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Effect of Silymarin and Quercetin in a Miniaturized Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease
[Image: see text] Silymarin and quercetin (SQ) are known antioxidants with substantial free radical scavenging activities. The efficacy of SQ activity is restricted due to poor absorption and availability. This study aims to increase the hepatoprotective activity of SQ by a newer delivery technique....
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374897/ https://www.ncbi.nlm.nih.gov/pubmed/34423182 http://dx.doi.org/10.1021/acsomega.1c00555 |
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author | Stephen Robert, Jaisheela Marry Peddha, Muthukumar Serva Srivastava, Alok Kumar |
author_facet | Stephen Robert, Jaisheela Marry Peddha, Muthukumar Serva Srivastava, Alok Kumar |
author_sort | Stephen Robert, Jaisheela Marry |
collection | PubMed |
description | [Image: see text] Silymarin and quercetin (SQ) are known antioxidants with substantial free radical scavenging activities. The efficacy of SQ activity is restricted due to poor absorption and availability. This study aims to increase the hepatoprotective activity of SQ by a newer delivery technique. We have optimized a technique, miniaturized scaffold (MS), for the delivery of active compounds of SQ. SQ molecules were embedded in MS and characterized by morphology, particle size, miniaturization efficiency, and functional group. Further, the hepatoprotective effects of MSQ were investigated through in vitro and in vivo methods. Hepatotoxicity was induced in rats by carbon tetrachloride (CCl(4)), and subsequently, hepatotoxic rats were treated with the miniaturized scaffold of SQ (MSQ) for 8 weeks. The body weight were significantly high in groups fed with MSQ. A substantial decrease in triglyceride, total cholesterol, low-density lipoprotein, alanine aminotransferase, and aspartate aminotransferase activities were observed in rats treated with MSQ. Similarly, rats treated with MSQ exhibited lower lipid accumulation in the hepatocytes. The experiments clearly demonstrated the efficacy of MSQ as a superior hepatoprotective agent against non-alcoholic fatty liver disease simulated through toxicity induced by CCl(4). |
format | Online Article Text |
id | pubmed-8374897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-83748972021-08-20 Effect of Silymarin and Quercetin in a Miniaturized Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease Stephen Robert, Jaisheela Marry Peddha, Muthukumar Serva Srivastava, Alok Kumar ACS Omega [Image: see text] Silymarin and quercetin (SQ) are known antioxidants with substantial free radical scavenging activities. The efficacy of SQ activity is restricted due to poor absorption and availability. This study aims to increase the hepatoprotective activity of SQ by a newer delivery technique. We have optimized a technique, miniaturized scaffold (MS), for the delivery of active compounds of SQ. SQ molecules were embedded in MS and characterized by morphology, particle size, miniaturization efficiency, and functional group. Further, the hepatoprotective effects of MSQ were investigated through in vitro and in vivo methods. Hepatotoxicity was induced in rats by carbon tetrachloride (CCl(4)), and subsequently, hepatotoxic rats were treated with the miniaturized scaffold of SQ (MSQ) for 8 weeks. The body weight were significantly high in groups fed with MSQ. A substantial decrease in triglyceride, total cholesterol, low-density lipoprotein, alanine aminotransferase, and aspartate aminotransferase activities were observed in rats treated with MSQ. Similarly, rats treated with MSQ exhibited lower lipid accumulation in the hepatocytes. The experiments clearly demonstrated the efficacy of MSQ as a superior hepatoprotective agent against non-alcoholic fatty liver disease simulated through toxicity induced by CCl(4). American Chemical Society 2021-08-03 /pmc/articles/PMC8374897/ /pubmed/34423182 http://dx.doi.org/10.1021/acsomega.1c00555 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Stephen Robert, Jaisheela Marry Peddha, Muthukumar Serva Srivastava, Alok Kumar Effect of Silymarin and Quercetin in a Miniaturized Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title | Effect of Silymarin and Quercetin in a Miniaturized
Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title_full | Effect of Silymarin and Quercetin in a Miniaturized
Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title_fullStr | Effect of Silymarin and Quercetin in a Miniaturized
Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title_full_unstemmed | Effect of Silymarin and Quercetin in a Miniaturized
Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title_short | Effect of Silymarin and Quercetin in a Miniaturized
Scaffold in Wistar Rats against Non-alcoholic Fatty Liver Disease |
title_sort | effect of silymarin and quercetin in a miniaturized
scaffold in wistar rats against non-alcoholic fatty liver disease |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8374897/ https://www.ncbi.nlm.nih.gov/pubmed/34423182 http://dx.doi.org/10.1021/acsomega.1c00555 |
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