Genetic differences in cholesterol absorption in 129/Sv and C57BL/6 mice: effect on cholesterol responsiveness
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This study compared the cholesterolemic response of two strains of mice with genetically determined differences in cholesterol absorption. When fed a basal low-cholesterol diet, 129/Sv mice absorbed cholesterol twice as efficiently as did C57BL/6 mice (44% vs. 20%). Total lipid absorption, in contrast, averaged 80–82% in both strains. The higher level of cholesterol absorption in the 129/Sv animals was reflected in an adaptive reduction in hepatic and intestinal sterol synthesis. When fed lipid-enriched diets, the 129/Sv mice became significantly more hypercholesterolemic and had twofold higher hepatic cholesterol concentrations than did the C57BL/6 animals even though the conversion of cholesterol to bile acids was stimulated equally in both strains. The difference in cholesterol absorption between these mouse strains was not the result of physicochemical factors relating to the size and composition of the intestinal bile acid pool but more likely reflects an inherited difference in one or more of the biochemical steps that facilitate the translocation of sterol across the epithelial cell.
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The C57BL/6J inbred strain and the 129/Sv substrains inherently manage peripheral cholesterol metabolism differently.
“The C57BL/6J inbred strain and the 129/Sv substrains inherently manage peripheral cholesterol metabolism differently36.”
From A suppressor screen in Mecp2 mutant mice implicates cholesterol metabolism in Rett syndrome (2013) · cites this paper as [36]
The Results report an inherent difference in cholesterol absorption between 129/Sv and C57BL/6 mice, with corresponding differences in intestinal and liver cholesterol synthesis and in plasma and liver responses to cholesterol-rich diets. The Discussion says the higher absorption also appears in other 129 sublines. The paper does not establish a difference in cholesterol metabolism across peripheral tissues generally, so the claim is broader than the findings. (LLM, conf=0.82)
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Self-citation
- Authors
- Jolley, C. D., Dietschy, J. M., & Turley, S. D.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Venue
- American Journal of Physiology-Gastrointestinal and Liver Physiology
- Publisher
- American Physiological Society
- Published
- 1999-05-01
- Volume
- 276
- Issue
- 5
- Pages
- G1117-G1124
- ISSN
- 0193-1857 (ISSN-L)
- 1522-1547
- OpenAlex
- W2188696427
- Cited by
- 53
- References
- 0
- Citations by year
- 2022: 1 · 2021: 2 · 2020: 2 · 2019: 1 · 2017: 1 · 2016: 2 · 2015: 1 · 2014: 1 · 2013: 3 · 2012: 2
- FWCI
- 6.24
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- American Journal of Physiology-Gastrointestinal and Liver Physiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Heart, Lung, and Blood Institute (HL09610)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK 07745)
- Topics
- Health Sciences › Medicine › Surgery › Cholesterol and Lipid Metabolism
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Lipid metabolism and disorders
- Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
- Keywords
- cholesterol absorption, 129/Sv mice, C57BL/6 mice, genetic strain differences, bile acid synthesis, hypercholesterolemia, fat absorption, bile acid pool
- MeSH terms
- Animals, Bile Acids and Salts, Cholesterol, Cholesterol Esters, Cholesterol, Dietary, Fasting, Feces, Hypercholesterolemia, Intestinal Absorption, Intestinal Mucosa, Liver, Mice, Inbred C57BL, Species Specificity, Sterols, Lipid Metabolism, Mice
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