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本文引用的文献

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A molecularly defined amygdala-independent tetra-synaptic forebrain-to-hindbrain pathway for odor-driven innate fear and anxiety.一种分子定义的杏仁核独立的四突触前脑-后脑通路,用于气味驱动的先天恐惧和焦虑。
Nat Neurosci. 2024 Mar;27(3):514-526. doi: 10.1038/s41593-023-01562-7. Epub 2024 Feb 12.
2
Parabrachial-to-parasubthalamic nucleus pathway mediates fear-induced suppression of feeding in male mice.臂旁核到苍白球内侧核通路介导雄性小鼠恐惧诱导的摄食抑制。
Nat Commun. 2022 Dec 30;13(1):7913. doi: 10.1038/s41467-022-35634-2.
3
An inter-organ neural circuit for appetite suppression.一个抑制食欲的器官间神经回路。
Cell. 2022 Jul 7;185(14):2478-2494.e28. doi: 10.1016/j.cell.2022.05.007. Epub 2022 Jun 2.
4
A discrete parasubthalamic nucleus subpopulation plays a critical role in appetite suppression.一个离散的苍白球内侧核亚群在抑制食欲方面起着关键作用。
Elife. 2022 May 4;11:e75470. doi: 10.7554/eLife.75470.
5
Dissecting a disynaptic central amygdala-parasubthalamic nucleus neural circuit that mediates cholecystokinin-induced eating suppression.解析介导胆囊收缩素诱导摄食抑制的双突触杏仁中央核-苍白球内侧部神经回路。
Mol Metab. 2022 Apr;58:101443. doi: 10.1016/j.molmet.2022.101443. Epub 2022 Jan 20.
6
At the heart of the interoception network: Influence of the parasubthalamic nucleus on autonomic functions and motivated behaviors.内脏感知网络的核心:旁丘脑底核对自主功能和动机行为的影响。
Neuropharmacology. 2022 Feb 15;204:108906. doi: 10.1016/j.neuropharm.2021.108906. Epub 2021 Nov 29.
7
Posterior subthalamic nucleus (PSTh) mediates innate fear-associated hypothermia in mice.PSTh 介导了小鼠先天恐惧相关的体温降低。
Nat Commun. 2021 May 11;12(1):2648. doi: 10.1038/s41467-021-22914-6.
8
Thiazoline-related innate fear stimuli orchestrate hypothermia and anti-hypoxia via sensory TRPA1 activation.噻唑啉相关的先天恐惧刺激通过感觉 TRPA1 激活来调节体温过低和抗缺氧。
Nat Commun. 2021 Apr 6;12(1):2074. doi: 10.1038/s41467-021-22205-0.
9
Dissociable control of unconditioned responses and associative fear learning by parabrachial CGRP neurons.臂旁核 CGRP 神经元对非条件反应和条件性恐惧学习的可分离控制。
Elife. 2020 Aug 28;9:e59799. doi: 10.7554/eLife.59799.
10
A basal ganglia-like cortical-amygdalar-hypothalamic network mediates feeding behavior.基底神经节样皮质-杏仁核-下丘脑网络介导摄食行为。
Proc Natl Acad Sci U S A. 2020 Jul 7;117(27):15967-15976. doi: 10.1073/pnas.2004914117. Epub 2020 Jun 22.

表达速激肽-1的底丘脑旁核神经元对气味诱导的食欲抑制是必需的。

Tachykinin-1-expressing parasubthalamic nucleus neurons are necessary for odorant-induced appetite suppression.

作者信息

Kaegi Zoe E, Carter Matthew E

机构信息

Department of Biology, Williams College, Williamstown, MA, 01267 USA.

Department of Biology, Williams College, Williamstown, MA, 01267 USA.

出版信息

Physiol Behav. 2025 Apr 1;292:114836. doi: 10.1016/j.physbeh.2025.114836. Epub 2025 Jan 31.

DOI:10.1016/j.physbeh.2025.114836
PMID:39892639
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11846689/
Abstract

Odorants play a critical role in regulating feeding behavior by signaling potential threats or food sources in the environment. However, the neural mechanisms by which odorants affect feeding are not well understood. Tachykinin-1-expressing neurons in the parasubthalamic nucleus (PSTN neurons) are critical for reducing food intake in response to internal appetite-suppressing hormones, gastric distension, and external cues that signal danger. Therefore, we tested the hypothesis that activity in these neurons is modulated by exposure to aversive, attractive, and neutral odorants. Using fiber photometry in mice, we found that PSTN neurons increase activity in response to the aversive predator odorants 2-methyl-2-thiazoline (2MT) and 2,5-dihydro-2,4,5-trimethylthiazoline (TMT), but not to neutral or attractive odorants. This activation correlates with a reduction in food intake and an increase in the latency to initiate feeding. Furthermore, chemogenetic inhibition of PSTN neurons blocks the suppression of feeding caused by 2MT and TMT. These findings highlight the specificity of PSTN neurons in processing aversive olfactory signals and their critical role in integrating external threat cues with internal signals that regulate appetite.

摘要

气味剂通过传递环境中的潜在威胁或食物来源信号,在调节进食行为中发挥关键作用。然而,气味剂影响进食的神经机制尚未得到充分理解。下丘脑旁核中表达速激肽-1的神经元(PSTN神经元)对于响应内部食欲抑制激素、胃扩张以及危险信号的外部线索而减少食物摄入至关重要。因此,我们测试了这样一个假设,即这些神经元的活动会受到厌恶、吸引和中性气味剂暴露的调节。利用小鼠的纤维光度法,我们发现PSTN神经元对厌恶的捕食者气味剂2-甲基-2-噻唑啉(2MT)和2,5-二氢-2,4,5-三甲基噻唑啉(TMT)有反应,活动增加,但对中性或吸引性气味剂无反应。这种激活与食物摄入量的减少和开始进食潜伏期的增加相关。此外,PSTN神经元的化学遗传学抑制可阻断2MT和TMT引起的进食抑制。这些发现突出了PSTN神经元在处理厌恶嗅觉信号方面的特异性,以及它们在将外部威胁线索与调节食欲的内部信号整合中的关键作用。