Peking University-Tsinghua University-NIBS Joint Graduate Program, School of Life Sciences, Tsinghua University, Beijing, China.
National Institute of Biological Sciences (NIBS), Beijing, China.
Nat Commun. 2021 May 11;12(1):2648. doi: 10.1038/s41467-021-22914-6.
The neural mechanisms of fear-associated thermoregulation remain unclear. Innate fear odor 2-methyl-2-thiazoline (2MT) elicits rapid hypothermia and elevated tail temperature, indicative of vasodilation-induced heat dissipation, in wild-type mice, but not in mice lacking Trpa1-the chemosensor for 2MT. Here we report that Trpa1 mice show diminished 2MT-evoked c-fos expression in the posterior subthalamic nucleus (PSTh), external lateral parabrachial subnucleus (PBel) and nucleus of the solitary tract (NTS). Whereas tetanus toxin light chain-mediated inactivation of NTS-projecting PSTh neurons suppress, optogenetic activation of direct PSTh-rostral NTS pathway induces hypothermia and tail vasodilation. Furthermore, selective opto-stimulation of 2MT-activated, PSTh-projecting PBel neurons by capturing activated neuronal ensembles (CANE) causes hypothermia. Conversely, chemogenetic suppression of vGlut2 neurons in PBel or PSTh, or PSTh-projecting PBel neurons attenuates 2MT-evoked hypothermia and tail vasodilation. These studies identify PSTh as a major thermoregulatory hub that connects PBel to NTS to mediate 2MT-evoked innate fear-associated hypothermia and tail vasodilation.
恐惧相关体温调节的神经机制尚不清楚。内源性恐惧气味 2-甲基-2-噻唑啉(2MT)在野生型小鼠中引起快速体温降低和尾巴温度升高,表明血管扩张引起的热量散失,但在缺乏 Trpa1 的小鼠中则没有。在这里,我们报告 Trpa1 小鼠在丘脑下核(PSTh)、外侧臂旁外侧亚核(PBel)和孤束核(NTS)中 2MT 诱导的 c-fos 表达减少。虽然肉毒杆菌毒素轻链介导的 NTS 投射 PSTh 神经元失活抑制,但直接 PSTh-前 NTS 途径的光遗传激活诱导体温降低和尾巴血管扩张。此外,通过捕获激活的神经元集合(CANE)选择性光刺激 2MT 激活的、投射 PSTh 的 PBel 神经元会导致体温降低。相反,在 PBel 或 PSTh 或 PSTh 投射 PBel 神经元中化学遗传抑制 vGlut2 神经元会减弱 2MT 诱导的体温降低和尾巴血管扩张。这些研究确定 PSTh 是一个主要的体温调节中枢,它将 PBel 与 NTS 连接起来,介导 2MT 诱导的先天恐惧相关的体温降低和尾巴血管扩张。