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

Abstract 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....

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Main Authors: Md. Mahmudul Hasan, Most. Sayla Tasmin, Ahmed M. El-Shehawi, Mona M. Elseehy, Md. Abu Reza, Ariful Haque
Format: Article
Language:English
Published: BMC 2021-09-01
Series:BMC Complementary Medicine and Therapies
Subjects:
Online Access:https://doi.org/10.1186/s12906-021-03398-9
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spelling doaj-9abdaed595a04463bd486e5db8e6c5a82021-09-05T11:46:30ZengBMCBMC Complementary Medicine and Therapies2662-76712021-09-0121111210.1186/s12906-021-03398-9R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stressMd. Mahmudul Hasan0Most. Sayla Tasmin1Ahmed M. El-Shehawi2Mona M. Elseehy3Md. Abu Reza4Ariful Haque5Molecular Biology and Protein Science Laboratory, Department of Genetic Engineering and Biotechnology, Faculty of Life and Earth Sciences, University of RajshahiMolecular Pathology Laboratory, Institute of Biological Sciences, University of RajshahiDepartment of Biotechnology, College of Science, Taif UniversityDepartment of Genetics, Faculty of Agriculture, Alexandria UniversityMolecular Biology and Protein Science Laboratory, Department of Genetic Engineering and Biotechnology, Faculty of Life and Earth Sciences, University of RajshahiMolecular Pathology Laboratory, Institute of Biological Sciences, University of RajshahiAbstract 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 (H2O2) 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 IC50 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 H2O2 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.https://doi.org/10.1186/s12906-021-03398-9CisplatinR. vesicariusMiceKidneyHK-2 cellsOxidative stress
collection DOAJ
language English
format Article
sources DOAJ
author Md. Mahmudul Hasan
Most. Sayla Tasmin
Ahmed M. El-Shehawi
Mona M. Elseehy
Md. Abu Reza
Ariful Haque
spellingShingle Md. Mahmudul Hasan
Most. Sayla Tasmin
Ahmed M. El-Shehawi
Mona M. Elseehy
Md. Abu Reza
Ariful Haque
R. vesicarius L. exerts nephroprotective effect against cisplatin-induced oxidative stress
BMC Complementary Medicine and Therapies
Cisplatin
R. vesicarius
Mice
Kidney
HK-2 cells
Oxidative stress
author_facet Md. Mahmudul Hasan
Most. Sayla Tasmin
Ahmed M. El-Shehawi
Mona M. Elseehy
Md. Abu Reza
Ariful Haque
author_sort Md. Mahmudul Hasan
title 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_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_sort r. vesicarius l. exerts nephroprotective effect against cisplatin-induced oxidative stress
publisher BMC
series BMC Complementary Medicine and Therapies
issn 2662-7671
publishDate 2021-09-01
description Abstract 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 (H2O2) 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 IC50 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 H2O2 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.
topic Cisplatin
R. vesicarius
Mice
Kidney
HK-2 cells
Oxidative stress
url https://doi.org/10.1186/s12906-021-03398-9
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