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长期给予阿魏酸对体内β-淀粉样肽毒性的保护作用。

Protection against beta-amyloid peptide toxicity in vivo with long-term administration of ferulic acid.

作者信息

Yan J J, Cho J Y, Kim H S, Kim K L, Jung J S, Huh S O, Suh H W, Kim Y H, Song D K

机构信息

Department of Pharmacology, College of Medicine, Institute of Natural Medicine, Hallym University, Chunchon, 200-702, S. Korea.

出版信息

Br J Pharmacol. 2001 May;133(1):89-96. doi: 10.1038/sj.bjp.0704047.

Abstract
  1. beta-Amyloid peptide (A beta), a 39 -- 43 amino acid peptide, is believed to induce oxidative stress and inflammation in the brain, which are postulated to play important roles in the pathogenesis of Alzheimer's disease. Ferulic acid is an antioxidant and anti-inflammatory agent derived from plants; therefore, the potential protective activity of ferulic acid against A beta toxicity in vivo was examined. 2. Mice were allowed free access to drinking water (control) or water containing ferulic acid (0.006%). After 4 weeks, A beta 1-42 (410 pmol) was administered via intracerebroventricular injection. 3. Injection of control mice with A beta 1-42 impaired performance on the passive avoidance test (35% decrease in step-through latency), the Y-maze test (19% decrease in alternation behaviour), and the water maze test (32% decrease in percentage time in platform-quadrant). In contrast, mice treated with ferulic acid prior to A beta 1-42 administration were protected from these changes (9% decrease in step-through latency; no decrease in alternation behaviour; 14% decrease in percentage time in platform-quadrant). A beta 1-42 induced 31% decrease in acetylcholine level in the cortex, which was tended to be ameliorated by ferulic acid. 4. In addition, A beta 1-42 increased immunoreactivities of the astrocyte marker glial fibrillary acidic protein (GFAP) and interleukin-1 beta (IL-1 beta) in the hippocampus, effects also suppressed by pretreatment with ferulic acid. 5. Administration of ferulic acid per se unexpectedly induced a transient and slight increase in GFAP and IL-1 beta immunoreactivity in the hippocampus on day 14, which returned to basal levels on day 28. A slight (8%) decrease in alternation behaviour was observed on day 14. 6. These results demonstrate that long-term administration of ferulic acid induces resistance to A beta 1-42 toxicity in the brain, and suggest that ferulic acid may be a useful chemopreventive agent against Alzheimer's disease.
摘要
  1. β-淀粉样肽(Aβ)是一种由39 - 43个氨基酸组成的肽,被认为会在大脑中引发氧化应激和炎症,据推测这些在阿尔茨海默病的发病机制中起重要作用。阿魏酸是一种源自植物的抗氧化剂和抗炎剂;因此,研究了阿魏酸在体内对Aβ毒性的潜在保护活性。2. 让小鼠自由饮用饮用水(对照组)或含有阿魏酸(0.006%)的水。4周后,通过脑室内注射给予Aβ1-42(410皮摩尔)。3. 给对照组小鼠注射Aβ1-42会损害其在被动回避试验(穿通潜伏期减少35%)、Y迷宫试验(交替行为减少19%)和水迷宫试验(在平台象限的时间百分比减少32%)中的表现。相比之下,在给予Aβ1-42之前用阿魏酸处理的小鼠免受这些变化的影响(穿通潜伏期减少9%;交替行为无减少;在平台象限的时间百分比减少14%)。Aβ1-42导致皮质中乙酰胆碱水平降低31%,阿魏酸倾向于改善这种情况。4. 此外,Aβ1-42增加了海马体中星形胶质细胞标志物胶质纤维酸性蛋白(GFAP)和白细胞介素-1β(IL-1β)的免疫反应性,阿魏酸预处理也能抑制这些作用。5. 阿魏酸本身的给药在第14天意外地导致海马体中GFAP和IL-1β免疫反应性短暂轻微增加,在第28天恢复到基础水平。在第14天观察到交替行为轻微减少(8%)。6. 这些结果表明,长期给予阿魏酸可诱导大脑对Aβ1-42毒性产生抗性,并表明阿魏酸可能是一种有用的预防阿尔茨海默病的化学预防剂。

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