Therapeutic Perspectives of Inhibitors of Endocannabinoid Degradation

被引:19
作者
Ortega-Gutierrez, Silvia [1 ]
机构
[1] Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain
关键词
Endocannabinoids; anandamide; 2-arachidonoylglycerol; fatty acid amide hydrolase; monoglycerol lipase; endocannabinoid uptake;
D O I
10.2174/156800705774933032
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The study of the cannabinoids can be established in the middle sixties with the elucidation of the structure of the active principle of Cannabis sativa plant, the Delta(9)-tetrahydrocannabinol. However, the existence of an endogenous cannabinoid system (ECS) has not been unequivocally accepted until recently. The last two decades have witnessed an impressive advance in the knowledge about cannabinoids, their chemistry, the enzymes involved in their metabolism, and their physiological and pathological roles. In particular, we have made progress in modifying the activity of the ECS with selective compounds, validating the ECS as a new therapeutic target. Endocannabinoids play a role in physiological and pathological processes, and their levels are affected in several disorders. Therefore, it should be possible to ameliorate these pathologies by correcting their altered levels. This review focuses on the current therapeutic opportunities of endocannabinoid-directed drugs, and pays special attention to the therapeutic possibilities underlying the inhibition of the endocannabinoid inactivation. The strategy of manipulating the ECS might open new avenues in the development of therapeutic approaches for a number of disorders, both central and peripheral, that lack as yet effective treatments.
引用
收藏
页码:697 / 707
页数:11
相关论文
共 143 条
[1]  
Alger BE, 2002, PROG NEUROBIOL, V68, P247
[2]   Circuitry for associative plasticity in the amygdala involves endocannabinoid signaling [J].
Azad, SC ;
Monory, K ;
Marsicano, G ;
Cravatt, BF ;
Lutz, B ;
Zieglgänsberger, W ;
Rammes, G .
JOURNAL OF NEUROSCIENCE, 2004, 24 (44) :9953-9961
[3]   Endocannabinoids control spasticity in a multiple sclerosis model [J].
Baker, D ;
Pryce, G ;
Croxford, JL ;
Brown, P ;
Pertwee, RG ;
Makriyannis, A ;
Khanolkar, A ;
Layward, L ;
Fezza, F ;
Bisogno, T ;
Di Marzo, V .
FASEB JOURNAL, 2001, 15 (02) :300-302
[4]   Cannabinoids control spasticity and tremor in a multiple sclerosis model [J].
Baker, D ;
Pryce, G ;
Croxford, JL ;
Brown, P ;
Pertwee, RG ;
Huffman, JW ;
Layward, L .
NATURE, 2000, 404 (6773) :84-87
[5]   Functional role of high-affinity anandamide transport, as revealed by selective inhibition [J].
Beltramo, M ;
Stella, N ;
Calignano, A ;
Lin, SY ;
Makriyannis, A ;
Piomelli, D .
SCIENCE, 1997, 277 (5329) :1094-1097
[6]   Carrier-mediated transport and enzymatic hydrolysis of the endogenous cannabinoid 2-arachidonylglycerol [J].
Beltramo, M ;
Piomelli, D .
NEUROREPORT, 2000, 11 (06) :1231-1235
[7]   Reversal of dopamine D2 receptor responses by an anandamide transport inhibitor [J].
Beltramo, M ;
de Fonseca, FR ;
Navarro, M ;
Calignano, A ;
Gorriti, MA ;
Grammatikopoulos, G ;
Sadile, AG ;
Giuffrida, A ;
Piomelli, D .
JOURNAL OF NEUROSCIENCE, 2000, 20 (09) :3401-3407
[8]   Involvement of the opioid system in the anxiolytic-like effects induced by Δ9-tetrahydrocannabinol [J].
Berrendero, F ;
Maldonado, R .
PSYCHOPHARMACOLOGY, 2002, 163 (01) :111-117
[9]   Tetrahydrocannabinol and endocannabinoids in feeding and appetite [J].
Berry, EM ;
Mechoulam, R .
PHARMACOLOGY & THERAPEUTICS, 2002, 95 (02) :185-190
[10]   Cloning of the first sn1-DAG lipases points to the spatial and temporal regulation of endocannabinoid signaling in the brain [J].
Bisogno, T ;
Howell, F ;
Williams, G ;
Minassi, A ;
Cascio, MG ;
Ligresti, A ;
Matias, I ;
Schiano-Moriello, A ;
Paul, P ;
Williams, EJ ;
Gangadharan, U ;
Hobbs, C ;
Di Marzo, V ;
Doherty, P .
JOURNAL OF CELL BIOLOGY, 2003, 163 (03) :463-468