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Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy
Use of the chemotherapeutic agent cisplatin (CDDP) in cancer patients is limited by the occurrence of acute kidney injury (AKI); however, no protective therapy is available. We aimed to investigate the renoprotective effects of Dendropanax morbifera water extract (DM) on CDDP-induced AKI. Male Sprag...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721194/ https://www.ncbi.nlm.nih.gov/pubmed/31366146 http://dx.doi.org/10.3390/antiox8080256 |
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author | Kim, Ji Su Kim, Kyeong Seok Son, Ji Yeon Kim, Hae Ri Park, Jae Hyeon Lee, Su Hyun Lee, Da Eun Kim, In Su Lee, Kwang Youl Lee, Byung Mu Kwak, Jong Hwan Kim, Hyung Sik |
author_facet | Kim, Ji Su Kim, Kyeong Seok Son, Ji Yeon Kim, Hae Ri Park, Jae Hyeon Lee, Su Hyun Lee, Da Eun Kim, In Su Lee, Kwang Youl Lee, Byung Mu Kwak, Jong Hwan Kim, Hyung Sik |
author_sort | Kim, Ji Su |
collection | PubMed |
description | Use of the chemotherapeutic agent cisplatin (CDDP) in cancer patients is limited by the occurrence of acute kidney injury (AKI); however, no protective therapy is available. We aimed to investigate the renoprotective effects of Dendropanax morbifera water extract (DM) on CDDP-induced AKI. Male Sprague-Dawley rats (six animals/group) received: Vehicle (control); CDDP (6 mg/kg, intraperitoneally (i.p.); DM (25 mg/kg, oral); or DM + CDDP injection. CDDP treatment significantly increased blood urea nitrogen (BUN), serum creatinine (sCr), and pro-inflammatory cytokines (IL-6 and TNF-α), and severely damaged the kidney architecture. Urinary excretion of protein-based AKI biomarkers also increased in the CDDP-treated group. In contrast, DM ameliorated CDDP-induced AKI biomarkers. It markedly protected against CDDP-induced oxidative stress by increasing the activity of endogenous antioxidants and reducing the levels of pro-inflammatory cytokines (IL-6 and TNF-α). The protective effect of DM in the proximal tubules was evident upon histopathological examination. In a tumor xenograft model, administration of DM enhanced the chemotherapeutic activity of CDDP and exhibited renoprotective effects against CDDP-induced nephrotoxicity without altering chemotherapeutic efficacy. Our data demonstrate that DM may be an adjuvant therapy with CDDP in solid tumor patients to preserve renal function. |
format | Online Article Text |
id | pubmed-6721194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67211942019-09-10 Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy Kim, Ji Su Kim, Kyeong Seok Son, Ji Yeon Kim, Hae Ri Park, Jae Hyeon Lee, Su Hyun Lee, Da Eun Kim, In Su Lee, Kwang Youl Lee, Byung Mu Kwak, Jong Hwan Kim, Hyung Sik Antioxidants (Basel) Article Use of the chemotherapeutic agent cisplatin (CDDP) in cancer patients is limited by the occurrence of acute kidney injury (AKI); however, no protective therapy is available. We aimed to investigate the renoprotective effects of Dendropanax morbifera water extract (DM) on CDDP-induced AKI. Male Sprague-Dawley rats (six animals/group) received: Vehicle (control); CDDP (6 mg/kg, intraperitoneally (i.p.); DM (25 mg/kg, oral); or DM + CDDP injection. CDDP treatment significantly increased blood urea nitrogen (BUN), serum creatinine (sCr), and pro-inflammatory cytokines (IL-6 and TNF-α), and severely damaged the kidney architecture. Urinary excretion of protein-based AKI biomarkers also increased in the CDDP-treated group. In contrast, DM ameliorated CDDP-induced AKI biomarkers. It markedly protected against CDDP-induced oxidative stress by increasing the activity of endogenous antioxidants and reducing the levels of pro-inflammatory cytokines (IL-6 and TNF-α). The protective effect of DM in the proximal tubules was evident upon histopathological examination. In a tumor xenograft model, administration of DM enhanced the chemotherapeutic activity of CDDP and exhibited renoprotective effects against CDDP-induced nephrotoxicity without altering chemotherapeutic efficacy. Our data demonstrate that DM may be an adjuvant therapy with CDDP in solid tumor patients to preserve renal function. MDPI 2019-07-30 /pmc/articles/PMC6721194/ /pubmed/31366146 http://dx.doi.org/10.3390/antiox8080256 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Kim, Ji Su Kim, Kyeong Seok Son, Ji Yeon Kim, Hae Ri Park, Jae Hyeon Lee, Su Hyun Lee, Da Eun Kim, In Su Lee, Kwang Youl Lee, Byung Mu Kwak, Jong Hwan Kim, Hyung Sik Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title | Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title_full | Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title_fullStr | Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title_full_unstemmed | Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title_short | Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy |
title_sort | protective effects of dendropanax morbifera against cisplatin-induced nephrotoxicity without altering chemotherapeutic efficacy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6721194/ https://www.ncbi.nlm.nih.gov/pubmed/31366146 http://dx.doi.org/10.3390/antiox8080256 |
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