Alzheimer's disease; taking the edge off with cannabinoids?

被引:96
作者
Campbell, V. A. [1 ]
Gowran, A.
机构
[1] Univ Dublin Trinity Coll, Dept Physiol, Dublin 2, Ireland
[2] Univ Dublin Trinity Coll, Trinity Coll, Inst Neurosci, Dublin 2, Ireland
关键词
Alzheimer's disease; cannabinoid; CB1; receptor; CB2; beta-amyloid; neurodegeneration;
D O I
10.1038/sj.bjp.0707446
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Alzheimer's disease is an age-related neurodegenerative condition associated with cognitive decline. The pathological hallmarks of the disease are the deposition of beta-amyloid protein and hyperphosphorylation of tau, which evoke neuronal cell death and impair inter-neuronal communication. The disease is also associated with neuroinflammation, excitotoxicity and oxidative stress. In recent years the proclivity of cannabinoids to exert a neuroprotective influence has received substantial interest as a means to mitigate the symptoms of neurodegenerative conditions. In brains obtained from Alzheimer's patients alterations in components of the cannabinoid system have been reported, suggesting that the cannabinoid system either contributes to, or is altered by, the pathophysiology of the disease. Certain cannabinoids can protect neurons from the deleterious effects of beta-amyloid and are capable of reducing tau phosphorylation. The propensity of cannabinoids to reduce beta-amyloid-evoked oxidative stress and neurodegeneration, whilst stimulating neurotrophin expression neurogenesis, are interesting properties that may be beneficial in the treatment of Alzheimer's disease. Delta(9)-tetrahydrocannabinol can also inhibit acetylcholinesterase activity and limit amyloidogenesis which may improve cholinergic transmission and delay disease progression. Targeting cannabinoid receptors on microglia may reduce the neuroinflammation that is a feature of Alzheimer's disease, without causing psychoactive effects. Thus, cannabinoids offer a multi-faceted approach for the treatment of Alzheimer's disease by providing neuroprotection and reducing neuroinflammation, whilst simultaneously supporting the brain's intrinsic repair mechanisms by augmenting neurotrophin expression and enhancing neurogenesis. The evidence supporting a potential role for the cannabinoid system as a therapeutic target for the treatment of Alzheimer's disease will be reviewed herewith.
引用
收藏
页码:655 / 662
页数:8
相关论文
共 88 条
[11]   Memantine in the treatment of mild-to-moderate Alzheimer's disease [J].
Cosman, Kelly M. ;
Boyle, Llsa L. ;
Porsteinsson, Anton P. .
EXPERT OPINION ON PHARMACOTHERAPY, 2007, 8 (02) :203-214
[12]   The non-psychoactive cannabis constituent cannabidiol is an orally effective therapeutic agent in rat chronic inflammatory and neuropathic pain [J].
Costa, Barbara ;
Trovato, Anna Elisa ;
Comelli, Francesca ;
Giagnoni, Gabriella ;
Colleoni, Mariapia .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2007, 556 (1-3) :75-83
[13]   FORMATION AND INACTIVATION OF ENDOGENOUS CANNABINOID ANANDAMIDE IN CENTRAL NEURONS [J].
DIMARZO, V ;
FONTANA, A ;
CADAS, H ;
SCHINELLI, S ;
CIMINO, G ;
SCHWARTZ, JC ;
PIOMELLI, D .
NATURE, 1994, 372 (6507) :686-691
[14]   Excitotoxicity in a chronic model of multiple sclerosis:: Neuroprotective effects of cannabinoids through CB1 and CB2 receptor activation [J].
Docagne, Fabian ;
Muneton, Vilma ;
Clemente, Diego ;
Ali, Carine ;
Loria, Frida ;
Correa, Fernando ;
Hernangomez, Miriam ;
Mestre, Leyre ;
Vivien, Denis ;
Guaza, Carmen .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2007, 34 (04) :551-561
[15]   Modulation of hippocampal cell proliferation, memory, and amyloid plaque deposition in APPsw (Tg2576) mutant mice by isolation stress [J].
Dong, H ;
Goico, B ;
Martin, M ;
Csernansky, CA ;
Bertchume, A ;
Csernansky, JG .
NEUROSCIENCE, 2004, 127 (03) :601-609
[16]   Stimulation of cannabinoid receptor 2 (CB2) suppresses microglial activation [J].
Ehrhart, Jared ;
Obregon, Demian ;
Mori, Takashi ;
Hou, Huayan ;
Sun, Nan ;
Bai, Yun ;
Klein, Thomas ;
Fernandez, Francisco ;
Tan, Jun ;
Shytle, R. Douglas .
JOURNAL OF NEUROINFLAMMATION, 2005, 2 (1)
[17]   HU-211, A NON-PSYCHOTROPIC CANNABINOID, RESCUES CORTICAL-NEURONS FROM EXCITATORY AMINO-ACID TOXICITY IN CULTURE [J].
ESHHAR, N ;
STRIEM, S ;
BIEGON, A .
NEUROREPORT, 1993, 5 (03) :237-240
[18]   The marijuana component cannabidiol inhibits β-amyloid-induced tau protein hyperphosphorylation through Wnt/β-catenin pathway rescue in PC12 cells [J].
Esposito, G ;
De Filippis, D ;
Carnuccio, R ;
Izzo, AA ;
Iuvone, T .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2006, 84 (03) :253-258
[19]   Cannabidiol inhibits inducible nitric oxide synthase protein expression and nitric oxide production in β-amyloid stimulated PC12 neurons through p38 MAP kinase and NF-κB involvement [J].
Esposito, Giuseppe ;
De Filippis, Daniele ;
Maiuri, Maria Chiara ;
De Stefano, Daniela ;
Carnuccio, Rosa ;
Iuvone, Teresa .
NEUROSCIENCE LETTERS, 2006, 399 (1-2) :91-95
[20]   A molecular link between the active component of marijuana and Alzheimer's disease pathology [J].
Eubanks, Lisa M. ;
Rogers, Claude J. ;
Beuscher, Albert E. ;
Koob, George F. ;
Olson, Arthur J. ;
Dickerson, Tobin J. ;
Janda, Kim D. .
MOLECULAR PHARMACEUTICS, 2006, 3 (06) :773-777