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Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines

BACKGROUND: Hepatitis C virus (HCV) is estimated to infect 200 million individuals in the globe, including approximately 10 million in Pakistan causing both acute and chronic hepatitis. The standard treatment against HCV is pegylated interferon therapy in combination with a nucleoside analogue ribav...

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Autores principales: Ali, Liaqat, Idrees, Muhammad, Ali, Muhammad, Hussain, Abrar, Rehman, Irshad Ur, Ali, Amjad, Iqbal, Syed Abbas, Kamel, Eyad Hassan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996148/
https://www.ncbi.nlm.nih.gov/pubmed/24742271
http://dx.doi.org/10.1186/1756-0500-7-247
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author Ali, Liaqat
Idrees, Muhammad
Ali, Muhammad
Hussain, Abrar
Rehman, Irshad Ur
Ali, Amjad
Iqbal, Syed Abbas
Kamel, Eyad Hassan
author_facet Ali, Liaqat
Idrees, Muhammad
Ali, Muhammad
Hussain, Abrar
Rehman, Irshad Ur
Ali, Amjad
Iqbal, Syed Abbas
Kamel, Eyad Hassan
author_sort Ali, Liaqat
collection PubMed
description BACKGROUND: Hepatitis C virus (HCV) is estimated to infect 200 million individuals in the globe, including approximately 10 million in Pakistan causing both acute and chronic hepatitis. The standard treatment against HCV is pegylated interferon therapy in combination with a nucleoside analogue ribavirin. In addition, several herbal extracts and phytochemicals derivatives are used traditionally in the treatment of liver diseases as well as HCV infection. The present study determines the inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines. METHODS: Huh-7 cell lines were used for the in vitro HCV replication by using HCV positive sera from different patients with known HCV genotypes and viral titer/load. Total RNA was extracted from these infected cells and was quantified by real-time polymerase chain reaction (Real-time PCR). The viral titer was compared with the control samples to determine the anti-HCV activity of kaolin derived compounds. Kaolin is a group of clay minerals, with the chemical composition Al(2) Si(2)O(5) (OH)(4). RESULTS: The results showed promising effectiveness of local kaolin derived anti-HCV compounds by causing 28% to 77% decrease in the HCV titer, when applied to infected Huh-7 cell lines. This study provides the basis for future work on these compounds especially to determine the specific pathway and mechanism for inhibitory action in the replicon systems of viral hepatitis. CONCLUSIONS: Kaolin mineral derivatives show promising inhibitory effects against HCV genotypes 3a and 1a infection, which suggests its possible use as complementary and alternative medicine for HCV viral infection.
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spelling pubmed-39961482014-04-24 Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines Ali, Liaqat Idrees, Muhammad Ali, Muhammad Hussain, Abrar Rehman, Irshad Ur Ali, Amjad Iqbal, Syed Abbas Kamel, Eyad Hassan BMC Res Notes Research Article BACKGROUND: Hepatitis C virus (HCV) is estimated to infect 200 million individuals in the globe, including approximately 10 million in Pakistan causing both acute and chronic hepatitis. The standard treatment against HCV is pegylated interferon therapy in combination with a nucleoside analogue ribavirin. In addition, several herbal extracts and phytochemicals derivatives are used traditionally in the treatment of liver diseases as well as HCV infection. The present study determines the inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines. METHODS: Huh-7 cell lines were used for the in vitro HCV replication by using HCV positive sera from different patients with known HCV genotypes and viral titer/load. Total RNA was extracted from these infected cells and was quantified by real-time polymerase chain reaction (Real-time PCR). The viral titer was compared with the control samples to determine the anti-HCV activity of kaolin derived compounds. Kaolin is a group of clay minerals, with the chemical composition Al(2) Si(2)O(5) (OH)(4). RESULTS: The results showed promising effectiveness of local kaolin derived anti-HCV compounds by causing 28% to 77% decrease in the HCV titer, when applied to infected Huh-7 cell lines. This study provides the basis for future work on these compounds especially to determine the specific pathway and mechanism for inhibitory action in the replicon systems of viral hepatitis. CONCLUSIONS: Kaolin mineral derivatives show promising inhibitory effects against HCV genotypes 3a and 1a infection, which suggests its possible use as complementary and alternative medicine for HCV viral infection. BioMed Central 2014-04-17 /pmc/articles/PMC3996148/ /pubmed/24742271 http://dx.doi.org/10.1186/1756-0500-7-247 Text en Copyright © 2014 Ali et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Ali, Liaqat
Idrees, Muhammad
Ali, Muhammad
Hussain, Abrar
Rehman, Irshad Ur
Ali, Amjad
Iqbal, Syed Abbas
Kamel, Eyad Hassan
Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title_full Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title_fullStr Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title_full_unstemmed Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title_short Inhibitory effect of kaolin minerals compound against hepatitis C virus in Huh-7 cell lines
title_sort inhibitory effect of kaolin minerals compound against hepatitis c virus in huh-7 cell lines
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996148/
https://www.ncbi.nlm.nih.gov/pubmed/24742271
http://dx.doi.org/10.1186/1756-0500-7-247
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