首页> 美国卫生研究院文献>The Journal of Neuroscience >Roles of Endocannabinoids in Heterosynaptic Long-Term Depression of Excitatory Synaptic Transmission in Visual Cortex of Young Mice
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Roles of Endocannabinoids in Heterosynaptic Long-Term Depression of Excitatory Synaptic Transmission in Visual Cortex of Young Mice

机译:内源性大麻素在年轻小鼠视觉皮层兴奋性突触传递异质突触长期抑制中的作用

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摘要

Tetanic stimulation of one of two afferent pathways converging to neurons in the visual cortex induces long-term depression (LTD) of synaptic transmission in the other, nonactivated pathway under a certain condition. This form of synaptic plasticity called heterosynaptic LTD (hetero-LTD) was not systematically investigated in previous studies, whereas homosynaptic LTD has been extensively studied. To determine whether hetero-LTD is induced in visual cortical slices of mice and, if so, through what mechanisms, we recorded EPSPs evoked in layer II/III neurons by alternating test stimulation of two sites in layer IV at 0.05 Hz. After theta-burst stimulation of one site, EPSPs evoked by test stimulation of the other site were depressed for a long time in most of the neurons, whereas homosynaptic long-term potentiation was induced at activated synapses. Such a hetero-LTD was induced in most mice at postnatal day 7–20 (P7–P20), but not induced in mice at P35–P41. Tests using the paired-pulse stimulation protocol and coefficient of variation analysis suggested that hetero-LTD was expressed at presynaptic sites. Pharmacological analysis indicated that this form of LTD was induced through activation of the type 5 of metabotropic glutamate receptors, not through the NMDA type of glutamate receptors. Additional analysis using a cannabinoid type 1 receptor agonist and an antagonist suggested that endocannabinoids (eCBs) are involved in this type of LTD. Moreover, results suggest that brain-derived neurotrophic factor, which may be released from strongly activated presynaptic sites, prevents eCBs from suppressing the release of transmitters from these sites.
机译:在一定条件下,在视觉皮层中收敛到神经元的两个传入通路之一的强直刺激会在另一条非激活通路中诱导突触传递的长期抑制(LTD)。在以前的研究中,尚未系统地研究这种形式的称为突触突触有限公司(hetero-LTD)的突触可塑性,而对突触突触有限公司进行了广泛的研究。为了确定是否在小鼠的视觉皮层切片中诱导了异LTD,并且,如果通过何种机制,我们通过在0.05 Hz下交替测试IV层中的两个位点来记录II / III层神经元中诱发的EPSP。在一个部位受到θ-爆发刺激后,大多数神经元长时间抑制了另一部位的测试刺激所诱发的EPSP,而在激活的突触中诱导了高突触的长期增强。在出生后的第7-20天(P7–P20),大多数小鼠都诱导出这种异质LTD,而在P35–P41的小鼠中却没有诱导出这种异质LTD。使用成对脉冲刺激方案和变异系数分析的测试表明,异质LTD在突触前位点表达。药理分析表明,这种形式的LTD是通过激活5型代谢型谷氨酸受体而不是通过NMDA型谷氨酸受体来诱导的。使用1型大麻素受体激动剂和拮抗剂进行的其他分析表明,内源性大麻素(eCBs)参与了该类型的LTD。此外,结果表明,可能从强烈激活的突触前位点释放的脑源性神经营养因子阻止eCB抑制这些位点释放递质。

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