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Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis

OBJECTIVE: It is very important to develop a new therapeutic strategy to cope with the increasing morbidity and mortality of chronic kidney disease (CKD). As a kind of physical therapy, low intensity pulsed ultrasound (LIPUS) has remarkable anti-inflammatory and repair-promoting effects and is expec...

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Autores principales: Ouyang, Zhi-Qiang, Shao, Li-shi, Wang, Wei-peng, Ke, Teng-fei, Chen, Dong, Zheng, Guang-rong, Duan, Xi-rui, Chu, Ji-xiang, Zhu, Yu, Yang, Lu, Shan, Hai-yan, Huang, Lin, Liao, Cheng-de
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472869/
https://www.ncbi.nlm.nih.gov/pubmed/37652897
http://dx.doi.org/10.1080/13510002.2023.2251237
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author Ouyang, Zhi-Qiang
Shao, Li-shi
Wang, Wei-peng
Ke, Teng-fei
Chen, Dong
Zheng, Guang-rong
Duan, Xi-rui
Chu, Ji-xiang
Zhu, Yu
Yang, Lu
Shan, Hai-yan
Huang, Lin
Liao, Cheng-de
author_facet Ouyang, Zhi-Qiang
Shao, Li-shi
Wang, Wei-peng
Ke, Teng-fei
Chen, Dong
Zheng, Guang-rong
Duan, Xi-rui
Chu, Ji-xiang
Zhu, Yu
Yang, Lu
Shan, Hai-yan
Huang, Lin
Liao, Cheng-de
author_sort Ouyang, Zhi-Qiang
collection PubMed
description OBJECTIVE: It is very important to develop a new therapeutic strategy to cope with the increasing morbidity and mortality of chronic kidney disease (CKD). As a kind of physical therapy, low intensity pulsed ultrasound (LIPUS) has remarkable anti-inflammatory and repair-promoting effects and is expected to become a new therapeutic method for CKD. This study aims to clarify the treatment effect of LIPUS on CKD-related renal inflammation and fibrosis, and to further explore the potential signal network of LIPUS treatment for ameliorating chronic renal injury. METHODS: A rat model simulating the progress of CKD was established by twice tail-vein injection of Adriamycin (ADR). Under anesthesia, bilateral kidneys of CKD rats were continuously stimulated by LIPUS for four weeks. The parameters of LIPUS were 1.0 MHz, 60 mW/cm(2), 50% duty cycle and 20 min/d. RESULTS: LIPUS treatment effectively inhibited ADR-induced renal inflammation and fibrosis, and improved CKD-related to oxidative stress and ferroptosis. In addition, the therapeutic effect of LIPUS is closely related to the regulation of TGF-β(1)/Smad and Nrf2/keap1/HO-1 signalling pathways. DISCUSSION: This study provides a new direction for further mechanism research and lays an important foundation for clinical trials.
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spelling pubmed-104728692023-09-02 Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis Ouyang, Zhi-Qiang Shao, Li-shi Wang, Wei-peng Ke, Teng-fei Chen, Dong Zheng, Guang-rong Duan, Xi-rui Chu, Ji-xiang Zhu, Yu Yang, Lu Shan, Hai-yan Huang, Lin Liao, Cheng-de Redox Rep Research Article OBJECTIVE: It is very important to develop a new therapeutic strategy to cope with the increasing morbidity and mortality of chronic kidney disease (CKD). As a kind of physical therapy, low intensity pulsed ultrasound (LIPUS) has remarkable anti-inflammatory and repair-promoting effects and is expected to become a new therapeutic method for CKD. This study aims to clarify the treatment effect of LIPUS on CKD-related renal inflammation and fibrosis, and to further explore the potential signal network of LIPUS treatment for ameliorating chronic renal injury. METHODS: A rat model simulating the progress of CKD was established by twice tail-vein injection of Adriamycin (ADR). Under anesthesia, bilateral kidneys of CKD rats were continuously stimulated by LIPUS for four weeks. The parameters of LIPUS were 1.0 MHz, 60 mW/cm(2), 50% duty cycle and 20 min/d. RESULTS: LIPUS treatment effectively inhibited ADR-induced renal inflammation and fibrosis, and improved CKD-related to oxidative stress and ferroptosis. In addition, the therapeutic effect of LIPUS is closely related to the regulation of TGF-β(1)/Smad and Nrf2/keap1/HO-1 signalling pathways. DISCUSSION: This study provides a new direction for further mechanism research and lays an important foundation for clinical trials. Taylor & Francis 2023-08-31 /pmc/articles/PMC10472869/ /pubmed/37652897 http://dx.doi.org/10.1080/13510002.2023.2251237 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Ouyang, Zhi-Qiang
Shao, Li-shi
Wang, Wei-peng
Ke, Teng-fei
Chen, Dong
Zheng, Guang-rong
Duan, Xi-rui
Chu, Ji-xiang
Zhu, Yu
Yang, Lu
Shan, Hai-yan
Huang, Lin
Liao, Cheng-de
Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title_full Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title_fullStr Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title_full_unstemmed Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title_short Low intensity pulsed ultrasound ameliorates Adriamycin-induced chronic renal injury by inhibiting ferroptosis
title_sort low intensity pulsed ultrasound ameliorates adriamycin-induced chronic renal injury by inhibiting ferroptosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10472869/
https://www.ncbi.nlm.nih.gov/pubmed/37652897
http://dx.doi.org/10.1080/13510002.2023.2251237
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