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Strain: SHR

Symbol: SHR
Strain: SHR
Full Name: Spontaneously Hypertensive Rat
Ontology ID: RS:0000015
Alleles: Agtr1b;   Ephx2;   Cd36
Type: inbred
Source: Not Available
Origin: Okamoto 1963 from outbred Wistar Kyoto rats. Bred from a male with mild hypertension, mated with a female with high blood pressure. Brother x sister mating with continued selection for high blood pressure (Okamoto 1969, Okamoto et al 1972). A number of sublines have been developed with a tendency to develop cardiovascular lesions and stroke (see particularly SHRSP) (Nagaoka et al 1976), and hypercholesterolemia (Yamori 1984). For a recent review see Yamori, (1994). However, there is no evidence for substrain differentiation among SHR stocks from the major commercial suppliers in the USA both respect to phenotype and DNA fingerprints (Blizard et al, 1991). Strain WKY, developed from the same base populations is sometimes used as a normotensive control, though its use as such must be questioned as it differs at many genetic marker loci (Festing and Bender 1984, and see also strain WKY). Stelzin et al (1992) found that SHR and WKY shared only 50% of their DNA fingerprint bands, whereas SS and SR shared about 80% of bands. Most authorities suggest that WKY alone is not a good control strain, and that for most comparative studies several normotensive strains should be used. There is an extensive literature on the characteristics of SHR. DeJong (1984) provides a useful comparative review of this and other hypertensive strains, and there are regular symposia on hypertensive rat strains (see J. Hypertension 4(suppl):S1-S541, 1986, and Jpn. Heart J. 28:567-648).
Genetic Markers: c
Coat Color: Albino
Inbred Generations: F70 (NIH 1989)
Last Known Status: Unknown


Disease Annotations
Phenotype Annotations
Experimental Data Annotations
Phenotype Values via Phenominer
References - curated


Strain QTL Data

Additional Information

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RGD Object Information
RGD ID: 61000
Created: 2000-06-01
Species: Rattus norvegicus
Last Modified: 2000-06-01
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.