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链脲佐菌素诱导的慢性糖尿病大鼠外周神经中磷脂的代谢:磷脂酰肌醇-4,5-二磷酸周转增加。

Metabolism of phospholipids in peripheral nerve from rats with chronic streptozotocin-induced diabetes: increased turnover of phosphatidylinositol-4,5-bisphosphate.

作者信息

Bell M E, Peterson R G, Eichberg J

出版信息

J Neurochem. 1982 Jul;39(1):192-200. doi: 10.1111/j.1471-4159.1982.tb04718.x.

Abstract

The effect of chronic streptozotocin-induced diabetes on phospholipid metabolism in rat sciatic nerve in vitro was investigated. In normal nerve incubated for 2 h in Krebs-Ringer-bicarbonate buffer containing [32P]orthophosphate, radioactivity was primarily incorporated into phosphatidylinositol-4,5-bisphosphate and phosphatidylcholine. Smaller amounts were present in phosphatidylinositol-4-phosphate, phosphatidylinositol, and phosphatidic acid. As compared to controls, phosphatidylinositol-4,5-bisphosphate in nerves from animals made diabetic 2, 10, and 20 weeks earlier accounted for 30-46% more of the isotope, expressed as a percentage, incorporated into all phospholipids. In contrast, the proportion of radioactivity in phosphatidylcholine decreased by 10-25%. When the results were expressed as the quantity of phosphorus incorporated into phospholipid, only phosphatidylinositol-4,5-bisphosphate displayed a change. The amount of isotope which entered this lipid increased 60% and 67% for 2- and 10-week diabetic animals, respectively. Increased phosphatidylinositol-4,5-bisphosphate labeling was observed when epineurial-free preparations were used or when the composition of the incubation medium was varied. Sciatic and caudal nerve conduction velocities were decreased after 10 and 20 weeks but were unchanged after 2 weeks. We conclude that an increase in the turnover of phosphatidylinositol-4,5-bisphosphate in sciatic nerve from streptozotocin-diabetic rats appears relatively early and persists throughout the course of the disease. This metabolic alteration may be related to a primary defect responsible for the accompanying deficient peripheral nerve function.

摘要

研究了慢性链脲佐菌素诱导的糖尿病对大鼠坐骨神经体外磷脂代谢的影响。在含有[32P]正磷酸盐的Krebs-Ringer-碳酸氢盐缓冲液中孵育2小时的正常神经中,放射性主要掺入磷脂酰肌醇-4,5-二磷酸和磷脂酰胆碱。磷脂酰肌醇-4-磷酸、磷脂酰肌醇和磷脂酸中的含量较少。与对照组相比,提前2周、10周和20周患糖尿病动物的神经中,磷脂酰肌醇-4,5-二磷酸占掺入所有磷脂的同位素的百分比多30%-46%。相反,磷脂酰胆碱中的放射性比例下降了10%-25%。当结果以掺入磷脂的磷量表示时,只有磷脂酰肌醇-4,5-二磷酸显示出变化。对于2周和10周患糖尿病的动物,进入这种脂质的同位素量分别增加了60%和67%。当使用无神经外膜的制剂或改变孵育培养基的组成时,观察到磷脂酰肌醇-4,5-二磷酸标记增加。10周和20周后坐骨神经和尾神经传导速度降低,但2周后未改变。我们得出结论,链脲佐菌素诱导的糖尿病大鼠坐骨神经中磷脂酰肌醇-4,5-二磷酸的周转率增加相对较早,并在疾病过程中持续存在。这种代谢改变可能与伴随的周围神经功能缺陷的原发性缺陷有关。

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