Pugliese G, Tilton R G, Speedy A, Santarelli E, Eades D M, Province M A, Kilo C, Sherman W R, Williamson J R
Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110.
Diabetes. 1990 Mar;39(3):312-22. doi: 10.2337/diab.39.3.312.
To assess the potential of myo-inositol-supplemented diets to prevent diabetes-induced vascular functional changes, we examined the effects of diets supplemented with 0.5, 1, or 2% myo-inositol on blood flow and vascular filtration function in nondiabetic control rats and rats with streptozocin-induced diabetes (STZ-D). After 1 mo of diabetes and dietary myo-inositol supplementation, 1) 131I-labeled bovine serum albumin (BSA) permeation of vessels was assessed in multiple tissues, 2) glomerular filtration rate (GFR) was estimated as renal plasma clearance of 57Co-labeled EDTA, 3) regional blood flows were measured with 15-microns 85Sr-labeled microspheres, and 4) endogenous albumin and IgG urinary excretion rates were quantified by radial immunodiffusion assay. In STZ-D rats, 131I-BSA tissue clearance increased significantly (2- to 4-fold) in the anterior uvea, choroid-sclera, retina, sciatic nerve, aorta, new granulation tissue, diaphragm, and kidney but was unchanged in skin, forelimb muscle, and heart. myo-Inositol-supplemented diets reduced diabetes-induced increases in 131I-BSA clearance (in a dose-dependent manner) in all tissues; however, only in new granulation tissue and diaphragm did the 2% myo-inositol diet completely normalize vascular albumin permeation. Diabetes-induced increases in GFR and in urinary albumin and IgG excretion were also substantially reduced or normalized by dietary myo-inositol supplements. Increased blood flow in anterior uvea, choroid-sclera, kidney, new granulation tissue, and skeletal muscle in STZ-D rats also was substantially reduced or normalized by the 2% myo-inositol diet. myo-Inositol had minimal if any effects on the above parameters in control rats. These observations indicate that diabetes-induced increases in regional blood flow, 131I-BSA permeation, GFR, and urinary protein excretion can be markedly reduced or normalized by consumption of myo-inositol-supplemented diets that raise plasma myo-inositol levels approximately fivefold. The failure of the 2% myo-inositol diet to normalize GFR and blood flow and albumin permeation in several tissues despite markedly elevated plasma myo-inositol levels and normal or elevated tissue myo-inositol levels indicates that if vascular functional changes in these tissues are linked to altered myo-inositol levels, they are resistant to normalization by elevation of plasma myo-inositol levels. These results suggest that other factors independent of changes in relative or absolute tissue myo-inositol levels may play an important role in the pathogenesis of diabetes-induced vascular functional changes in these tissues.(ABSTRACT TRUNCATED AT 400 WORDS)
为评估补充肌醇的饮食预防糖尿病引起的血管功能变化的潜力,我们研究了补充0.5%、1%或2%肌醇的饮食对非糖尿病对照大鼠和链脲佐菌素诱导的糖尿病大鼠(STZ-D)的血流和血管滤过功能的影响。在糖尿病及饮食补充肌醇1个月后,1)在多个组织中评估131I标记的牛血清白蛋白(BSA)在血管中的渗透;2)通过57Co标记的EDTA的肾血浆清除率估算肾小球滤过率(GFR);3)用15微米的85Sr标记微球测量局部血流量;4)通过放射免疫扩散测定法定量内源性白蛋白和IgG的尿排泄率。在STZ-D大鼠中,前葡萄膜、脉络膜-巩膜、视网膜、坐骨神经、主动脉、新生肉芽组织、膈肌和肾脏中131I-BSA的组织清除率显著增加(2至4倍),但皮肤、前肢肌肉和心脏中则无变化。补充肌醇的饮食可降低糖尿病引起的所有组织中131I-BSA清除率的增加(呈剂量依赖性);然而,只有2%肌醇饮食能使新生肉芽组织和膈肌中的血管白蛋白渗透完全恢复正常。饮食补充肌醇还可显著降低或使糖尿病引起的GFR以及尿白蛋白和IgG排泄增加恢复正常。2%肌醇饮食也可使STZ-D大鼠前葡萄膜、脉络膜-巩膜、肾脏、新生肉芽组织和骨骼肌中增加的血流量显著降低或恢复正常。肌醇对对照大鼠的上述参数影响极小(若有影响)。这些观察结果表明,食用使血浆肌醇水平升高约五倍的补充肌醇的饮食,可显著降低或使糖尿病引起的局部血流量增加、131I-BSA渗透、GFR和尿蛋白排泄增加恢复正常。尽管血浆肌醇水平显著升高且组织肌醇水平正常或升高,但2%肌醇饮食未能使几个组织中的GFR、血流和白蛋白渗透恢复正常,这表明如果这些组织中的血管功能变化与肌醇水平改变有关,那么它们对通过升高血浆肌醇水平来恢复正常具有抗性。这些结果表明,与相对或绝对组织肌醇水平变化无关的其他因素可能在糖尿病引起的这些组织血管功能变化的发病机制中起重要作用。(摘要截短至400字)