Department of Surgery, Division of Otolaryngology-Head & Neck Surgery, University of Wisconsin-Madison, 1300 University Ave, Madison, WI, 53706, USA.
Department of Communication Sciences and Disorders, University of Wisconsin-Madison, 1975 Willow Drive, Madison, WI, 53706, USA.
Dysphagia. 2023 Oct;38(5):1382-1397. doi: 10.1007/s00455-023-10567-0. Epub 2023 Mar 22.
Early motor and non-motor signs of Parkinson disease (PD) include dysphagia, gastrointestinal dysmotility, and constipation. However, because these often manifest prior to formal diagnosis, the study of PD-related swallow and GI dysfunction in early stages is difficult. To overcome this limitation, we used the Pink1-/- rat, a well-established early-onset genetic rat model of PD to assay swallowing and GI motility deficits. Thirty male rats were tested at 4 months (Pink1-/- = 15, wildtype (WT) control = 15) and 6 months (Pink1-/- = 7, WT = 6) of age; analogous to early-stage PD in humans. Videofluoroscopy of rats ingesting a peanut-butter-barium mixture was used to measure mastication rate and oropharyngeal and pharyngoesophageal bolus speeds. Abnormal swallowing behaviors were also quantified. A second experiment tracked barium contents through the stomach, small intestine, caecum, and colon at hours 0-6 post-barium gavage. Number and weight of fecal emissions over 24 h were also collected. Compared to WTs, Pink1-/- rats showed slower mastication rates, slower pharyngoesophageal bolus speeds, and more abnormal swallowing behaviors. Pink1-/- rats demonstrated significantly delayed motility through the caecum and colon. Pink1-/- rats also had significantly lower fecal pellet count and higher fecal pellet weight after 24 h at 6 months of age. Results demonstrate that swallowing dysfunction occurs early in Pink1-/- rats. Delayed transit to the colon and constipation-like signs are also evident in this model. The presence of these early swallowing and GI deficits in Pink1-/- rats are analogous to those observed in human PD.
帕金森病(PD)的早期运动和非运动症状包括吞咽困难、胃肠动力障碍和便秘。然而,由于这些症状通常在正式诊断之前出现,因此研究早期 PD 相关的吞咽和胃肠道功能障碍具有一定难度。为了克服这一局限性,我们使用 Pink1-/- 大鼠,这是一种已建立的早发性遗传 PD 大鼠模型,以检测吞咽和胃肠道运动功能障碍。30 只雄性大鼠在 4 个月(Pink1-/-=15,野生型(WT)对照组=15)和 6 个月(Pink1-/-=7,WT=6)龄时进行测试;这与人类的早期 PD 相似。通过视频荧光透视法观察大鼠摄入花生酱-钡混合物,测量咀嚼速度以及口咽和咽食管食团速度。还对异常吞咽行为进行了定量分析。第二个实验通过跟踪胃、小肠、盲肠和结肠中钡的含量来评估胃排空。在 24 小时内收集粪便的数量和重量。与 WT 相比,Pink1-/-大鼠的咀嚼速度较慢,咽食管食团速度较慢,并且有更多异常的吞咽行为。Pink1-/-大鼠的盲肠和结肠运动明显延迟。在 6 个月龄时,Pink1-/-大鼠的粪便颗粒计数和重量明显降低,24 小时后粪便颗粒数量和重量显著降低。结果表明,吞咽功能障碍在 Pink1-/-大鼠中很早就出现了。在该模型中也存在向结肠转移延迟和类似便秘的症状。在 Pink1-/-大鼠中存在这些早期的吞咽和胃肠道缺陷类似于在人类 PD 中观察到的缺陷。