Motor function is not impaired in all components of the oral phase of feeding in a rat rotenone model of Parkinson’s disease

IF 5.3 2区 医学 Q1 PHYSIOLOGY Physiology Pub Date : 2024-05-01 DOI:10.1152/physiol.2024.39.s1.1117
Francois Gould, Ireneusz D. Wojtas, Nicole Charles
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Abstract

Parkinson’s disease results in pathological swallowing, or dysphagia, in up to 90% of cases. Severity and extent of functional impairment of feeding is highly variable in this disease. Feeding is a multi step neuromuscular process of tightly coordinated orofacial behaviors -transport, food reduction, pharyngeal swallowing- involving multiple musculoskeletal systems — tongue, jaw muscles, hyolaryngeal muscles — innervated by multiple cranial and cervical spinal nerves. The type of food being ingested further affects this sequence. The pesticide rotenone, a type II mitochondrial inhibitor, has been epidemiologically linked to Parkinson’s disease. The goal of this project is to identify how parkinsonian neurodegeneration affects this sequence in an animal model. We hypothesize that not all elements of the sequence will be equally affected. Twelve young adult male Lewis rats received daily intraperitoneal injections of either 2.75 mg/kg of rotenone or vehicle control for 8 days. The rats were trained to eat breakfast cereal and drink water mixed with barium in front of a high speed (200 fps) videofluoroscope. From the high speed video recording duration of intraoral transport and chewing of solid food as well as lick duration for liquid drinking were measured for multiple swallows per individual on day 0 (before injection), day 1, day 4, and day 7. On day 8 animals were perfused and brains harvested, sliced, stained with immunofluorescent markers for striatal tyrosine hydroxylase to confirm effectiveness of the model. Mixed model ANOVA was used to test the hypothesis that duration of the phases varied over the course of treatment. Duration of intra oral transport changed in neither control nor rotenone treated animals (p=0.1136), but duration of chewing increased in rotenone treated rats only by day 4 (p<0.001). Duration of licks increased in liquid drinking rats from day 0. Different components of the oral feeding process vary in degree and timing of impairment in the rat rotenone model of Parkinson’s disease, with coordinated rhythmic tongue and jaw movements (licking and chewing) being most sensitive. The neurological basis for this differential sensitivity remains unclear. Internal Rowan funds to Dr. Gould supported this work. This is the full abstract presented at the American Physiology Summit 2024 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.
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在帕金森病大鼠鱼藤酮模型中,口服阶段的所有进食成分都不会损害运动功能
高达 90% 的帕金森病患者会出现病理性吞咽或吞咽困难。在这种疾病中,进食功能障碍的严重程度和范围差异很大。进食是一个多步骤的神经肌肉过程,其中包括紧密协调的口面部行为--运输、减少食物、咽部吞咽--涉及多个肌肉骨骼系统--舌、下颌肌、舌咽肌,由多个颅神经和颈脊神经支配。摄入食物的种类会进一步影响这一顺序。杀虫剂鱼藤酮是一种线粒体抑制剂,从流行病学角度看,它与帕金森病有关。本项目的目标是确定帕金森病神经变性如何影响动物模型中的这一序列。我们假设,并非该序列的所有元素都会受到同样的影响。12 只年轻的成年雄性 Lewis 大鼠每天腹腔注射 2.75 毫克/千克鱼藤酮或药物对照,共注射 8 天。训练大鼠在高速(200 帧/秒)视频荧光屏前吃早餐谷物和喝混有钡的水。通过高速视频记录,测量每个个体在第 0 天(注射前)、第 1 天、第 4 天和第 7 天多次吞咽固体食物的口腔内运输和咀嚼持续时间,以及舔饮液体的持续时间。第 8 天对动物进行脑灌注,收获大脑并切片,用纹状体酪氨酸羟化酶免疫荧光标记物染色,以确认模型的有效性。混合模型方差分析用于检验阶段持续时间随治疗过程而变化的假设。对照组和经鱼藤酮处理的动物的口腔内运输持续时间均无变化(p=0.1136),但经鱼藤酮处理的大鼠的咀嚼持续时间仅在第 4 天时有所增加(p<0.001)。饮液大鼠的舔食持续时间从第 0 天开始增加。在帕金森病大鼠的鱼藤酮模型中,口腔进食过程的不同组成部分在受损程度和时间上各不相同,其中舌头和下颌的协调节律运动(舔食和咀嚼)最为敏感。这种不同敏感性的神经学基础尚不清楚。古尔德博士的罗文内部基金支持了这项工作。本文是在 2024 年美国生理学峰会(American Physiology Summit 2024)上发表的摘要全文,只有 HTML 格式。本摘要没有附加版本或附加内容。生理学》未参与同行评审过程。
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来源期刊
Physiology
Physiology 医学-生理学
CiteScore
14.50
自引率
0.00%
发文量
37
期刊介绍: Physiology journal features meticulously crafted review articles penned by esteemed leaders in their respective fields. These articles undergo rigorous peer review and showcase the forefront of cutting-edge advances across various domains of physiology. Our Editorial Board, comprised of distinguished leaders in the broad spectrum of physiology, convenes annually to deliberate and recommend pioneering topics for review articles, as well as select the most suitable scientists to author these articles. Join us in exploring the forefront of physiological research and innovation.
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