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Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis

The therapeutic effects of low intensity pulsed ultrasound (LIPUS) on renal ischemia/reperfusion injury (IRI) with acute kidney injury (AKI) are still unclear. A renal tubule cell model under H(2)O(2) or hypoxia/reoxygenation (H/R) conditions with or without LIPUS pre-treatment (1 MHz, 30 and 100 mW...

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Autores principales: Chiang, Chih-Kang, Loh, Jui-Zhi, Yang, Ting-Hua, Huang, Kuo-Tong, Wu, Cheng-Tien, Guan, Siao-Syun, Liu, Shing-Hwa, Hung, Kuan-Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459306/
https://www.ncbi.nlm.nih.gov/pubmed/32868865
http://dx.doi.org/10.1038/s41598-020-71330-1
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author Chiang, Chih-Kang
Loh, Jui-Zhi
Yang, Ting-Hua
Huang, Kuo-Tong
Wu, Cheng-Tien
Guan, Siao-Syun
Liu, Shing-Hwa
Hung, Kuan-Yu
author_facet Chiang, Chih-Kang
Loh, Jui-Zhi
Yang, Ting-Hua
Huang, Kuo-Tong
Wu, Cheng-Tien
Guan, Siao-Syun
Liu, Shing-Hwa
Hung, Kuan-Yu
author_sort Chiang, Chih-Kang
collection PubMed
description The therapeutic effects of low intensity pulsed ultrasound (LIPUS) on renal ischemia/reperfusion injury (IRI) with acute kidney injury (AKI) are still unclear. A renal tubule cell model under H(2)O(2) or hypoxia/reoxygenation (H/R) conditions with or without LIPUS pre-treatment (1 MHz, 30 and 100 mW/cm(2), 15 min) was used to test the in vitro effects of LIPUS. An AKI mouse model of unilateral IRI with nephrectomy of the contralateral kidney for 48 h with or without LIPUS treatment (3 MHz, 100 mW/cm(2), 20 min/day) 5 day before IRI were used to investigate the in vivo effects of LIPUS. LIPUS significantly protected the renal tubule cell viability and prevented inflammatory signals against H(2)O(2) challenge. LIPUS could inhibit the apoptosis-related molecular signals and increase the protein levels of endogenous antioxidant enzymes, α-Klotho, and Sirt1 in renal tubule cells after H/R challenge. LIPUS alleviated the increases in the serum levels of blood urea nitrogen, creatinine, and cystatin C, renal pathological changes and apoptosis-related molecular signals, and impaired antioxidant enzymes in AKI mice. The IRI-induced inflammatory responses in the kidneys and spleens could be reversed by LIPUS. These findings suggest that LIPUS treatment displays the benefits for renal protection in IRI-induced AKI mice.
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spelling pubmed-74593062020-09-01 Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis Chiang, Chih-Kang Loh, Jui-Zhi Yang, Ting-Hua Huang, Kuo-Tong Wu, Cheng-Tien Guan, Siao-Syun Liu, Shing-Hwa Hung, Kuan-Yu Sci Rep Article The therapeutic effects of low intensity pulsed ultrasound (LIPUS) on renal ischemia/reperfusion injury (IRI) with acute kidney injury (AKI) are still unclear. A renal tubule cell model under H(2)O(2) or hypoxia/reoxygenation (H/R) conditions with or without LIPUS pre-treatment (1 MHz, 30 and 100 mW/cm(2), 15 min) was used to test the in vitro effects of LIPUS. An AKI mouse model of unilateral IRI with nephrectomy of the contralateral kidney for 48 h with or without LIPUS treatment (3 MHz, 100 mW/cm(2), 20 min/day) 5 day before IRI were used to investigate the in vivo effects of LIPUS. LIPUS significantly protected the renal tubule cell viability and prevented inflammatory signals against H(2)O(2) challenge. LIPUS could inhibit the apoptosis-related molecular signals and increase the protein levels of endogenous antioxidant enzymes, α-Klotho, and Sirt1 in renal tubule cells after H/R challenge. LIPUS alleviated the increases in the serum levels of blood urea nitrogen, creatinine, and cystatin C, renal pathological changes and apoptosis-related molecular signals, and impaired antioxidant enzymes in AKI mice. The IRI-induced inflammatory responses in the kidneys and spleens could be reversed by LIPUS. These findings suggest that LIPUS treatment displays the benefits for renal protection in IRI-induced AKI mice. Nature Publishing Group UK 2020-08-31 /pmc/articles/PMC7459306/ /pubmed/32868865 http://dx.doi.org/10.1038/s41598-020-71330-1 Text en © The Author(s) 2020 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chiang, Chih-Kang
Loh, Jui-Zhi
Yang, Ting-Hua
Huang, Kuo-Tong
Wu, Cheng-Tien
Guan, Siao-Syun
Liu, Shing-Hwa
Hung, Kuan-Yu
Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title_full Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title_fullStr Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title_full_unstemmed Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title_short Prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
title_sort prevention of acute kidney injury by low intensity pulsed ultrasound via anti-inflammation and anti-apoptosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7459306/
https://www.ncbi.nlm.nih.gov/pubmed/32868865
http://dx.doi.org/10.1038/s41598-020-71330-1
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