Institute of Biophysics, State Key Laboratory of Brain and Cognitive Science, Center for Excellence in Biomacromolecules, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
Institute of Biophysics, State Key Laboratory of Brain and Cognitive Science, Center for Excellence in Biomacromolecules, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China; Sino-Danish Center for Education and Research, Beijing 100190, China.
Cell Rep. 2024 Jun 25;43(6):114282. doi: 10.1016/j.celrep.2024.114282. Epub 2024 May 24.
The suppressive effect of insulin on food intake has been documented for decades. However, whether insulin signals can encode a certain type of nutrients to regulate nutrient-specific feeding behavior remains elusive. Here, we show that in female Drosophila, a pair of dopaminergic neurons, tritocerebrum 1-dopaminergic neurons (T1-DANs), are directly activated by a protein-intake-induced insulin signal from insulin-producing cells (IPCs). Intriguingly, opto-activating IPCs elicits feeding inhibition for both protein and sugar, while silencing T1-DANs blocks this inhibition only for protein food. Elevating insulin signaling in T1-DANs or opto-activating these neurons is sufficient to mimic protein satiety. Furthermore, this signal is conveyed to local neurons of the protocerebral bridge (PB-LNs) and specifically suppresses protein intake. Therefore, our findings reveal that a brain-derived insulin signal encodes protein satiety and suppresses feeding behavior in a nutrient-specific manner, shedding light on the functional specificity of brain insulin signals in regulating behaviors.
几十年来,人们已经证实胰岛素对摄食具有抑制作用。然而,胰岛素信号是否可以编码特定类型的营养物质来调节特定营养物质的摄食行为仍然难以捉摸。在这里,我们发现在雌性果蝇中,一对多巴胺能神经元,即三叉神经 1 型多巴胺能神经元(T1-DANs),可被来自胰岛素分泌细胞(IPCs)的蛋白摄入诱导的胰岛素信号直接激活。有趣的是,光激活 IPCs 会引起蛋白和糖的摄食抑制,而沉默 T1-DANs 则仅阻断对蛋白食物的这种抑制。在 T1-DANs 中升高胰岛素信号或光激活这些神经元足以模拟蛋白饱腹感。此外,这种信号被传递到protocerebral bridge(PB-LNs)的局部神经元,并特异性地抑制蛋白摄入。因此,我们的研究结果表明,源自大脑的胰岛素信号编码蛋白饱腹感,并以特定的营养物质特异性方式抑制摄食行为,为调节行为的大脑胰岛素信号的功能特异性提供了线索。