Selection of Mouse Strains Showing High and Low Incidences of Alloxan-induced Diabetes
To produce an experimental model of diabetes in animals, ICR mice were inbred until the 20th generation by two-way selection toward the high-and low-incidences of alloxan-induced diabetes. Changes in successive generations in the incidence of such diabetes, in blood glucose levels, growth patterns a...
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Veröffentlicht in: | Experimental Animals 1991/01/01, Vol.40(1), pp.61-67 |
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Sprache: | eng |
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Zusammenfassung: | To produce an experimental model of diabetes in animals, ICR mice were inbred until the 20th generation by two-way selection toward the high-and low-incidences of alloxan-induced diabetes. Changes in successive generations in the incidence of such diabetes, in blood glucose levels, growth patterns and reproductive performance were studied. The incidence of alloxan-induced diabetes was 41.1% in the basal population ; in the high-incidence strain, it was 98.7% in F13, ranging between 90 and 99% in later generations ; and in the low-incidence strain, it reached 0 % in F 7, remaining near that level in later generations. The heritability of the incidence of alloxan-induced diabetes determined at the beginning of selection was 50-60%. The blood glucose level was 251 ± 19mg/dl in the basal population ; in the highincidence strain, it was 423±11mg/dl in F13, ranging thereafter between 340 and 455 mg/dl ; and in the low-incidence strain, it was 128±4mg/dl in F7, then varying from 120 to 140mg/dl in following generations. The heritability of the blood glucose level determined at the beginning of selection was 40-60%. No marked decrease in growth or reproductive performance accompanied successive selections. Successive generations of the high-incidence mice, however, tended to become heavier than the lowincidence animals. The high-and low-incidence strains, established in the 20 th generation, were named the ALS (alloxan-induced diabetes-susceptible) and ALR (alloxan-induced diabetes-resistant) strains, respectively. |
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ISSN: | 0007-5124 1881-7122 |
DOI: | 10.1538/expanim1978.40.1_61 |