Department of Physiology and Biophysics, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, Brazil.
Department of Pharmacology, Instituto de Ciencias Biomedicas, Universidade de Sao Paulo, Sao Paulo, Brazil.
Am J Physiol Lung Cell Mol Physiol. 2024 Oct 1;327(4):L452-L463. doi: 10.1152/ajplung.00155.2024. Epub 2024 Aug 6.
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 V (5.4 ± 0.35, vs. RTN/pFRG stimulation: 7.77 ± 0.21 mL/kg) without changing in a condition of KF inhibition. However, inhibition of the VGlut2 neurons in the KF did affect the 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. 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.
考虑到梯形核/呼吸口面区(RTN/pFRG)可能是中枢神经系统中参与维持和调节呼吸活动的重要中心,我们假设该核中的神经元也通过与脑桥 Kölliker-Fuse(KF)区的连接参与呼吸周期的后吸气(post-I)阶段。在这里,我们在 VGlut2-cre、Ai6 清醒小鼠中进行了遗传药理学操作(AAV-hM3D(Gq)-mCherry 或 AAV-hM4D(Gi)-mCherry),通过全身 plethysmography 在基础条件下(常氧:[Formula: see text] = 0.21)或在高碳酸血症或低氧血症挑战下评估呼吸参数([Formula: see text] = 0.07 或 [Formula: see text] = 0.08)。在常氧下,选择性刺激 RTN/pFRG 导致 V̇e 的增加较小(1,272 ± 102.5,与 RTN/pFRG 刺激相比:1,878 ± 122.1 mL/kg/min),这是由于 V 的增加较小(5.4 ± 0.35,与 RTN/pFRG 刺激相比:7.77 ± 0.21 mL/kg),而在 KF 抑制的情况下没有改变。然而,抑制 KF 中的 VGlut2 神经元会影响选择性激活 RTN/pFRG 产生的(119.9 ± 2.53,与 RTN/pFRG 刺激相比:104 ± 2.46 ms)。抑制表达 VGlut2 的 KF 神经元后,高碳酸血症和低氧血症的通气反应均降低。因此,与解剖学投影一致,RTN/pFRG 神经元通过控制呼吸的各个方面来调节肺通气,即呼吸频率、吸气、后吸气和主动呼气。所有的调节似乎都依赖于 KF 区域中谷氨酸能神经元的完整性。我们的研究揭示了梯形核/呼吸口面区(RTN/pFRG)和脑桥 Kölliker-Fuse(KF)区在控制呼吸阶段中的特定作用和相互作用。RTN/pFRG 神经元是调节呼吸各个方面的关键,包括频率、吸气、后吸气和主动呼气。这种调节取决于 KF 区域中谷氨酸能神经元的功能完整性,与解剖学投影一致。