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Bueno, C.A.; Michelini, F.M.; Pertino, M.W.; Gómez, C.A.; Schmeda-Hirschmann, G.; Alché, L.E. "Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway" (2015) Medical Microbiology and Immunology. 204(5):575-584
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Abstract:

The pathogenesis of many viral infections lies on the damage caused by the immune response against the virus. Current antiviral drugs do not act on the inflammatory component of the disease. Thus, new compounds that inhibit both viral multiplication and the immunopathology elicited by the virus are an approach that should be considered. In the present study, we identified two jatropholones (2A and 5B) and one carnosic acid derivative (9C) that significantly inhibited multiplication of TK+ and TK− strains of HSV-1 in Vero cells. Compounds 2A, 5B and 9C also prevented HSV-1- and TLRs-induced inflammatory response in cultivated murine macrophages. In macrophages infected with HSV-1, the inhibitory effect of compounds 2A, 5B and 9C on TNF-α and IL-6 production could be associated with the block of ERK pathway, whereas NF-κB pathway was not hampered by any of the compounds. Besides, 2A, 5B and 9C also inhibited ERK pathway and reduced TNF-α production in macrophages stimulated with TLR2, TLR4 or TLR9 agonists and were able to hinder IL-6 secretion after activation with TLR2 or TLR4, but not with TLR9. The immunomodulatory effect of 2A, 5B and 9C in macrophages infected with HSV-1 may be a consequence of the inhibition of ERK pathway activated by TLRs. The availability of compounds with both antiviral and immunomodulatory properties which affect TLR signaling pathways might be a useful strategy to control the progress of virus-induced disease. © 2014, Springer-Verlag Berlin Heidelberg.

Registro:

Documento: Artículo
Título:Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway
Autor:Bueno, C.A.; Michelini, F.M.; Pertino, M.W.; Gómez, C.A.; Schmeda-Hirschmann, G.; Alché, L.E.
Filiación:Laboratorio de Virología, Departamento de Química Biológica-IQUIBICEN, Universidad de Buenos Aires, Pabellón II, Piso 4º, Ciudad Universitaria, C-1428GBA, Buenos Aires, Argentina
Laboratorio de Química de Productos Naturales, Instituto de Química de Recursos Naturales, Universidad de Talca, Casilla 747, Talca, Chile
Palabras clave:Antiviral; Carnosic acid; ERK pathway; HSV-1; Immunomodulatory; Jatropholones; carnosic acid; carnosic acid derivative; diterpenoid; immunoglobulin enhancer binding protein; interleukin 6; jatropholone; jatropholone A; jatropholone B; mitogen activated protein kinase; toll like receptor; toll like receptor 2; toll like receptor 4; toll like receptor 9; toll like receptor agonist; tumor necrosis factor alpha; unclassified drug; antivirus agent; cytokine; diterpene; immunosuppressive agent; animal cell; antiviral activity; Article; controlled study; cytokine production; cytokine release; disease course; drug activity; drug effect; drug structure; Herpes simplex virus 1; immunomodulatory activity; inflammation; macrophage activation; macrophage culture; nonhuman; priority journal; signal transduction; Vero cell line; virus inhibition; virus strain; animal; antagonists and inhibitors; cell line; Chlorocebus aethiops; drug effects; immunology; mouse; physiology; signal transduction; virus replication; Animals; Antiviral Agents; Cell Line; Cercopithecus aethiops; Cytokines; Diterpenes; Herpesvirus 1, Human; Immunosuppressive Agents; MAP Kinase Signaling System; Mice; Virus Replication
Año:2015
Volumen:204
Número:5
Página de inicio:575
Página de fin:584
DOI: http://dx.doi.org/10.1007/s00430-014-0383-9
Título revista:Medical Microbiology and Immunology
Título revista abreviado:Med. Microbiol. Immunol.
ISSN:03008584
CODEN:MMIYA
CAS:carnosic acid, 3650-09-7; mitogen activated protein kinase, 142243-02-5; toll like receptor, 409141-78-2; toll like receptor 2, 203811-81-8; toll like receptor 4, 203811-83-0; toll like receptor 9, 352486-49-8, 390883-32-6; Antiviral Agents; Cytokines; Diterpenes; Immunosuppressive Agents
Registro:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_03008584_v204_n5_p575_Bueno

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Citas:

---------- APA ----------
Bueno, C.A., Michelini, F.M., Pertino, M.W., Gómez, C.A., Schmeda-Hirschmann, G. & Alché, L.E. (2015) . Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway. Medical Microbiology and Immunology, 204(5), 575-584.
http://dx.doi.org/10.1007/s00430-014-0383-9
---------- CHICAGO ----------
Bueno, C.A., Michelini, F.M., Pertino, M.W., Gómez, C.A., Schmeda-Hirschmann, G., Alché, L.E. "Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway" . Medical Microbiology and Immunology 204, no. 5 (2015) : 575-584.
http://dx.doi.org/10.1007/s00430-014-0383-9
---------- MLA ----------
Bueno, C.A., Michelini, F.M., Pertino, M.W., Gómez, C.A., Schmeda-Hirschmann, G., Alché, L.E. "Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway" . Medical Microbiology and Immunology, vol. 204, no. 5, 2015, pp. 575-584.
http://dx.doi.org/10.1007/s00430-014-0383-9
---------- VANCOUVER ----------
Bueno, C.A., Michelini, F.M., Pertino, M.W., Gómez, C.A., Schmeda-Hirschmann, G., Alché, L.E. Natural and semisynthetic diterpenoids with antiviral and immunomodulatory activities block the ERK signaling pathway. Med. Microbiol. Immunol. 2015;204(5):575-584.
http://dx.doi.org/10.1007/s00430-014-0383-9