Blackshear P J, Alberti K G
Biochem J. 1974 Jan;138(1):107-17. doi: 10.1042/bj1380107.
Male rats rendered diabetic by the intravenous injection of streptozotocin (150mg/kg) were treated with a long-acting insulin for 1 week, then allowed to develop ketoacidosis. By using sampling techniques designed to avoid the use of anaesthesia and extended anoxic periods, sequential measurements of metabolic intermediates were made in blood, liver, cerebrospinal fluid and brain at 24h intervals after the last insulin injection. Measurements in blood and liver suggested a rapid increase in hepatic glycogenolysis and gluconeogenesis and peripheral-depot lipolysis between 24 and 48h after the last insulin injection, whereas blood and liver ketone-body and triglyceride concentrations rose more slowly. The changing metabolic patterns occurring with increasing time of insulin deprivation stress the importance of sequential compared with static measurements in experimental diabetes. Data are presented for brain metabolic intermediates in diabetic ketoacidosis, and support recent evidence that glucose plays a less important role in brain oxidative metabolism in ketotic states.
通过静脉注射链脲佐菌素(150mg/kg)使雄性大鼠患糖尿病,用长效胰岛素治疗1周,然后使其发生酮症酸中毒。通过采用旨在避免使用麻醉和延长缺氧期的采样技术,在最后一次注射胰岛素后每隔24小时对血液、肝脏、脑脊液和大脑中的代谢中间产物进行连续测量。血液和肝脏的测量结果表明,在最后一次注射胰岛素后的24至48小时之间,肝糖原分解、糖异生和外周脂肪分解迅速增加,而血液和肝脏中的酮体和甘油三酯浓度上升得较慢。随着胰岛素缺乏时间的增加而出现的代谢模式变化强调了在实验性糖尿病中进行连续测量而非静态测量的重要性。本文给出了糖尿病酮症酸中毒时脑代谢中间产物的数据,并支持了最近的证据,即葡萄糖在酮症状态下的脑氧化代谢中起的作用较小。