Aims: Hyperlipidaemia model animals have been used to elucidate the role of infection in atherosclerosis. The aims of this study were to investigate the proatherogenic effect of multiple infections in ApoB100only/LDLR mice which based on lipid profile can be regarded as the most suitable mouse model of human hypercholesterolemia and to compare the lesion development to that in a major atherosclerosis model ApoE mice.
Methods And Results: Aorta samples of ApoB100only/LDLR mice infected three times with were subjected to morphometric analyses. Morphometric evaluation disclosed that infections exacerbated atherosclerosis development in the aortic root and descending aorta of the mice fed with normal diet. Viable Cpn was detected in the ascending aorta by RT-PCR. Chlamydial 16SrRNA expression showed the presence of viable in the aorta of infected animals. A similar rate of acceleration of atherosclerosis was observed when the infection protocol was applied in ApoB100only/LDLR and in ApoE mice.
Conclusion: Similar to ApoE mice, ApoB100only/LDLR mice with more human-relevant serum lipoprotein composition develop increased atherosclerosis after infections; thus this mouse strain can be used as a model of infection-related atherosclerosis enhancement and can provide further evidence for the proatherogenic influence of in mice.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5889898 | PMC |
http://dx.doi.org/10.1155/2018/8325915 | DOI Listing |
Biomed Res Int
September 2018
Department of Medical Microbiology and Immunobiology, University of Szeged, Dóm Tér 10, Szeged 6720, Hungary.
Aims: Hyperlipidaemia model animals have been used to elucidate the role of infection in atherosclerosis. The aims of this study were to investigate the proatherogenic effect of multiple infections in ApoB100only/LDLR mice which based on lipid profile can be regarded as the most suitable mouse model of human hypercholesterolemia and to compare the lesion development to that in a major atherosclerosis model ApoE mice.
Methods And Results: Aorta samples of ApoB100only/LDLR mice infected three times with were subjected to morphometric analyses.
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