Rice Kevin M, Wu Miaozong, Blough Eric R
Department of Biological Sciences, College of Science, Marshall University, USA.
J Pharmacol Sci. 2008 Dec;108(4):393-8. doi: 10.1254/jphs.08r02cp.
Aging is now recognized as one of major risk factors for cardiovascular disease (CVD). It is well documented that elderly populations show increased incidence of CVD symptomology but whether these changes are directly related to aging is not well understood since the possibility exists that other age-associated pathologies in different organ systems could impact on cardiovascular function. Hence, the development of an aging model with reduced systemic illness could invigorate efforts to understand the direct role of aging in CVD progression. The Fischer 344 / NNIaHSD x Brown Norway / BiNia rat (F344BN) has been proposed as a potential model for aging that exhibits reduced systemic pathology and increased longevity compared to other models. Here we examine the current literature regarding the F344BN, focusing on age-associated changes in aortic structure and function.
衰老现已被公认为心血管疾病(CVD)的主要风险因素之一。有充分的文献记载,老年人群中心血管疾病症状的发生率有所增加,但这些变化是否与衰老直接相关尚不清楚,因为不同器官系统中其他与年龄相关的病理状况可能会影响心血管功能。因此,开发一种全身性疾病较少的衰老模型可以促进人们努力了解衰老在心血管疾病进展中的直接作用。Fischer 344 / NNIaHSD x Brown Norway / BiNia大鼠(F344BN)已被提议作为一种潜在的衰老模型,与其他模型相比,该模型表现出较少的全身性病理变化和更长的寿命。在此,我们研究了有关F344BN的现有文献,重点关注主动脉结构和功能与年龄相关的变化。