Your browser doesn't support javascript.
loading
Compatibility of geniposide and ginsenoside rgl: their regulating roles in secretion of anoxia induction injured microglia inflammatory cytokines / 中国中西医结合杂志
Article en Zh | WPRIM | ID: wpr-231594
Biblioteca responsable: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To clarify the protective roles of compatibility of geniposide and ginsenoside (Rg1) in regulating ischemia injured microglia homeostasis by comparing the difference in regulatory roles of geniposide, Rg1, or ginsenoside + Rg1 in balancing secretion of oxygen glucose deprivation induced microglia inflammatory cytokines.</p><p><b>METHODS</b>The mimic ischemia injured microglia model was induced by oxygen-glucose deprivation (OGD). Then geniposide, Rg1, or ginsenoside + Rg1 (Tongluo Jiunao Injection, TJI) was respectively added. The NO content was determined by Griess Reagent. The cyto activity was detected using cell count kit. Contents of TNF-alpha and TGF-beta and their expression levels were detected by ELISA and Western blot.</p><p><b>RESULTS</b>Geniposide + Rg1 could significantly inhibit the release of NO, elevate the TGF-beta level, and decrease the content of TNF-alpha without influencing the cell survival. The two active ingredients played different therapeutic roles. The compatible use was obviously superior to use any one of the two active ingredients alone.</p><p><b>CONCLUSIONS</b>Geniposide, Rg1, or Ginsenoside + Rg1 had regulating roles in balancing ischemia injured microglia homeostasis. Its mechanisms might be related to up-regulating the TGF-beta expression and down-regulating TNF-alpha expression.</p>
Asunto(s)
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / Factor de Crecimiento Transformador beta / Factor de Necrosis Tumoral alfa / Microglía / Iridoides / Ginsenósidos / Hipoxia / Metabolismo / Óxido Nítrico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: Zh Revista: Zhongguo Zhong Xi Yi Jie He Za Zhi Año: 2014 Tipo del documento: Article
Texto completo: 1 Base de datos: WPRIM Asunto principal: Farmacología / Factor de Crecimiento Transformador beta / Factor de Necrosis Tumoral alfa / Microglía / Iridoides / Ginsenósidos / Hipoxia / Metabolismo / Óxido Nítrico Tipo de estudio: Prognostic_studies Límite: Animals Idioma: Zh Revista: Zhongguo Zhong Xi Yi Jie He Za Zhi Año: 2014 Tipo del documento: Article