Department of Pharmacology and Toxicology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
College of Animal Science and Veterinary Medicine, Shanxi Agricultural University, Taigu, China.
J Biochem Mol Toxicol. 2020 Nov;34(11):e22564. doi: 10.1002/jbt.22564. Epub 2020 Jul 8.
Multiple sclerosis (MS) is a well-known neurodegenerative disorder, causing toxicity in different organs, such as spinal cord tissue. The goal of this study was to investigate the protective effect of ellagic acid (EA) against spinal cord and sciatica function in cuprizone (Cup)-induced demyelination model. Animals were divided into six equal groups. The first group received tap water as the control. Cup group was treated with Cup (0.2% w/w in fed). EA 100 group was orally treated with EA (100 mg/kg). EA + Cup groups were orally treated with three doses of 5, 50, and 100 mg/kg of EA plus Cup (0.2% w/w). All groups received treatment for 42 days. Open field, rotarod, and gait tests were done to evaluate the behavioral changes following Cup and/or EA treatment. Also, lipid peroxidation, reactive oxygen species (ROS) content, antioxidant capacity, superoxide dismutase (SOD), and catalase enzymes activity in spinal cord was evaluated. Luxol fast blue (LFB) staining also the behavioral tests were performed to evaluate the model. Cup increased ROS levels and oxidative stress in their spinal cord tissues. Also, Cup reduced antioxidant capacity, SOD, and catalase activity. EA (especially at 100 mg/kg) prevented these abnormal changes. EA co-treatment dose-dependently was able to ameliorate behavioral impairments in mice that received Cup. EA might act as a protective agent in MS by modulating spinal cord function.
多发性硬化症(MS)是一种众所周知的神经退行性疾病,会导致不同器官(如脊髓组织)中毒。本研究的目的是研究鞣花酸(EA)对杯状(Cup)诱导脱髓鞘模型中脊髓和坐骨神经功能的保护作用。动物被分为六组。第一组接受自来水作为对照。杯组用 Cup(饲料中 0.2%w/w)处理。EA100 组用 EA(100mg/kg)口服治疗。EA+杯组用 5、50 和 100mg/kg EA 加 Cup(0.2%w/w)口服治疗三剂。所有组均接受治疗 42 天。进行旷场、旋转棒和步态测试,以评估 Cup 和/或 EA 治疗后行为变化。还评估了脊髓中的脂质过氧化、活性氧(ROS)含量、抗氧化能力、超氧化物歧化酶(SOD)和过氧化氢酶酶活性。卢索快速蓝(LFB)染色和行为测试也用于评估模型。Cup 增加了其脊髓组织中的 ROS 水平和氧化应激。此外,Cup 降低了抗氧化能力、SOD 和过氧化氢酶活性。EA(尤其是 100mg/kg)预防了这些异常变化。EA 共同治疗以剂量依赖性方式改善了接受 Cup 的小鼠的行为损伤。EA 可能通过调节脊髓功能在 MS 中发挥保护作用。