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Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals

OBJECTIVE: Oxidized cholesterol derivatives are thought to exert atherogenic effect thus adversely affecting vascular endothelium. The aim of the study was to assess the effect of 5α,6α-epoxycholesterol on experimentally induced hypercholesterolemia in rabbits, and the levels of homocysteine (HCY),...

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Autores principales: Wielkoszyński, Tomasz, Zalejska-Fiolka, Jolanta, Strzelczyk, Joanna K., Owczarek, Aleksander J., Cholewka, Armand, Furmański, Marcin, Stanek, Agata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866902/
https://www.ncbi.nlm.nih.gov/pubmed/29713239
http://dx.doi.org/10.1155/2018/2784701
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author Wielkoszyński, Tomasz
Zalejska-Fiolka, Jolanta
Strzelczyk, Joanna K.
Owczarek, Aleksander J.
Cholewka, Armand
Furmański, Marcin
Stanek, Agata
author_facet Wielkoszyński, Tomasz
Zalejska-Fiolka, Jolanta
Strzelczyk, Joanna K.
Owczarek, Aleksander J.
Cholewka, Armand
Furmański, Marcin
Stanek, Agata
author_sort Wielkoszyński, Tomasz
collection PubMed
description OBJECTIVE: Oxidized cholesterol derivatives are thought to exert atherogenic effect thus adversely affecting vascular endothelium. The aim of the study was to assess the effect of 5α,6α-epoxycholesterol on experimentally induced hypercholesterolemia in rabbits, and the levels of homocysteine (HCY), asymmetric dimethylarginine (ADMA), paraoxonase-1 (PON-1), and inflammatory parameters (IL-6, TNF-α, CRP). MATERIAL AND METHODS: The rabbits were divided into 3 groups, 8 animals each, and fed with basic fodder (C), basic fodder plus cholesterol (Ch) or basic fodder plus 5α,6α-epoxycholesterol, and unoxidized cholesterol (ECh). Serum concentrations of studied parameters were determined at 45-day intervals. The study was continued for six months. RESULTS: We demonstrated that adding 5α,6α-epoxycholesterol to basic fodder significantly affected lipid status of the experimental animals, increasing total cholesterol and LDL cholesterol levels, as well as HCY and ADMA levels, whilst leaving the PON-1 activity unaffected. Additionally, the ECh group presented with significantly higher concentrations of inflammatory biomarkers (IL-6, TNF-α, and CRP). In the Ch group, lower yet significant (as compared to the C group) changes of levels of studied parameters were observed. CONCLUSION: Exposure of animals with experimentally induced hypercholesterolemia to 5α,6α-epoxycholesterol increases dyslipidaemia, endothelial dysfunction, and inflammatory response.
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spelling pubmed-58669022018-04-30 Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals Wielkoszyński, Tomasz Zalejska-Fiolka, Jolanta Strzelczyk, Joanna K. Owczarek, Aleksander J. Cholewka, Armand Furmański, Marcin Stanek, Agata Mediators Inflamm Research Article OBJECTIVE: Oxidized cholesterol derivatives are thought to exert atherogenic effect thus adversely affecting vascular endothelium. The aim of the study was to assess the effect of 5α,6α-epoxycholesterol on experimentally induced hypercholesterolemia in rabbits, and the levels of homocysteine (HCY), asymmetric dimethylarginine (ADMA), paraoxonase-1 (PON-1), and inflammatory parameters (IL-6, TNF-α, CRP). MATERIAL AND METHODS: The rabbits were divided into 3 groups, 8 animals each, and fed with basic fodder (C), basic fodder plus cholesterol (Ch) or basic fodder plus 5α,6α-epoxycholesterol, and unoxidized cholesterol (ECh). Serum concentrations of studied parameters were determined at 45-day intervals. The study was continued for six months. RESULTS: We demonstrated that adding 5α,6α-epoxycholesterol to basic fodder significantly affected lipid status of the experimental animals, increasing total cholesterol and LDL cholesterol levels, as well as HCY and ADMA levels, whilst leaving the PON-1 activity unaffected. Additionally, the ECh group presented with significantly higher concentrations of inflammatory biomarkers (IL-6, TNF-α, and CRP). In the Ch group, lower yet significant (as compared to the C group) changes of levels of studied parameters were observed. CONCLUSION: Exposure of animals with experimentally induced hypercholesterolemia to 5α,6α-epoxycholesterol increases dyslipidaemia, endothelial dysfunction, and inflammatory response. Hindawi 2018-03-11 /pmc/articles/PMC5866902/ /pubmed/29713239 http://dx.doi.org/10.1155/2018/2784701 Text en Copyright © 2018 Tomasz Wielkoszyński et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wielkoszyński, Tomasz
Zalejska-Fiolka, Jolanta
Strzelczyk, Joanna K.
Owczarek, Aleksander J.
Cholewka, Armand
Furmański, Marcin
Stanek, Agata
Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title_full Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title_fullStr Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title_full_unstemmed Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title_short Oxysterols Increase Inflammation, Lipid Marker Levels and Reflect Accelerated Endothelial Dysfunction in Experimental Animals
title_sort oxysterols increase inflammation, lipid marker levels and reflect accelerated endothelial dysfunction in experimental animals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5866902/
https://www.ncbi.nlm.nih.gov/pubmed/29713239
http://dx.doi.org/10.1155/2018/2784701
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