Fighting neurodegeneration with rapamycin: mechanistic insights

被引:413
作者
Bove, Jordi [1 ]
Martinez-Vicente, Marta [1 ]
Vila, Miquel [1 ,2 ,3 ]
机构
[1] Vall Hebron Res Inst CIBERNED, Neurodegenerat Dis Res Grp, Barcelona 08035, Spain
[2] Catalan Inst Res & Adv Studies ICREA, Barcelona 08010, Spain
[3] Autonomous Univ Barcelona, Dept Biochem & Mol Biol, E-08193 Barcelona, Spain
关键词
AMYOTROPHIC-LATERAL-SCLEROSIS; LIFE-SPAN EXTENSION; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE MOUSE MODEL; LYSOSOMAL MEMBRANE PERMEABILIZATION; CAP-DEPENDENT TRANSLATION; AGGREGATE-PRONE PROTEINS; RENAL-CELL CARCINOMA; PARKINSONS-DISEASE; HUNTINGTONS-DISEASE; ALPHA-SYNUCLEIN;
D O I
10.1038/nrn3068
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A growing number of studies point to rapamycin as a pharmacological compound that is able to provide neuroprotection in several experimental models of neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, Huntington's disease and spinocerebellar ataxia type 3. In addition, rapamycin exerts strong anti-ageing effects in several species, including mammals. By inhibiting the activity of mammalian target of rapamycin (mTOR), rapamycin influences a variety of essential cellular processes, such as cell growth and proliferation, protein synthesis and autophagy. Here, we review the molecular mechanisms underlying the neuroprotective effects of rapamycin and discuss the therapeutic potential of this compound for neurodegenerative diseases.
引用
收藏
页码:437 / 452
页数:16
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