Department of Neurobiology, Harvard Medical School, 220 Longwood Ave., Boston, MA 02115, USA.
J Neurophysiol. 2011 Feb;105(2):958-63. doi: 10.1152/jn.00980.2010. Epub 2010 Nov 17.
Endocannabinoids are potent regulators of synaptic strength. They are generally thought to modify neurotransmitter release through retrograde activation of presynaptic type 1 cannabinoid receptors (CB1Rs). In the cerebellar cortex, CB1Rs regulate several forms of synaptic plasticity at synapses onto Purkinje cells, including presynaptically expressed short-term plasticity and, somewhat paradoxically, a postsynaptic form of long-term depression (LTD). Here we have generated mice in which CB1Rs were selectively eliminated from cerebellar granule cells, whose axons form parallel fibers. We find that in these mice, endocannabinoid-dependent short-term plasticity is eliminated at parallel fiber, but not inhibitory interneuron, synapses onto Purkinje cells. Further, parallel fiber LTD is not observed in these mice, indicating that presynaptic CB1Rs regulate long-term plasticity at this synapse.
内源性大麻素是突触强度的有效调节剂。它们通常被认为通过逆行激活突触前 1 型大麻素受体 (CB1R) 来调节神经递质的释放。在小脑皮层中,CB1R 调节着与浦肯野细胞形成突触的几种形式的突触可塑性,包括突触前表达的短期可塑性,以及有些矛盾的是,一种突触后的长时程抑制 (LTD)。在这里,我们生成了 CB1R 选择性地从形成平行纤维的小脑颗粒细胞中消除的小鼠。我们发现,在这些小鼠中,内源性大麻素依赖性的短期可塑性在平行纤维上被消除,但在抑制性中间神经元上没有被消除。此外,在这些小鼠中没有观察到平行纤维 LTD,表明突触前 CB1R 调节着这个突触的长期可塑性。