期刊文献+

抗阿尔茨海默症海藻天然产物及其药理机制研究进展

Advances in the treatment effect of the marine algae-derived compounds on Alzheimer’s Disease and its pharmacological mechanism
原文传递
导出
摘要 阿尔茨海默症(AD)是老年人群发病率最高的神经退性疾病,主要以语言、学习、记忆等认知功能受损及人格改变为特征,目前还没有治疗AD的特效药物,其给社会带来的经济和健康问题日益突出。AD的发病机制十分复杂,人们普遍认为有β淀粉样蛋白沉积假说、tau蛋白假说、神经炎性损伤假说、胆碱能缺失假说和氧化应激假说等多种机制。海洋蕴藏着大量的藻类生物,研究表明来源于海藻的天然产物具有神经保护作用,具有开发成为治疗AD药物的潜力。中国自主研发的昆布来源的甘露寡糖二酸GV971已进入抗AD临床Ⅲ期实验,为AD患者带来了新希望。本文从AD不同发病机制假说角度综述具有抗AD潜力海藻来源的天然产物及其作用机理,为抗AD海藻药物开发提供参考。 Alzheimer’s disease(AD)is the most common neurodegenerative disease in the elderly.It is characterized by impaired cognitive function and personality changes such as language,learning,and memory.Currently,there is no specific drug for treating AD.The economic and health problems that have arisen have become increasingly prominent.The pathogenesis of AD is very complicated.It is generally believed that there are many mechanisms such asβamyloid deposition theory,tau protein theory,neuroinflammatory injury theory,cholinergic loss theory and oxidative stress.The sea contains a large number of algae plants.Studies have shown that the natural products derived from algae have neuroprotective effects and have the potential to be developed into AD drugs.The algae-derived mannooligosaccharide GV971,which has been independently developed in China,has entered the phase III trial of anti-Alzheimer’s clinical trials.these have brought new hope to AD patients.In this paper,we review the natural products derived from algae with anti-AD potential and their mechanism of action from the perspective of different pathogenesis hypotheses of AD,and provide reference for the development of anti-AD seaweed drugs.
作者 扆雪涛 于德志 方选 张琪 YI Xue-tao;YU De-zhi;FANG Xuan;ZHANG Qi(Food and drug safety evaluation center,Qingdao Institute for Food and Drug Control,Qingdao 266071,China)
出处 《中国海洋药物》 CAS CSCD 2020年第2期93-100,共8页 Chinese Journal of Marine Drugs
关键词 阿尔茨海默症 海藻天然产物 神经保护 药理机制 Alzheimer’s disease marine algae-derived compounds neuroprotection pharmacological mechanism
  • 相关文献

参考文献4

二级参考文献31

  • 1WimoA, Winblad B, Jonsson L. The worldwide societal costs of dementia: Estimates for 2009. Alzheimers Dement 2010; 6: 98-103.
  • 2Sloane PD, Zimmerman S, Suchindran C, Reed P, Wang L, Boustani M, et al. The public health impact of Alzheimer's disease, 2000-2050: potential implication of treatment advances. Annu Rev Public Health 2002; 23: 213-31.
  • 3Cras P, Kawai M, Lowery D, Gonzalez DP, Greenberg B, Perry G. Senile plaque neurites in Alzheimer disease accumulate amyloid precursor peptide. Proc Natl Acad Sci U S A 1991; 88: 7552-6.
  • 4Btanquet V, Gotdgaber D, Turleau C, Creau GN, Delabar J, Sinet PM, et al. The beta amyloid peptide (AD-AP) cDNA hybridizes in normal and Alzheimer individuals near the interface of 21q21 and q22.1. Ann Genet 1987; 30: 68-9.
  • 5Ove A. The bittersweet promise of glycobiology. Nat Biotechnol 2001; 19: 913-7.
  • 6Sasaki T, Takasuka N. Further study of the structure of lentinan, an anti-tumor polysaccharide from Lentinus edodes. Carbohydr Res 1976; 47: 99-104.
  • 7Schaefer D J, Krylov VS. Anti-HIV activity of extracts and compounds from algae and cyanobacteria. Ecotoxicol Environ Saf 2000; 45: 208-27.
  • 8Kim HM, KangJS, Kim JY. Evaluation ofantidiabetic activity of polysaccharide isolated from Phellinus linteus in non-obese diabetic mouse. Int Immunopharmacol 2010; 10: 72-8.
  • 9Ho YS, Yu MS, Yang XF, So KF, Yuen WH, Chang RC. Neuroprotective effects of polysaccharides from wolfberry, the fruits of Lycium barbarum, against homocysteine-induced toxicity in rat cortica neurons. J Alzhiermers Dis 2010; 19: 813-27.
  • 10Townsend M, Cleary JP, Mehta T, Hofmeister J, Lesne S, Selkoe D J, et al. Orally available compound prevents deficits in memory caused by the Alzheimer amyloid-3 oligomers. Ann Neurol 2006; 60: 668-76.

共引文献53

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部