Molecular model of cannabis sensitivity in developing neuronal circuits

被引:68
|
作者
Keimpema, Erik [1 ]
Mackie, Ken [2 ,3 ]
Harkany, Tibor [1 ,4 ]
机构
[1] Univ Aberdeen, European Neurosci Inst Aberdeen, Aberdeen AB25 2ZD, Scotland
[2] Indiana Univ, Gill Ctr Neurosci, Bloomington, IN 47405 USA
[3] Indiana Univ, Dept Psychol & Brain Sci, Bloomington, IN 47405 USA
[4] Karolinska Inst, Dept Med Biochem & Biophys, Div Mol Neurobiol, S-17177 Stockholm, Sweden
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
DIACYLGLYCEROL LIPASE-ALPHA; PRENATAL MARIJUANA EXPOSURE; GENE-EXPRESSION; MONOACYLGLYCEROL LIPASE; PERINATAL EXPOSURE; DOWN-REGULATION; COGNITIVE DEFICITS; AXONAL GROWTH; LIPID RAFTS; RECEPTOR;
D O I
10.1016/j.tips.2011.05.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Prenatal cannabis exposure can complicate in utero development of the nervous system. Cannabis impacts the formation and functions of neuronal circuitries by targeting cannabinoid receptors. Endocannabinoid signaling emerges as a signaling cassette that orchestrates neuronal differentiation programs through the precisely timed interaction of endocannabinoid ligands with their cognate cannabinoid receptors. By indiscriminately prolonging the 'switched-on' period of cannabinoid receptors, cannabis can hijack endocannabinoid signals to evoke molecular rearrangements, leading to the erroneous wiring of neuronal networks. Here, we formulate a hierarchical network design necessary and sufficient to describe the molecular underpinnings of cannabis-induced neural growth defects. We integrate signalosome components, deduced from genome- and proteome-wide arrays and candidate analyses, to propose a mechanistic hypothesis of how cannabis-induced ectopic cannabinoid receptor activity overrides physiological neurodevelopmental endocannabinoid signals, affecting the timely formation of synapses.
引用
收藏
页码:551 / 561
页数:11
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