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外周传入神经至脊髓的神经回路改变:链脲佐菌素诱导 1 型糖尿病大鼠糖尿病多发性神经病的可能意义。

Alterations in the neural circuits from peripheral afferents to the spinal cord: possible implications for diabetic polyneuropathy in streptozotocin-induced type 1 diabetic rats.

机构信息

Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, The Fourth Military Medical University Xi'an, China.

出版信息

Front Neural Circuits. 2014 Jan 29;8:6. doi: 10.3389/fncir.2014.00006. eCollection 2014.

Abstract

Diabetic polyneuropathy (DPN) presents as a wide variety of sensorimotor symptoms and affects approximately 50% of diabetic patients. Changes in the neural circuits may occur in the early stages in diabetes and are implicated in the development of DPN. Therefore, we aimed to detect changes in the expression of isolectin B4 (IB4, the marker for nonpeptidergic unmyelinated fibers and their cell bodies) and calcitonin gene-related peptide (CGRP, the marker for peptidergic fibers and their cell bodies) in the dorsal root ganglion (DRG) and spinal cord of streptozotocin (STZ)-induced type 1 diabetic rats showing alterations in sensory and motor function. We also used cholera toxin B subunit (CTB) to show the morphological changes of the myelinated fibers and motor neurons. STZ-induced diabetic rats exhibited hyperglycemia, decreased body weight gain, mechanical allodynia and impaired locomotor activity. In the DRG and spinal dorsal horn, IB4-labeled structures decreased, but both CGRP immunostaining and CTB labeling increased from day 14 to day 28 in diabetic rats. In spinal ventral horn, CTB labeling decreased in motor neurons in diabetic rats. Treatment with intrathecal injection of insulin at the early stages of DPN could alleviate mechanical allodynia and impaired locomotor activity in diabetic rats. The results suggest that the alterations of the neural circuits between spinal nerve and spinal cord via the DRG and ventral root might be involved in DPN.

摘要

糖尿病性多发性神经病(DPN)表现为多种感觉运动症状,影响约 50%的糖尿病患者。在糖尿病的早期阶段,神经回路可能会发生变化,并且与 DPN 的发展有关。因此,我们旨在检测在表现出感觉和运动功能改变的链脲佐菌素(STZ)诱导的 1 型糖尿病大鼠的背根神经节(DRG)和脊髓中异凝集素 B4(IB4,无髓神经纤维及其细胞体的标记物)和降钙素基因相关肽(CGRP,肽能纤维及其细胞体的标记物)表达的变化。我们还使用霍乱毒素 B 亚单位(CTB)显示有髓纤维和运动神经元的形态变化。STZ 诱导的糖尿病大鼠表现出高血糖、体重增加减少、机械性痛觉过敏和运动活动受损。在 DRG 和脊髓背角,IB4 标记的结构减少,但在糖尿病大鼠中,从第 14 天到第 28 天,CGRP 免疫染色和 CTB 标记均增加。在脊髓腹角,糖尿病大鼠运动神经元中的 CTB 标记减少。在 DPN 的早期阶段通过鞘内注射胰岛素治疗可以缓解糖尿病大鼠的机械性痛觉过敏和运动活动受损。结果表明,通过背根神经节和腹根,脊髓神经和脊髓之间的神经回路的改变可能与 DPN 有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4073/3905201/26ae8375a404/fncir-08-00006-g0001.jpg

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