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糖尿病神经病理性疼痛大鼠脊髓糖质液系统水通道蛋白-4 极性的恢复

Restoration of aquaporin-4 polarization in the spinal glymphatic system by metformin in rats with painful diabetic neuropathy.

机构信息

Departments of Anesthesiology.

Radiology, the Affiliated Hospital of North Sichuan Medical College, Nanchong, China.

出版信息

Neuroreport. 2023 Feb 1;34(3):190-197. doi: 10.1097/WNR.0000000000001880. Epub 2023 Jan 20.

DOI:10.1097/WNR.0000000000001880
PMID:36719843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9981323/
Abstract

Painful diabetic neuropathy (PDN) is a common complication in patients with diabetes, and its underlying mechanism remains unclear. Aquaporin-4 (AQP4) plays a crucial role in removing metabolic waste in the glymphatic system. In this study, we aimed to explore the relationship between the spinal glymphatic system and the effect of metformin on PDN. Male Sprague-Dawley rats were randomly allocated into the control group ( n = 10), the PDN group ( n = 10), and the metformin group ( n = 10). A high-fat and high-glucose diet combined with low-dose streptozotocin was used to induce PDN rats. We detected the clearance rate of the contrast agent in the spinal cord of each rat by MRI to reflect the function of the glymphatic system. Immunofluorescence was used to detect the localization of perivascular AQP4 in astrocyte endfeet. Furthermore, we measured the expression of AQP4 in the spinal cord by Western blot. Compared with the rats in the control group, PDN rats exhibited enhanced mechanical allodynia, decreased clearance rate of the contrast agent in the spinal glymphatic system, reversed AQP4 polarization, and increased expression of AQP4. After being treated with metformin, the rats showed opposite changes in the above characteristics. The analgesic effect of metformin on PDN may be related to its ability to restore spinal AQP4 polarization, thus promoting the function of the spinal glymphatic system.

摘要

糖尿病性周围神经痛(PDN)是糖尿病患者常见的并发症,其发病机制尚不清楚。水通道蛋白-4(AQP4)在糖质淋系统中清除代谢废物中起着关键作用。在本研究中,我们旨在探讨脊髓糖质淋系统与二甲双胍对 PDN 的影响之间的关系。雄性 Sprague-Dawley 大鼠随机分为对照组(n = 10)、PDN 组(n = 10)和二甲双胍组(n = 10)。采用高脂高糖饮食联合小剂量链脲佐菌素诱导 PDN 大鼠。我们通过 MRI 检测每只大鼠脊髓中对比剂的清除率,以反映糖质淋系统的功能。免疫荧光用于检测血管周 AQP4 在星形胶质细胞足突中的定位。此外,我们通过 Western blot 测量脊髓中 AQP4 的表达。与对照组大鼠相比,PDN 大鼠表现出机械性痛觉过敏增强,脊髓糖质淋系统中对比剂清除率降低,AQP4 极化逆转,AQP4 表达增加。用二甲双胍治疗后,上述特征出现相反变化。二甲双胍对 PDN 的镇痛作用可能与其恢复脊髓 AQP4 极化的能力有关,从而促进脊髓糖质淋系统的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/0ff2d72fc2da/nr-34-190-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/30894aab037b/nr-34-190-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/9c25b885b304/nr-34-190-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/c1e0ce7275c3/nr-34-190-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/eebb152bfe64/nr-34-190-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/0ff2d72fc2da/nr-34-190-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/30894aab037b/nr-34-190-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/9c25b885b304/nr-34-190-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/c1e0ce7275c3/nr-34-190-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/eebb152bfe64/nr-34-190-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/917d/9981323/0ff2d72fc2da/nr-34-190-g005.jpg

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