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糖尿病高脂饮食/链脲佐菌素模型中疼痛反应的特征及抗糖尿病治疗的镇痛作用。

Characterisation of pain responses in the high fat diet/streptozotocin model of diabetes and the analgesic effects of antidiabetic treatments.

作者信息

Byrne Frederika Maria, Cheetham Sharon, Vickers Steven, Chapman Victoria

机构信息

School of Life Sciences, University of Nottingham, Nottingham NG7 2UH, UK.

RenaSci Ltd., BioCity Nottingham, Pennyfoot Street, Nottingham NG1 1GF, UK.

出版信息

J Diabetes Res. 2015;2015:752481. doi: 10.1155/2015/752481. Epub 2015 Feb 9.

DOI:10.1155/2015/752481
PMID:25759824
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4338392/
Abstract

Chronic pain is a common complication of diabetes. The aim of the present study was to characterise pain behaviour in a high fat diet/streptozotocin (HFD/STZ) model of diabetes in the rat, investigate spinal mechanisms, and determine the effects of antidiabetic interventions. Three-week consumption of a high fat diet followed by single injection of STZ (45 mgkg(-1)) produced sustained changes in plasma insulin and glucose until day 120. Hindpaw mechanical withdrawal thresholds were significantly lowered in the model, but mechanically evoked responses of spinal neurones were unaltered, compared to HFD/vehicle rats. HFD/STZ rats had significantly lower numbers of spinal Iba-1 positive cells (morphologically identified as activated microglia) and spinal GFAP immunofluorescence (a marker of astrogliosis) in the spinal cord at day 50, compared to time-matched controls. The PPARγ ligand pioglitazone (10 mgkg(-1)) did not alter HFD/STZ induced metabolic changes or hindpaw withdrawal thresholds of HFD/STZ rats. Daily linagliptin (3 mgkg(-1)) and metformin (200 mgkg(-1)) from day 4 after model induction did not alter plasma glucose or insulin in HFD/STZ rats but significantly prevented changes in the mechanical withdrawal thresholds. The demonstration that currently prescribed antidiabetic drugs prevent aberrant pain behaviour supports the use of this model to investigate pain mechanisms associated with diabetes.

摘要

慢性疼痛是糖尿病的常见并发症。本研究的目的是描述大鼠高脂饮食/链脲佐菌素(HFD/STZ)糖尿病模型中的疼痛行为,研究脊髓机制,并确定抗糖尿病干预措施的效果。连续三周食用高脂饮食,随后单次注射STZ(45 mgkg(-1)),可使血浆胰岛素和葡萄糖持续变化至第120天。与HFD/溶媒组大鼠相比,该模型中后爪机械性退缩阈值显著降低,但脊髓神经元的机械诱发反应未改变。与时间匹配的对照组相比,HFD/STZ大鼠在第50天时脊髓中Iba-1阳性细胞(形态学上鉴定为活化的小胶质细胞)数量和脊髓GFAP免疫荧光(星形胶质细胞增生的标志物)显著降低。PPARγ配体吡格列酮(10 mgkg(-1))并未改变HFD/STZ诱导的代谢变化或HFD/STZ大鼠的后爪退缩阈值。从模型诱导后第4天开始每日给予利格列汀(3 mgkg(-1))和二甲双胍(200 mgkg(-1)),并未改变HFD/STZ大鼠的血糖或胰岛素水平,但显著预防了机械性退缩阈值的变化。目前处方的抗糖尿病药物可预防异常疼痛行为,这一证明支持使用该模型来研究与糖尿病相关的疼痛机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/e7231c0fb203/JDR2015-752481.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/62d3c5de75cb/JDR2015-752481.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/125e283246dd/JDR2015-752481.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/07256e4e7a8e/JDR2015-752481.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/31bc0cfe9709/JDR2015-752481.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/e7231c0fb203/JDR2015-752481.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/62d3c5de75cb/JDR2015-752481.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/125e283246dd/JDR2015-752481.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/07256e4e7a8e/JDR2015-752481.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/31bc0cfe9709/JDR2015-752481.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d57/4338392/e7231c0fb203/JDR2015-752481.005.jpg

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