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Trilobatin, an Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in Mice
[Image: see text] Although naturally occurring flavonoids have shown beneficial effects on the side effects caused by cisplatin, there are few reports on the protective effect of dihydrochalcone on the cisplatin-induced toxicity. Trilobatin (TLB), as the major sweetener and active ingredient in Lith...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607670/ https://www.ncbi.nlm.nih.gov/pubmed/36312396 http://dx.doi.org/10.1021/acsomega.2c04142 |
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author | Duan, Yue-yang Mi, Xiao-jie Su, Wen-ya Tang, Shan Jiang, Shuang Wang, Zi Zhao, Li-Chun Li, Wei |
author_facet | Duan, Yue-yang Mi, Xiao-jie Su, Wen-ya Tang, Shan Jiang, Shuang Wang, Zi Zhao, Li-Chun Li, Wei |
author_sort | Duan, Yue-yang |
collection | PubMed |
description | [Image: see text] Although naturally occurring flavonoids have shown beneficial effects on the side effects caused by cisplatin, there are few reports on the protective effect of dihydrochalcone on the cisplatin-induced toxicity. Trilobatin (TLB), as the major sweetener and active ingredient in Lithocarpus polystachyus Rehd, is a dihydrochalcone-like compound that can be present in concentrations of up to 10% or more in tender leaves. Herein, a cisplatin-induced acute kidney injury (AKI) model was established to investigate the protective effect and mechanism of TLB against the cisplatin-induced nephrotoxicity in mice. The results showed that TLB significantly reversed the inhibition of CRE, BUN, and MDA levels compared with the cisplatin group. Furthermore, TLB treatment (50 and 100 mg/kg) for 10 days significantly alleviated cisplatin-induced renal pathological changes. TUNEL staining showed that TLB administration can effectively improve the occurrence of apoptosis of renal tissue cells caused by cisplatin exposure. Importantly, western blot analysis verified that TLB alleviated cisplatin-induced nephrotoxicity by regulating the AKT/MAPK signaling pathway and apoptosis. In summary, our findings showed clearly that TLB has a significant preventive effect on cisplatin-induced AKI. |
format | Online Article Text |
id | pubmed-9607670 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96076702022-10-28 Trilobatin, an Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in Mice Duan, Yue-yang Mi, Xiao-jie Su, Wen-ya Tang, Shan Jiang, Shuang Wang, Zi Zhao, Li-Chun Li, Wei ACS Omega [Image: see text] Although naturally occurring flavonoids have shown beneficial effects on the side effects caused by cisplatin, there are few reports on the protective effect of dihydrochalcone on the cisplatin-induced toxicity. Trilobatin (TLB), as the major sweetener and active ingredient in Lithocarpus polystachyus Rehd, is a dihydrochalcone-like compound that can be present in concentrations of up to 10% or more in tender leaves. Herein, a cisplatin-induced acute kidney injury (AKI) model was established to investigate the protective effect and mechanism of TLB against the cisplatin-induced nephrotoxicity in mice. The results showed that TLB significantly reversed the inhibition of CRE, BUN, and MDA levels compared with the cisplatin group. Furthermore, TLB treatment (50 and 100 mg/kg) for 10 days significantly alleviated cisplatin-induced renal pathological changes. TUNEL staining showed that TLB administration can effectively improve the occurrence of apoptosis of renal tissue cells caused by cisplatin exposure. Importantly, western blot analysis verified that TLB alleviated cisplatin-induced nephrotoxicity by regulating the AKT/MAPK signaling pathway and apoptosis. In summary, our findings showed clearly that TLB has a significant preventive effect on cisplatin-induced AKI. American Chemical Society 2022-10-13 /pmc/articles/PMC9607670/ /pubmed/36312396 http://dx.doi.org/10.1021/acsomega.2c04142 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Duan, Yue-yang Mi, Xiao-jie Su, Wen-ya Tang, Shan Jiang, Shuang Wang, Zi Zhao, Li-Chun Li, Wei Trilobatin, an Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in Mice |
title | Trilobatin, an
Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity
via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in
Mice |
title_full | Trilobatin, an
Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity
via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in
Mice |
title_fullStr | Trilobatin, an
Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity
via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in
Mice |
title_full_unstemmed | Trilobatin, an
Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity
via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in
Mice |
title_short | Trilobatin, an
Active Dihydrochalcone from Lithocarpus polystachyus, Prevents Cisplatin-Induced Nephrotoxicity
via Mitogen-Activated Protein Kinase Pathway-Mediated Apoptosis in
Mice |
title_sort | trilobatin, an
active dihydrochalcone from lithocarpus polystachyus, prevents cisplatin-induced nephrotoxicity
via mitogen-activated protein kinase pathway-mediated apoptosis in
mice |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9607670/ https://www.ncbi.nlm.nih.gov/pubmed/36312396 http://dx.doi.org/10.1021/acsomega.2c04142 |
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