Department of Basic Neuroscience, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Department of Basic Neuroscience, Faculty of Medicine, University of Geneva, Geneva, Switzerland; Clinic of Neurology, Department of Clinical Neurosciences, Geneva University Hospital, Geneva, Switzerland.
Neuron. 2020 Jul 8;107(1):158-172.e4. doi: 10.1016/j.neuron.2020.03.029. Epub 2020 Apr 24.
Overeating typically follows periods of energy deficit, but it is also sustained by highly palatable foods, even without metabolic demand. Dopamine D1 receptor-expressing medium spiny neurons (D1-MSNs) of the nucleus accumbens shell (NAcSh) project to the lateral hypothalamus (LH) to authorize feeding when inhibited. Whether plasticity at these synapses can affect food intake is unknown. Here, ex vivo electrophysiology recordings reveal that D1-MSN-to-LH inhibitory transmission is depressed in circumstances in which overeating is promoted. Endocannabinoid signaling is identified as the induction mechanism, since inhibitory plasticity and concomitant overeating were blocked or induced by CB1R antagonism or agonism, respectively. D1-MSN-to-LH projectors were largely non-overlapping with D1-MSNs targeting ventral pallidum or ventral midbrain, providing an anatomical basis for distinct circuit plasticity mechanisms. Our study reveals a critical role for plasticity at D1-MSN-to-LH synapses in adaptive feeding control, which may underlie persistent overeating of unhealthy foods, a major risk factor for developing obesity.
进食过量通常发生在能量不足之后,但即使没有代谢需求,高可口性的食物也能维持进食过量。伏隔核壳部表达多巴胺 D1 受体的中型棘状神经元(D1-MSNs)投射到外侧下丘脑(LH),当受到抑制时,它们会授权进食。这些突触的可塑性是否会影响食物摄入尚不清楚。在这里,离体电生理学记录显示,在促进进食过量的情况下,D1-MSN 到 LH 的抑制性传递被抑制。内源性大麻素信号被确定为诱导机制,因为抑制性可塑性和随之而来的进食过量分别被 CB1R 拮抗剂或激动剂阻断或诱导。D1-MSN 到 LH 的投射者与靶向苍白球腹侧部或中脑腹侧部的 D1-MSN 基本上没有重叠,为不同的回路可塑性机制提供了解剖学基础。我们的研究揭示了 D1-MSN 到 LH 突触可塑性在适应性摄食控制中的关键作用,这可能是持续进食不健康食物的基础,而不健康食物是肥胖发生的一个主要危险因素。