DAMGO 对纹状体中表达 D1 和 D2 多巴胺受体的中型棘突神经元的区域性和细胞类型特异性影响。
Regional and cell-type-specific effects of DAMGO on striatal D1 and D2 dopamine receptor-expressing medium-sized spiny neurons.
机构信息
Stefan Shirley Hatos Center for Neuropharmacology, David Geffen School of Medicine, University of California Los Angeles, USA.
出版信息
ASN Neuro. 2012 Mar 8;4(2):e00077. doi: 10.1042/AN20110063.
The striatum can be divided into the DLS (dorsolateral striatum) and the VMS (ventromedial striatum), which includes NAcC (nucleus accumbens core) and NAcS (nucleus accumbens shell). Here, we examined differences in electrophysiological properties of MSSNs (medium-sized spiny neurons) based on their location, expression of DA (dopamine) D1/D2 receptors and responses to the μ-opioid receptor agonist, DAMGO {[D-Ala(2)-MePhe(4)-Gly(ol)(5)]enkephalin}. The main differences in morphological and biophysical membrane properties occurred among striatal sub-regions. MSSNs in the DLS were larger, had higher membrane capacitances and lower Rin (input resistances) compared with cells in the VMS. RMPs (resting membrane potentials) were similar among regions except for D2 cells in the NAcC, which displayed a significantly more depolarized RMP. In contrast, differences in frequency of spontaneous excitatory synaptic inputs were more prominent between cell types, with D2 cells receiving significantly more excitatory inputs than D1 cells, particularly in the VMS. Inhibitory inputs were not different between D1 and D2 cells. However, MSSNs in the VMS received more inhibitory inputs than those in the DLS. Acute application of DAMGO reduced the frequency of spontaneous excitatory and inhibitory postsynaptic currents, but the effect was greater in the VMS, in particular in the NAcS, where excitatory currents from D2 cells and inhibitory currents from D1 cells were inhibited by the largest amount. DAMGO also increased cellular excitability in the VMS, as shown by reduced threshold for evoking APs (action potentials). Together the present findings help elucidate the regional and cell-type-specific substrate of opioid actions in the striatum and point to the VMS as a critical mediator of DAMGO effects.
纹状体可分为背外侧纹状体 (DLS) 和腹内侧纹状体 (VMS),后者包括伏隔核核心 (NAcC) 和伏隔核壳 (NAcS)。在这里,我们根据位置、多巴胺 D1/D2 受体表达和对 μ 阿片受体激动剂 DAMGO [D-Ala(2)-MePhe(4)-Gly(ol)(5)]脑啡肽的反应,检查了中型棘突神经元 (MSSN) 的电生理特性差异。形态和生物物理膜特性的主要差异发生在纹状体亚区之间。与 VMS 中的细胞相比,DLS 中的 MSSN 较大,膜电容较高,Rin (输入电阻) 较低。除 NAcC 中的 D2 细胞外,各区的 RMPs (静息膜电位) 相似,D2 细胞的 RMP 明显更去极化。相比之下,自发兴奋性突触传入的频率差异在细胞类型之间更为明显,D2 细胞的兴奋性传入明显多于 D1 细胞,特别是在 VMS 中。D1 和 D2 细胞之间的抑制性输入没有差异。然而,VMS 中的 MSSN 接收的抑制性输入多于 DLS 中的 MSSN。急性应用 DAMGO 降低了自发兴奋性和抑制性突触后电流的频率,但 VMS 的效果更大,特别是在 NAcS 中,D2 细胞的兴奋性电流和 D1 细胞的抑制性电流受到的抑制最大。DAMGO 还降低了 VMS 中动作电位 (AP) 的诱发阈值,从而增加了细胞兴奋性。综上所述,本研究结果有助于阐明纹状体中阿片作用的区域和细胞类型特异性底物,并表明 VMS 是 DAMGO 作用的关键中介。