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Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice

Background. Diabetes is associated with increased cardiovascular disease, but the underlying cellular and molecular mechanisms are poorly understood. One proposed mechanism is that diabetes aggravates atherosclerosis by enhancing plaque inflammation. The Akita mouse has recently been adopted as a re...

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Autores principales: Engelbertsen, Daniel, To, Fong, Dunér, Pontus, Kotova, Olga, Söderberg, Ingrid, Alm, Ragnar, Gomez, Maria F., Nilsson, Jan, Bengtsson, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515907/
https://www.ncbi.nlm.nih.gov/pubmed/23243415
http://dx.doi.org/10.1155/2012/176162
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author Engelbertsen, Daniel
To, Fong
Dunér, Pontus
Kotova, Olga
Söderberg, Ingrid
Alm, Ragnar
Gomez, Maria F.
Nilsson, Jan
Bengtsson, Eva
author_facet Engelbertsen, Daniel
To, Fong
Dunér, Pontus
Kotova, Olga
Söderberg, Ingrid
Alm, Ragnar
Gomez, Maria F.
Nilsson, Jan
Bengtsson, Eva
author_sort Engelbertsen, Daniel
collection PubMed
description Background. Diabetes is associated with increased cardiovascular disease, but the underlying cellular and molecular mechanisms are poorly understood. One proposed mechanism is that diabetes aggravates atherosclerosis by enhancing plaque inflammation. The Akita mouse has recently been adopted as a relevant model for microvascular complications of diabetes. Here we investigate the development of atherosclerosis and inflammation in vessels of Akita mice on LDLr (−/−) background. Methods and Results. Akita-LDLr (−/−) and LDLr (−/−) mice were fed high-fat diet from 6 to 24 weeks of age. Blood glucose levels were higher in both male and female Akita-LDLr (−/−) mice (137% and 70%, resp.). Male Akita-LDLr (−/−) mice had markedly increased plasma cholesterol and triglyceride levels, a three-fold increase in atherosclerosis, and enhanced accumulation of macrophages and T-cells in plaques. In contrast, female Akita-LDLr (−/−) mice demonstrated a modest 29% increase in plasma cholesterol and no significant increase in triglycerides, atherosclerosis, or inflammatory cells in lesions. Male Akita-LDLr (−/−) mice had increased levels of plasma IL-1β compared to nondiabetic mice, whereas no such difference was seen between female diabetic and nondiabetic mice. Conclusion. Akita-LDLr (−/−) mice display considerable gender differences in the development of diabetic atherosclerosis. In addition, the increased atherosclerosis in male Akita-LDLr (−/−) mice is associated with an increase in inflammatory cells in lesions.
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spelling pubmed-35159072012-12-14 Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice Engelbertsen, Daniel To, Fong Dunér, Pontus Kotova, Olga Söderberg, Ingrid Alm, Ragnar Gomez, Maria F. Nilsson, Jan Bengtsson, Eva Exp Diabetes Res Research Article Background. Diabetes is associated with increased cardiovascular disease, but the underlying cellular and molecular mechanisms are poorly understood. One proposed mechanism is that diabetes aggravates atherosclerosis by enhancing plaque inflammation. The Akita mouse has recently been adopted as a relevant model for microvascular complications of diabetes. Here we investigate the development of atherosclerosis and inflammation in vessels of Akita mice on LDLr (−/−) background. Methods and Results. Akita-LDLr (−/−) and LDLr (−/−) mice were fed high-fat diet from 6 to 24 weeks of age. Blood glucose levels were higher in both male and female Akita-LDLr (−/−) mice (137% and 70%, resp.). Male Akita-LDLr (−/−) mice had markedly increased plasma cholesterol and triglyceride levels, a three-fold increase in atherosclerosis, and enhanced accumulation of macrophages and T-cells in plaques. In contrast, female Akita-LDLr (−/−) mice demonstrated a modest 29% increase in plasma cholesterol and no significant increase in triglycerides, atherosclerosis, or inflammatory cells in lesions. Male Akita-LDLr (−/−) mice had increased levels of plasma IL-1β compared to nondiabetic mice, whereas no such difference was seen between female diabetic and nondiabetic mice. Conclusion. Akita-LDLr (−/−) mice display considerable gender differences in the development of diabetic atherosclerosis. In addition, the increased atherosclerosis in male Akita-LDLr (−/−) mice is associated with an increase in inflammatory cells in lesions. Hindawi Publishing Corporation 2012 2012-11-28 /pmc/articles/PMC3515907/ /pubmed/23243415 http://dx.doi.org/10.1155/2012/176162 Text en Copyright © 2012 Daniel Engelbertsen et al. https://creativecommons.org/licenses/by/3.0/ 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
Engelbertsen, Daniel
To, Fong
Dunér, Pontus
Kotova, Olga
Söderberg, Ingrid
Alm, Ragnar
Gomez, Maria F.
Nilsson, Jan
Bengtsson, Eva
Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title_full Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title_fullStr Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title_full_unstemmed Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title_short Increased Inflammation in Atherosclerotic Lesions of Diabetic Akita-LDLr (−/−) Mice Compared to Nondiabetic LDLr (−/−) Mice
title_sort increased inflammation in atherosclerotic lesions of diabetic akita-ldlr (−/−) mice compared to nondiabetic ldlr (−/−) mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3515907/
https://www.ncbi.nlm.nih.gov/pubmed/23243415
http://dx.doi.org/10.1155/2012/176162
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