Hotchkiss Brain Institute and the Department of Physiology and Pharmacology, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
J Neurosci. 2011 Aug 17;31(33):12011-20. doi: 10.1523/JNEUROSCI.2925-11.2011.
Endocannabinoids (eCBs) are feedback messengers in the nervous system that act at the presynaptic nerve terminal to inhibit transmitter release. Here we report that in brain slices from rat, eCBs are released from vasopressin (VP) neurons in the paraventricular nucleus of the hypothalamus following coincident bursts of presynaptic and postsynaptic spiking. eCBs transiently depress glutamate release from excitatory terminals and, in doing so, prevent the synapses from undergoing long-term depression (LTD). Specifically, we show that blockade of CB1 receptors unmasks LTD following coincident presynaptic and postsynaptic activity. This LTD is presynaptic in nature, but requires the release of the opioid peptide dynorphin from the postsynaptic neuron. Dynorphin release and subsequent LTD require the activation of postsynaptic metabotropic glutamate receptors (mGluRs). Our findings indicate that eCBs, by transiently depressing glutamate release, limit mGluR activation and indirectly gate release of dynorphin from the postsynaptic neuron. We propose that eCBs, in addition to their well described role in the rapid modulation of transmitter release from the nerve terminal, also regulate the release of other retrograde transmitters and thus encode for multiple temporal windows of synaptic plasticity.
内源性大麻素 (eCBs) 是神经系统中的反馈信使,作用于突触前神经末梢以抑制递质释放。在这里,我们报告在大鼠脑片中,在下丘脑室旁核的加压素 (VP) 神经元中,在突触前和突触后放电的同时爆发会释放 eCBs。eCBs 会短暂抑制谷氨酸从兴奋性末梢释放,并由此防止突触发生长时程抑制 (LTD)。具体而言,我们发现阻断 CB1 受体可在突触前和突触后活动同时发生时揭示 LTD。这种 LTD 本质上是突触前的,但需要从突触后神经元释放阿片肽 dynorphin。dynorphin 释放和随后的 LTD 需要激活突触后代谢型谷氨酸受体 (mGluRs)。我们的研究结果表明,eCBs 通过短暂抑制谷氨酸释放,限制 mGluR 的激活,并间接控制 dynorphin 从突触后神经元的释放。我们提出,eCBs 除了在快速调节神经末梢递质释放方面的作用外,还调节其他逆行递质的释放,从而编码多个突触可塑性的时间窗口。