Publications

Detailed Information

Suppression of Allergic Diarrhea in Murine Ovalbumin-Induced Allergic Diarrhea Model by PG102, a Water-Soluble Extract Prepared from Actinidia arguta

DC Field Value Language
dc.contributor.authorKim, Donghyun-
dc.contributor.authorKim, Seon Hee-
dc.contributor.authorPark, Eun-Jin-
dc.contributor.authorKim, Jiyoung-
dc.contributor.authorKagawa, Junko-
dc.contributor.authorJun, Kunisawa-
dc.contributor.authorKim, Sunyoung-
dc.contributor.authorKiyono, Hiroshi-
dc.contributor.authorArai, Naoko-
dc.contributor.authorCho, Sang-Heon-
dc.date.accessioned2012-05-24T01:07:21Z-
dc.date.available2012-05-24T01:07:21Z-
dc.date.issued2009-
dc.identifier.citationINTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY; Vol.150 2; 164-171ko_KR
dc.identifier.issn1018-2438-
dc.identifier.urihttps://hdl.handle.net/10371/76373-
dc.description.abstractBackground: Allergic reactions to food can involve diarrhea, vomiting, nausea and abnormal pain. PG102 has previously been shown to control various factors involved in allergy pathogenesis, including IgE and various Th1 and Th2 cytokines, in vivo as well as in vitro [Park EJ, et al.: J Allergy Clin Immunol 2005; 116: 1151-1157; Park EJ, et al.: J Invest Dermatol 2007; 127: 1154-1160]. These data indicate that PG102 might have antiallergic effects on allergic diarrhea. Here, we investigated whether PG102 could prevent allergic diarrhea in the murine ovalbumin (OVA)-induced allergic diarrhea model. Methods: BALB/c mice were orally treated with PG102, dexamethasone or water for 9 days on a daily basis, followed by subcutaneous injection with OVA on day 0. Animals were orally administrated with OVA from day 7, 3 times a week, over a period of approximately 20 days. Incidence of diarrhea, serum, OVA-restimulated splenocytes and lamina propria lymphocytes were analyzed. Results: Oral administration of PG102 could suppress the incidence of diarrhea in a murine allergic diarrhea model. The amelioration of allergic diarrhea by PG102 was accompanied with the inhibition of mast cell infiltration into the large intestine. The serum level of IgE, IL-6 and MCP-1 was decreased in PG102-treated mice. When splenocytes were isolated from respective groups and cultured in the presence of OVA, cells from PG102-administrated animals produced lesser amounts of IL-6 and MCP-1. Conclusions: PG102 has the potential to be used as a preventive for food allergic diseases. Copyright (C) 2009 S. Karger AG, Baselko_KR
dc.language.isoenko_KR
dc.publisherKARGERko_KR
dc.subjectActinidia argutako_KR
dc.subjectPG102ko_KR
dc.subjectMCP-1ko_KR
dc.subjectIL-10ko_KR
dc.subjectIL-6ko_KR
dc.subjectIgEko_KR
dc.subjectFood allergyko_KR
dc.subjectDiarrheako_KR
dc.subjectAntiallergyko_KR
dc.titleSuppression of Allergic Diarrhea in Murine Ovalbumin-Induced Allergic Diarrhea Model by PG102, a Water-Soluble Extract Prepared from Actinidia argutako_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor김동현-
dc.contributor.AlternativeAuthor김선희-
dc.contributor.AlternativeAuthor박은진-
dc.contributor.AlternativeAuthor김지영-
dc.contributor.AlternativeAuthor조상헌-
dc.contributor.AlternativeAuthor김선영-
dc.identifier.doi10.1159/000218119-
dc.citation.journaltitleINTERNATIONAL ARCHIVES OF ALLERGY AND IMMUNOLOGY-
dc.description.citedreferenceKim D, 2009, CLIN EXP ALLERGY, V39, P280, DOI 10.1111/j.1365-2222.2008.03124.x-
dc.description.citedreferenceBloemen K, 2007, IMMUNOL LETT, V113, P6, DOI 10.1016/j.imlet.2007.07.010-
dc.description.citedreferenceKurashima Y, 2007, J IMMUNOL, V179, P1577-
dc.description.citedreferencePark EJ, 2007, J INVEST DERMATOL, V127, P1154, DOI 10.1038/sj.jid.5700658-
dc.description.citedreferenceScheller J, 2006, MED MICROBIOL IMMUN, V195, P173, DOI 10.1007/s00430-006-0019-9-
dc.description.citedreferenceWan YSY, 2006, IMMUNOL REV, V212, P114-
dc.description.citedreferenceAkdis M, 2005, J ALLERGY CLIN IMMUN, V116, P961, DOI 10.1016/j.jaci.2005.09.004-
dc.description.citedreferencePark EJ, 2005, J ALLERGY CLIN IMMUN, V116, P1151, DOI 10.1016/j.jaci.2005.07.024-
dc.description.citedreferenceDoganci A, 2005, CLIN REV ALLERG IMMU, V28, P257-
dc.description.citedreferenceDetournay O, 2005, HUM IMMUNOL, V66, P460, DOI 10.1016/j.humimm.2005.01.012-
dc.description.citedreferenceSeibold F, 2005, DIGESTION, V71, P251, DOI 10.1159/000087051-
dc.description.citedreferenceAKDIS M, 2005, J ALLERGY CLIN IMMUN, V116, P969-
dc.description.citedreferenceSampson HA, 2004, J ALLERGY CLIN IMMUN, V113, P805, DOI 10.1016/j.jaci.2004.03.014-
dc.description.citedreferenceRose CE, 2003, MICROCIRCULATION, V10, P273, DOI 10.1038/sj.mn.7800193-
dc.description.citedreferenceLeung DYM, 2003, NEW ENGL J MED, V348, P986, DOI 10.1056/NEJMoa022613-
dc.description.citedreferencePasare C, 2003, SCIENCE, V299, P1033, DOI 10.1126/science.1078231-
dc.description.citedreferenceGilliet M, 2002, J EXP MED, V195, P695-
dc.description.citedreferenceHelm RM, 2002, ANN NY ACAD SCI, V964, P139-
dc.description.citedreferenceStrobel S, 2001, PEDIATR ALLERGY IMMU, V12, P43, DOI 10.1034/j.1399-3038.2001.121410.x-
dc.description.citedreferenceKweon MN, 2001, DIGESTION, V63, P1-
dc.description.citedreferenceKweon MN, 2000, J CLIN INVEST, V106, P199-
dc.description.citedreferenceAsseman C, 1999, J EXP MED, V190, P995-
dc.description.citedreferenceJones SA, 1999, J EXP MED, V189, P599-
dc.description.citedreferenceKweon MN, 1998, J IMMUNOL, V160, P1687-
dc.description.citedreferenceLOETSCHER P, 1994, FASEB J, V8, P1055-
dc.description.citedreferenceHIRANO T, 1989, J IMMUNOL METHODS, V119, P145-
dc.description.tc3-
Appears in Collections:
Files in This Item:
There are no files associated with this item.

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share