Non-psychotropic plant cannabinoids: new therapeutic opportunities from an ancient herb

被引:621
作者
Izzo, Angelo A. [1 ]
Borrelli, Francesca [1 ]
Capasso, Raffaele [1 ]
Di Marzo, Vincenzo [2 ]
Mechoulam, Raphael [3 ]
机构
[1] Univ Naples Federico II, Dept Expt Pharmacol, Naples, Italy
[2] CNR, Inst Biomol Chem, Pozzuoli, NA, Italy
[3] Hebrew Univ Jerusalem, Fac Med, Dept Med Chem & Nat Prod, Jerusalem, Israel
关键词
CANNABIDIOL-INDUCED APOPTOSIS; EQUILIBRATIVE NUCLEOSIDE TRANSPORTER; LITHIUM-PAIRED CONTEXT; CONSTITUENT CANNABIDIOL; ANTITUMOR-ACTIVITY; IN-VIVO; RECEPTOR; INHIBITION; DELTA(9)-TETRAHYDROCANNABIVARIN; CELLS;
D O I
10.1016/j.tips.2009.07.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Delta(9)-tetrahydrocannabinol binds cannabinoid (CB1 and CB2) receptors, which are activated by endogenous compounds (endocannabinoids) and are involved in a wide range of physiopathological processes (e.g. modulation of neurotransmitter release, regulation of pain perception, and of cardiovascular, gastrointestinal and liver functions). The well-known psychotropic effects of Delta(9)-tetra hydrocannabinol, which are mediated by activation of brain CB1 receptors, have greatly limited its clinical use. However, the plant Cannabis contains many cannabinoids with weak or no psychoactivity that, therapeutically, might be more promising than Delta(9)-tetra hydrocannabinol. Here, we provide an overview of the recent pharmacological advances, novel mechanisms of action, and potential therapeutic applications of such non-psychotropic plant-derived cannabinoids. Special emphasis is given to cannabidiol, the possible applications of which have recently emerged in inflammation, diabetes, cancer, affective and neurodegenerative diseases, and to Delta(9)-tetrahydrocannabivarin, a novel CB1 antagonist which exerts potentially useful actions in the treatment of epilepsy and obesity.
引用
收藏
页码:515 / 527
页数:13
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