Rivas-Arancibia S, Rodríguez A I, Zigova T, Willing A E, Brown W D, Cahill D W, Sanberg P R
Dept. of Neurosurgery, College of Medicine, University of South Florida, Tampa, FL 33612, USA.
Int J Neurosci. 2001 Aug;108(1-2):55-67. doi: 10.3109/00207450108986505.
Taurine acts as an antioxidant protecting neurons from free radical-mediated cellular damage. 3-nitropropionic acid (3-NP) inhibits energy metabolism, initiating oxidative stress. With the objective to examine whether taurine can protect glia and neurons from damage produced by 3-NP, male Wistar and Sprague-Dawley rats were treated with either (1) saline, (2) taurine (3) 3-NP and saline, or (4) 3-NP and taurine for 4 days. Survival was determined and brains were processed immunohistochemically. Large striatal lesions and increased GFAP, SOD, and taurine immunoreactivity were detected in the 3-NP group when compared with control groups. In contrast, animals receiving 3-NP and taurine exhibited less GFAP, SOD, and taurine immunoreactivity, along with increased survival rates. Results indicate that taurine treatment after 3-NP administration protects the striatum from damage.
牛磺酸作为一种抗氧化剂,可保护神经元免受自由基介导的细胞损伤。3-硝基丙酸(3-NP)抑制能量代谢,引发氧化应激。为了研究牛磺酸是否能保护神经胶质细胞和神经元免受3-NP产生的损伤,将雄性Wistar和Sprague-Dawley大鼠分为四组进行处理,分别为:(1)生理盐水组;(2)牛磺酸组;(3)3-NP与生理盐水组;(4)3-NP与牛磺酸组,处理4天。测定大鼠存活率,并对大脑进行免疫组织化学处理。与对照组相比,3-NP组出现大面积纹状体损伤,且胶质纤维酸性蛋白(GFAP)、超氧化物歧化酶(SOD)和牛磺酸免疫反应性增加。相反,接受3-NP和牛磺酸处理的动物,其GFAP、SOD和牛磺酸免疫反应性降低,存活率提高。结果表明,3-NP给药后给予牛磺酸治疗可保护纹状体免受损伤。