dc.creatorEberlin, S
dc.creatordos Santos, LMB
dc.creatorQueiroz, MLS
dc.date2005
dc.dateJUL
dc.date2014-11-16T10:19:45Z
dc.date2015-11-26T17:24:31Z
dc.date2014-11-16T10:19:45Z
dc.date2015-11-26T17:24:31Z
dc.date.accessioned2018-03-29T00:11:49Z
dc.date.available2018-03-29T00:11:49Z
dc.identifierInternational Immunopharmacology. Elsevier Science Bv, v. 5, n. 41858, n. 1235, n. 1246, 2005.
dc.identifier1567-5769
dc.identifierWOS:000229714300013
dc.identifier10.1016/j.intimp.2005.03.001
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/73361
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/73361
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/73361
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1284098
dc.descriptionIn this study, we demonstrated that Uncaria tomentosa extract (UTE) protects mice from a lethal dose of Listeria monocytogenes when administered prophytactically at 50, 100, 150 and 200 mg/kg for 7 days, with survival rates up to 35%. These doses also prevented the myelosuppression and the splenomegaly caused by a sublethal infection with L. monocytogenes, due to increased numbers of granulocyte-macrophage progenitors (CFU-GM) in the bone marrow. Non-infected mice treated with 100 mg/kg UTE also presented higher numbers of CFU-GM in the bone marrow than the controls. Investigation of the production of colony-stimulating factors revealed increased colony-stimulating activity (CSA) in the serum of normal and infected mice pre-treated with UTE. Moreover, stimulation of myelopoiesis and CSA occurred in a dose-dependent manner, a plateaux being reached with the dose of 100 mg/kg. Further studies to investigate the levels of factors such as IL-1 and IL-6 were undertaken. We observed increases in the levels of IL-1 and IL-6 in mice infected with L. monocytogenes and treated with 100 mg/kg of UTE. White blood cells (WI3Q and differential counting were also performed, and our results demonstrated no significant changes in these data, when infected mice were pre-treated with 100 mg/kg of UTE. All together, our results suggest that UTE indirectly modulates immune activity and probably disengages Listeria-induced supression of these responses by inducing a higher reserve of myeloid progenitors in the bone marrow in consequence of biologically active cytokine release (CSFs, IL-1 and IL-6). (C) 2005 Elsevier B.V. All rights reserved.
dc.description5
dc.description41858
dc.description1235
dc.description1246
dc.languageen
dc.publisherElsevier Science Bv
dc.publisherAmsterdam
dc.publisherHolanda
dc.relationInternational Immunopharmacology
dc.relationInt. Immunopharmacol.
dc.rightsfechado
dc.rightshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.sourceWeb of Science
dc.subjectUncaria tomentosa
dc.subjectListeria monocytogenes
dc.subjecthematopoiesis
dc.subjectCFU-GM
dc.subjectCSA
dc.subjectIL-1
dc.subjectIL-6
dc.subjectColony-stimulating Factor
dc.subjectPentacyclic Oxindole Alkaloids
dc.subjectNf-kappa-b
dc.subjectCats-claw
dc.subjectMurine Listeriosis
dc.subjectBacterial-infection
dc.subjectSusceptible Mice
dc.subjectProtects Mice
dc.subjectAntiinflammatory Activity
dc.subjectHematopoietic Response
dc.titleUncaria tomentosa extract increases the number of myeloid progenitor cells in the bone marrow of mice infected with Listeria monocytogenes
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución