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1型和2型糖尿病患者骨间后神经中的自噬:一项超微结构研究。

Autophagy in the posterior interosseous nerve of patients with type 1 and type 2 diabetes mellitus: an ultrastructural study.

作者信息

Osman Ayman A M, Dahlin Lars B, Thomsen Niels O B, Mohseni Simin

机构信息

Department of Clinical and Experimental Medicine, Division of Cell Biology, Linköping University, SE-581 83, Linköping, Sweden.

出版信息

Diabetologia. 2015 Mar;58(3):625-32. doi: 10.1007/s00125-014-3477-4. Epub 2014 Dec 19.

Abstract

AIMS/HYPOTHESIS: We addressed the question of whether the autophagy pathway occurs in human peripheral nerves and whether this pathway is associated with peripheral neuropathy in diabetes mellitus.

METHODS

By using electron microscopy, we evaluated the presence of autophagy-related structures and neuropathy in the posterior interosseous nerve of patients who had undergone carpal tunnel release and had type 1 or type 2 diabetes mellitus, and in patients with no diabetes (controls).

RESULTS

Autophagy-related ultrastructures were observed in the samples taken from all patients of the three groups. The number of autophagy-associated structures was significantly higher (p < 0.05) in the nerves of patients with type 1 than type 2 diabetes. Qualitative and quantitative evaluations of fascicle area, diameter of myelinated and unmyelinated nerve fibres, the density of myelinated and unmyelinated fibres and the g-ratio of myelinated fibres were performed. We found degeneration and regeneration of a few myelinated axons in controls, and a well-developed neuropathy with the loss of large myelinated axons and the presence of many small ones in patients with diabetes. The pathology in type 1 diabetes was more extensive than in type 2 diabetes.

CONCLUSIONS/INTERPRETATION: The results of this study show that the human peripheral nerves have access to the autophagy machinery, and this pathway may be regulated differently in type 1 and type 2 diabetes; insulin, presence of extensive neuropathy, and/or other factors such as duration of diabetes and HbA1c level may underlie this differential regulation.

摘要

目的/假设:我们探讨了自噬途径是否在人类周围神经中发生,以及该途径是否与糖尿病周围神经病变相关。

方法

通过电子显微镜,我们评估了接受腕管松解术的1型或2型糖尿病患者以及无糖尿病患者(对照组)的骨间后神经中自噬相关结构和神经病变的存在情况。

结果

在三组所有患者的样本中均观察到自噬相关超微结构。1型糖尿病患者神经中自噬相关结构的数量显著高于2型糖尿病患者(p < 0.05)。对束面积、有髓和无髓神经纤维直径、有髓和无髓纤维密度以及有髓纤维的g比值进行了定性和定量评估。我们在对照组中发现了一些有髓轴突的退变和再生,而在糖尿病患者中则出现了明显的神经病变,表现为大的有髓轴突丢失和许多小的有髓轴突存在。1型糖尿病的病理改变比2型糖尿病更广泛。

结论/解读:本研究结果表明,人类周围神经能够利用自噬机制,并且该途径在1型和2型糖尿病中可能受到不同的调节;胰岛素、广泛神经病变的存在和/或其他因素,如糖尿病病程和糖化血红蛋白水平,可能是这种差异调节的基础。

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