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托芬那酸可减轻 3-硝基丙酸致小鼠的生化改变。

Tolfenamic Acid Attenuates 3-Nitropropionic Acid-Induced Biochemical Alteration in Mice.

机构信息

Department of Pharmacology, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenhe District, Shenyang, 110016, Liaoning, China.

Key Laboratory of Neurodegenerative Diseases (Capital Medical University), Ministry of Education, 45 Changchun Street, Xuanwu, Beijing, 100053, China.

出版信息

Neurochem Res. 2018 Oct;43(10):1938-1946. doi: 10.1007/s11064-018-2615-7. Epub 2018 Aug 17.

Abstract

Tolfenamic acid (TA), a nonsteroidal anti-inflammatory drug, shows neuroprotective effects and alleviates cognitive deficits in transgenic mouse models of Alzheimer's disease. However, whether TA can prevent the biochemical alterations induced by intraperitoneal injection of 3-nitropropionic acid (3-NP) in mice is still unknown. In this study, the striatal lesion area was measured by 2,3,5-triphenyltetrazolium chloride staining. Glutamate, SDH and ATP levels were tested using colorimetric assay kits. The neuroinflammatory cytokine levels were tested by ELISA kits. The expression of synaptic proteins and the subtypes of the NMDA receptor were tested by western blotting. TA was orally administered 10 days before 3-NP injection (pretreatment) or on the same day as 3-NP injection (co-treatment). TA pretreatment showed the strongest neuroprotective effects: pretreatment significantly attenuated the 3-NP-induced muscular weakness in the forelimb and alterations in glutamate level, mitochondrial function, and pro-inflammatory cytokine release in the brains of mice. These results suggest that TA has preventive and protective effects on 3-NP-induced neurotoxicity.

摘要

托芬那酸(TA)是一种非甾体抗炎药,具有神经保护作用,并能减轻阿尔茨海默病转基因小鼠模型的认知缺陷。然而,TA 是否能预防腹腔注射 3-硝基丙酸(3-NP)在小鼠中引起的生化改变尚不清楚。在本研究中,通过 2,3,5-三苯基氯化四氮唑染色测量纹状体损伤面积。使用比色法试剂盒测试谷氨酸、SDH 和 ATP 水平。通过 ELISA 试剂盒测试神经炎症细胞因子水平。通过 Western 印迹法测试突触蛋白的表达和 NMDA 受体的亚型。TA 在 3-NP 注射前 10 天(预处理)或与 3-NP 注射同一天(共同处理)口服给药。TA 预处理显示出最强的神经保护作用:预处理显著减轻了 3-NP 诱导的小鼠前肢肌肉无力以及大脑中谷氨酸水平、线粒体功能和促炎细胞因子释放的改变。这些结果表明 TA 对 3-NP 诱导的神经毒性具有预防和保护作用。

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