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Rehmannia Glutinosa Pharmacopuncture Solution Regulates Functional Activation, FcεRI Expression, and Signaling Events in Mast Cells.
Kang, Kyung-Hwa; Lee, Kyung-Hee; Yoon, Hyun-Min; Jang, Kyung-Jeon; Song, Chun-; Kim, Cheol-Hong.
Afiliación
  • Kang KH; Department of Oriental Physiology, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
  • Lee KH; Department of Acupuncture & Moxibustion, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
  • Yoon HM; Department of Acupuncture & Moxibustion, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
  • Jang KJ; Department of Acupuncture & Moxibustion, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
  • Song C; Department of Acupuncture & Moxibustion, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
  • Kim CH; Department of Acupuncture & Moxibustion, Dong-Eui University College of Oriental Medicine and Research Institute of Oriental Medicine, Busan, Korea.
J Pharmacopuncture ; 15(4): 32-41, 2012 Dec.
Article en En | MEDLINE | ID: mdl-25780652
OBJECTIVES: Rehmannia glutinosa pharmacopuncture solution (RGPS) was investigated to determine both its anti-allergic inflammatory effects on mast cells and its detailed mechanism of actions. METHODS: We investigated whether RGPS suppress cytokines, enzymes, FcεRI expression and FcεRImediated signaling in RBL-2H3 cells stimulated with anti-DNP IgE/DNP-HSA. The suppressive effects of RGPS on the levels of cytokines such as IL-1ß, IL-6 and GM-CSF were measured using emzyme-linked immunospecific assay (ELISA). The mRNA expression levels of cytokines, enzymes (HDC2, COX-1, COX-2 and 5LO) and FcεRI αßγsubunits were measured using reverse transcription polymerase chain reaction (RTPCR) method. The activation of FcεRI-mediated signaling was examined using Western blot analyses. RESULTS: RGPS suppressed production of proinflamm-atory cytokines (IL-1ß, IL-6, and GM-CSF) in stimulated RBL-2H3 cells significantly (p< 0.05). RGPS also suppressed mRNA expression of inflammatory enzymes (HDC2, COX-1, COX-2, 5LO). In addition, mRNA expression levels of FcεRIα, FcεRIßand FcεRIγ were lowered by treatment with RGPS. Finally, RGPS prevented phosphrylation of Lyn, Syk, LAT, Gab2, PLC γ1/2, PI3K, Akt, cPLA2 and IκBα. CONCLUSIONS: RGPS effectively suppresses mast cell activations such as degranulation and inflammatory response via down-regulation of the FcεRI-mediated signaling pathways in IgE/Ag-stimulated mast cells.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Pharmacopuncture Año: 2012 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Pharmacopuncture Año: 2012 Tipo del documento: Article