Graduate Program in Health Sciences, University of Brasilia, Brasilia, Brazil.
Graduate Program in Health Sciences and Technologies, University of Brasilia, Brasilia, Brazil.
Respir Physiol Neurobiol. 2024 May;323:104239. doi: 10.1016/j.resp.2024.104239. Epub 2024 Feb 22.
This study aimed to evaluate the timing and frequency of spontaneous apneas during breathing and swallowing by using cineradiography on mouse models of early/initial or late/advanced Parkinson's disease (PD). C57BL/6 J mice received either 6-OHDA or vehicle injections into their right striatum, followed by respiratory movement recordings during spontaneous breathing and swallowing, and a stress challenge, two weeks later. Experimental group animals showed a significantly lower respiratory rate (158.66 ± 32.88 breaths/minute in late PD, 173.16 ± 25.19 in early PD versus 185.27 ± 25.36 in controls; p<0.001) and a significantly higher frequency of apneas (median 1 apnea/minute in both groups versus 0 in controls; p<0.001). Other changes included reduced food intake and the absence of swallow apneas in experimental mice. 6-OHDA-induced nigrostriatal degeneration in mice disrupted respiratory control, swallowing, stress responsiveness, and feeding behaviors, potentially hindering airway protection and elevating the risk of aspiration.
本研究旨在通过对早期/初始和晚期/进展期帕金森病(PD)的小鼠模型进行动态射线照相,评估呼吸和吞咽过程中自发性呼吸暂停的时间和频率。C57BL/6J 小鼠接受右侧纹状体的 6-OHDA 或载体注射,两周后进行自发性呼吸和吞咽以及应激挑战期间的呼吸运动记录。实验组动物的呼吸频率明显降低(晚期 PD 为 158.66±32.88 次/分钟,早期 PD 为 173.16±25.19 次/分钟,对照组为 185.27±25.36 次/分钟;p<0.001),呼吸暂停的频率明显升高(两组的中位数均为 1 次/分钟,而对照组为 0 次/分钟;p<0.001)。其他变化包括实验组小鼠的食物摄入量减少和吞咽性呼吸暂停缺失。6-OHDA 诱导的小鼠黑质纹状体变性破坏了呼吸控制、吞咽、应激反应和摄食行为,可能阻碍气道保护并增加吸入风险。