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Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression

Hepatitis A virus (HAV) infection is one of the major causes of acute hepatitis and acute liver failure in developing and developed countries. Although effective vaccines for HAV infection are available, outbreaks of HAV infection still cause deaths, even in developed countries. One approach to cont...

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Autores principales: Win, Nan Nwe, Kanda, Tatsuo, Nakamoto, Shingo, Moriyama, Mitsuhiko, Jiang, Xia, Suganami, Akiko, Tamura, Yutaka, Okamoto, Hiroaki, Shirasawa, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097272/
https://www.ncbi.nlm.nih.gov/pubmed/30123052
http://dx.doi.org/10.7150/ijms.27489
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author Win, Nan Nwe
Kanda, Tatsuo
Nakamoto, Shingo
Moriyama, Mitsuhiko
Jiang, Xia
Suganami, Akiko
Tamura, Yutaka
Okamoto, Hiroaki
Shirasawa, Hiroshi
author_facet Win, Nan Nwe
Kanda, Tatsuo
Nakamoto, Shingo
Moriyama, Mitsuhiko
Jiang, Xia
Suganami, Akiko
Tamura, Yutaka
Okamoto, Hiroaki
Shirasawa, Hiroshi
author_sort Win, Nan Nwe
collection PubMed
description Hepatitis A virus (HAV) infection is one of the major causes of acute hepatitis and acute liver failure in developing and developed countries. Although effective vaccines for HAV infection are available, outbreaks of HAV infection still cause deaths, even in developed countries. One approach to control HAV infection is prevention through diet, which can inhibit HAV propagation and replication. Glucose-regulated protein 78 (GRP78) is a member of the heat shock protein 70 family of molecular chaperone required for endoplasmic reticulum stress and stress-induced autophagy. We previously showed that the elevation of GRP78 expression inhibits HAV replication. It has been reported that Japanese miso extracts, which was made from rice-koji, enhance GRP78 expression. In the present study, we used human hepatoma Huh7 cells and human hepatocyte PXB cells to examine the efficacy of Japanese miso extracts as antiviral agents against HAV. Japanese miso extracts enhanced GRP78 expression and inhibited HAV replication in human hepatocytes. Together, these results demonstrate that Japanese miso extracts may partly modulate GRP78 expression and additively or synergistically work as antivirals against HAV infection. Japanese miso extracts can be used as effective dietary supplements for severe hepatitis A.
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spelling pubmed-60972722018-08-17 Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression Win, Nan Nwe Kanda, Tatsuo Nakamoto, Shingo Moriyama, Mitsuhiko Jiang, Xia Suganami, Akiko Tamura, Yutaka Okamoto, Hiroaki Shirasawa, Hiroshi Int J Med Sci Short Research Communication Hepatitis A virus (HAV) infection is one of the major causes of acute hepatitis and acute liver failure in developing and developed countries. Although effective vaccines for HAV infection are available, outbreaks of HAV infection still cause deaths, even in developed countries. One approach to control HAV infection is prevention through diet, which can inhibit HAV propagation and replication. Glucose-regulated protein 78 (GRP78) is a member of the heat shock protein 70 family of molecular chaperone required for endoplasmic reticulum stress and stress-induced autophagy. We previously showed that the elevation of GRP78 expression inhibits HAV replication. It has been reported that Japanese miso extracts, which was made from rice-koji, enhance GRP78 expression. In the present study, we used human hepatoma Huh7 cells and human hepatocyte PXB cells to examine the efficacy of Japanese miso extracts as antiviral agents against HAV. Japanese miso extracts enhanced GRP78 expression and inhibited HAV replication in human hepatocytes. Together, these results demonstrate that Japanese miso extracts may partly modulate GRP78 expression and additively or synergistically work as antivirals against HAV infection. Japanese miso extracts can be used as effective dietary supplements for severe hepatitis A. Ivyspring International Publisher 2018-07-30 /pmc/articles/PMC6097272/ /pubmed/30123052 http://dx.doi.org/10.7150/ijms.27489 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Short Research Communication
Win, Nan Nwe
Kanda, Tatsuo
Nakamoto, Shingo
Moriyama, Mitsuhiko
Jiang, Xia
Suganami, Akiko
Tamura, Yutaka
Okamoto, Hiroaki
Shirasawa, Hiroshi
Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title_full Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title_fullStr Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title_full_unstemmed Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title_short Inhibitory effect of Japanese rice-koji miso extracts on hepatitis A virus replication in association with the elevation of glucose-regulated protein 78 expression
title_sort inhibitory effect of japanese rice-koji miso extracts on hepatitis a virus replication in association with the elevation of glucose-regulated protein 78 expression
topic Short Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6097272/
https://www.ncbi.nlm.nih.gov/pubmed/30123052
http://dx.doi.org/10.7150/ijms.27489
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