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在2型糖尿病小鼠模型中,用鲱鱼油丰富饮食或用消退素D1每日治疗对神经病变的影响。

Effect of enriching the diet with menhaden oil or daily treatment with resolvin D1 on neuropathy in a mouse model of type 2 diabetes.

作者信息

Shevalye Hanna, Yorek Matthew S, Coppey Lawrence J, Holmes Amey, Harper Matthew M, Kardon Randy H, Yorek Mark A

机构信息

Department of Internal Medicine, University of Iowa, Iowa City, Iowa;

Department of Veterans Affairs Iowa City Health Care System, Iowa City, Iowa; Veterans Affairs Center for the Prevention and Treatment of Visual Loss, Iowa City, Iowa; and

出版信息

J Neurophysiol. 2015 Jul;114(1):199-208. doi: 10.1152/jn.00224.2015. Epub 2015 Apr 29.

Abstract

The purpose of this study was to determine the effect of supplementing the diet of a mouse model of type 2 diabetes with menhaden (fish) oil or daily treatment with resolvin D1 on diabetic neuropathy. The end points evaluated included motor and sensory nerve conduction velocity, thermal sensitivity, innervation of sensory nerves in the cornea and skin, and the retinal ganglion cell complex thickness. Menhaden oil is a natural source for n-3 polyunsaturated fatty acids, which have been shown to have beneficial effects in other diseases. Resolvin D1 is a metabolite of docosahexaenoic acid and is known to have anti-inflammatory and neuroprotective properties. To model type 2 diabetes, mice were fed a high-fat diet for 8 wk followed by a low dosage of streptozotocin. After 8 wk of hyperglycemia, mice in experimental groups were treated for 6 wk with menhaden oil in the diet or daily injections of 1 ng/g body wt resolvin D1. Our findings show that menhaden oil or resolvin D1 did not improve elevated blood glucose, HbA1C, or glucose utilization. Untreated diabetic mice were thermal hypoalgesic, had reduced motor and sensory nerve conduction velocities, had decreased innervation of the cornea and skin, and had thinner retinal ganglion cell complex. These end points were significantly improved with menhaden oil or resolvin D1 treatment. Exogenously, resolvin D1 stimulated neurite outgrowth from primary cultures of dorsal root ganglion neurons from normal mice. These studies suggest that n-3 polyunsaturated fatty acids derived from fish oil could be an effective treatment for diabetic neuropathy.

摘要

本研究的目的是确定用鲱鱼油补充2型糖尿病小鼠模型的饮食或用消退素D1每日治疗对糖尿病性神经病变的影响。评估的终点包括运动和感觉神经传导速度、热敏感性、角膜和皮肤中感觉神经的神经支配以及视网膜神经节细胞复合体厚度。鲱鱼油是n-3多不饱和脂肪酸的天然来源,已证明其在其他疾病中具有有益作用。消退素D1是二十二碳六烯酸的代谢产物,已知具有抗炎和神经保护特性。为了模拟2型糖尿病,给小鼠喂食高脂饮食8周,然后给予低剂量链脲佐菌素。在高血糖8周后,对实验组的小鼠用饮食中的鲱鱼油或每日注射1 ng/g体重的消退素D1进行6周的治疗。我们的研究结果表明,鲱鱼油或消退素D1并不能改善血糖升高、糖化血红蛋白或葡萄糖利用情况。未经治疗的糖尿病小鼠存在热感觉减退,运动和感觉神经传导速度降低,角膜和皮肤的神经支配减少,视网膜神经节细胞复合体变薄。用鲱鱼油或消退素D1治疗后,这些终点指标有显著改善。在体外,消退素D1刺激正常小鼠背根神经节神经元原代培养物中的神经突生长。这些研究表明,鱼油衍生的n-3多不饱和脂肪酸可能是治疗糖尿病性神经病变的有效方法。

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