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Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice

Aerobic exercise training (AET) improves the reverse cholesterol transport (RCT) in cholesteryl ester transfer protein-transgenic (CETP-tg) mice. We aimed at investigating the role of AET in the expression of genes and proteins involved in lipid flux in the aorta and macrophages of CETP-tg mice. Thr...

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Autores principales: Pinto, Paula R., da Silva, Karolline S., Iborra, Rodrigo T., Okuda, Ligia S., Gomes-Kjerulf, Diego, Ferreira, Guilherme S., Machado-Lima, Adriana, Rocco, Debora D. F. M., Nakandakare, Edna R., Machado, Ubiratan F., Correa-Giannella, Maria L., Catanozi, Sergio, Passarelli, Marisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952009/
https://www.ncbi.nlm.nih.gov/pubmed/29867549
http://dx.doi.org/10.3389/fphys.2018.00502
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author Pinto, Paula R.
da Silva, Karolline S.
Iborra, Rodrigo T.
Okuda, Ligia S.
Gomes-Kjerulf, Diego
Ferreira, Guilherme S.
Machado-Lima, Adriana
Rocco, Debora D. F. M.
Nakandakare, Edna R.
Machado, Ubiratan F.
Correa-Giannella, Maria L.
Catanozi, Sergio
Passarelli, Marisa
author_facet Pinto, Paula R.
da Silva, Karolline S.
Iborra, Rodrigo T.
Okuda, Ligia S.
Gomes-Kjerulf, Diego
Ferreira, Guilherme S.
Machado-Lima, Adriana
Rocco, Debora D. F. M.
Nakandakare, Edna R.
Machado, Ubiratan F.
Correa-Giannella, Maria L.
Catanozi, Sergio
Passarelli, Marisa
author_sort Pinto, Paula R.
collection PubMed
description Aerobic exercise training (AET) improves the reverse cholesterol transport (RCT) in cholesteryl ester transfer protein-transgenic (CETP-tg) mice. We aimed at investigating the role of AET in the expression of genes and proteins involved in lipid flux in the aorta and macrophages of CETP-tg mice. Three-month-old male mice were randomly divided into trained (T; treadmill 15 m/min; 30 min/day) and sedentary (S) groups. After 6 weeks, peritoneal macrophages and the aortic arch were obtained immediately (0 h) or 48 h after the last exercise session. mRNA was determined by RT-qPCR, protein levels by immunoblot and (14)C-cholesterol efflux determined in macrophages. AET did not change body weight, plasma cholesterol, triglycerides, glucose and CETP activity. In macrophages, at time 0 h, a higher expression of genes that encode PPAR gamma, ABCA-1 and a lower expression of MCP-1 and IL-10, was observed in T as compared to S. After 48 h, lower expressions of MCP-1 and PPAR gamma genes were observed in T mice. Increase in ABCA-1, SR-BI and IL-6 and decrease of LOX-1, MCP-1, TNF and IL-10 gene expression was observed in the aorta of T compared to S mice (0 h) and LOX-1 and MCP-1 remained diminished after 48 h. The protein level of MCP-1 and SR-BI in the aortic arch was unchanged in T animals after 48 h as compared to S, but LOX-1 was reduced confirming data of gene expression. The apo A-I and the HDL(2) mediated-cholesterol efflux (8 and 24 h) were not different between T and S animals. In the presence of CETP, AET positively influences gene expression in the arterial wall and macrophages of CETP-tg mice contributing to the RCT and prevention of atherosclerosis. These changes were perceptible immediately after the exercise session and were influenced by the presence of CETP although independent of changes in its activity. Reductions in gene and protein expression of LOX-1 were parallel and reflect the ability of exercise training in reducing the uptake of modified LDL by the arterial wall macrophages.
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spelling pubmed-59520092018-06-04 Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice Pinto, Paula R. da Silva, Karolline S. Iborra, Rodrigo T. Okuda, Ligia S. Gomes-Kjerulf, Diego Ferreira, Guilherme S. Machado-Lima, Adriana Rocco, Debora D. F. M. Nakandakare, Edna R. Machado, Ubiratan F. Correa-Giannella, Maria L. Catanozi, Sergio Passarelli, Marisa Front Physiol Physiology Aerobic exercise training (AET) improves the reverse cholesterol transport (RCT) in cholesteryl ester transfer protein-transgenic (CETP-tg) mice. We aimed at investigating the role of AET in the expression of genes and proteins involved in lipid flux in the aorta and macrophages of CETP-tg mice. Three-month-old male mice were randomly divided into trained (T; treadmill 15 m/min; 30 min/day) and sedentary (S) groups. After 6 weeks, peritoneal macrophages and the aortic arch were obtained immediately (0 h) or 48 h after the last exercise session. mRNA was determined by RT-qPCR, protein levels by immunoblot and (14)C-cholesterol efflux determined in macrophages. AET did not change body weight, plasma cholesterol, triglycerides, glucose and CETP activity. In macrophages, at time 0 h, a higher expression of genes that encode PPAR gamma, ABCA-1 and a lower expression of MCP-1 and IL-10, was observed in T as compared to S. After 48 h, lower expressions of MCP-1 and PPAR gamma genes were observed in T mice. Increase in ABCA-1, SR-BI and IL-6 and decrease of LOX-1, MCP-1, TNF and IL-10 gene expression was observed in the aorta of T compared to S mice (0 h) and LOX-1 and MCP-1 remained diminished after 48 h. The protein level of MCP-1 and SR-BI in the aortic arch was unchanged in T animals after 48 h as compared to S, but LOX-1 was reduced confirming data of gene expression. The apo A-I and the HDL(2) mediated-cholesterol efflux (8 and 24 h) were not different between T and S animals. In the presence of CETP, AET positively influences gene expression in the arterial wall and macrophages of CETP-tg mice contributing to the RCT and prevention of atherosclerosis. These changes were perceptible immediately after the exercise session and were influenced by the presence of CETP although independent of changes in its activity. Reductions in gene and protein expression of LOX-1 were parallel and reflect the ability of exercise training in reducing the uptake of modified LDL by the arterial wall macrophages. Frontiers Media S.A. 2018-05-08 /pmc/articles/PMC5952009/ /pubmed/29867549 http://dx.doi.org/10.3389/fphys.2018.00502 Text en Copyright © 2018 Pinto, da Silva, Iborra, Okuda, Gomes-Kjerulf, Ferreira, Machado-Lima, Rocco, Nakandakare, Machado, Correa-Giannella, Catanozi and Passarelli. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Pinto, Paula R.
da Silva, Karolline S.
Iborra, Rodrigo T.
Okuda, Ligia S.
Gomes-Kjerulf, Diego
Ferreira, Guilherme S.
Machado-Lima, Adriana
Rocco, Debora D. F. M.
Nakandakare, Edna R.
Machado, Ubiratan F.
Correa-Giannella, Maria L.
Catanozi, Sergio
Passarelli, Marisa
Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title_full Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title_fullStr Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title_full_unstemmed Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title_short Exercise Training Favorably Modulates Gene and Protein Expression That Regulate Arterial Cholesterol Content in CETP Transgenic Mice
title_sort exercise training favorably modulates gene and protein expression that regulate arterial cholesterol content in cetp transgenic mice
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5952009/
https://www.ncbi.nlm.nih.gov/pubmed/29867549
http://dx.doi.org/10.3389/fphys.2018.00502
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