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Calcium transport and vitamin D in three breeds of spontaneously hypertensive rats.
Author(s) -
Harold P. Schedl,
Helen Wilson,
R.L. Horst
Publication year - 1988
Publication title -
hypertension
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.986
H-Index - 265
eISSN - 1524-4563
pISSN - 0194-911X
DOI - 10.1161/01.hyp.12.3.310
Subject(s) - medicine , endocrinology , calcium , sodium , chemistry , vitamin d and neurology , receptor , breeder (animal) , organic chemistry , archaeology , blanket , history
Conflicting results have been published by different laboratories comparing the rate of intestinal calcium transport and concentration of circulating 1,25-dihydroxyvitamin D (1,25-[OH]2D) in the spontaneously hypertensive rat (SHR) and control Wistar-Kyoto rat (WKY): They have been reported to be greater, the same, or lower in the SHR than in the WKY. We tested the possibility that the conflicting results might be breeder-related by measuring 1) the rate of intestinal mucosal calcium transport, 2) the concentration of circulating 25-hydroxyvitamin D (25-OH-D) and 1,25-(OH)2D, and 3) the concentration of intestinal mucosal receptor for 1,25-(OH)2D in the two strains of animals from three different breeders. Sodium and water transport were also measured because of their relevance to hypertension. Blood pressure was always higher and calcium, as well as mean sodium and water transport, was always lower in the SHR than in the WKY. The concentration of 1,25-(OH)2D was the same, higher, or lower in the SHR than in the WKY and was age- and breeder-dependent. Mean mucosal 1,25-(OH)2D receptor concentration was higher in the SHR and was variable, depending on breeder. We conclude that 1) the rate of calcium transport is lower in the SHR than in the WKY and independent of breeder and concentration of 1,25-(OH)2D in serum, 2) the variability in 1,25-(OH)2D concentration among investigators may be breeder-dependent, and 3) the higher receptor concentration in the intestinal mucosa of the SHR could be a compensatory response to the decreased rate of calcium transport. These differences in calcium and sodium transport may be an expression in the enterocyte of factors etiological for hypertension.

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