖三天,总DAG和[3H]-棕榈酸标记的DAG水平分别增加了35±8%和50±8%(p<0.05)。d-α-生育酚(50μg/ml)的存在可防止暴露于22mM葡萄糖的细胞中总DAG和[3H]-棕榈酸标记的DAG水平增加。这些发现表明,d-α-生育酚的作用机制似乎是通过使高血糖诱导的DAG-PKC途径激活正常化来介导的,这导致糖尿病中异常视网膜血流正常化。

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