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杜氏肌营养不良症(DMSXL)转基因小鼠模型呼吸衰竭的功能和组织病理学鉴定。

Functional and histopathological identification of the respiratory failure in a DMSXL transgenic mouse model of myotonic dystrophy.

机构信息

Department of Clinical Neurosciences, University Hospital, 1011 Lausanne, Switzerland.

出版信息

Dis Model Mech. 2013 May;6(3):622-31. doi: 10.1242/dmm.010512. Epub 2012 Nov 23.

Abstract

Acute and chronic respiratory failure is one of the major and potentially life-threatening features in individuals with myotonic dystrophy type 1 (DM1). Despite several clinical demonstrations showing respiratory problems in DM1 patients, the mechanisms are still not completely understood. This study was designed to investigate whether the DMSXL transgenic mouse model for DM1 exhibits respiratory disorders and, if so, to identify the pathological changes underlying these respiratory problems. Using pressure plethysmography, we assessed the breathing function in control mice and DMSXL mice generated after large expansions of the CTG repeat in successive generations of DM1 transgenic mice. Statistical analysis of breathing function measurements revealed a significant decrease in the most relevant respiratory parameters in DMSXL mice, indicating impaired respiratory function. Histological and morphometric analysis showed pathological changes in diaphragmatic muscle of DMSXL mice, characterized by an increase in the percentage of type I muscle fibers, the presence of central nuclei, partial denervation of end-plates (EPs) and a significant reduction in their size, shape complexity and density of acetylcholine receptors, all of which reflect a possible breakdown in communication between the diaphragmatic muscles fibers and the nerve terminals. Diaphragm muscle abnormalities were accompanied by an accumulation of mutant DMPK RNA foci in muscle fiber nuclei. Moreover, in DMSXL mice, the unmyelinated phrenic afferents are significantly lower. Also in these mice, significant neuronopathy was not detected in either cervical phrenic motor neurons or brainstem respiratory neurons. Because EPs are involved in the transmission of action potentials and the unmyelinated phrenic afferents exert a modulating influence on the respiratory drive, the pathological alterations affecting these structures might underlie the respiratory impairment detected in DMSXL mice. Understanding mechanisms of respiratory deficiency should guide pharmaceutical and clinical research towards better therapy for the respiratory deficits associated with DM1.

摘要

急性和慢性呼吸衰竭是肌强直性营养不良 1 型(DM1)患者的主要潜在致命特征之一。尽管有几项临床研究表明 DM1 患者存在呼吸问题,但这些机制仍不完全清楚。本研究旨在探讨 DM1 的 DMSXL 转基因小鼠模型是否存在呼吸障碍,如果存在,确定这些呼吸问题的基础病理变化。我们使用压力容积描记法评估了对照组小鼠和经过几代 DM1 转基因小鼠中 CTG 重复序列大量扩增后产生的 DMSXL 小鼠的呼吸功能。对呼吸功能测量的统计分析显示,DMSXL 小鼠的大多数相关呼吸参数显著下降,表明呼吸功能受损。组织学和形态计量学分析显示 DMSXL 小鼠膈肌存在病理变化,特征为 I 型肌纤维比例增加、中央核存在、终板(EP)部分去神经支配以及其大小、形状复杂性和乙酰胆碱受体密度显著降低,所有这些都反映了膈肌纤维和神经末梢之间的通讯可能中断。膈肌肌肉异常伴有肌纤维核中突变 DMPK RNA 焦点的积累。此外,在 DMSXL 小鼠中,无髓肋间传入神经明显减少。在这些小鼠中,颈椎膈神经运动神经元或脑干呼吸神经元也未检测到明显的神经元病。因为 EP 参与动作电位的传递,无髓肋间传入神经对呼吸驱动施加调节影响,所以影响这些结构的病理改变可能是 DMSXL 小鼠呼吸障碍的基础。了解呼吸缺陷的机制应该指导药物和临床研究,以寻求更好的治疗 DM1 相关呼吸缺陷的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c86/3634646/ce954e0324ea/DMM010512F1.jpg

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