Neuropharmacology of the endocannabinoid signaling system-molecular mechanisms, biological actions and synaptic plasticity

被引:82
作者
Basavarajappa, Balapal S.
机构
[1] Nathan S Kline Inst Psychiat Res, Orangeburg, NY 10962 USA
[2] New York State Psychiat Inst & Hosp, Div Analyt Psychopharmacol, New York, NY 10032 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Psychiat, New York, NY 10032 USA
关键词
alcoholism; endocannabinoids; CNS; synaptic plasticity; reward; CB1; receptors; alcohol-drinking behavior; therapy;
D O I
10.2174/157015907780866910
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tile endocannabinoid signaling system is composed of the cannabinoid receptors; their endogenous ligands, the enclocannabinoids; the enzymes that produce and inactivate the endocannabinoids; and die endocannabinoid transporters. The enclocannabinoids are a new family of lipidic signal mediators, which includes amides, esters, and ethers of long-chain polyunsaturated fatty acids. Endocannabinoids signal through the same cell surface receptors that are targeted by Delta(9)-tetrahydrocannabinol (Delta(9)-THC), the active principles of cannabis sativa preparations like hashish and marijuana. The biosynthetic pathways for the synthesis and release of endocannabinoids are still rather uncertain. Unlike neurotransmitter molecules that are typically held in vesicles before synaptic release, enclocannabinoids are synthesized oil demand within the plasma membrane. Once released, they travel in a retrograde direction and transiently suppress presynaptic neurotransmitter release through activation of cannabinoid receptors. The endocannabinoid signaling system is being found to be involved in all increasing number of pathological conditions. In the brain, endocannabinoid signaling is mostly inhibitory and suggests a role for cannabinoids as therapeutic agents in central nervous system (CNS) disease. Their ability to modulate synaptic efficacy has a wide range of functional consequences and provides unique therapeutic possibilities. The present review is focused on new information regarding the endocannabinoid signaling system in the brain. First, the structure, anatomical distribution, and signal transduction mechanisms of cannabinoid receptors are described. Second, the synthetic pathways of enclocannabinoids are discussed, along with the putative mechanisms of their release, uptake, and degradation. Finally, the role of the endocannabinoid signaling system in the CNS and its polential as a therapeutic target in various CNS disease conditions, including alcoholism, are discussed.
引用
收藏
页码:81 / 97
页数:17
相关论文
共 321 条
  • [41] Recent progress toward the identification of genes related to risk for alcoholism
    Buck, KJ
    [J]. MAMMALIAN GENOME, 1998, 9 (12) : 927 - 928
  • [42] Buck KJ, 1997, J NEUROSCI, V17, P3946
  • [43] BUCKLEY NE, 1997, P S CANN INT CANN RE
  • [44] Oxidative metabolism of anandamide
    Burstein, SH
    Rossetti, RG
    Yagen, B
    Zurier, RB
    [J]. PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2000, 61 (1-2): : 29 - 41
  • [45] Drugs and immunity: cannabinoids and their role in decreased resistance to infectious disease
    Cabral, GA
    Pettit, DAD
    [J]. JOURNAL OF NEUROIMMUNOLOGY, 1998, 83 (1-2) : 116 - 123
  • [46] Cadas H, 1997, J NEUROSCI, V17, P1226
  • [47] Dual intracellular signaling pathways mediated by the human cannabinoid CB1 receptor
    Calandra, B
    Portier, M
    Kernéis, A
    Delpech, M
    Carillon, C
    Le Fur, G
    Ferrara, P
    Shire, D
    [J]. EUROPEAN JOURNAL OF PHARMACOLOGY, 1999, 374 (03) : 445 - 455
  • [48] Cultured rat microglial cells synthesize the endocannabinoid 2-arachidonylglycerol, which increases proliferation via a CB2 receptor-dependent mechanism
    Carrier, EJ
    Kearn, CS
    Barkmeier, AJ
    Breese, NM
    Yang, WQ
    Nithipatikom, K
    Pfister, SL
    Campbell, WB
    Hillard, CJ
    [J]. MOLECULAR PHARMACOLOGY, 2004, 65 (04) : 999 - 1007
  • [49] Regulation of neurotransmitter release by metabotropic glutamate receptors
    Cartmell, J
    Schoepp, DD
    [J]. JOURNAL OF NEUROCHEMISTRY, 2000, 75 (03) : 889 - 907
  • [50] NEUROTRANSMITTERS INHIBIT THE OMEGA-CONOTOXIN-SENSITIVE COMPONENT OF CA CURRENT IN NEUROBLASTOMA X GLIOMA HYBRID (NG 108-15) CELLS, NOT THE NIFEDIPINE-SENSITIVE COMPONENT
    CAULFIELD, MP
    ROBBINS, J
    BROWN, DA
    [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1992, 420 (5-6): : 486 - 492