Animal Toxicology and Physiology Specialty Research Unit (ATPSRU), Department of Zoology, Faculty of Science, Kasetsart University, 50 Ngam Wong Wan Road, Jatujak, Bangkok 10900, Thailand.
Exp Anim. 2024 Jul 9;73(3):259-269. doi: 10.1538/expanim.23-0165. Epub 2024 Feb 1.
We investigated the effect of gallic acid (Gal) against neurodegenerative pathophysiology relevant to Parkinsion's disease (PD) in mice with rotenone-induced toxicity. Forty male institute of cancer research (ICR) mice were randomly divided into four groups: sham-veh, PD-veh (received subcutaneous injection with 2.5 mg/kg/48 h of rotenone); PD-Gal50; and PD-Gal100 (the latter two groups received subcutaneous injection with 2.5 mg/kg/48 h of rotenone and oral gavage with gallic acid 50 and 100 mg/kg/48 h, respectively). All treatments continued for 5 weeks with motor ability assessments once per week using hanging and rotarod tests. Brain tissue evaluation of oxidative status, together with striatal and substantia nigra par compacta (SNc) histological and immunohistological assessments were performed. The results indicate that rotenone significantly induced muscle weakness and motor coordination deficit from the first week of rotenone injection, and a significant increase in neuronal degeneration was presented in both the striatum and SNc. Decreased tyrosine hydroxylase and increment of glia fibrillary acidic protein expression in SNc were depicted. The deteriorating effects of rotenone were ameliorated by gallic acid treatment, especially 100 mg/kg dose. Rotenone did not induce a significant change of lipid peroxidation indicated, but gallic acid exhibited a significant inhibitory effect on the lipid peroxidation increment. Rotenone showed a significant reduction of superoxide dismutase activity, and neither 50 nor 100 mg/kg of gallic acid could alleviate this enzyme activity. In conclusion, gallic acid ameliorated motor deficits and preserving SNc neurons which led to maintaining of the dopaminergic source, including a nurturing effect on supporting astrocytes in mice with rotenone-induced neurodegeneration.
我们研究了没食子酸(GA)对鱼藤酮诱导毒性的小鼠帕金森病(PD)相关神经退行性病理生理学的影响。40 只雄性 ICR 小鼠随机分为四组:假手术-veh(接受皮下注射 2.5mg/kg/48h 鱼藤酮);PD-veh(接受皮下注射 2.5mg/kg/48h 鱼藤酮);PD-Gal50;和 PD-Gal100(后两组分别接受皮下注射 2.5mg/kg/48h 鱼藤酮和口服 50 和 100mg/kg/48h 没食子酸)。所有治疗持续 5 周,每周进行一次运动能力评估,使用悬挂和旋转棒测试。进行大脑组织氧化状态评估,以及纹状体和黑质致密部(SNc)组织学和免疫组织化学评估。结果表明,鱼藤酮从注射鱼藤酮的第一周开始显著引起肌肉无力和运动协调缺陷,并且在纹状体和 SNc 中均出现神经元变性的显著增加。SNc 中酪氨酸羟化酶减少和胶质纤维酸性蛋白表达增加。GA 处理改善了鱼藤酮的恶化作用,特别是 100mg/kg 剂量。鱼藤酮没有引起脂质过氧化的显著变化,但 GA 对脂质过氧化的增加表现出显著的抑制作用。鱼藤酮显著降低超氧化物歧化酶活性,GA 的 50 或 100mg/kg 剂量均不能缓解这种酶活性。总之,GA 改善了运动缺陷并保护了 SNc 神经元,从而维持了多巴胺能来源,包括对鱼藤酮诱导的神经退行性变小鼠中支持星形胶质细胞的营养作用。