Cannabidiol for neurodegenerative disorders: important new clinical applications for this phytocannabinoid?

被引:247
作者
Fernandez-Ruiz, Javier [1 ,2 ,3 ]
Sagredo, Onintza [1 ,2 ,3 ]
Ruth Pazos, M. [4 ]
Garcia, Concepcion [1 ,2 ,3 ]
Pertwee, Roger [5 ]
Mechoulam, Raphael [6 ]
Martinez-Orgado, Jose [4 ,7 ]
机构
[1] Univ Complutense, Fac Med, Dept Bioquim & Biol Mol 3, Inst Univ Invest Neuroquim, E-28040 Madrid, Spain
[2] Hosp Univ Puerta Hierro, Ctr Invest Biomed Red Enfermedades Neurodegenerat, Madrid 28222, Spain
[3] Hosp Univ Puerta Hierro, IRYCIS, Madrid 28222, Spain
[4] Hosp Univ Puerta Hierro, Fdn Invest Biomed, Unidad Expt, Madrid 28222, Spain
[5] Univ Aberdeen, Inst Med Sci, Sch Med Sci, Aberdeen, Scotland
[6] Hebrew Univ Jerusalem, Fac Med, Inst Drug Res, IL-91120 Jerusalem, Israel
[7] Hosp Univ Puerta Hierro, Dept Pediat, Serv Neonatol, Madrid 28222, Spain
关键词
cannabidiol; cannabinoid signalling system; Huntington's disease; neonatal ischaemia; neuroprotection; Parkinson's disease; NONPSYCHOACTIVE CANNABINOID CANNABIDIOL; DYSTONIC MOVEMENT-DISORDERS; COLLAGEN-INDUCED ARTHRITIS; HOUSE MUSK SHREW; HUNTINGTONS-DISEASE; PARKINSONS-DISEASE; 5-HT1A RECEPTORS; IN-VITRO; CB2; RECEPTOR; NEUROPROTECTIVE ANTIOXIDANTS;
D O I
10.1111/j.1365-2125.2012.04341.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cannabidiol (CBD) is a phytocannabinoid with therapeutic properties for numerous disorders exerted through molecular mechanisms that are yet to be completely identified. CBD acts in some experimental models as an anti-inflammatory, anticonvulsant, anti-oxidant, anti-emetic, anxiolytic and antipsychotic agent, and is therefore a potential medicine for the treatment of neuroinflammation, epilepsy, oxidative injury, vomiting and nausea, anxiety and schizophrenia, respectively. The neuroprotective potential of CBD, based on the combination of its anti-inflammatory and anti-oxidant properties, is of particular interest and is presently under intense preclinical research in numerous neurodegenerative disorders. In fact, CBD combined with ?9-tetrahydrocannabinol is already under clinical evaluation in patients with Huntington's disease to determine its potential as a disease-modifying therapy. The neuroprotective properties of CBD do not appear to be exerted by the activation of key targets within the endocannabinoid system for plant-derived cannabinoids like ?9-tetrahydrocannabinol, i.e. CB1 and CB2 receptors, as CBD has negligible activity at these cannabinoid receptors, although certain activity at the CB2 receptor has been documented in specific pathological conditions (i.e. damage of immature brain). Within the endocannabinoid system, CBD has been shown to have an inhibitory effect on the inactivation of endocannabinoids (i.e. inhibition of FAAH enzyme), thereby enhancing the action of these endogenous molecules on cannabinoid receptors, which is also noted in certain pathological conditions. CBD acts not only through the endocannabinoid system, but also causes direct or indirect activation of metabotropic receptors for serotonin or adenosine, and can target nuclear receptors of the PPAR family and also ion channels.
引用
收藏
页码:323 / 333
页数:11
相关论文
共 109 条
[41]   Neuroprotective effect of cannabidiol, a non-psychoactive component from Cannabis sativa, on β-amyloid-induced toxicity in PC12 cells [J].
Iuvone, T ;
Esposito, G ;
Esposito, R ;
Santamaria, R ;
Di Rosa, M ;
Izzo, AA .
JOURNAL OF NEUROCHEMISTRY, 2004, 89 (01) :134-141
[42]   Cannabidiol: A Promising Drug for Neurodegenerative Disorders? [J].
Iuvone, Teresa ;
Esposito, Giuseppe ;
De Filippis, Daniele ;
Scuderi, Caterina ;
Steardo, Luca .
CNS NEUROSCIENCE & THERAPEUTICS, 2009, 15 (01) :65-75
[43]   Δ9-Tetrahydrocannabinol and cannabidiol modulate mitogen-induced tryptophan degradation and neopterin formation in peripheral blood mononuclear cells in vitro [J].
Jenny, Marcel ;
Santer, Elisabeth ;
Pirich, Eberhard ;
Schennach, Harald ;
Fuchs, Dietmar .
JOURNAL OF NEUROIMMUNOLOGY, 2009, 207 (1-2) :75-82
[44]   Huntington's disease: progress toward effective disease-modifying treatments and a cure [J].
Johnson, Carl D. ;
Davidson, Beverly L. .
HUMAN MOLECULAR GENETICS, 2010, 19 :R98-R102
[45]  
Juknat A, 2012, BR J PHARM IN PRESS
[46]   Cannabinoids attenuate norepinephrine-induced melatonin biosynthesis in the rat pineal gland by reducing arylalkylamine N-acetyltransferase activity without involvement of cannabinoid receptors [J].
Koch, Marco ;
Dehghani, Faramarz ;
Habazettl, Iris ;
Schomerus, Christof ;
Korf, Horst-Werner .
JOURNAL OF NEUROCHEMISTRY, 2006, 98 (01) :267-278
[47]   Cannabidiol inhibits pathogenic T cells, decreases spinal microglial activation and ameliorates multiple sclerosis-like disease in C57BL/6 mice [J].
Kozela, Ewa ;
Lev, Nirit ;
Kaushansky, Nathali ;
Eilam, Raya ;
Rimmerman, Neta ;
Levy, Rivka ;
Ben-Nun, Avraham ;
Juknat, Ana ;
Vogel, Zvi .
BRITISH JOURNAL OF PHARMACOLOGY, 2011, 163 (07) :1507-1519
[48]   Cannabidiol-treated Rats Exhibited Higher Motor Score After Cryogenic Spinal Cord Injury [J].
Kwiatkoski, Marcelo ;
Guimaraes, Francisco Silveira ;
Del-Bel, Elaine .
NEUROTOXICITY RESEARCH, 2012, 21 (03) :271-280
[49]   A comparative analysis of the potential of cannabinoids and ondansetron to suppress cisplatin-induced emesis in the Suncus murinus (house musk shrew) [J].
Kwiatkowska, M ;
Parker, LA ;
Burton, P ;
Mechoulam, R .
PSYCHOPHARMACOLOGY, 2004, 174 (02) :254-259
[50]   Cannabidiol Reduces Brain Damage and Improves Functional Recovery After Acute Hypoxia-Ischemia in Newborn Pigs [J].
Lafuente, Hector ;
Alvarez, Francisco J. ;
Ruth Pazos, M. ;
Alvarez, Antonia ;
Carmen Rey-Santano, M. ;
Mielgo, Victoria ;
Murgia-Esteve, Xabier ;
Hilario, Enrique ;
Martinez-Orgado, Jose .
PEDIATRIC RESEARCH, 2011, 70 (03) :272-277