The endogenous cannabinoid system and the basal ganglia:: biochemical, pharmacological, and therapeutic aspects

被引:98
作者
Romero, J
Lastres-Becker, I
de Miguel, R
Berrendero, F
Ramos, JA
Fernández-Ruiz, J
机构
[1] Univ Complutense, Fac Med, Dept Bioquim & Biol Mol 3, E-28040 Madrid, Spain
[2] Fdn Hosp Alcorcon, Lab Apoyo Invest, Madrid 28922, Spain
关键词
cannabinoids; CB1; receptors; basal ganglia; motor disorders;
D O I
10.1016/S0163-7258(02)00253-X
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
New data strengthen the idea of a prominent role for endocannabinoids in the modulation of a wide variety of neurobiological functions. Among these, one of the most important is the control of movement. This finding is supported by 3 lines of evidence: (1) the demonstration of a powerful action, mostly inhibitory in nature, of synthetic and plant-derived cannabinoids and, more recently, of endocannabinoids on motor activity; (2) the presence of the cannabinoid CB1 receptor subtype and the recent description of endocannabinoids in the basal ganglia and the cerebellum, the areas that control movement; and (3) the fact that CB1 receptor binding was altered in the basal ganglia of humans affected by several neurological diseases and also of rodents with experimentally induced motor disorders. Based on this evidence, it has been suggested that new synthetic compounds that act at key steps of endocannabinoid activity (i.e., more-stable analogs of endocannabinoids, inhibitors of endocannabinoid reuptake or metabolism, antagonists of CB1 receptors) might be of interest for their potential use as therapeutic agents in a variety of pathologies affecting extrapyramidal structures, such as Parkinson's and Huntington's diseases. Currently, only a few data exist in the literature studying such relationships in humans, but an increasing number of journal articles are revealing the importance of this new neuromodulatory system and arguing in favour of the funding of more extensive research in this field. The present article will review the current knowledge of this neuromodulatory system, trying to establish the future lines for research on the therapeutic potential of the endocannabinoid system in motor disorders. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:137 / 152
页数:16
相关论文
共 169 条
[1]   (R)-METHANANDAMIDE - A CHIRAL NOVEL ANANDAMIDE POSSESSING HIGHER POTENCY AND METABOLIC STABILITY [J].
ABADJI, V ;
LIN, SY ;
TAHA, G ;
GRIFFIN, G ;
STEVENSON, LA ;
PERTWEE, RG ;
MAKRIYANNIS, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1994, 37 (12) :1889-1893
[2]   CANNABINOID PRECIPITATED WITHDRAWAL BY THE SELECTIVE CANNABINOID RECEPTOR ANTAGONIST, SR 141716A [J].
ACETO, MD ;
SCATES, SM ;
LOWE, JA ;
MARTIN, BR .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1995, 282 (1-3) :R1-R2
[3]   3-nitropropionic acid's lethal triplet: cooperative pathways of neurodegeneration [J].
Alexi, T ;
Hughes, PE ;
Faull, RLM ;
Williams, CE .
NEUROREPORT, 1998, 9 (11) :R57-R64
[4]   A comparison of the academic progress of students with EBD and students with LD [J].
Anderson, JA ;
Kutash, K ;
Duchnowski, AJ .
JOURNAL OF EMOTIONAL AND BEHAVIORAL DISORDERS, 2001, 9 (02) :106-115
[5]   The cloned rat hydrolytic enzyme responsible for the breakdown of anandamide also catalyzes its formation via the condensation of arachidonic acid and ethanolamine [J].
Arreaza, G ;
Devane, WA ;
Omeir, RL ;
Sajnani, G ;
Kunz, J ;
Cravatt, BF ;
Deutsch, DG .
NEUROSCIENCE LETTERS, 1997, 234 (01) :59-62
[6]   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
[7]   Selective blockade of type-1 metabotropic glutamate receptors induces neuroprotection by enhancing gabaergic transmission [J].
Battaglia, G ;
Bruno, V ;
Pisani, A ;
Centonze, D ;
Catania, MV ;
Calabresi, P ;
Nicoletti, F .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2001, 17 (06) :1071-1083
[8]   AGING, ENERGY, AND OXIDATIVE STRESS IN NEURODEGENERATIVE DISEASES [J].
BEAL, MF .
ANNALS OF NEUROLOGY, 1995, 38 (03) :357-366
[9]   HU-211, A NONPSYCHOTROPIC CANNABINOID, IMPROVES NEUROLOGICAL SIGNS AND REDUCES BRAIN-DAMAGE AFTER SEVERE FOREBRAIN ISCHEMIA IN RATS [J].
BELAYEV, L ;
BARJOSEPH, A ;
ADAMCHIK, J ;
BIEGON, A .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1995, 25 (01) :19-33
[10]   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