Literature DB >> 8454565

Comparative study of various genetic hypertensive rat strains: blood pressure, body weight, growth and organ weights.

M Kihara1, R Horie, W Lovenberg, Y Yamori.   

Abstract

In an attempt to compare various genetic strains of hypertensive rats, representative hypertensive strains and associated controls (male, 1-month-old, 6-10 of each strain and 18 strains in total) were collected at a single center (National Institutes of Health; NIH, United States), maintained under the same experimental conditions with normal sodium NIH open formula diet and studied by a single investigator using standard techniques. Animals were measured for blood pressure (BP) by a tail-cuff method without anesthesia and body weight (BW) at 10 and 12 weeks of age and killed to measure organ weights. Hypertension was severe (> 190 mmHg) in spontaneously hypertensive rats (SHR) and their stroke-prone substrains at 12 weeks of age but mild to moderate (145-160 mmHg) in the rest of the hypertensive strains (Dahl's, Milan, Lyon, Sabra, and New Zealand Strains). Regarding organ size, partial correlation analysis showed that organ weights, except for brain and adrenal glands, are good functions of BW and that weight of the left ventricle (LV) was the only one significantly linked to BP levels. A bivariate regression model for LV weight was obtained as follows: LV(mg) = 1.478 BW(g) + 2.13BP(mmHg) - 51(R = 0.878, P < 0.001). The presence of some genetic factor regulating relative organ size independently of BW and BP was suggested in LV weight as well as in the weight of the other organs. Among the strains, MHS was found to be unique for the smallest kidney size and New Zealand strains for the greatest relative LV size when adjusted to allow for the influence of BP.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1993        PMID: 8454565

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  15 in total

1.  Development of a strain of spontaneously hypertensive rats.

Authors:  K OKAMOTO; K AOKI
Journal:  Jpn Circ J       Date:  1963-03

2.  Molecular evidence of genetic heterogeneity in Wistar-Kyoto rats: implications for research with the spontaneously hypertensive rat.

Authors:  T W Kurtz; M Montano; L Chan; P Kabra
Journal:  Hypertension       Date:  1989-02       Impact factor: 10.190

3.  The hypertensive role of the kidney in spontaneously hypertensive rats.

Authors:  G Bianchi; U Fox; G F Di Francesco; U Bardi; M Radice
Journal:  Clin Sci Mol Med Suppl       Date:  1973-08

4.  Importance of genetic factors in stroke: an evidence obtained by selective breeding of stroke-prone and -resistant SHR.

Authors:  Y Yamori
Journal:  Jpn Circ J       Date:  1974-12

5.  Separation of two strains of rats with inbred dissimilar sensitivity to Doca-salt hypertension.

Authors:  D Ben-Ishay; R Saliternik; A Welner
Journal:  Experientia       Date:  1972-11-15

6.  Heart size in inbred strains of rats. Part 1. Genetic determination of the development of cardiovascular enlargement in rats.

Authors:  H Tanase; Y Yamori; C T Hansen; W Lovenberg
Journal:  Hypertension       Date:  1982 Nov-Dec       Impact factor: 10.190

7.  Hypothalamic pressor responses and salt-induced hypertension in Dahl rats.

Authors:  R D Buñag; J Butterfield; S Sasaki
Journal:  Hypertension       Date:  1983 Jul-Aug       Impact factor: 10.190

8.  Consequence of social isolation on blood pressure, cardiovascular reactivity and design in spontaneously hypertensive rats.

Authors:  M Hallbäck
Journal:  Acta Physiol Scand       Date:  1975-04

9.  Biological variability in Wistar-Kyoto rats. Implications for research with the spontaneously hypertensive rat.

Authors:  T W Kurtz; R C Morris
Journal:  Hypertension       Date:  1987-07       Impact factor: 10.190

10.  Development and characteristics of inbred strains of Dahl salt-sensitive and salt-resistant rats.

Authors:  J P Rapp; H Dene
Journal:  Hypertension       Date:  1985 May-Jun       Impact factor: 10.190

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  2 in total

1.  Congenic strain confirms putative quantitative trait locus for body weight in the rat.

Authors:  P Kovács; B Voigt; I Klöting
Journal:  Mamm Genome       Date:  1998-04       Impact factor: 2.957

2.  Cerebrovascular damage after midlife transient hypertension in non-transgenic and Alzheimer's disease rats.

Authors:  Aaron Y Lai; Illsung L Joo; Arunachala U Trivedi; Adrienne Dorr; Mary E Hill; Bojana Stefanovic; JoAnne McLaurin
Journal:  Brain Res       Date:  2021-02-12       Impact factor: 3.252

  2 in total

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