The endocannabinoid system controls key epileptogenic circuits in the hippocampus

被引:568
作者
Monory, Krisztina
Massa, Federico
Egertova, Michaela
Eder, Matthias
Blaudzun, Heike
Westenbroek, Ruth
Kelsch, Wolfgang
Jacob, Wolfgang
Marsch, Rudolf
Ekker, Marc
Long, Jason
Rubenstein, John L.
Goebbels, Sandra
Nave, Klaus-Armin
During, Matthew
Klugmann, Matthias
Woelfel, Barbara
Dodt, Hans-Ulrich
Zieglgaensberger, Walter
Wotjak, Carsten T.
Mackie, Ken
Elphick, Maurice R.
Marsicano, Giovanni
Lutz, Beat
机构
[1] Johannes Gutenberg Univ Mainz, Dept Physiol Chem, D-55099 Mainz, Germany
[2] Max Planck Inst Psychiat, D-80804 Munich, Germany
[3] Queen Mary Univ London, Sch Biol & Chem Sci, London E1 4NS, England
[4] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[5] Univ Ottawa, Dept Biol, Ctr Adv Res Environm Genom, Ottawa, ON K1N 6N5, Canada
[6] Univ Calif San Francisco, Nina Ireland Lab Dev Neurobiol, San Francisco, CA 94143 USA
[7] Max Planck Inst Expt Med, Dept Neurogenet, D-37075 Gottingen, Germany
[8] Univ Auckland, Sch Med, Dept Mol Med & Pathol, Auckland 92019, New Zealand
基金
英国生物技术与生命科学研究理事会;
关键词
D O I
10.1016/j.neuron.2006.07.006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Balanced control of neuronal activity is central in maintaining function and viability of neuronal circuits. The endocannabinoid system tightly controls neuronal excitability. Here, we show that endocannabinoids directly target hippocampal glutamatergic neurons to provide protection against acute epileptiform seizures in mice. Functional CB1 cannabinoid receptors are present on glutamatergic terminals of the hippocampal formation, colocalizing with vesicular glutamate transporter 1 (VGluT1). Conditional deletion of the CB1 gene either in cortical glutamatergic neurons or in forebrain GABAergic neurons, as well as virally induced deletion of the CB1 gene in the hippocampus, demonstrate that the presence of CB1 receptors in glutamatergic hippocampal neurons is both necessary and sufficient to provide substantial endogenous protection against kainic acid (KA)-induced seizures. The direct endocannabinoid-mediated control of hippocampal glutamatergic neurotransmission may constitute a promising therapeutic target for the treatment of disorders associated with excessive excitatory neuronal activity.
引用
收藏
页码:455 / 466
页数:12
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