Sochor M, Kunjara S, Greenbaum A L, McLean P
Biochem J. 1986 Mar 15;234(3):573-7. doi: 10.1042/bj2340573.
The effect of short-term diabetes, 5 days after the administration of streptozotocin, on renal growth and the activity of alternative pathways of glucose metabolism was studied in immature (21-day-old) rats and in adult rats. The kidney weight increased by 28% in the adult diabetic rats, but by only 10% in the immature diabetic rats, relative to their age-matched control groups. The flux of glucose via the pentose phosphate pathway was increased 2-3-fold in the adult diabetic rats, but was unchanged in the immature diabetic group. Enzymes of this pathway (glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase) increased by 29% and 77% respectively in adult diabetic rats; in the immature group they showed changes of +5% and +28% respectively. The rate of glucose phosphorylation increased significantly in both groups of diabetic rats; only minor changes were observed in oxidation via the tricarboxylic acid cycle. Increases of 40-50% were found in the activity of enzymes involved in UDP-glucose metabolism (phosphoglucomutase, UDPglucose pyrophosphorylase and UDPglucose dehydrogenase) and in lactate dehydrogenase in both young and adult animals. The results suggest a differential renal response to streptozotocin-diabetes according to the stage of renal growth and development, and it is proposed that the difference is related to the developmental emergence of aldose reductase. Enzymes involved in formation of ribose 5-phosphate and NADPH are strikingly increased in the adult diabetic, whereas metabolic functions dependent on a high ambient glucose concentration, e.g. synthesis of glycogen and glucuronate, are similarly affected in adult and immature diabetic groups, both showing certain aspects of 'glucose overutilization'.
研究了链脲佐菌素给药5天后短期糖尿病对未成熟(21日龄)大鼠和成年大鼠肾脏生长及葡萄糖代谢替代途径活性的影响。相对于年龄匹配的对照组,成年糖尿病大鼠的肾脏重量增加了28%,但未成熟糖尿病大鼠仅增加了10%。成年糖尿病大鼠中,通过磷酸戊糖途径的葡萄糖通量增加了2至3倍,但未成熟糖尿病组中该通量未发生变化。该途径的酶(葡萄糖-6-磷酸脱氢酶和6-磷酸葡萄糖酸脱氢酶)在成年糖尿病大鼠中分别增加了29%和77%;在未成熟组中,它们分别有5%和28%的变化。两组糖尿病大鼠的葡萄糖磷酸化速率均显著增加;通过三羧酸循环的氧化仅观察到微小变化。在幼年和成年动物中,参与UDP-葡萄糖代谢的酶(磷酸葡萄糖变位酶、UDP-葡萄糖焦磷酸化酶和UDP-葡萄糖脱氢酶)以及乳酸脱氢酶的活性均增加了40%至50%。结果表明,根据肾脏生长发育阶段,肾脏对链脲佐菌素诱导的糖尿病有不同反应,并且推测这种差异与醛糖还原酶的发育出现有关。在成年糖尿病大鼠中,参与核糖5-磷酸和NADPH形成的酶显著增加,而依赖于高环境葡萄糖浓度的代谢功能,如糖原和葡萄糖醛酸的合成,在成年和未成熟糖尿病组中受到类似影响,两者均表现出“葡萄糖过度利用”的某些方面。