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实验性糖尿病大鼠外周神经和骨骼肌中神经营养因子mRNA水平的改变

Altered neurotrophin mRNA levels in peripheral nerve and skeletal muscle of experimentally diabetic rats.

作者信息

Fernyhough P, Diemel L T, Brewster W J, Tomlinson D R

机构信息

Department of Pharmacology, Queen Mary and Westfield College, University of London, England.

出版信息

J Neurochem. 1995 Mar;64(3):1231-7. doi: 10.1046/j.1471-4159.1995.64031231.x.

Abstract

The levels of neurotrophin mRNA in sensory ganglia, sciatic nerve, and skeletal muscle were measured in the streptozotocin-diabetic rat using northern blotting. Periods of diabetes of 4, 6, and 12 weeks significantly elevated brain-derived neurotrophic factor (BDNF) mRNA levels in soleus muscle compared with age-matched controls, the increase being highest at 6 weeks. At all time periods studied, the levels of nerve growth factor (NGF) mRNA in soleus muscle were decreased by 21-47%. Following 12 weeks of diabetes, BDNF mRNA levels were increased approximately two- to threefold in L4 and L5 dorsal root ganglia (DRG), and in sciatic nerve, NGF mRNA levels were raised 1.65-fold. Intensive insulin treatment of diabetic rats for the final 4 weeks of the 12-week period of diabetes reversed the up-regulation of BDNF mRNA in DRG and muscle and NGF mRNA in sciatic nerve. All diabetes-induced changes in neurotrophin mRNA were not paralleled by similar alterations in the levels of beta-actin mRNA in muscle and nerve, or of GAP-43 mRNA in DRG and nerve. It is proposed that the up-regulation of neurotrophin mRNA is an endogenous protective and/or repair mechanism induced by insult and, as such, appears as an early marker of peripheral nerve and muscle damage in experimental diabetes.

摘要

采用Northern印迹法检测链脲佐菌素诱导的糖尿病大鼠感觉神经节、坐骨神经和骨骼肌中神经营养因子mRNA的水平。与年龄匹配的对照组相比,糖尿病4周、6周和12周时,比目鱼肌中脑源性神经营养因子(BDNF)mRNA水平显著升高,6周时升高最为明显。在所有研究时间段,比目鱼肌中神经生长因子(NGF)mRNA水平降低了21%-47%。糖尿病12周后,L4和L5背根神经节(DRG)中BDNF mRNA水平升高约2至3倍,坐骨神经中NGF mRNA水平升高1.65倍。在糖尿病12周期间的最后4周对糖尿病大鼠进行强化胰岛素治疗,可逆转DRG和肌肉中BDNF mRNA以及坐骨神经中NGF mRNA的上调。糖尿病诱导的神经营养因子mRNA的所有变化,在肌肉和神经中β-肌动蛋白mRNA水平,或DRG和神经中GAP-43 mRNA水平上均未出现类似改变。有人提出,神经营养因子mRNA的上调是由损伤诱导的一种内源性保护和/或修复机制,因此,它似乎是实验性糖尿病中周围神经和肌肉损伤的早期标志物。

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