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Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol

Context: Rutin (RUT) is an antioxidant flavonoid with well-known metal chelating potentials. Objective: This study was designed to evaluate the protective effects of RUT against cadmium (Cd) + ethanol (EtOH)-induced hepatic and renal toxicity in rats. Materials and methods: Wistar rats were treated...

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Autores principales: Abarikwu, Sunny O., Njoku, Rex-Clovis, Lawrence, Chiamaka J., Charles, Iniobong A., Ikewuchi, Jude C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130732/
https://www.ncbi.nlm.nih.gov/pubmed/29025321
http://dx.doi.org/10.1080/13880209.2017.1387575
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author Abarikwu, Sunny O.
Njoku, Rex-Clovis
Lawrence, Chiamaka J.
Charles, Iniobong A.
Ikewuchi, Jude C.
author_facet Abarikwu, Sunny O.
Njoku, Rex-Clovis
Lawrence, Chiamaka J.
Charles, Iniobong A.
Ikewuchi, Jude C.
author_sort Abarikwu, Sunny O.
collection PubMed
description Context: Rutin (RUT) is an antioxidant flavonoid with well-known metal chelating potentials. Objective: This study was designed to evaluate the protective effects of RUT against cadmium (Cd) + ethanol (EtOH)-induced hepatic and renal toxicity in rats. Materials and methods: Wistar rats were treated with Cd (50 mg/kg) alone or in combination with EtOH (5 mg/kg) and RUT (25, 50 and 100 mg/kg) for 15 days. After treatment, the liver, kidney and serum were removed for biochemical assays by spectrophotometric methods. Results: Serum, hepatic and renal malondialdehyde (MDA) levels were highest in the Cd + EtOH group and lowest in Cd + EtOH animals co-treated with the highest dose of RUT (2.98 ± 0.34, 10.08 ± 2.32, 4.99 ± 1.21 vs. 1.69 ± 0.33, 6.13 ± 0.28, 3.66 ± 1.12 μmol MDA/mg protein, respectively). The serum level of Cd was increased in the Cd + EtOH treated animals compared to Cd + EtOH animals co-treated with 100 mg/kg RUT (2.54 ± 0.08 vs. 1.28 ± 0.04 ppm). Furthermore, RUT at the highest dose protected against Cd + EtOH-induced elevation of bilirubin and uric acid levels as well as activities of lactate dehydrogenase and γ-glutamyl transferase (62.86 ± 2.74 vs. 122.52 ± 6.35 µmol/L; 1.77 ± 0.35 vs. 3.23 ± 0.55 mmol/L; 9.56 ± 1.22 vs. 16.21 ± 1.64 U/L; 288.92 ± 40.12 vs. 159.8 ± 18.01 U/L). The histo-pathological changes in the liver and kidney were also reduced in the Cd + EtOH animals co-treated with RUT in a dose-dependent manner. Discussion and conclusion: RUT protected against the combined effects of Cd + EtOH on hepatic and renal functions and improved the antioxidant defence system in the blood.
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spelling pubmed-61307322018-09-27 Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol Abarikwu, Sunny O. Njoku, Rex-Clovis Lawrence, Chiamaka J. Charles, Iniobong A. Ikewuchi, Jude C. Pharm Biol Research Article Context: Rutin (RUT) is an antioxidant flavonoid with well-known metal chelating potentials. Objective: This study was designed to evaluate the protective effects of RUT against cadmium (Cd) + ethanol (EtOH)-induced hepatic and renal toxicity in rats. Materials and methods: Wistar rats were treated with Cd (50 mg/kg) alone or in combination with EtOH (5 mg/kg) and RUT (25, 50 and 100 mg/kg) for 15 days. After treatment, the liver, kidney and serum were removed for biochemical assays by spectrophotometric methods. Results: Serum, hepatic and renal malondialdehyde (MDA) levels were highest in the Cd + EtOH group and lowest in Cd + EtOH animals co-treated with the highest dose of RUT (2.98 ± 0.34, 10.08 ± 2.32, 4.99 ± 1.21 vs. 1.69 ± 0.33, 6.13 ± 0.28, 3.66 ± 1.12 μmol MDA/mg protein, respectively). The serum level of Cd was increased in the Cd + EtOH treated animals compared to Cd + EtOH animals co-treated with 100 mg/kg RUT (2.54 ± 0.08 vs. 1.28 ± 0.04 ppm). Furthermore, RUT at the highest dose protected against Cd + EtOH-induced elevation of bilirubin and uric acid levels as well as activities of lactate dehydrogenase and γ-glutamyl transferase (62.86 ± 2.74 vs. 122.52 ± 6.35 µmol/L; 1.77 ± 0.35 vs. 3.23 ± 0.55 mmol/L; 9.56 ± 1.22 vs. 16.21 ± 1.64 U/L; 288.92 ± 40.12 vs. 159.8 ± 18.01 U/L). The histo-pathological changes in the liver and kidney were also reduced in the Cd + EtOH animals co-treated with RUT in a dose-dependent manner. Discussion and conclusion: RUT protected against the combined effects of Cd + EtOH on hepatic and renal functions and improved the antioxidant defence system in the blood. Taylor & Francis 2017-10-12 /pmc/articles/PMC6130732/ /pubmed/29025321 http://dx.doi.org/10.1080/13880209.2017.1387575 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Abarikwu, Sunny O.
Njoku, Rex-Clovis
Lawrence, Chiamaka J.
Charles, Iniobong A.
Ikewuchi, Jude C.
Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title_full Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title_fullStr Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title_full_unstemmed Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title_short Rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
title_sort rutin ameliorates oxidative stress and preserves hepatic and renal functions following exposure to cadmium and ethanol
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6130732/
https://www.ncbi.nlm.nih.gov/pubmed/29025321
http://dx.doi.org/10.1080/13880209.2017.1387575
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