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Hypertension. 1998;32:223-227

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(Hypertension. 1998;32:223-227.)
© 1998 American Heart Association, Inc.


Scientific Contributions

Effect of Genetic Deficiency of Angiotensinogen on the Renin-Angiotensin System

Kouichi Tamura; Satoshi Umemura; Yoichi Sumida; Nobuo Nyui; Shun-ichi Kobayashi; Tomoaki Ishigami; Minoru Kihara; Takeshi Sugaya; Akiyoshi Fukamizu; Hitoshi Miyazaki; Kazuo Murakami; ; Masao Ishii

From the Department of Internal Medicine II, Yokohama City University School of Medicine, Yokohama (K.T., S.U., Y.S., N.N., S.K., T.I., M.K., M.I.); Lead Generation Research Laboratories, Tanabe Seiyaku Co, Ltd, Osaka (T.S.); and the Institute of Applied Biochemistry (A.F., K.M.) and Gene Experiment Center (H.M.), University of Tsukuba, Ibaraki, Japan.

Correspondence to Kouichi Tamura, MD, Department of Internal Medicine II, Yokohama City University School of Medicine, 3–9, Fukuura, Kanazawa-ku, Yokohama 236, Japan. E-mail tamukou{at}yellow.med.yokohama-cu.ac.jp

Abstract—This study examined expression of renin-angiotensin system (RAS) component mRNAs in angiotensinogen gene knockout (Atg-/-) mice. Wild-type (Atg+/+) and Atg-/- mice were fed a normal-salt (0.3% NaCl) or high-salt (4% NaCl) diet for 2 weeks. Angiotensinogen, renin, angiotensin-converting enzyme (ACE), angiotensin II type 1a receptor (AT1A), and angiotensin II type 2 receptor (AT2) mRNA levels were measured by Northern blot analysis. In Atg+/+ mice, activities of circulating RAS and renal angiotensinogen mRNA level were decreased by salt loading, whereas levels of renal and cardiac ACE; renal, brain, and cardiac AT1A; and brain and cardiac AT2 mRNA were increased by salt loading. Although activities of circulating RAS were not detected in Atg-/- mice, salt loading increased blood pressure in Atg-/- mice. In Atg-/- mice, renal renin mRNA level was decreased by salt loading; in contrast, salt loading increased renal AT1A and cardiac AT2 mRNA levels in Atg-/- mice, and these activated levels in Atg-/- mice were higher than those in Atg+/+ mice fed the high-salt diet. Thus, expression of each component of the RAS is regulated in a tissue-specific manner that is distinct from other components of systemic and local RAS and that appears to be mediated by a mechanism other than changes in the circulating or tissue levels of angiotensin peptides.


Key Words: renin-angiotensin system • angiotensinogen • angiotensin-converting enzyme • receptors, angiotensin • RNA, messenger • sodium, dietary




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