1. Academic Validation
  2. Suppression of nuclear factor-kappa B and mitogen-activated protein kinase signalling pathways by goshonoside-F5 extracted from Rubi Fructus

Suppression of nuclear factor-kappa B and mitogen-activated protein kinase signalling pathways by goshonoside-F5 extracted from Rubi Fructus

  • Int Immunopharmacol. 2015 Feb;24(2):182-190. doi: 10.1016/j.intimp.2014.12.007.
Jian-Ming He 1 Shi-Cai Chen 2 Run-Ping Li 3 Liang-Xi Yuan 4 Jun-Min Bao 5 Mei-Li Guo 6
Affiliations

Affiliations

  • 1 Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, Shanghai 200433, China; School of Pharmacy, Fudan University, Shanghai 201203, China.
  • 2 Department of Otorhinolaryngology, Changhai Hospital, Shanghai 200433, China. Electronic address: docchen5775@yahoo.com.cn.
  • 3 Department of Diving Medicine, Faculty of Navy Medicine, Second Military Medical University, Shanghai 200433, China.
  • 4 Department of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • 5 Department of Vascular Surgery, Changhai Hospital, Second Military Medical University, Shanghai 200433, China. Electronic address: drbaojm@gmail.com.
  • 6 Department of Pharmacognosy, School of Pharmacy, Second Military Medical University, Shanghai 200433, China. Electronic address: mlguo@126.com.
Abstract

Rubi Fructus, a traditional Chinese medicine, was considered as an anti-inflammatory agent in folk medicine. In the present study, we investigated the signalling pathways involved in the anti-inflammatory effects of goshonoside-F5 (GF5), isolated from Rubi Fructus, in peritoneal macrophages and examined its therapeutic effect in a mouse endotoxic shock model. GF5 decreased NO and PGE2 production in LPS-stimulated macrophages (IC50=3.84 and 3.16μM). This effect involved the suppression of NOS-2 and COX-2 gene expression at the transcriptional level. Examination of the effects of GF5 on NF-κB signalling demonstrated that it inhibits the phosphorylation of IκB-α and IκB-β, blocking their degradation and the nuclear translocation of the NF-κB p65 subunit. Moreover, inhibition of MAPK signalling was also observed, and phosphorylation of p38 and JNK was suppressed in the presence of GF5. Inflammatory cytokines, including IL-6 and TNF-α, were down-regulated by this compound after activation with LPS (IC50=17.04 and 4.09μM). Additionally, GF5 (30 and 90mg/kg, i.p.) significantly reduced the circulating cytokine levels (IL-6 and TNF-α) and increased survival in a mouse model of endotoxemia. These results show that GF5 significantly inhibits the pro-inflammatory response induced by LPS, both in vitro and in vivo. Our results provide a strong pharmacological basis for further understanding the potential therapeutic role of GF5 in inflammatory disease and shed new LIGHT on the bioactivity of ent-labdane diterpene glucoside.

Keywords

Anti-inflammatory; Ent-labdane diterpene glucoside; MAPK; Macrophage; NF-κB; Rubi Fructus.

Figures
Products