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Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice

BACKGROUND: Toll-like receptor 4 (TLR4) is a pattern recognition receptor of the innate immune system. TLR4 contributes to many aging-related chronic diseases. However, whether TLR4 is involved in cardiovascular injury during the aging process has not been investigated. METHODS: The effects of TLR4...

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Autores principales: Liu, Huan, Chu, Shujuan, Wu, Zhilin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569991/
https://www.ncbi.nlm.nih.gov/pubmed/34740366
http://dx.doi.org/10.1186/s12979-021-00251-y
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author Liu, Huan
Chu, Shujuan
Wu, Zhilin
author_facet Liu, Huan
Chu, Shujuan
Wu, Zhilin
author_sort Liu, Huan
collection PubMed
description BACKGROUND: Toll-like receptor 4 (TLR4) is a pattern recognition receptor of the innate immune system. TLR4 contributes to many aging-related chronic diseases. However, whether TLR4 is involved in cardiovascular injury during the aging process has not been investigated. METHODS: The effects of TLR4 on the cardiovascular system of aged mice were investigated in TLR4(−/−) mice. An intraperitoneal glucose tolerance test (IPGTT) and insulin sensitivity test (IST) were conducted to evaluate global insulin sensitivity. Echocardiography was used to measure cardiac structure and performance. An isolated artery ring assay was used to measure the vasodilator function of the thoracic aorta. The inflammatory response was reflected by the serum concentration of cytokines. RESULTS: TLR4 expression increased in the hearts and aortas of mice in an age-dependent manner. Loss of TLR4 increased insulin sensitivity in aged mice. Moreover, loss of TLR4 improved cardiac performance and endothelium-dependent vascular relaxation in aged mice. Importantly, the increases in serum inflammatory cytokines and oxidative stress in the heart and aorta were also inhibited by TLR4 deficiency. CONCLUSION: In summary, loss of TLR4 improved cardiac performance and endothelium-dependent vascular relaxation in aged mice. The reduced inflammatory responses and oxidative stress may be the reason for the protective effects of TLR4 deficiency during aging. Our study indicates that targeting TLR4 is a potential therapeutic strategy for preventing aging-related cardiovascular disease.
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spelling pubmed-85699912021-11-08 Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice Liu, Huan Chu, Shujuan Wu, Zhilin Immun Ageing Research BACKGROUND: Toll-like receptor 4 (TLR4) is a pattern recognition receptor of the innate immune system. TLR4 contributes to many aging-related chronic diseases. However, whether TLR4 is involved in cardiovascular injury during the aging process has not been investigated. METHODS: The effects of TLR4 on the cardiovascular system of aged mice were investigated in TLR4(−/−) mice. An intraperitoneal glucose tolerance test (IPGTT) and insulin sensitivity test (IST) were conducted to evaluate global insulin sensitivity. Echocardiography was used to measure cardiac structure and performance. An isolated artery ring assay was used to measure the vasodilator function of the thoracic aorta. The inflammatory response was reflected by the serum concentration of cytokines. RESULTS: TLR4 expression increased in the hearts and aortas of mice in an age-dependent manner. Loss of TLR4 increased insulin sensitivity in aged mice. Moreover, loss of TLR4 improved cardiac performance and endothelium-dependent vascular relaxation in aged mice. Importantly, the increases in serum inflammatory cytokines and oxidative stress in the heart and aorta were also inhibited by TLR4 deficiency. CONCLUSION: In summary, loss of TLR4 improved cardiac performance and endothelium-dependent vascular relaxation in aged mice. The reduced inflammatory responses and oxidative stress may be the reason for the protective effects of TLR4 deficiency during aging. Our study indicates that targeting TLR4 is a potential therapeutic strategy for preventing aging-related cardiovascular disease. BioMed Central 2021-11-05 /pmc/articles/PMC8569991/ /pubmed/34740366 http://dx.doi.org/10.1186/s12979-021-00251-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Liu, Huan
Chu, Shujuan
Wu, Zhilin
Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title_full Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title_fullStr Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title_full_unstemmed Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title_short Loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
title_sort loss of toll-like receptor 4 ameliorates cardiovascular dysfunction in aged mice
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8569991/
https://www.ncbi.nlm.nih.gov/pubmed/34740366
http://dx.doi.org/10.1186/s12979-021-00251-y
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