Glomerular losartan (DuP 753)-sensitive angiotensin II receptor density is increased in young spontaneously hypertensive rats

R. M. Haws, P. W. Shaul, B. S. Arant, B. A. Atiyeh, M. G. Seikaly

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14 Scopus citations


There is increasing evidence that an activated intrarenal renin- angiotensin system (RAS) alters renal hemodynamics and fluid balance and that such events may lead to the development of hypertension. To examine the role of the glomerular RAS in the development of hypertension in the spontaneously hypertensive (SHR) rat, we studied angiotensin (ANG) II receptors in isolated glomeruli from young (4- to 5-wk-old) and adult (10- to 12-wk-old) SHR and from age-matched, normotensive Wistar-Kyoto (WKY) rats. Glomerular ANG II receptor density in young SHR is 3-fold higher than in age-matched WKY rats (2033 ± 154 versus 742 ± 151 receptors/μm2; p < 0.05) and 1.5-fold higher than in adult SHR and WKY rats (1128 ± 85 and 1198 ± 181 receptors/μm2, respectively; p < 0.05). Additional studies demonstrated that the differences in receptor density are not related to disparity in receptor occupancy and that they are also independent of systemic ANG levels. Suppression of RAS by ANG converting enzyme inhibitors resulted in a 3-fold increase in receptor density in young SHR rats and a 4.5-fold increase in young WKY rats; receptor density remained greater in young SHR rats (5915 ± 318 versus 3358 ± 234 receptors/μm2, p < 0.05). Furthermore, competitive binding experiments using the nonpeptide ANG II antagonists losartan (AT1) and PD 123319 (AT2) indicate that the greater ANG II receptor density in the young SHR rats represents an increase in the number of a single population of AT1 receptors. We postulate that increased glomerular ANG II receptor density in the young SHR rats may contribute to the initiation of hypertension in this animal model.

Original languageEnglish (US)
Pages (from-to)671-676
Number of pages6
JournalPediatric Research
Issue number6
Publication statusPublished - 1994


ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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