实验动物高血压遗传模型。

Y Yagil, C Yagil
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引用次数: 14

摘要

遗传动物模型是阐明高血压的病理生理和遗传基础的核心。大鼠是实验性高血压的主要物种。高血压大鼠模型有多种,包括自交系、同源系、转基因动物和重组自交系。这些模型中的每一个都被设计来表达不同的表型,包括自发性高血压、盐敏感性、应激敏感性和终末器官损伤的易感性。所有这些模型在寻找高血压的生理机制方面都非常有用,但其中一些模型是专门为检测高血压基因而设计的。后一项任务在自发性高血压中非常复杂,但遗传动物模型可以通过关注特定表型来简化这项任务。尽管经过近30年的努力,高血压的遗传基础至今尚未在大鼠或其他物种中揭晓。最近大鼠基因组的密集定位,分子遗传学新策略和新技术的发展,包括差异基因表达,表达序列标签和DNA生物芯片,使人们希望鉴定新的高血压候选基因的艰巨任务将向前迈进一大步。一旦确定了这些基因,就必须利用功能基因组策略和生物信息学来确定它们在高血压中的功能和作用。最后,在高血压遗传动物模型中的发现将不得不通过同源性和合成作图策略外推到人类。
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Genetic models of hypertension in experimental animals.

Genetic animal models are central to ongoing efforts to elucidate the pathophysiology and genetic basis of hypertension. The rat is the leading species in experimental hypertension. Several rat models of hypertension are available for research, including inbred strains, congenic lines, transgenic animals and recombinant inbred strains. Each of these models has been designed to express different phenotypes, including spontaneous hypertension, salt sensitivity, stress sensitivity and susceptibility to end-organ damage. All these models have been extremely useful in the search for the physiological mechanisms that underlie hypertension, but some of them have been specifically designed for detecting the hypertension genes. This latter task is extremely complex in spontaneous hypertension, but genetic animal models may simplify the task by enabling to focus on specific phenotypes. Despite intensive efforts over nearly 3 decades, the genetic basis of hypertension has not been unveiled so far in the rat or in other species. Recent dense mapping of the rat genome, the development of new strategies and technologies in molecular genetics including differential gene expression, expressed sequence tags and DNA biochips render hope that the formidable task of identification of new candidate genes in hypertension will move another major step forward. Once these genes are identified, their function and role in hypertension will have to be determined, utilizing functional genomic strategies and bioinformatics. Finally, the findings in genetic animal models of hypertension will have to be extrapolated to humans by homology and syntenic mapping strategies.

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