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退行性悬韧带腱炎是一种以蛋白聚糖积聚为特征的全身性疾病。

Degenerative suspensory ligament desmitis as a systemic disorder characterized by proteoglycan accumulation.

作者信息

Halper Jaroslava, Kim Byoungjae, Khan Ahrar, Yoon Jung Hae, Mueller P O Eric

机构信息

Department of Pathology, College of Veterinary Medicine, The University of Georgia, Athens, GA 30602, USA.

出版信息

BMC Vet Res. 2006 Apr 12;2:12. doi: 10.1186/1746-6148-2-12.

Abstract

BACKGROUND

Degenerative suspensory ligament desmitis (DSLD) is a debilitating disorder thought to be limited to suspensory ligaments of Peruvian Pasos, Peruvian Paso crosses, Arabians, American Saddlebreds, American Quarter Horses, Thoroughbreds, and some European breeds. It frequently leads to persistent, incurable lameness and need to euthanize affected horses. The pathogenesis remains unclear, though the disease appears to run in families. Treatment and prevention are empirical and supportive, and not effective in halting the progression of the disease. Presently, the presumptive diagnosis of DSLD is obtained from patient signalment and history, clinical examination, and ultrasonographic examination of clinically affected horses, and is confirmed at post mortem examination. Presently, there are no reliable methods of diagnosing DSLD in asymptomatic horses. The goal of this study was to characterize and define the disorder in terms of tissue involvement at the macroscopic and microscopic levels.

RESULTS

We examined tissues and organs from 28 affected horses (22 Peruvian Pasos, 6 horses of other breeds) and from 8 control horses. Histopathological examination revealed the presence of excessive amounts of proteoglycans in the following tissues removed from DSLD-affected horses: suspensory ligaments, superficial and deep digital flexor tendons, patellar and nuchal ligaments, cardiovascular system, and sclerae. Electron microscopy demonstrated changes in diameters of collagen fibrils in the tendon, and in smooth muscle cells of the media of the aorta compatible with increased cell permeability in DSLD-affected cells. Separation of tendon extracts by gel chromatography revealed the presence of additional proteoglycan(s) in extracts from affected, but not control extracts.

CONCLUSION

This study demonstrates for the first time that DSLD, a disease process previously thought to be limited to the suspensory ligaments of the distal limbs of affected horses, is in fact a systemic disorder involving tissues and organs with significant connective tissue component. Abnormal accumulation of proteoglycans between collagen and elastic fibers rather than specific collagen fibril abnormalities is the most prominent histological feature of DSLD. Because of this observation and because of the involvement of many other tendons and ligaments beside the suspensory ligament, and of non-ligamentous tissue we, therefore, propose that equine systemic proteoglycan accumulation or ESPA rather than DSLD is a more appropriate name for this condition.

摘要

背景

退行性悬韧带腱炎(DSLD)是一种使人衰弱的疾病,被认为仅限于秘鲁帕索马、秘鲁帕索杂交马、阿拉伯马、美国鞍马、美国夸特马、纯种马以及一些欧洲品种马的悬韧带。它常导致持续无法治愈的跛行,患病马匹往往需要实施安乐死。尽管该病似乎具有家族遗传性,但其发病机制仍不清楚。治疗和预防措施都是经验性的且只是支持性的,无法有效阻止疾病进展。目前,DSLD的推测性诊断是根据患病马匹的病史、临床检查以及对临床患病马匹的超声检查做出的,并在尸检时得到证实。目前,尚无可靠方法用于诊断无症状马匹是否患有DSLD。本研究的目的是从宏观和微观层面的组织受累情况来描述和界定这种疾病。

结果

我们检查了28匹患病马(22匹秘鲁帕索马,6匹其他品种马)以及8匹对照马的组织和器官。组织病理学检查显示,从患有DSLD的马匹身上取下的以下组织中存在过量蛋白聚糖:悬韧带、浅深指屈肌腱、髌韧带和项韧带、心血管系统以及巩膜。电子显微镜检查显示,患病马匹的肌腱中胶原纤维直径以及主动脉中膜平滑肌细胞发生了变化,这与患病细胞中细胞通透性增加相符。通过凝胶色谱法分离肌腱提取物发现,患病马匹提取物中存在额外的蛋白聚糖,而对照提取物中没有。

结论

本研究首次表明,DSLD这种此前被认为仅限于患病马匹远端肢体悬韧带的疾病过程,实际上是一种涉及具有大量结缔组织成分的组织和器官的全身性疾病。蛋白聚糖在胶原纤维和弹性纤维之间异常蓄积而非特定胶原纤维异常,是DSLD最显著的组织学特征。基于这一观察结果,以及除悬韧带外还有许多其他肌腱和韧带以及非韧带组织受累,因此我们提议将马全身性蛋白聚糖蓄积症(ESPA)而非DSLD作为这种病症更合适的名称。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0fa1/1459153/150ca060b64e/1746-6148-2-12-1.jpg

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