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spelling todo:paper_01681702_v141_n1_p47_Bueno2023-10-03T15:06:11Z A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent Bueno, C.A. Barquero, A.A. Di Cónsoli, H. Maier, M.S. Alché, L.E. Antiviral Cytokine HSV Immunomodulatory Medicinal plants NF-κB 1 cinnamoyl 3,11 dihydroxymeliacarpin I kappa B alpha immunoglobulin enhancer binding protein interleukin 6 lipopolysaccharide triterpenoid tumor necrosis factor alpha unclassified drug animal cell antiviral activity article controlled study cornea cell cytokine release Herpes simplex virus 1 human human cell immunomodulation macrophage nonhuman priority journal protein degradation Animals Antiviral Agents Cell Line Cells, Cultured Cornea Cytokines Herpesvirus 1, Human Humans Keratitis, Herpetic Limonins Macrophages Melia azedarach Mice Human herpesvirus 1 Melia azedarach Murinae Mus Simplexvirus Meliacine (MA), an antiviral principle present in partially purified leaf extracts of Melia azedarach L., prevents the development of herpetic stromal keratitis (HSK) in mice by diminishing the viral load in the eye and the severity of lesions caused by a virus-induced immunopathological reaction. The tetranortriterpenoid 1-cinnamoyl-3,11-dihydroxymeliacarpin (CDM), obtained from MA purification, displays anti-herpetic activity and impedes nuclear factor κB (NF-κB) activation in HSV-1 infected conjunctival cells. To extend our understanding about CDM biological properties, we investigated its anti-HSV-1 activity as well as the effect on NF-κB activation and cytokine secretion induced by viral (HSV-1) and no-viral (LPS) stimuli, in corneal cells and macrophages. CDM exerted a potent anti-HSV-1 effect on corneal cells and inhibited NF-κB translocation to the nucleus, leading to a decrease in IL-6 production. Besides, CDM seemed to modulate IL-6 and TNF-α responses in macrophages, whether they were infected with HSV-1 or stimulated with LPS. However, CDM did not affect NF-κB activation in these cells, suggesting that an alternative NF-κB cell signaling pathway would be involved in the modulation of cytokine production. We conclude that, in addition to its antiviral effect, CDM would be acting as an immunomodulating compound which would be responsible for the improvement of murine HSK already reported. © 2008 Elsevier B.V. All rights reserved. Fil:Bueno, C.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Barquero, A.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Maier, M.S. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Alché, L.E. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_01681702_v141_n1_p47_Bueno
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Antiviral
Cytokine
HSV
Immunomodulatory
Medicinal plants
NF-κB
1 cinnamoyl 3,11 dihydroxymeliacarpin
I kappa B alpha
immunoglobulin enhancer binding protein
interleukin 6
lipopolysaccharide
triterpenoid
tumor necrosis factor alpha
unclassified drug
animal cell
antiviral activity
article
controlled study
cornea cell
cytokine release
Herpes simplex virus 1
human
human cell
immunomodulation
macrophage
nonhuman
priority journal
protein degradation
Animals
Antiviral Agents
Cell Line
Cells, Cultured
Cornea
Cytokines
Herpesvirus 1, Human
Humans
Keratitis, Herpetic
Limonins
Macrophages
Melia azedarach
Mice
Human herpesvirus 1
Melia azedarach
Murinae
Mus
Simplexvirus
spellingShingle Antiviral
Cytokine
HSV
Immunomodulatory
Medicinal plants
NF-κB
1 cinnamoyl 3,11 dihydroxymeliacarpin
I kappa B alpha
immunoglobulin enhancer binding protein
interleukin 6
lipopolysaccharide
triterpenoid
tumor necrosis factor alpha
unclassified drug
animal cell
antiviral activity
article
controlled study
cornea cell
cytokine release
Herpes simplex virus 1
human
human cell
immunomodulation
macrophage
nonhuman
priority journal
protein degradation
Animals
Antiviral Agents
Cell Line
Cells, Cultured
Cornea
Cytokines
Herpesvirus 1, Human
Humans
Keratitis, Herpetic
Limonins
Macrophages
Melia azedarach
Mice
Human herpesvirus 1
Melia azedarach
Murinae
Mus
Simplexvirus
Bueno, C.A.
Barquero, A.A.
Di Cónsoli, H.
Maier, M.S.
Alché, L.E.
A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
topic_facet Antiviral
Cytokine
HSV
Immunomodulatory
Medicinal plants
NF-κB
1 cinnamoyl 3,11 dihydroxymeliacarpin
I kappa B alpha
immunoglobulin enhancer binding protein
interleukin 6
lipopolysaccharide
triterpenoid
tumor necrosis factor alpha
unclassified drug
animal cell
antiviral activity
article
controlled study
cornea cell
cytokine release
Herpes simplex virus 1
human
human cell
immunomodulation
macrophage
nonhuman
priority journal
protein degradation
Animals
Antiviral Agents
Cell Line
Cells, Cultured
Cornea
Cytokines
Herpesvirus 1, Human
Humans
Keratitis, Herpetic
Limonins
Macrophages
Melia azedarach
Mice
Human herpesvirus 1
Melia azedarach
Murinae
Mus
Simplexvirus
description Meliacine (MA), an antiviral principle present in partially purified leaf extracts of Melia azedarach L., prevents the development of herpetic stromal keratitis (HSK) in mice by diminishing the viral load in the eye and the severity of lesions caused by a virus-induced immunopathological reaction. The tetranortriterpenoid 1-cinnamoyl-3,11-dihydroxymeliacarpin (CDM), obtained from MA purification, displays anti-herpetic activity and impedes nuclear factor κB (NF-κB) activation in HSV-1 infected conjunctival cells. To extend our understanding about CDM biological properties, we investigated its anti-HSV-1 activity as well as the effect on NF-κB activation and cytokine secretion induced by viral (HSV-1) and no-viral (LPS) stimuli, in corneal cells and macrophages. CDM exerted a potent anti-HSV-1 effect on corneal cells and inhibited NF-κB translocation to the nucleus, leading to a decrease in IL-6 production. Besides, CDM seemed to modulate IL-6 and TNF-α responses in macrophages, whether they were infected with HSV-1 or stimulated with LPS. However, CDM did not affect NF-κB activation in these cells, suggesting that an alternative NF-κB cell signaling pathway would be involved in the modulation of cytokine production. We conclude that, in addition to its antiviral effect, CDM would be acting as an immunomodulating compound which would be responsible for the improvement of murine HSK already reported. © 2008 Elsevier B.V. All rights reserved.
format JOUR
author Bueno, C.A.
Barquero, A.A.
Di Cónsoli, H.
Maier, M.S.
Alché, L.E.
author_facet Bueno, C.A.
Barquero, A.A.
Di Cónsoli, H.
Maier, M.S.
Alché, L.E.
author_sort Bueno, C.A.
title A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
title_short A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
title_full A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
title_fullStr A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
title_full_unstemmed A natural tetranortriterpenoid with immunomodulating properties as a potential anti-HSV agent
title_sort natural tetranortriterpenoid with immunomodulating properties as a potential anti-hsv agent
url http://hdl.handle.net/20.500.12110/paper_01681702_v141_n1_p47_Bueno
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