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Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity

Atherogenic events promote changes in vessel walls, with alteration of the redox state, and increased activity of matrix metalloproteinases (MMPs). Thus, this study aims to evaluate aortic remodeling, MMP activity, and reactive oxygen species (ROS) levels after treatment with doxycycline in ApoE(-⁄-...

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Autores principales: Rodrigues, Keuri E., Azevedo, Aline, Gonçalves, Pricila R., Pontes, Maria H. B., Alves, Gustavo M., Oliveira, Ruan R., Amarante, Cristine B., Issa, João P. M., Gerlach, Raquel F., Prado, Alejandro F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910467/
https://www.ncbi.nlm.nih.gov/pubmed/35269673
http://dx.doi.org/10.3390/ijms23052532
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author Rodrigues, Keuri E.
Azevedo, Aline
Gonçalves, Pricila R.
Pontes, Maria H. B.
Alves, Gustavo M.
Oliveira, Ruan R.
Amarante, Cristine B.
Issa, João P. M.
Gerlach, Raquel F.
Prado, Alejandro F.
author_facet Rodrigues, Keuri E.
Azevedo, Aline
Gonçalves, Pricila R.
Pontes, Maria H. B.
Alves, Gustavo M.
Oliveira, Ruan R.
Amarante, Cristine B.
Issa, João P. M.
Gerlach, Raquel F.
Prado, Alejandro F.
author_sort Rodrigues, Keuri E.
collection PubMed
description Atherogenic events promote changes in vessel walls, with alteration of the redox state, and increased activity of matrix metalloproteinases (MMPs). Thus, this study aims to evaluate aortic remodeling, MMP activity, and reactive oxygen species (ROS) levels after treatment with doxycycline in ApoE(-⁄-) and ovariectomized mice (OVX). Female ApoE(-⁄-)-knockout mice (5 weeks) were submitted to ovariectomy surgery to induce experimental menopause. They then received chow enriched with 1% cholesterol to induce hypercholesterolemia. The animals were divided into two experimental groups: ApoE(-⁄-)/OVX vehicle and ApoE(-⁄-)/OVX doxycycline (30 mg/kg) administered by gavage once a day for 28 days (15th to the 18th week of life). Blood samples were collected to measure total cholesterol and fractions. The aorta was used for morphometry and to measure the activity and expression of MMP-2 and ROS levels. The ApoE(-⁄-)/OVX doxycycline group showed no change in total and fraction cholesterol levels. However, there was a reduction in ROS levels, MMP-2 expression, and activity that correlated with a decrease in atherosclerotic lesions relative to the ApoE(-⁄-)/OVX vehicle (p > 0.05). Therefore, we conclude that doxycycline in ApoE(-⁄-)/OVX animals promotes a reduction in atherosclerotic lesions by reducing ROS and MMP-2 activity and expression.
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spelling pubmed-89104672022-03-11 Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity Rodrigues, Keuri E. Azevedo, Aline Gonçalves, Pricila R. Pontes, Maria H. B. Alves, Gustavo M. Oliveira, Ruan R. Amarante, Cristine B. Issa, João P. M. Gerlach, Raquel F. Prado, Alejandro F. Int J Mol Sci Article Atherogenic events promote changes in vessel walls, with alteration of the redox state, and increased activity of matrix metalloproteinases (MMPs). Thus, this study aims to evaluate aortic remodeling, MMP activity, and reactive oxygen species (ROS) levels after treatment with doxycycline in ApoE(-⁄-) and ovariectomized mice (OVX). Female ApoE(-⁄-)-knockout mice (5 weeks) were submitted to ovariectomy surgery to induce experimental menopause. They then received chow enriched with 1% cholesterol to induce hypercholesterolemia. The animals were divided into two experimental groups: ApoE(-⁄-)/OVX vehicle and ApoE(-⁄-)/OVX doxycycline (30 mg/kg) administered by gavage once a day for 28 days (15th to the 18th week of life). Blood samples were collected to measure total cholesterol and fractions. The aorta was used for morphometry and to measure the activity and expression of MMP-2 and ROS levels. The ApoE(-⁄-)/OVX doxycycline group showed no change in total and fraction cholesterol levels. However, there was a reduction in ROS levels, MMP-2 expression, and activity that correlated with a decrease in atherosclerotic lesions relative to the ApoE(-⁄-)/OVX vehicle (p > 0.05). Therefore, we conclude that doxycycline in ApoE(-⁄-)/OVX animals promotes a reduction in atherosclerotic lesions by reducing ROS and MMP-2 activity and expression. MDPI 2022-02-25 /pmc/articles/PMC8910467/ /pubmed/35269673 http://dx.doi.org/10.3390/ijms23052532 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Rodrigues, Keuri E.
Azevedo, Aline
Gonçalves, Pricila R.
Pontes, Maria H. B.
Alves, Gustavo M.
Oliveira, Ruan R.
Amarante, Cristine B.
Issa, João P. M.
Gerlach, Raquel F.
Prado, Alejandro F.
Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title_full Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title_fullStr Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title_full_unstemmed Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title_short Doxycycline Decreases Atherosclerotic Lesions in the Aorta of ApoE(-⁄-) and Ovariectomized Mice with Correlation to Reduced MMP-2 Activity
title_sort doxycycline decreases atherosclerotic lesions in the aorta of apoe(-⁄-) and ovariectomized mice with correlation to reduced mmp-2 activity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8910467/
https://www.ncbi.nlm.nih.gov/pubmed/35269673
http://dx.doi.org/10.3390/ijms23052532
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