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高血压和低血压基因工程小鼠的开发。

Development of genetically engineered mice with hypertension and hypotension.

作者信息

Sugiyama F

机构信息

Laboratory Animal Research Center, University of Tsukuba, Ibaraki, Japan.

出版信息

Exp Anim. 1997 Jul;46(3):171-82. doi: 10.1538/expanim.46.171.

Abstract

Human essential hypertension is generally recognized as a multifactorial disease involving the interplay of environmental factors based on genetic diathesis. Spontaneously hypertensive rats (SHR) and Dahl rats are widely used as animal models for human essential hypertension and salt-sensitive hypertension, respectively. The definitive genetic factor ruling the development of hypertension in these strains remains unclear, but recently advances in embryonic engineering and molecular biological techniques may make it possible for transgenic mice and gene-targeted mice to become important pathological models defined genetically and functionally for human disease. The author developed two types of genetically engineered mice that may serve as such models: a transgenic mouse with hypertension caused by enhancing the renin-angiotensin system and a gene-targeted mouse with hypotension caused by disrupting the renin-angiotensin system.

摘要

原发性高血压通常被认为是一种多因素疾病,涉及基于遗传素质的环境因素之间的相互作用。自发性高血压大鼠(SHR)和 Dahl 大鼠分别被广泛用作人类原发性高血压和盐敏感性高血压的动物模型。决定这些品系高血压发展的决定性遗传因素仍不清楚,但最近胚胎工程和分子生物学技术的进展可能使转基因小鼠和基因敲除小鼠成为从基因和功能上定义人类疾病的重要病理模型。作者开发了两种可能用作此类模型的基因工程小鼠:一种通过增强肾素 - 血管紧张素系统导致高血压的转基因小鼠,以及一种通过破坏肾素 - 血管紧张素系统导致低血压的基因敲除小鼠。

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