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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Mashhad University of Medical Sciences
2022
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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. |
format | Online Article Text |
id | pubmed-9148410 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Mashhad University of Medical Sciences |
record_format | MEDLINE/PubMed |
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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