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首页> 外文期刊>Human gene therapy >Peripheral gene transfer of glial cell-derived neurotrophic factor ameliorates neuropathic deficits in diabetic rats.
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Peripheral gene transfer of glial cell-derived neurotrophic factor ameliorates neuropathic deficits in diabetic rats.

机译:胶质细胞源性神经营养因子的外周基因转移改善了糖尿病大鼠的神经性缺陷。

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摘要

Deprivation of neurotrophic factors contributes to the pathogenesis of diabetic neuropathy. However, the role of glial cell-derived neurotrophic factor (GDNF) in the pathogenesis of diabetic neuropathy remains unclear. The present study evaluated the pathogenic role of GDNF deficiency and the therapeutic potential of GDNF gene transfer for diabetic neuropathy. After injection of streptozotocin (STZ) for 2 weeks, diabetic rats displayed significant alteration in electrophysiological parameters, which was associated with structural changes and defective myelination in the sciatic nerves. The early diabetic neuropathy was accompanied by attenuation of the GDNF/GFRalpha1/Akt signaling cascade and depletion of sensory neuropeptides in the peripheral nerves. After detection of neuropathy, intramuscular GDNF gene transfer reversed the deficiency of GDNF/Akt signaling in the sciatic nerve and improved the neurological functions of diabetic rats. Moreover, GDNF gene delivery alleviated the axonal demyelination and restored the sensory neuropeptide levels in the sciatic nerve of diabetic rats. In summary, peripheral GDNF gene delivery ameliorates the diabetes-induced downregulation of the GDNF signaling complex in the peripheral nervous system and holds promises for treatment of diabetic neuropathy.
机译:剥夺神经营养因子有助于糖尿病性神经病的发病机理。然而,胶质细胞源性神经营养因子(GDNF)在糖尿病性神经病的发病机制中的作用仍不清楚。本研究评估了GDNF缺乏的致病作用和GDNF基因转移对糖尿病性神经病的治疗潜力。注射链脲佐菌素(STZ)2周后,糖尿病大鼠显示出明显的电生理参数改变,这与坐骨神经的结构改变和髓鞘化不良有关。早期糖尿病性神经病变伴有GDNF / GFRalpha1 / Akt信号级联的减弱和周围神经中感觉神经肽的消耗。在检测到神经病后,肌内GDNF基因转移逆转了坐骨神经中GDNF / Akt信号转导的缺乏,并改善了糖尿病大鼠的神经功能。而且,GDNF基因的递送减轻了糖尿病大鼠坐骨神经中的轴突脱髓鞘并恢复了感觉神经肽水平。总之,外周GDNF基因递送改善了糖尿病诱导的外周神经系统中GDNF信号传导复合物的下调,并且有望用于治疗糖尿病性神经病。

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