| Literature DB >> 26549014 |
Satoru Morishita1,2, Hiroaki Kawaguchi3, Tomoji Ono1,4, Naoki Miura5, Michiaki Murakoshi1,6, Keikichi Sugiyama1,7, Hisanori Kato2, Akihide Tanimoto3, Hoyoku Nishino6.
Abstract
Previously, we found that enteric lactoferrin (eLF) could reduce the visceral fat accumulation known to associate strongly with metabolic syndrome symptoms and consequently with an increased risk of atherosclerosis. In this study, the atherosclerosis-preventive potential of LF was assessed in a high-fat and high-cholesterol diet (HFCD)-induced hypercholesterolemia and atherosclerosis model using Microminipig™. Eight-week orally administered eLF remarkably reduced the HFCD-induced serum total and low-density lipoprotein cholesterol levels but not high-density lipoprotein cholesterol levels. A histological analysis of 15 arteries revealed that eLF systemically inhibited the development of atherosclerotic lesions. Pathway analysis using identified genes that characterized eLF administration in liver revealed significant changes in the steroid biosynthesis pathway (ssc00100) and all affected genes in this pathway were upregulated, suggesting that cholesterol synthesis inhibited by HFCD was recovered by eLF. In summary, eLF could potentially prevent the hypercholesterolemia and atherosclerosis through protecting homeostasis from HFCD-induced dysfunction of cholesterol metabolism.Entities:
Keywords: DNA microarray; LDL cholesterol; atherosclerosis; lactoferrin; microminipig
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Year: 2015 PMID: 26549014 DOI: 10.1080/09168451.2015.1091713
Source DB: PubMed Journal: Biosci Biotechnol Biochem ISSN: 0916-8451 Impact factor: 2.043