Reddi A S
Biochim Biophys Acta. 1986 Jun 3;882(1):71-6. doi: 10.1016/0304-4165(86)90057-7.
Riboflavin nutritional status was assessed on the basis of activity coefficients of glutathione reductase in erythrocyte hemolysates of normal and streptozotocin-diabetic rats. Activity coefficient values higher than 1.3 were regarded as evidence of riboflavin deficiency. All diabetic animals were found to be riboflavin-deficient, with activity coefficient values of 1.47-2.11. Treatment of diabetic rats with either insulin or riboflavin returned their activity coefficients to normal. Rats fed a restricted diet had normal activity coefficient values. The erythrocyte glutathione reductase activity was significantly lower in diabetic rats, and the augmentation of enzyme activity in the presence of flavin-adenine dinucleotide (FAD) was 72% compared to 16% in normal rats. Hepatic activities of glutathione reductase and succinate dehydrogenase, both FAD-containing enzymes, were significantly lower in diabetic than in normal rats. Like activity coefficient values, all enzyme activities were normalized after insulin or riboflavin treatments. These data suggest that insulin and riboflavin enhance the synthesis of erythrocyte and hepatic FAD. The results of the present study suggest that experimental diabetes causes riboflavin deficiency, which in turn decreases erythrocyte and hepatic flavoprotein enzyme activities. These changes can be corrected for by either insulin or riboflavin. The pathogenesis of riboflavin deficiency in diabetes mellitus is not clearly understood. The data of the present study provide evidence in addition to the previous findings of an increased prevalence of riboflavin deficiency in genetically diabetic KK mice.
基于正常大鼠和链脲佐菌素诱导的糖尿病大鼠红细胞溶血产物中谷胱甘肽还原酶的活性系数,评估核黄素营养状况。活性系数值高于1.3被视为核黄素缺乏的证据。所有糖尿病动物均被发现存在核黄素缺乏,活性系数值为1.47 - 2.11。用胰岛素或核黄素治疗糖尿病大鼠可使其活性系数恢复正常。喂食受限饮食的大鼠活性系数值正常。糖尿病大鼠的红细胞谷胱甘肽还原酶活性显著降低,与正常大鼠的16%相比,在黄素腺嘌呤二核苷酸(FAD)存在下酶活性的增强为72%。谷胱甘肽还原酶和琥珀酸脱氢酶这两种含FAD的酶的肝脏活性,糖尿病大鼠显著低于正常大鼠。与活性系数值一样,胰岛素或核黄素治疗后所有酶活性均恢复正常。这些数据表明胰岛素和核黄素可增强红细胞和肝脏FAD的合成。本研究结果表明,实验性糖尿病会导致核黄素缺乏,进而降低红细胞和肝脏黄素蛋白酶的活性。这些变化可用胰岛素或核黄素纠正。糖尿病中核黄素缺乏的发病机制尚不清楚。本研究的数据除了之前在遗传性糖尿病KK小鼠中核黄素缺乏患病率增加的研究结果外,还提供了证据。