Center for Neural Science, New York University, 4 Washington Place, New York, NY 10003, USA.
Center for Neural Science, New York University, 4 Washington Place, New York, NY 10003, USA.
Cell Rep. 2019 Aug 27;28(9):2256-2263.e3. doi: 10.1016/j.celrep.2019.07.074.
We examine synaptic connectivity and cocaine-evoked plasticity at specific networks within the nucleus accumbens (NAc). We identify distinct subpopulations of D1+ medium spiny neurons (MSNs) that project to either the ventral pallidum (D1+) or the ventral tegmental area (D1+). We show that inputs from the ventral hippocampus (vHPC), but not the basolateral amygdala (BLA), are initially biased onto D1+ MSNs. However, repeated cocaine exposure eliminates the bias of vHPC inputs onto D1+ MSNs, while strengthening BLA inputs onto D1+ MSNs. Our results reveal that connectivity and plasticity depend on the specific inputs and outputs of D1+ MSNs and highlight the complexity of cocaine-evoked circuit level adaptations in the NAc.
我们研究了伏隔核(NAc)内特定网络的突触连接和可卡因诱导的可塑性。我们确定了投射到腹侧苍白球(D1+)或腹侧被盖区(D1+)的不同亚群 D1+ 中型棘突神经元(MSNs)。我们表明,来自腹侧海马体(vHPC)的输入,但不是基底外侧杏仁核(BLA)的输入,最初偏向 D1+MSNs。然而,反复可卡因暴露消除了 vHPC 输入对 D1+MSNs 的偏向,同时增强了 BLA 输入对 D1+MSNs 的作用。我们的结果表明,连接和可塑性取决于 D1+MSNs 的特定输入和输出,并强调了 NAc 中可卡因诱导的电路水平适应的复杂性。