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R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress

BACKGROUND: Cisplatin is an outstanding anticancer drug, but its use has been decreased remarkably due to sever nephrotoxicity. R. vesicarius L. is a leafy vegetable that is evident with anti-angeogenic, anti-inflammatory, anti-proliferative, hepatoprotective, and nephroprotective potential. Therefo...

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Autores principales: Hasan, Md. Mahmudul, Tasmin, Most. Sayla, El-Shehawi, Ahmed M., Elseehy, Mona M., Reza, Md. Abu, Haque, Ariful
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417970/
https://www.ncbi.nlm.nih.gov/pubmed/34481509
http://dx.doi.org/10.1186/s12906-021-03398-9
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author Hasan, Md. Mahmudul
Tasmin, Most. Sayla
El-Shehawi, Ahmed M.
Elseehy, Mona M.
Reza, Md. Abu
Haque, Ariful
author_facet Hasan, Md. Mahmudul
Tasmin, Most. Sayla
El-Shehawi, Ahmed M.
Elseehy, Mona M.
Reza, Md. Abu
Haque, Ariful
author_sort Hasan, Md. Mahmudul
collection PubMed
description BACKGROUND: Cisplatin is an outstanding anticancer drug, but its use has been decreased remarkably due to sever nephrotoxicity. R. vesicarius L. is a leafy vegetable that is evident with anti-angeogenic, anti-inflammatory, anti-proliferative, hepatoprotective, and nephroprotective potential. Therefore, this study was designed to inspect its methanol extract (RVE) for possible nephroprotective effect. METHODS: Primarily, in vitro antioxidant activity of RVE was confirmed based on 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging aptitude. Thereafter, Swiss Albino male mice were treated with cisplatin (2.5 mg/kg) for 5 successive days to induce nephrotoxicity. Recovery from nephrotoxicity was scrutinized by treating the animals with RVE (25, 50, and 100 mg/kg) intraperitoneally (i.p.) for the next 5 consecutive days. After completion of treatment, mice were sacrificed and kidneys were collected. Part of it was homogenized in sodium phosphate buffer for evaluating malondialdehyde (MDA) level, another part was used to evaluate gene (NQO1, p53, and Bcl-2) expression. Moreover, the hydrogen peroxide (H(2)O(2)) neutralizing capacity of RVE was evaluated in HK-2 cells in vitro. Finally, bioactive phytochemicals in RVE were determined using gas chromatography–mass spectrometry (GC-MS). RESULTS: RVE showed in vitro antioxidant activity in a dose-dependent fashion with 37.39 ± 1.89 μg/mL IC(50) value. Treatment with RVE remarkably (p < 0.05) decreased MDA content in kidney tissue. Besides, the expression of NQO, p53, and Bcl-2 genes was significantly (p < 0.05) mitigated in a dose-dependent manner due to the administration of RVE. RVE significantly (p < 0.05) reversed the H(2)O(2) level in HK-2 cells to almost normal. From GC-MS, ten compounds including three known antioxidants “4H-Pyran-4-one, 2, 3-dihydro-3,5-dihydroxy-6-methyl-”, “Hexadecanoic acid”, and “Squalene” were detected. The extract was rich with an alkaloid “13-Docosenamide”. CONCLUSION: Overall, RVE possesses a protective effect against cisplatin-induced kidney damage.
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spelling pubmed-84179702021-09-09 R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress Hasan, Md. Mahmudul Tasmin, Most. Sayla El-Shehawi, Ahmed M. Elseehy, Mona M. Reza, Md. Abu Haque, Ariful BMC Complement Med Ther Research BACKGROUND: Cisplatin is an outstanding anticancer drug, but its use has been decreased remarkably due to sever nephrotoxicity. R. vesicarius L. is a leafy vegetable that is evident with anti-angeogenic, anti-inflammatory, anti-proliferative, hepatoprotective, and nephroprotective potential. Therefore, this study was designed to inspect its methanol extract (RVE) for possible nephroprotective effect. METHODS: Primarily, in vitro antioxidant activity of RVE was confirmed based on 2, 2-diphenyl-1-picrylhydrazyl (DPPH) free radical scavenging aptitude. Thereafter, Swiss Albino male mice were treated with cisplatin (2.5 mg/kg) for 5 successive days to induce nephrotoxicity. Recovery from nephrotoxicity was scrutinized by treating the animals with RVE (25, 50, and 100 mg/kg) intraperitoneally (i.p.) for the next 5 consecutive days. After completion of treatment, mice were sacrificed and kidneys were collected. Part of it was homogenized in sodium phosphate buffer for evaluating malondialdehyde (MDA) level, another part was used to evaluate gene (NQO1, p53, and Bcl-2) expression. Moreover, the hydrogen peroxide (H(2)O(2)) neutralizing capacity of RVE was evaluated in HK-2 cells in vitro. Finally, bioactive phytochemicals in RVE were determined using gas chromatography–mass spectrometry (GC-MS). RESULTS: RVE showed in vitro antioxidant activity in a dose-dependent fashion with 37.39 ± 1.89 μg/mL IC(50) value. Treatment with RVE remarkably (p < 0.05) decreased MDA content in kidney tissue. Besides, the expression of NQO, p53, and Bcl-2 genes was significantly (p < 0.05) mitigated in a dose-dependent manner due to the administration of RVE. RVE significantly (p < 0.05) reversed the H(2)O(2) level in HK-2 cells to almost normal. From GC-MS, ten compounds including three known antioxidants “4H-Pyran-4-one, 2, 3-dihydro-3,5-dihydroxy-6-methyl-”, “Hexadecanoic acid”, and “Squalene” were detected. The extract was rich with an alkaloid “13-Docosenamide”. CONCLUSION: Overall, RVE possesses a protective effect against cisplatin-induced kidney damage. BioMed Central 2021-09-04 /pmc/articles/PMC8417970/ /pubmed/34481509 http://dx.doi.org/10.1186/s12906-021-03398-9 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Hasan, Md. Mahmudul
Tasmin, Most. Sayla
El-Shehawi, Ahmed M.
Elseehy, Mona M.
Reza, Md. Abu
Haque, Ariful
R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title_full R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title_fullStr R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title_full_unstemmed R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title_short R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
title_sort r. vesicarius l. exerts nephroprotective effect against cisplatin-induced oxidative stress
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8417970/
https://www.ncbi.nlm.nih.gov/pubmed/34481509
http://dx.doi.org/10.1186/s12906-021-03398-9
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