Center for Integrative Brain Research, Seattle Children's Research Institute, Seattle, WA 98101.
Department of Neurological Surgery, School of Medicine, University of Louisville, Louisville, KY 40202.
Proc Natl Acad Sci U S A. 2022 Jul 19;119(29):e2121095119. doi: 10.1073/pnas.2121095119. Epub 2022 Jul 14.
The coordination of swallowing with breathing, in particular inspiration, is essential for homeostasis in most organisms. While much has been learned about the neuronal network critical for inspiration in mammals, the pre-Bötzinger complex (preBötC), little is known about how this network interacts with swallowing. Here we activate within the preBötC excitatory neurons (defined as and neurons) and inhibitory neurons (defined as neurons) and inhibit and activate neurons defined by the transcription factor to gain an understanding of the coordination between the preBötC and swallow behavior. We found that stimulating inhibitory preBötC neurons did not mimic the premature shutdown of inspiratory activity caused by water swallows, suggesting that swallow-induced suppression of inspiratory activity is not directly mediated by the inhibitory neurons in the preBötC. By contrast, stimulation of preBötC neurons delayed laryngeal closure of the swallow sequence. Inhibition of neurons increased laryngeal closure duration and stimulation of neurons pushed swallow occurrence to later in the respiratory cycle, suggesting that excitatory neurons from the preBötC connect to the laryngeal motoneurons and contribute to the timing of swallowing. Interestingly, the delayed swallow sequence was also caused by chronic intermittent hypoxia (CIH), a model for sleep apnea, which is 1) known to destabilize inspiratory activity and 2) associated with dysphagia. This delay was not present when inhibiting Dbx1 neurons. We propose that a stable preBötC is essential for normal swallow pattern generation and disruption may contribute to the dysphagia seen in obstructive sleep apnea.
吞咽与呼吸的协调,特别是吸气,对大多数生物体的内稳态至关重要。虽然人们已经了解了哺乳动物呼吸所必需的关键神经元网络——前脑桥背外侧复合体(preBötC),但对于该网络如何与吞咽相互作用却知之甚少。在这里,我们激活 preBötC 中的兴奋性神经元(定义为 和 神经元)和抑制性神经元(定义为 神经元),并抑制和激活转录因子 定义的神经元,以了解 preBötC 与吞咽行为之间的协调。我们发现,刺激抑制性 preBötC 神经元并不能模拟水吞咽引起的吸气活动过早停止,这表明吞咽引起的吸气活动抑制不是直接由 preBötC 中的抑制性神经元介导的。相比之下,刺激 preBötC 神经元会延迟吞咽序列中的喉闭合。抑制 神经元会增加喉闭合持续时间,而刺激 神经元会将吞咽发生时间推迟到呼吸周期的后期,这表明来自 preBötC 的兴奋性神经元与喉运动神经元相连,并有助于吞咽的时间安排。有趣的是,慢性间歇性缺氧(CIH)——一种睡眠呼吸暂停模型,也会导致吞咽序列延迟,CIH 1)已知会使吸气活动不稳定,2)与吞咽困难有关。当抑制 Dbx1 神经元时,这种延迟就不会出现。我们提出,稳定的 preBötC 对于正常的吞咽模式产生是必不可少的,而中断可能会导致阻塞性睡眠呼吸暂停中出现的吞咽困难。