首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Compartment-specific localization of cannabinoid 1 (CB1) and mu-opioid receptors in rat nucleus accumbens.
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Compartment-specific localization of cannabinoid 1 (CB1) and mu-opioid receptors in rat nucleus accumbens.

机译:在大鼠伏隔核中大麻素1(CB1)和μ阿片受体的房室特异性定位。

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摘要

Interactions between cannabinoid and opioid systems have been implicated in reward and drug seeking behaviors involving neuronal circuitry in the nucleus accumbens (Acb) shell and core. To determine the relevant sites, we examined the electron microscopic localization of cannabinoid type-1 (CB1) receptors and mu-opioid receptors in each Acb compartment in rat brain. CB1 receptor immunogold labeling was seen on the plasma membrane and within the cytoplasm of neuronal and glial profiles throughout the Acb. These neuronal profiles included somata and dendrites as well as axon terminals, many of which formed excitatory-type, asymmetric synapses with notable perforations that are often associated with synaptic plasticity. The number of CB1-labeled terminals within the neuropil of the Acb shell was significantly greater than in the core. Mu-opioid receptors were also detected in axonal and dendritic profiles. These dendrites were most prevalent in the Acb shell, where mu-receptors also were located in 21% ofthe dendritic profiles and 3% of the axon terminals containing CB1 receptors. More of the CB1-labeled terminals contacted dendrites expressing mu-opioid receptors in the shell (19%) compared with the core (13%). Conversely, of the synaptic mu-labeled terminals, 20% in the shell and 10% in the core contacted dendrites containing CB1 receptors. These findings provide ultrastructural evidence that cannabinoid-opioid interactions are mediated by activation of CB1 and mu-opioid receptors within the same or synaptically linked neurons in the Acb shell and core. They also suggest a particularly important role for presynaptic CB1 receptors in the reward circuit of the Acb shell.
机译:大麻素和阿片类药物系统之间的相互作用已牵涉到伏伏核(Acb)壳和核中涉及神经元回路的奖励和寻求药物的行为。为了确定相关位点,我们检查了大鼠大脑每个Acb区室中1型大麻素(CB1)受体和μ阿片受体的电子显微镜定位。 CB1受体免疫金标记可见于整个Acb的质膜以及神经元和神经胶质分布的细胞质内。这些神经元特征包括躯体和树突以及轴突末端,其中许多形成兴奋型,不对称突触,并具有明显的穿孔,这些穿孔通常与突触可塑性有关。 Acb壳的神经纤维中CB1标记的末端数量明显多于核心。在轴突和树突状分布中也检测到了阿片类药物受体。这些树突在Acb壳中最普遍,其中mu受体也位于21%的树突轮廓和3%的包含CB1受体的轴突末端。与核心(13%)相比,更多的CB1标记的末端接触了在壳中表达μ阿片受体的树突(19%)。相反,在突触mu标记的末端中,在壳中20%和在核心中10%接触含有CB1受体的树突。这些发现提供了超结构证据,表明大麻素-阿片类药物相互作用是由Acb壳和核中相同或突触连接的神经元内CB1和mu-阿片类受体的激活介导的。他们还暗示突触前CB1受体在Acb壳的奖励回路中具有特别重要的作用。

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