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Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice

OBJECTIVE(S): Cisplatin (CDDP) is a highly effective chemotherapeutic agent, but its clinical application has been limited by nephrotoxicity. Tanshinone Ⅰ (T-I), a phenanthrenequinone compound extracted from the Chinese herb Danshen, has been used to improve circulation and treat cardiovascular dise...

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Autores principales: Wang, Yan, Zhang, Yun-hui, Tang, Yin-ru, Lan, Jie, Huang, Zhi-ying, Tian, Wei, Huang, Qian, Peng, Yan, Gao, Yuan, Hu, Yue-qin, Zhang, Xue-nong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148410/
https://www.ncbi.nlm.nih.gov/pubmed/35656184
http://dx.doi.org/10.22038/IJBMS.2022.58959.13102
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author Wang, Yan
Zhang, Yun-hui
Tang, Yin-ru
Lan, Jie
Huang, Zhi-ying
Tian, Wei
Huang, Qian
Peng, Yan
Gao, Yuan
Hu, Yue-qin
Zhang, Xue-nong
author_facet Wang, Yan
Zhang, Yun-hui
Tang, Yin-ru
Lan, Jie
Huang, Zhi-ying
Tian, Wei
Huang, Qian
Peng, Yan
Gao, Yuan
Hu, Yue-qin
Zhang, Xue-nong
author_sort Wang, Yan
collection PubMed
description OBJECTIVE(S): Cisplatin (CDDP) is a highly effective chemotherapeutic agent, but its clinical application has been limited by nephrotoxicity. Tanshinone Ⅰ (T-I), a phenanthrenequinone compound extracted from the Chinese herb Danshen, has been used to improve circulation and treat cardiovascular diseases. The aim of this study was to investigate the protective effect of T-I on CDDP-induced nephrotoxicity in mice. MATERIALS AND METHODS: The BALB/c mouse models of nephrotoxicity were established by a single intraperitoneal injection of 20 mg/kg CDDP on the first day of the experiment. Three hours prior to CDDP administration, the mice were dosed with 10 mg/kg and 30 mg/kg T-I for 3 consecutive days intraperitoneally to explore nephroprotection of T-I. RESULTS: Treatment with T-I significantly reduced blood urea nitrogen and creatinine levels in serum observed in CDDP-administered mice, especially at a dose of 30 mg/kg. T-I at 30 mg/kg significantly decreased malondialdehyde levels and increased glutathione levels and the enzymatic activity of catalase in kidney tissue compared to CDDP. Additionally, T-I (30 mg/kg) significantly reversed the CDDP-decreased expression level of superoxide dismutase 2 protein in renal tissue. Histopathological evaluation of the kidneys further confirmed the protective effect of T-I. CONCLUSION: The findings of this study demonstrate that T-I can protect against CDDP-induced nephrotoxicity through suppression of oxidative stress.
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spelling pubmed-91484102022-06-01 Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice Wang, Yan Zhang, Yun-hui Tang, Yin-ru Lan, Jie Huang, Zhi-ying Tian, Wei Huang, Qian Peng, Yan Gao, Yuan Hu, Yue-qin Zhang, Xue-nong Iran J Basic Med Sci Short Communication OBJECTIVE(S): Cisplatin (CDDP) is a highly effective chemotherapeutic agent, but its clinical application has been limited by nephrotoxicity. Tanshinone Ⅰ (T-I), a phenanthrenequinone compound extracted from the Chinese herb Danshen, has been used to improve circulation and treat cardiovascular diseases. The aim of this study was to investigate the protective effect of T-I on CDDP-induced nephrotoxicity in mice. MATERIALS AND METHODS: The BALB/c mouse models of nephrotoxicity were established by a single intraperitoneal injection of 20 mg/kg CDDP on the first day of the experiment. Three hours prior to CDDP administration, the mice were dosed with 10 mg/kg and 30 mg/kg T-I for 3 consecutive days intraperitoneally to explore nephroprotection of T-I. RESULTS: Treatment with T-I significantly reduced blood urea nitrogen and creatinine levels in serum observed in CDDP-administered mice, especially at a dose of 30 mg/kg. T-I at 30 mg/kg significantly decreased malondialdehyde levels and increased glutathione levels and the enzymatic activity of catalase in kidney tissue compared to CDDP. Additionally, T-I (30 mg/kg) significantly reversed the CDDP-decreased expression level of superoxide dismutase 2 protein in renal tissue. Histopathological evaluation of the kidneys further confirmed the protective effect of T-I. CONCLUSION: The findings of this study demonstrate that T-I can protect against CDDP-induced nephrotoxicity through suppression of oxidative stress. Mashhad University of Medical Sciences 2022-03 /pmc/articles/PMC9148410/ /pubmed/35656184 http://dx.doi.org/10.22038/IJBMS.2022.58959.13102 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Wang, Yan
Zhang, Yun-hui
Tang, Yin-ru
Lan, Jie
Huang, Zhi-ying
Tian, Wei
Huang, Qian
Peng, Yan
Gao, Yuan
Hu, Yue-qin
Zhang, Xue-nong
Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title_full Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title_fullStr Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title_full_unstemmed Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title_short Protective effects of tanshinone Ⅰ against cisplatin-induced nephrotoxicity in mice
title_sort protective effects of tanshinone ⅰ against cisplatin-induced nephrotoxicity in mice
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148410/
https://www.ncbi.nlm.nih.gov/pubmed/35656184
http://dx.doi.org/10.22038/IJBMS.2022.58959.13102
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