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Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)

In the current study, the hepatoprotective activity of vanillic acid, silymarin, and vanillic acid-loaded silver nanoparticles (AgNPs) against CCl(4)-induced hepatotoxicity was tested in male rats for four weeks. Thirty male rats were divided into five groups (n = 6). The 1st group was a negative co...

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Autores principales: Alamri, Eman S., El Rabey, Haddad A., Alzahrani, Othman R., Almutairi, Fahad M., Attia, Eman S., Bayomy, Hala M., Albalwi, Renad A., Rezk, Samar M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737075/
https://www.ncbi.nlm.nih.gov/pubmed/36500401
http://dx.doi.org/10.3390/molecules27238308
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author Alamri, Eman S.
El Rabey, Haddad A.
Alzahrani, Othman R.
Almutairi, Fahad M.
Attia, Eman S.
Bayomy, Hala M.
Albalwi, Renad A.
Rezk, Samar M.
author_facet Alamri, Eman S.
El Rabey, Haddad A.
Alzahrani, Othman R.
Almutairi, Fahad M.
Attia, Eman S.
Bayomy, Hala M.
Albalwi, Renad A.
Rezk, Samar M.
author_sort Alamri, Eman S.
collection PubMed
description In the current study, the hepatoprotective activity of vanillic acid, silymarin, and vanillic acid-loaded silver nanoparticles (AgNPs) against CCl(4)-induced hepatotoxicity was tested in male rats for four weeks. Thirty male rats were divided into five groups (n = 6). The 1st group was a negative control, the 2nd group was a positive control, the 3rd group was treated with 100 mg/kg b.w. of vanillic acid, the 4th group was treated with 100 mg/kg b.w. of vanillic acid–AgNPs, and the 5th group was treated with 50 mg/kg b.w. of silymarin. The CCl(4)-induced hepatic toxicity in the 2nd group was revealed by the liver function and all other biochemical tests. Liver enzymes, bilirubin, lipid peroxidation, lactate dehydrogenase, and interleukin-6 were elevated, whereas, total protein, antioxidant enzymes, and irisin were decreased compared to the negative control. The hepatic tissues were also injured as a result of the CCl(4)-induced hepatotoxicity. Treating the hepatotoxic rats with vanillic acid moderately protected the rats of the 3rd group, whereas treatment with vanillic AgNPs and silymarin in G4 and G5, respectively, greatly protected the rats against the CCl(4) hepatotoxicity, approaching the normal biochemical levels and liver tissue appearance. The biochemical tests were confirmed by the histological investigations of liver tissue.
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spelling pubmed-97370752022-12-11 Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs) Alamri, Eman S. El Rabey, Haddad A. Alzahrani, Othman R. Almutairi, Fahad M. Attia, Eman S. Bayomy, Hala M. Albalwi, Renad A. Rezk, Samar M. Molecules Article In the current study, the hepatoprotective activity of vanillic acid, silymarin, and vanillic acid-loaded silver nanoparticles (AgNPs) against CCl(4)-induced hepatotoxicity was tested in male rats for four weeks. Thirty male rats were divided into five groups (n = 6). The 1st group was a negative control, the 2nd group was a positive control, the 3rd group was treated with 100 mg/kg b.w. of vanillic acid, the 4th group was treated with 100 mg/kg b.w. of vanillic acid–AgNPs, and the 5th group was treated with 50 mg/kg b.w. of silymarin. The CCl(4)-induced hepatic toxicity in the 2nd group was revealed by the liver function and all other biochemical tests. Liver enzymes, bilirubin, lipid peroxidation, lactate dehydrogenase, and interleukin-6 were elevated, whereas, total protein, antioxidant enzymes, and irisin were decreased compared to the negative control. The hepatic tissues were also injured as a result of the CCl(4)-induced hepatotoxicity. Treating the hepatotoxic rats with vanillic acid moderately protected the rats of the 3rd group, whereas treatment with vanillic AgNPs and silymarin in G4 and G5, respectively, greatly protected the rats against the CCl(4) hepatotoxicity, approaching the normal biochemical levels and liver tissue appearance. The biochemical tests were confirmed by the histological investigations of liver tissue. MDPI 2022-11-28 /pmc/articles/PMC9737075/ /pubmed/36500401 http://dx.doi.org/10.3390/molecules27238308 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Alamri, Eman S.
El Rabey, Haddad A.
Alzahrani, Othman R.
Almutairi, Fahad M.
Attia, Eman S.
Bayomy, Hala M.
Albalwi, Renad A.
Rezk, Samar M.
Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title_full Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title_fullStr Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title_full_unstemmed Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title_short Enhancement of the Protective Activity of Vanillic Acid against Tetrachloro-Carbon (CCl(4)) Hepatotoxicity in Male Rats by the Synthesis of Silver Nanoparticles (AgNPs)
title_sort enhancement of the protective activity of vanillic acid against tetrachloro-carbon (ccl(4)) hepatotoxicity in male rats by the synthesis of silver nanoparticles (agnps)
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9737075/
https://www.ncbi.nlm.nih.gov/pubmed/36500401
http://dx.doi.org/10.3390/molecules27238308
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