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In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment

Biliverdin (BY) is a bile pigment having anti‐allergic properties. We examined the effect of BV on human immunodeficiency virus type 1 (HIV‐1) in vitro. BV completely inhibited the cytopathic effect of HIV‐1 in MT‐4 cells at concentrations of 22.2 μg/ml or more. This inhibitory effect was also obser...

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Autores principales: Mori, Haruyo, Otake, Toru, Morimoto, Motoko, Ueba, Noboru, Kunita, Nobuharu, Nakagami, Tatsuyoshi, Yamasaki, Non, Taji, Shiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 1991
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918533/
https://www.ncbi.nlm.nih.gov/pubmed/1715337
http://dx.doi.org/10.1111/j.1349-7006.1991.tb02698.x
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author Mori, Haruyo
Otake, Toru
Morimoto, Motoko
Ueba, Noboru
Kunita, Nobuharu
Nakagami, Tatsuyoshi
Yamasaki, Non
Taji, Shiro
author_facet Mori, Haruyo
Otake, Toru
Morimoto, Motoko
Ueba, Noboru
Kunita, Nobuharu
Nakagami, Tatsuyoshi
Yamasaki, Non
Taji, Shiro
author_sort Mori, Haruyo
collection PubMed
description Biliverdin (BY) is a bile pigment having anti‐allergic properties. We examined the effect of BV on human immunodeficiency virus type 1 (HIV‐1) in vitro. BV completely inhibited the cytopathic effect of HIV‐1 in MT‐4 cells at concentrations of 22.2 μg/ml or more. This inhibitory effect was also observed when BV was present during the adsorption period of HIV‐1. However, BV was cytotoxic to MT‐4 cells at concentrations above 800 μg/ml. At a concentration of 66.7 μg/ml, BV completely inhibited syncytia formation by HIV‐infected and uninfected MOLT‐4 cells. Moreover, after exposure of HIV‐1 particles to BV for 2 h, the infectivity of the virus was reduced in a dose‐dependent manner. It is speculated that the anti‐HIV activity of BV is due to direct inactivation of virions and inhibition of virus binding to target cells.
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spelling pubmed-59185332018-05-11 In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment Mori, Haruyo Otake, Toru Morimoto, Motoko Ueba, Noboru Kunita, Nobuharu Nakagami, Tatsuyoshi Yamasaki, Non Taji, Shiro Jpn J Cancer Res Rapid Communication Biliverdin (BY) is a bile pigment having anti‐allergic properties. We examined the effect of BV on human immunodeficiency virus type 1 (HIV‐1) in vitro. BV completely inhibited the cytopathic effect of HIV‐1 in MT‐4 cells at concentrations of 22.2 μg/ml or more. This inhibitory effect was also observed when BV was present during the adsorption period of HIV‐1. However, BV was cytotoxic to MT‐4 cells at concentrations above 800 μg/ml. At a concentration of 66.7 μg/ml, BV completely inhibited syncytia formation by HIV‐infected and uninfected MOLT‐4 cells. Moreover, after exposure of HIV‐1 particles to BV for 2 h, the infectivity of the virus was reduced in a dose‐dependent manner. It is speculated that the anti‐HIV activity of BV is due to direct inactivation of virions and inhibition of virus binding to target cells. Blackwell Publishing Ltd 1991-07 /pmc/articles/PMC5918533/ /pubmed/1715337 http://dx.doi.org/10.1111/j.1349-7006.1991.tb02698.x Text en
spellingShingle Rapid Communication
Mori, Haruyo
Otake, Toru
Morimoto, Motoko
Ueba, Noboru
Kunita, Nobuharu
Nakagami, Tatsuyoshi
Yamasaki, Non
Taji, Shiro
In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title_full In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title_fullStr In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title_full_unstemmed In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title_short In vitro Anti‐human Immunodeficiency Virus Type 1 Activity of Biliverdin, a Bile Pigment
title_sort in vitro anti‐human immunodeficiency virus type 1 activity of biliverdin, a bile pigment
topic Rapid Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5918533/
https://www.ncbi.nlm.nih.gov/pubmed/1715337
http://dx.doi.org/10.1111/j.1349-7006.1991.tb02698.x
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