GABA 和神经降压素共同释放对视前神经元活动和体温的相反作用。
Opposing actions of co-released GABA and neurotensin on the activity of preoptic neurons and on body temperature.
机构信息
Scintillon Institute, San Diego, United States.
出版信息
Elife. 2024 Aug 29;13:RP98677. doi: 10.7554/eLife.98677.
Neurotensin (Nts) is a neuropeptide acting as a neuromodulator in the brain. Pharmacological studies have identified Nts as a potent hypothermic agent. The medial preoptic area, a region that plays an important role in the control of thermoregulation, contains a high density of neurotensinergic neurons and Nts receptors. The conditions in which neurotensinergic neurons play a role in thermoregulation are not known. In this study, optogenetic stimulation of preoptic Nts neurons induced a small hyperthermia. In vitro, optogenetic stimulation of preoptic Nts neurons resulted in synaptic release of GABA and net inhibition of the preoptic pituitary adenylate cyclase-activating polypeptide (Adcyap1) neurons firing activity. GABA-A receptor antagonist or genetic deletion of Slc32a1 (VGAT) in Nts neurons unmasked also an excitatory effect that was blocked by a Nts receptor 1 antagonist. Stimulation of preoptic Nts neurons lacking resulted in excitation of neurons and hypothermia. Mice lacking expression in Nts neurons presented changes in the fever response and in the responses to heat or cold exposure as well as an altered circadian rhythm of body temperature. Chemogenetic activation of all Nts neurons in the brain induced a 4-5°C hypothermia, which could be blocked by Nts receptor antagonists in the preoptic area. Chemogenetic activation of preoptic neurotensinergic projections resulted in robust excitation of preoptic neurons. Taken together, our data demonstrate that endogenously released Nts can induce potent hypothermia and that excitation of preoptic neurons is the cellular mechanism that triggers this response.
神经降压素(Nts)是一种在大脑中充当神经调质的神经肽。药理学研究已经确定 Nts 是一种有效的解热剂。中脑前区(MPOA)在体温调节控制中起着重要作用,其中含有高密度的神经降压素能神经元和 Nts 受体。目前尚不清楚神经降压素能神经元在体温调节中发挥作用的条件。在这项研究中,MPOA 神经降压素神经元的光遗传学刺激诱导了轻度发热。在体外,MPOA 神经降压素神经元的光遗传学刺激导致 GABA 的突触释放和垂体腺苷酸环化酶激活肽 1(Adcyap1)神经元放电活动的净抑制。Nts 神经元中的 GABA-A 受体拮抗剂或 Slc32a1(VGAT)的基因缺失也揭示了一种兴奋性作用,该作用被 Nts 受体 1 拮抗剂阻断。缺乏 的 MPOA 神经降压素神经元的刺激导致 神经元的兴奋和体温降低。在 Nts 神经元中缺乏 表达的小鼠表现出发热反应的变化,以及对热或冷暴露的反应以及体温昼夜节律的改变。大脑中所有 Nts 神经元的化学遗传激活导致 4-5°C 的体温降低,该降低可被 MPOA 中的 Nts 受体拮抗剂阻断。MPOA 神经降压素能投射的化学遗传激活导致 MPOA 中的 神经元强烈兴奋。总之,我们的数据表明,内源性释放的 Nts 可以诱导强烈的解热作用,并且 MPOA 神经元的兴奋是触发这种反应的细胞机制。