Münster Alexandra, Votteler Angeline, Sommer Susanne, Hauber Wolfgang
Systems Neurobiology Research Unit, University of Stuttgart, Stuttgart D-70569, Germany.
Department of Neurobiology, University of Stuttgart, Stuttgart D-70569, Germany.
Cereb Cortex Commun. 2020 Nov 26;1(1):tgaa086. doi: 10.1093/texcom/tgaa086. eCollection 2020.
The posterior subdivision of the medial orbitofrontal cortex (mOFC-p) mediates the willingness to expend effort to reach a selected goal. However, the neural circuitry through which the mOFC-p modulates effort-related function is as yet unknown. The mOFC-p projects prominently to the posterior ventral tegmental area (pVTA). Therefore, we analyzed the role of the mOFC-p and interactions with the pVTA in effort-related responding using a combination of behavioral, pharmacological, and neural circuit analysis methods in rats. Pharmacological inhibition of the mOFC-p was found to increase lever pressing for food under a progressive ratio (PR) schedule of reinforcement. These findings provide further support for a modulation of effort-related function by the mOFC-p. Then, we investigated effects of disconnecting the mOFC-p and pVTA on PR responding using unilateral pharmacological inhibition of both areas. This asymmetric intervention was also found to increase PR responding suggesting that the mOFC-p controls effort-related function through interactions with the pVTA. Possibly, a reduced excitatory mOFC-p drive on pVTA gamma-aminobutyric acid (GABA)ergic relays disinhibits VTA dopamine neurons which are known to support PR responding. Collectively, our findings suggest that the mOFC-p and pVTA are key components of a neural circuit mediating the willingness to expend effort to reach a goal.
内侧眶额皮质的后部细分区域(mOFC-p)介导了为实现选定目标而付出努力的意愿。然而,mOFC-p调节与努力相关功能的神经回路尚不清楚。mOFC-p显著投射到腹侧被盖区后部(pVTA)。因此,我们结合行为学、药理学和神经回路分析方法,分析了mOFC-p在与努力相关反应中的作用以及与pVTA的相互作用。发现在渐进比率(PR)强化程序下,对mOFC-p进行药理学抑制会增加大鼠为获取食物而按压杠杆的行为。这些发现为mOFC-p对与努力相关功能的调节提供了进一步支持。然后,我们通过对这两个区域进行单侧药理学抑制,研究了切断mOFC-p和pVTA对PR反应的影响。这种不对称干预也被发现会增加PR反应,表明mOFC-p通过与pVTA的相互作用来控制与努力相关的功能。可能是mOFC-p对pVTAγ-氨基丁酸(GABA)能中继的兴奋性驱动减弱,解除了对VTA多巴胺能神经元的抑制,已知这些神经元支持PR反应。总体而言,我们的研究结果表明,mOFC-p和pVTA是介导为实现目标而付出努力意愿的神经回路的关键组成部分。