id paper:paper_00426822_v309_n1_p75_Benencia
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spelling paper:paper_00426822_v309_n1_p75_Benencia2023-06-08T15:04:51Z Nitric oxide and HSV vaginal infection in BALB/c mice aminoguanidine macrophage inflammatory protein 2 messenger RNA n acetyl s nitrosopenicillamine nitric oxide nitric oxide donor nitric oxide synthase nitric oxide synthase inhibitor RANTES animal cell animal experiment animal model animal tissue article cell count controlled study enzyme activation exudate female Herpes simplex virus 2 histopathology inguinal lymph node mouse nonhuman polymorphonuclear cell priority journal protein expression reverse transcription polymerase chain reaction vaginitis virus replication virus titration Animalia Human herpesvirus 2 Simplexvirus Here we study the role of nitric oxide in the vaginal infection of Balb/c mice with herpes simplex virus type 2. Inducible nitric oxide synthase (iNOS) mRNA was detected by RT-PCR in vaginal tissue and inguinal lymph nodes early postinfection. iNOS was also found to be activated in cells recovered from vaginal washings of infected animals. Animals treated with aminoguanidine (AG), an iNOS inhibitor, showed a dose-dependent increase in vaginal pathology after viral infection compared to controls. Viral titers in vaginal washings and vaginas were higher in AG-treated mice. Treated animals presented higher PMN counts in vaginal washings compared to controls. Histopathology studies revealed a profound inflammatory exudate in vaginal tissue of treated animals. Finally, RT-PCR analysis showed increased expression of the chemokines MIP-2 and RANTES in vaginal tissue and inguinal lymph nodes of these animals. © 2003 Elsevier Science (USA). All rights reserved. 2003 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00426822_v309_n1_p75_Benencia http://hdl.handle.net/20.500.12110/paper_00426822_v309_n1_p75_Benencia
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic aminoguanidine
macrophage inflammatory protein 2
messenger RNA
n acetyl s nitrosopenicillamine
nitric oxide
nitric oxide donor
nitric oxide synthase
nitric oxide synthase inhibitor
RANTES
animal cell
animal experiment
animal model
animal tissue
article
cell count
controlled study
enzyme activation
exudate
female
Herpes simplex virus 2
histopathology
inguinal lymph node
mouse
nonhuman
polymorphonuclear cell
priority journal
protein expression
reverse transcription polymerase chain reaction
vaginitis
virus replication
virus titration
Animalia
Human herpesvirus 2
Simplexvirus
spellingShingle aminoguanidine
macrophage inflammatory protein 2
messenger RNA
n acetyl s nitrosopenicillamine
nitric oxide
nitric oxide donor
nitric oxide synthase
nitric oxide synthase inhibitor
RANTES
animal cell
animal experiment
animal model
animal tissue
article
cell count
controlled study
enzyme activation
exudate
female
Herpes simplex virus 2
histopathology
inguinal lymph node
mouse
nonhuman
polymorphonuclear cell
priority journal
protein expression
reverse transcription polymerase chain reaction
vaginitis
virus replication
virus titration
Animalia
Human herpesvirus 2
Simplexvirus
Nitric oxide and HSV vaginal infection in BALB/c mice
topic_facet aminoguanidine
macrophage inflammatory protein 2
messenger RNA
n acetyl s nitrosopenicillamine
nitric oxide
nitric oxide donor
nitric oxide synthase
nitric oxide synthase inhibitor
RANTES
animal cell
animal experiment
animal model
animal tissue
article
cell count
controlled study
enzyme activation
exudate
female
Herpes simplex virus 2
histopathology
inguinal lymph node
mouse
nonhuman
polymorphonuclear cell
priority journal
protein expression
reverse transcription polymerase chain reaction
vaginitis
virus replication
virus titration
Animalia
Human herpesvirus 2
Simplexvirus
description Here we study the role of nitric oxide in the vaginal infection of Balb/c mice with herpes simplex virus type 2. Inducible nitric oxide synthase (iNOS) mRNA was detected by RT-PCR in vaginal tissue and inguinal lymph nodes early postinfection. iNOS was also found to be activated in cells recovered from vaginal washings of infected animals. Animals treated with aminoguanidine (AG), an iNOS inhibitor, showed a dose-dependent increase in vaginal pathology after viral infection compared to controls. Viral titers in vaginal washings and vaginas were higher in AG-treated mice. Treated animals presented higher PMN counts in vaginal washings compared to controls. Histopathology studies revealed a profound inflammatory exudate in vaginal tissue of treated animals. Finally, RT-PCR analysis showed increased expression of the chemokines MIP-2 and RANTES in vaginal tissue and inguinal lymph nodes of these animals. © 2003 Elsevier Science (USA). All rights reserved.
title Nitric oxide and HSV vaginal infection in BALB/c mice
title_short Nitric oxide and HSV vaginal infection in BALB/c mice
title_full Nitric oxide and HSV vaginal infection in BALB/c mice
title_fullStr Nitric oxide and HSV vaginal infection in BALB/c mice
title_full_unstemmed Nitric oxide and HSV vaginal infection in BALB/c mice
title_sort nitric oxide and hsv vaginal infection in balb/c mice
publishDate 2003
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00426822_v309_n1_p75_Benencia
http://hdl.handle.net/20.500.12110/paper_00426822_v309_n1_p75_Benencia
_version_ 1768542212570742784