Department of Biology, University of Virginia, Charlottesville, VA 22904, USA.
Departments of Pharmacology and Psychiatry and Behavioral Sciences, University of Washington, 1959 NE Pacific Street, Seattle, WA 98195, USA.
Cell Rep. 2022 Nov 29;41(9):111718. doi: 10.1016/j.celrep.2022.111718.
Obesity comorbidities such as diabetes and cardiovascular disease are pressing public health concerns. Overconsumption of calories leads to weight gain; however, neural mechanisms underlying excessive food consumption are poorly understood. Here, we demonstrate that dopamine receptor D1 (Drd1) expressed in the agouti-related peptide/neuropeptide Y (AgRP/NPY) neurons of the arcuate hypothalamus is required for appropriate responses to a high-fat diet (HFD). Stimulation of Drd1 and AgRP/NPY co-expressing arcuate neurons is sufficient to induce voracious feeding. Delivery of a HFD after food deprivation acutely induces dopamine (DA) release in the ARC, whereas animals that lack Drd1 expression in ARC neurons (Drd1-KO) exhibit attenuated foraging and refeeding of HFD. These results define a role for the DA input to the ARC that encodes acute responses to food and position Drd1 signaling in the ARC neurons as an integrator of the hedonic and homeostatic neuronal feeding circuits.
肥胖症的合并症,如糖尿病和心血管疾病,是当前迫切的公共健康关注点。卡路里摄入过多会导致体重增加;然而,人们对导致过度进食的神经机制知之甚少。在这里,我们证明了在弓状核的刺鼠相关肽/神经肽 Y(AgRP/NPY)神经元中表达的多巴胺受体 D1(Drd1)对于对高脂肪饮食(HFD)的适当反应是必需的。刺激表达 Drd1 和 AgRP/NPY 的弓状核神经元足以诱导暴食。在禁食后给予高脂肪饮食会急性诱导 ARC 中的多巴胺(DA)释放,而缺乏 ARC 神经元中 Drd1 表达的动物(Drd1-KO)表现出觅食减少和重新进食 HFD。这些结果定义了 DA 输入到 ARC 的作用,该作用编码了对食物的急性反应,并将 Drd1 信号在 ARC 神经元中的定位作为享乐和稳态神经元进食回路的整合者。