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Atherogenesis and metabolic dysregulation in LDL receptor-knockout rats.

Authors: Sithu, Srinivas D  Malovichko, Marina V  Riggs, Krista A  Wickramasinghe, Nalinie S  Winner, Millicent G  Agarwal, Abhinav  Hamed-Berair, Rihab E  Kalani, Anuradha  Riggs, Daniel W  Bhatnagar, Aruni  Srivastava, Sanjay 
Citation: Sithu SD, etal., JCI Insight. 2017 May 4;2(9). pii: 86442. doi: 10.1172/jci.insight.86442.
Pubmed: (View Article at PubMed) PMID:28469073
DOI: Full-text: DOI:10.1172/jci.insight.86442

Mechanisms of atherogenesis have been studied extensively in genetically engineered mice with disturbed cholesterol metabolism such as those lacking either the LDL receptor (Ldlr) or apolipoprotein E (apoe). Few other animal models of atherosclerosis are available. WT rabbits or rats, even on high-fat or high-cholesterol diets, develop sparse atherosclerotic lesions. We examined the effects of Ldlr deletion on lipoprotein metabolism and atherosclerotic lesion formation in Sprague-Dawley rats. Deletion of Ldlr resulted in the loss of the LDLR protein and caused a significant increase in plasma total cholesterol and triglycerides. On normal chow, Ldlr-KO rats gained more weight and were more glucose intolerant than WT rats. Plasma proprotein convertase subtilisin kexin 9 (PCSK9) and leptin levels were higher and adiponectin levels were lower in KO than WT rats. On the Western diet, the KO rats displayed exaggerated obesity and age-dependent increases in glucose intolerance. No appreciable aortic lesions were observed in KO rats fed normal chow for 64 weeks or Western diet for 16 weeks; however, after 34-52 weeks of Western diet, the KO rats developed exuberant atherosclerotic lesions in the aortic arch and throughout the abdominal aorta. The Ldlr-KO rat may be a useful model for studying obesity, insulin resistance, and early-stage atherosclerosis.


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CRRD Object Information
CRRD ID: 12910100
Created: 2017-06-08
Species: All species
Last Modified: 2017-06-08
Status: ACTIVE


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