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Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals

This study was done to investigate the possible nephroprotective effect of an ethanolic root extract of Polyalthia Longifolia (PL) on vancomycin-induced nephrotoxicity using curative and protective models. Vancomycin (150 mg/kg, intravenous) was given to healthy Wistar albino rats in the curative mo...

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Autores principales: Das, Kuntal, Muthukumar, A., Almuqbil, Mansour, Imran, Mohd., Rabaan, Ali A., Halwani, Muhammad A., Garout, Mohammed, Alsaleh, Abdulmonem A., Alissa, Mohammed, Alwashmi, Ameen S. S., Alshehri, Ahmad A., Alsayyah, Ahmed, Bhavani, Keserla, Mittal, Swati, Gayathri, R., Alomar, Nasser Fawzan, Rabbani, Syed Imam, Basheeruddin Asdaq, Syed Mohammed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900101/
https://www.ncbi.nlm.nih.gov/pubmed/36755952
http://dx.doi.org/10.3389/fphar.2023.1107435
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author Das, Kuntal
Muthukumar, A.
Almuqbil, Mansour
Imran, Mohd.
Rabaan, Ali A.
Halwani, Muhammad A.
Garout, Mohammed
Alsaleh, Abdulmonem A.
Alissa, Mohammed
Alwashmi, Ameen S. S.
Alshehri, Ahmad A.
Alsayyah, Ahmed
Bhavani, Keserla
Mittal, Swati
Gayathri, R.
Alomar, Nasser Fawzan
Rabbani, Syed Imam
Basheeruddin Asdaq, Syed Mohammed
author_facet Das, Kuntal
Muthukumar, A.
Almuqbil, Mansour
Imran, Mohd.
Rabaan, Ali A.
Halwani, Muhammad A.
Garout, Mohammed
Alsaleh, Abdulmonem A.
Alissa, Mohammed
Alwashmi, Ameen S. S.
Alshehri, Ahmad A.
Alsayyah, Ahmed
Bhavani, Keserla
Mittal, Swati
Gayathri, R.
Alomar, Nasser Fawzan
Rabbani, Syed Imam
Basheeruddin Asdaq, Syed Mohammed
author_sort Das, Kuntal
collection PubMed
description This study was done to investigate the possible nephroprotective effect of an ethanolic root extract of Polyalthia Longifolia (PL) on vancomycin-induced nephrotoxicity using curative and protective models. Vancomycin (150 mg/kg, intravenous) was given to healthy Wistar albino rats in the curative model before the start of treatment, whereas the protective group received vancomycin at the conclusion of the 10-day treatment procedure. Animals were divided into six groups for both models; group I served as the normal control, while groups II, III, IV, V, and VI were kept as toxic control, standard (selenium, 6 mg/kg), LDPL (low dose of PL 200 mg/kg), HDPL (high dose of PL 400 mg/kg), and HDPL + selenium (interactive) groups, respectively. Renal biomarkers [(uric acid, creatinine, blood urea nitrogen (BUN), serum proteins], and blood electrolyte levels were measured for all tested groups. When compared to the vancomycin group, the HDPL significantly (p < 0.01) showed greater effectiveness in lowering the BUN, potassium, and calcium levels. Additionally, in the curative model, there was a significant (p < 0.05) decrease in the blood levels of uric acid, creatinine, BUN, potassium, and calcium in the animals who received the combination of selenium and HDPL. Both LDPL and HDPL did not provide any distinguishable effect in the protective model, but groups that received HDPL with selenium did provide detectable protection by significantly lowering their levels of uric acid, BUN, serum potassium, and total serum protein in comparison to the vancomycin control group. These findings indicate that, whether administered before or after renal damage is induced, the Polyalthia longifolia root extract provided only modest protection to nephrons, which require selenium support to prevent vancomycin-induced kidney damage.
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spelling pubmed-99001012023-02-07 Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals Das, Kuntal Muthukumar, A. Almuqbil, Mansour Imran, Mohd. Rabaan, Ali A. Halwani, Muhammad A. Garout, Mohammed Alsaleh, Abdulmonem A. Alissa, Mohammed Alwashmi, Ameen S. S. Alshehri, Ahmad A. Alsayyah, Ahmed Bhavani, Keserla Mittal, Swati Gayathri, R. Alomar, Nasser Fawzan Rabbani, Syed Imam Basheeruddin Asdaq, Syed Mohammed Front Pharmacol Pharmacology This study was done to investigate the possible nephroprotective effect of an ethanolic root extract of Polyalthia Longifolia (PL) on vancomycin-induced nephrotoxicity using curative and protective models. Vancomycin (150 mg/kg, intravenous) was given to healthy Wistar albino rats in the curative model before the start of treatment, whereas the protective group received vancomycin at the conclusion of the 10-day treatment procedure. Animals were divided into six groups for both models; group I served as the normal control, while groups II, III, IV, V, and VI were kept as toxic control, standard (selenium, 6 mg/kg), LDPL (low dose of PL 200 mg/kg), HDPL (high dose of PL 400 mg/kg), and HDPL + selenium (interactive) groups, respectively. Renal biomarkers [(uric acid, creatinine, blood urea nitrogen (BUN), serum proteins], and blood electrolyte levels were measured for all tested groups. When compared to the vancomycin group, the HDPL significantly (p < 0.01) showed greater effectiveness in lowering the BUN, potassium, and calcium levels. Additionally, in the curative model, there was a significant (p < 0.05) decrease in the blood levels of uric acid, creatinine, BUN, potassium, and calcium in the animals who received the combination of selenium and HDPL. Both LDPL and HDPL did not provide any distinguishable effect in the protective model, but groups that received HDPL with selenium did provide detectable protection by significantly lowering their levels of uric acid, BUN, serum potassium, and total serum protein in comparison to the vancomycin control group. These findings indicate that, whether administered before or after renal damage is induced, the Polyalthia longifolia root extract provided only modest protection to nephrons, which require selenium support to prevent vancomycin-induced kidney damage. Frontiers Media S.A. 2023-01-23 /pmc/articles/PMC9900101/ /pubmed/36755952 http://dx.doi.org/10.3389/fphar.2023.1107435 Text en Copyright © 2023 Das, Muthukumar, Almuqbil, Imran, Rabaan, Halwani, Garout, Alsaleh, Alissa, Alwashmi, Alshehri, Alsayyah, Bhavani, Mittal, Gayathri, Alomar, Rabbani and Basheeruddin Asdaq. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Das, Kuntal
Muthukumar, A.
Almuqbil, Mansour
Imran, Mohd.
Rabaan, Ali A.
Halwani, Muhammad A.
Garout, Mohammed
Alsaleh, Abdulmonem A.
Alissa, Mohammed
Alwashmi, Ameen S. S.
Alshehri, Ahmad A.
Alsayyah, Ahmed
Bhavani, Keserla
Mittal, Swati
Gayathri, R.
Alomar, Nasser Fawzan
Rabbani, Syed Imam
Basheeruddin Asdaq, Syed Mohammed
Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title_full Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title_fullStr Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title_full_unstemmed Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title_short Nephroprotective potential of Polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
title_sort nephroprotective potential of polyalthia longifolia roots against vancomycin-induced renal toxicity in experimental animals
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9900101/
https://www.ncbi.nlm.nih.gov/pubmed/36755952
http://dx.doi.org/10.3389/fphar.2023.1107435
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