The pontine Kölliker-Fuse nucleus is important for reduced postinspiratory airflow elicited by stimulation of the ventral respiratory parafacial region.

IF 3.6 2区 医学 Q1 PHYSIOLOGY American journal of physiology. Lung cellular and molecular physiology Pub Date : 2024-10-01 Epub Date: 2024-08-06 DOI:10.1152/ajplung.00155.2024
Karine C Flor, Octavio A C Maia, Ana C Takakura, Thiago S Moreira
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Abstract

Considering that the retrotrapezoid nucleus/respiratory parafacial region (RTN/pFRG) would be an important center in the central nervous system involved in the maintenance and modulation of respiratory activity, we hypothesized that neurons in this nucleus would also be involved in the postinspiratory (post-I) phase of the respiratory cycle through a connection with the pontine Kölliker-Fuse (KF) region. Here, we performed pharmacogenetic manipulation (AAV-hM3D(Gq)-mCherry or AAV-hM4D(Gi)-mCherry) in VGlut2-cre, Ai6 conscious mice to evaluate breathing parameters through whole body plethysmography under baseline conditions (normoxia: [Formula: see text] = 0.21) or under hypercapnia or hypoxia challenges ([Formula: see text] = 0.07 or [Formula: see text] = 0.08). Under normoxia, selective stimulation of RTN/pFRG resulted in a smaller increase in V̇e (1,272 ± 102.5, vs. RTN/pFRG stimulation: 1,878 ± 122.1 mL/kg/min), due to a smaller increase in VT (5.4 ± 0.35, vs. RTN/pFRG stimulation: 7.77 ± 0.21 mL/kg) without changing fR in a condition of KF inhibition. However, inhibition of the VGlut2 neurons in the KF did affect the TE1 produced by selective activation of RTN/pFRG (119.9 ± 2.53, vs. RTN/pFRG stimulation: 104 ± 2.46 ms). Both the hypercapnia and hypoxia ventilatory response were reduced after inhibition of VGlut2-expressing KF neurons. Therefore, consistent with anatomical projections RTN/pFRG neurons regulate lung ventilation by controlling all aspects of breathing, i.e., breathing frequency, inspiration, postinspiration, and active expiration. All the modulation seems to be dependent on the integrity of the glutamatergic neurons in the KF region.NEW & NOTEWORTHY Our research reveals specific roles and interactions between the retrotrapezoid nucleus/respiratory parafacial region (RTN/pFRG) and the pontine Kölliker-Fuse (KF) region in controlling respiratory phases. RTN/pFRG neurons are key in regulating all aspects of breathing, including frequency, inspiration, postinspiration, and active expiration. This regulation depends on the functional integrity of glutamatergic neurons in the KF region, aligning with anatomical projections.

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脑桥 Kölliker-Fuse 核对刺激腹侧呼吸面旁区引起的吸气后气流减少非常重要。
考虑到蛛网膜后核/呼吸面旁区(RTN/pFRG)是中枢神经系统中参与维持和调节呼吸活动的一个重要中枢,我们假设该核中的神经元也会通过与桥脑柯利克-傅斯(KF)区的连接参与呼吸周期的后吸气阶段。在此,我们对 VGlut2-cre、Ai6 意识清醒的小鼠进行了药物遗传学操作(AAV-hM3D(Gq)-mCherry 或 AAV-hM4D(Gi)-mCherry),在基线条件(常氧:FiO2 = 0.21)或高碳酸血症或低氧挑战(FiCO2 = 0.07 或 FiO2 = 0.08)下通过全身胸透评估呼吸参数。在常氧状态下,选择性刺激 RTN/pFRG 导致 VE 增加较少(1,272 ± 102.5,与 RTN/pFRG 刺激相比:1,878 ± 122.1 毫升/千克/分钟),这是因为在 KF 抑制条件下 VT 增加较少(5.4 ± 0.35,与 RTN/pFRG 刺激相比:7.77 ± 0.21 毫升/千克),而 fR 不变。然而,抑制 KF 中的 VGlut2 神经元确实会影响 RTN/pFRG 选择性激活产生的 TE1(119.9 ± 2.53,对比:RTN/pFRG 刺激:104 ± 2.46 ms)。抑制 VGlut2 表达的 KF 神经元后,高碳酸血症和低氧通气反应均减弱。因此,与解剖投射一致,RTN/pFRG 神经元通过控制呼吸的各个方面(即呼吸频率、吸气、吸气后和主动呼气)来调节肺通气。所有这些调节似乎都取决于 KF 区域谷氨酸能神经元的完整性。
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来源期刊
CiteScore
9.20
自引率
4.10%
发文量
146
审稿时长
2 months
期刊介绍: The American Journal of Physiology-Lung Cellular and Molecular Physiology publishes original research covering the broad scope of molecular, cellular, and integrative aspects of normal and abnormal function of cells and components of the respiratory system. Areas of interest include conducting airways, pulmonary circulation, lung endothelial and epithelial cells, the pleura, neuroendocrine and immunologic cells in the lung, neural cells involved in control of breathing, and cells of the diaphragm and thoracic muscles. The processes to be covered in the Journal include gas-exchange, metabolic control at the cellular level, intracellular signaling, gene expression, genomics, macromolecules and their turnover, cell-cell and cell-matrix interactions, cell motility, secretory mechanisms, membrane function, surfactant, matrix components, mucus and lining materials, lung defenses, macrophage function, transport of salt, water and protein, development and differentiation of the respiratory system, and response to the environment.
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