Key result
Specific triple-mutant lipoprotein pigs develop severe hypercholesterolemia and extensive three-vessel coronary atherosclerosis by 7 months.
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A strain of pigs bearing three immunogenetically defined lipoprotein-associated markers (allotypes), designated Lpb5, Lpr1, and Lpu1, has marked hypercholesterolemia on a low fat, cholesterol-free diet. Unlike individuals with familial hypercholesterolemia or WHHL rabbits, the affected pigs have normal low density lipoprotein receptor activity. The animals, by 7 months of age, have extensive atherosclerotic lesions in all three coronary arteries. This strain of pig represents an animal model for atherosclerosis and hypercholesterolemia associated with mutations affecting the structures of plasma lipoproteins. One of the variant apolipoproteins, Lpb5, is apolipoprotein-B. A second variant apolipoprotein (Lpr1), termed apo-R, is a 23-kilodalton protein present in both the very low density (d less than 1.006 g/ml) and the very high density (d greater than 1.21 g/ml) fractions of pig plasma. Isoforms of this protein correlate with two Lpr alleles, Lpr1 and Lpr2. The Lpr genes segregate independently of the Lpb5 and Lpu1 alleles. The Lpu1 allotype is a component of low density lipoprotein and is genetically linked to Lpb5.
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Rapacz et al. (1986) studied Hypercholesterolemia and atherosclerosis. Lipoprotein mutations (Lpb5, Lpr1, and Lpu1 allotypes) was evaluated on Hypercholesterolemia and coronary artery atherosclerotic lesions. Pigs bearing Lpb5, Lpr1, and Lpu1 lipoprotein mutations develop marked hypercholesterolemia and extensive atherosclerotic lesions in all 3 coronary arteries by 7 months of age.
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