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下丘脑 39 肽的分泌对冷刺激的反应至关重要:一种新的体温调节肽能机制。

Regulation of hypothalamic signaling by tuberoinfundibular peptide of 39 residues is critical for the response to cold: a novel peptidergic mechanism of thermoregulation.

机构信息

Section On Fundamental Neuroscience, National Institute Of Mental Health, National Institutes Of Health, Bethesda, Maryland 20892, USA.

出版信息

J Neurosci. 2011 Dec 7;31(49):18166-79. doi: 10.1523/JNEUROSCI.2619-11.2011.

DOI:10.1523/JNEUROSCI.2619-11.2011
PMID:22159128
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3258491/
Abstract

Euthermia is critical for mammalian homeostasis. Circuits within the preoptic hypothalamus regulate temperature, with fine control exerted via descending GABAergic inhibition of presympathetic motor neurons that control brown adipose tissue (BAT) thermogenesis and cutaneous vascular tone. The thermoregulatory role of hypothalamic excitatory neurons is less clear. Here we report peptidergic regulation of preoptic glutamatergic neurons that contributes to temperature regulation. Tuberoinfundibular peptide of 39 residues (TIP39) is a ligand for the parathyroid hormone 2 receptor (PTH2R). Both peptide and receptor are abundant in the preoptic hypothalamus. Based on PTH2R and vesicular glutamate transporter 2 (VGlut2) immunolabeling in animals with retrograde tracer injection, PTH2R-containing glutamatergic fibers are presynaptic to neurons projecting from the median preoptic nucleus (MnPO) to the dorsomedial hypothalamus. Transneuronal retrograde pathway tracing with pseudorabies virus revealed connectivity between MnPO VGlut2 and PTH2R neurons and BAT. MnPO injection of TIP39 increased body temperature by 2°C for several hours. Mice lacking TIP39 signaling, either because of PTH2R-null mutation or brain delivery of a PTH2R antagonist had impaired heat production upon cold exposure, but no change in basal temperature and no impairment in response to a hot environment. Thus, TIP39 appears to act on PTH2Rs present on MnPO glutamatergic terminals to regulate their activation of projection neurons and subsequent sympathetic BAT activation. This excitatory mechanism of heat production appears to be activated on demand, during cold exposure, and parallels the tonic inhibitory GABAergic control of body temperature.

摘要

体温稳定对哺乳动物的内环境平衡至关重要。视前下丘脑的神经回路可以调节体温,通过下行 GABA 能抑制交感运动神经元来精细控制体温,这些神经元控制棕色脂肪组织(BAT)产热和皮肤血管张力。下丘脑兴奋性神经元在体温调节中的作用尚不明确。本文报道了视前区谷氨酸能神经元的肽能调节在体温调节中的作用。39 个氨基酸的促甲状腺素释放肽(TIP39)是甲状旁腺素 2 受体(PTH2R)的配体。这种肽和受体在视前下丘脑都很丰富。基于示踪剂逆行注射动物的 PTH2R 和囊泡谷氨酸转运体 2(VGlut2)免疫标记,含有 PTH2R 的谷氨酸能纤维位于投射到下丘脑背内侧核的中视前核(MnPO)神经元的突触前。假狂犬病毒的顺行逆行示踪显示 MnPO VGlut2 和 PTH2R 神经元与 BAT 之间存在连接。MnPO 注射 TIP39 可使体温升高 2°C 并持续数小时。由于 PTH2R 基因突变或脑内给予 PTH2R 拮抗剂,TIP39 信号缺失的小鼠在寒冷暴露时产热受损,但基础体温无变化,对热环境无反应受损。因此,TIP39 似乎作用于 MnPO 谷氨酸能末梢上的 PTH2R,调节其对投射神经元的激活,进而激活 BAT 的交感神经。这种产热的兴奋性机制似乎是按需激活的,在寒冷暴露期间,与体温的 tonic 抑制性 GABA 能控制平行。

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本文引用的文献

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Tuberoinfundibular peptide of 39 residues- immunoreactive fibers in the zona incerta and the supraoptic decussations terminate in the neuroendocrine hypothalamus.39个氨基酸残基的结节漏斗肽免疫反应性纤维在未定带和视上交叉中终止于神经内分泌下丘脑。
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Tuberoinfundibular peptide of 39 residues is activated during lactation and participates in the suckling-induced prolactin release in rat.39 个氨基酸组成的下丘脑神经肽在哺乳期被激活,并参与大鼠吮吸诱导的催乳素释放。
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Tuberoinfundibular peptide of 39 residues modulates the mouse hypothalamic-pituitary-adrenal axis via paraventricular glutamatergic neurons.39 个氨基酸组成的结节漏斗肽通过室旁核谷氨酸能神经元调节小鼠的下丘脑-垂体-肾上腺轴。
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Tuberoinfundibular peptide of 39 residues (TIP39) signaling modulates acute and tonic nociception.39 个氨基酸的结节漏斗肽 (TIP39) 信号调节急性和持续痛觉。
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Inhibition of brown adipose tissue thermogenesis by neurons in the ventrolateral medulla and in the nucleus tractus solitarius.腹外侧延髓和孤束核神经元对棕色脂肪组织产热的抑制作用。
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Histamine influences body temperature by acting at H1 and H3 receptors on distinct populations of preoptic neurons.组胺通过作用于视前神经元中不同群体的 H1 和 H3 受体来影响体温。
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Dorsomedial hypothalamus mediates autonomic, neuroendocrine, and locomotor responses evoked from the medial preoptic area.背内侧下丘脑介导了来自内侧视前区的自主神经、神经内分泌和运动反应。
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