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生酮饮食可改善啮齿动物脊髓损伤后的前肢运动功能。

Ketogenic diet improves forelimb motor function after spinal cord injury in rodents.

作者信息

Streijger Femke, Plunet Ward T, Lee Jae H T, Liu Jie, Lam Clarrie K, Park Soeyun, Hilton Brett J, Fransen Bas L, Matheson Keely A J, Assinck Peggy, Kwon Brian K, Tetzlaff Wolfram

机构信息

International Collaboration on Repair Discoveries (ICORD), Blusson Spinal Cord Center, Vancouver, British Columbia, Canada.

出版信息

PLoS One. 2013 Nov 4;8(11):e78765. doi: 10.1371/journal.pone.0078765. eCollection 2013.

Abstract

High fat, low carbohydrate ketogenic diets (KD) are validated non-pharmacological treatments for some forms of drug-resistant epilepsy. Ketones reduce neuronal excitation and promote neuroprotection. Here, we investigated the efficacy of KD as a treatment for acute cervical spinal cord injury (SCI) in rats. Starting 4 hours following C5 hemi-contusion injury animals were fed either a standard carbohydrate based diet or a KD formulation with lipid to carbohydrate plus protein ratio of 3:1. The forelimb functional recovery was evaluated for 14 weeks, followed by quantitative histopathology. Post-injury 3:1 KD treatment resulted in increased usage and range of motion of the affected forepaw. Furthermore, KD improved pellet retrieval with recovery of wrist and digit movements. Importantly, after returning to a standard diet after 12 weeks of KD treatment, the improved forelimb function remained stable. Histologically, the spinal cords of KD treated animals displayed smaller lesion areas and more grey matter sparing. In addition, KD treatment increased the number of glucose transporter-1 positive blood vessels in the lesion penumbra and monocarboxylate transporter-1 (MCT1) expression. Pharmacological inhibition of MCTs with 4-CIN (α-cyano-4-hydroxycinnamate) prevented the KD-induced neuroprotection after SCI, In conclusion, post-injury KD effectively promotes functional recovery and is neuroprotective after cervical SCI. These beneficial effects require the function of monocarboxylate transporters responsible for ketone uptake and link the observed neuroprotection directly to the function of ketones, which are known to exert neuroprotection by multiple mechanisms. Our data suggest that current clinical nutritional guidelines, which include relatively high carbohydrate contents, should be revisited.

摘要

高脂肪、低碳水化合物的生酮饮食(KD)是经证实的针对某些形式耐药性癫痫的非药物治疗方法。酮类可降低神经元兴奋性并促进神经保护。在此,我们研究了KD作为大鼠急性颈脊髓损伤(SCI)治疗方法的疗效。在C5半横断损伤后4小时开始,动物被喂食标准的基于碳水化合物的饮食或脂质与碳水化合物加蛋白质比例为3:1的KD配方饮食。对前肢功能恢复情况进行了14周的评估,随后进行定量组织病理学分析。损伤后接受3:1 KD治疗导致受影响前爪的使用和活动范围增加。此外,KD改善了小球抓取能力,并恢复了手腕和手指的运动。重要的是,在KD治疗12周后恢复到标准饮食后,改善的前肢功能保持稳定。组织学上,接受KD治疗的动物脊髓显示出较小的损伤区域和更多的灰质保留。此外,KD治疗增加了损伤半暗带中葡萄糖转运蛋白-1阳性血管的数量以及单羧酸转运蛋白-1(MCT1)的表达。用4-CIN(α-氰基-4-羟基肉桂酸)对MCTs进行药理学抑制可防止SCI后KD诱导的神经保护作用。总之,损伤后KD能有效促进功能恢复,并在颈脊髓损伤后具有神经保护作用。这些有益作用需要负责酮摄取的单羧酸转运蛋白发挥功能,并将观察到的神经保护作用直接与酮的功能联系起来,已知酮可通过多种机制发挥神经保护作用。我们的数据表明,应重新审视目前包含相对较高碳水化合物含量的临床营养指南。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6d8f/3817084/a5d4cdfbb1a8/pone.0078765.g001.jpg

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