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醛糖还原酶抑制对糖尿病患者红细胞多元醇和半乳糖醇蓄积的影响。

The effect of aldose reductase inhibition on erythrocyte polyols and galactitol accumulation in diabetic patients.

作者信息

Airey C M, Price D E, Kemp J V, Perkins C M, Wales J K

机构信息

University Department of Medicine, Leeds, UK.

出版信息

Diabet Med. 1989 Dec;6(9):804-8. doi: 10.1111/j.1464-5491.1989.tb01283.x.

Abstract

Erythrocyte sorbitol level has previously been used as a measure of the efficacy of aldose reductase inhibitors, but its value is limited by fluctuations related to variations in blood glucose concentration. The aim of the study was to compare sorbitol content with the ability to accumulate galactitol during ex vivo incubation with galactose, of erythrocytes taken from diabetic patients following administration of a single 600 mg dose of the aldose reductase inhibitor, ponalrestat. Twelve patients were studied in a placebo-controlled crossover trial. Blood glucose levels were not statistically different during the placebo and ponalrestat treatment periods except at 1 h after the dose was taken (10.6 +/- 6.7 vs 7.7 +/- 4.6 mmol l-1 (+/- SD), p less than 0.05). Ponalrestat reduced erythrocyte sorbitol concentrations compared with placebo at 3, 5 and 7 h (0.82 +/- 0.36, 0.69 +/- 0.23, and 0.83 +/- 0.35 mg l-1 vs 1.79 +/- 0.67, 1.68 +/- 0.65, and 1.57 +/- 0.59 mg l-1 respectively, p less than 0.005) and 24 h post-dose (1.57 + 0.45 vs 2.01 + 0.73 mg l-1, p less than 0.05). Ponalrestat also reduced erythrocyte galactitol accumulation at 3, 5 and 24 h post-dose from 5.53 +/- 2.41, 5.43 +/- 1.89, and 5.42 +/- 1.96 mg l-1 2-h-1 to 1.47 +/- 0.30, 1.76 +/- 0.41, and 4.12 +/- 0.72 mg l-1 2-h-1 respectively, p less than 0.01. Galactitol accumulation rate appeared to be a less variable parameter than erythrocyte sorbitol and was not influenced by fluctuations in blood glucose.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

红细胞山梨醇水平此前一直被用作醛糖还原酶抑制剂疗效的一项衡量指标,但其价值受到与血糖浓度变化相关波动的限制。本研究的目的是比较服用单次600毫克剂量醛糖还原酶抑制剂泊那司他后,糖尿病患者红细胞在体外与半乳糖孵育期间的山梨醇含量和积累半乳糖醇的能力。在一项安慰剂对照的交叉试验中对12名患者进行了研究。在安慰剂和泊那司他治疗期间,除服药后1小时外,血糖水平无统计学差异(分别为10.6±6.7与7.7±(4.6毫摩尔/升)(±标准差),p<0.05)。与安慰剂相比,泊那司他在3、5和7小时以及给药后24小时降低了红细胞山梨醇浓度(分别为0.82±0.36、0.69±0.23和0.83±0.35毫克/升,对比1.79±0.67、1.68±0.65和1.57±0.59毫克/升,p<0.005)以及给药后24小时(1.57 + 0.45对比2.01 + 0.73毫克/升,p<0.05)。泊那司他在给药后3、5和24小时也将红细胞半乳糖醇积累量从5.53±2.41、5.43±1.89和5.42±1.96毫克/升·2小时-1分别降至1.47±0.30、1.76±0.41和4.12±0.72毫克/升·2小时-1,p<0.01。半乳糖醇积累率似乎是一个比红细胞山梨醇变异性更小的参数,且不受血糖波动的影响。(摘要截选至250词)

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