Claramunt Débora, Gil-Peña Helena, Fuente Rocío, Hernández-Frías Olaya, Santos Fernando
University of Oviedo, Spain.
Hospital Universitario Central de Asturias, Spain.
Nefrologia. 2015 Nov-Dec;35(6):517-22. doi: 10.1016/j.nefro.2015.08.004. Epub 2015 Oct 29.
Pediatric chronic kidney disease (CKD) has peculiar features. In particular, growth impairment is a major clinical manifestation of CKD that debuts in pediatric age because it presents in a large proportion of infants and children with CKD and has a profound impact on the self-esteem and social integration of the stunted patients. Several factors associated with CKD may lead to growth retardation by interfering with the normal physiology of growth plate, the organ where longitudinal growth rate takes place. The study of growth plate is hardly possible in humans and justifies the use of animal models. Young rats made uremic by 5/6 nephrectomy have been widely used as a model to investigate growth retardation in CKD. This article examines the characteristics of this model and analyzes the utilization of CKD induced by high adenine diet as an alternative research protocol.
小儿慢性肾脏病(CKD)具有独特的特征。特别是,生长发育迟缓是CKD的主要临床表现,始于儿童期,因为它在很大比例的CKD婴幼儿和儿童中出现,并对发育迟缓患者的自尊和社会融入产生深远影响。与CKD相关的几个因素可能通过干扰生长板的正常生理功能导致生长发育迟缓,生长板是纵向生长速率发生的器官。在人体中很难对生长板进行研究,这就说明了使用动物模型的合理性。通过5/6肾切除术导致尿毒症的幼鼠已被广泛用作研究CKD生长发育迟缓的模型。本文研究了该模型的特点,并分析了高腺嘌呤饮食诱导的CKD作为替代研究方案的应用。