The inhibitory effect of Aconiti Sinomontani Radix extracts on the proliferation and migration of human synovial fibroblast cell line SW982

J Ethnopharmacol. 2018 Mar 1:213:321-327. doi: 10.1016/j.jep.2017.11.029. Epub 2017 Nov 28.

Abstract

Ethnopharmacological relevance: Aconiti Sinomontani Radix is frequently used in the treatment of Bi syndrome in traditional Chinese medicine. Several reports indicate that Aconiti Sinomontani Radix has therapeutic effects for rheumatoid arthritis (RA). However, the cellular mode of action is still unclear. To investigate the effect of alkaloid extracts of Aconiti Sinomontani Radix on proliferation and migration of human synovial sarcoma SW982 cells as well as the molecular mechanism underlying.

Materials and methods: SW982 cells were examined for proliferation by a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) method. Wound scratch assays were performed to assess the migrated rate of SW982 cells. Quantitative real-time PCR was used to measure the mRNA expression levels of Wnt5a, Runx2, MMP3, and Bmp2. Western blotting was used to measure the phosphorylated levels of JNK and NF-κB as well as the expression of MMP3.

Results: The alkaloid extract from Aconiti Sinomontani Radix (MQA) and MQB, which removed lappaconitine from MQA significantly inhibited the proliferation of SW982 in a dose-dependent manner. The proliferation inhibitory effect of MQB was more potent. Incubation with 10μg/ml MQB for 12, 24, and 36h inhibited the migration of SW982 cells by 83%, 58%, and 42%, respectively. Treatment with different concentrations of MQB for 24h inhibited mRNA expression of Wnt5a, Runx2, and MMP3, but Bmp2 mRNA expression was elevated by MQB. Further, MQB inhibited phosphorylation of JNK and NF-κB p65 as well as MMP3 expression by Western blotting analysis.

Conclusion: The results showed that MQB inhibited proliferation and migration of SW982 cells possibly through suppressing Wnt5a-mediated JNK and NF-κB pathways. These results indicated that MQB might be an active extract of Aconiti Sinomontani Radix for targeting fibroblast-like synoviocytes (FLS) and be potential for RA therapy.

Keywords: Aconiti Sinomontani Radix; Celastrol (PubChem CID: 122724); DMSO (PubChem CID: 679); Fibroblast-like synoviocytes; Lappaconitine (PubChem CID: 90479327); Migration; Penicillin (PubChem CID: 5904); Proliferation; Streptomycin (PubChem CID: 19649); acetonitrile (PubChem CID: 6342); formic acid (PubChem CID: 284); l-glutamine (PubChem CID: 5961).

MeSH terms

  • Aconitum / chemistry*
  • Bone Morphogenetic Protein 2 / biosynthesis
  • Cell Line
  • Cell Migration Assays
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects*
  • Core Binding Factor Alpha 1 Subunit / biosynthesis
  • Dose-Response Relationship, Drug
  • Fibroblasts / cytology
  • Fibroblasts / drug effects*
  • Gene Expression / drug effects
  • Humans
  • JNK Mitogen-Activated Protein Kinases / metabolism
  • Matrix Metalloproteinase 3 / biosynthesis
  • NF-kappa B / metabolism
  • Phosphorylation / drug effects
  • Plant Extracts / pharmacology*
  • Synoviocytes / cytology*
  • Synoviocytes / drug effects*
  • Wnt-5a Protein / biosynthesis

Substances

  • BMP2 protein, human
  • Bone Morphogenetic Protein 2
  • Core Binding Factor Alpha 1 Subunit
  • NF-kappa B
  • Plant Extracts
  • RUNX2 protein, human
  • WNT5A protein, human
  • Wnt-5a Protein
  • JNK Mitogen-Activated Protein Kinases
  • MMP3 protein, human
  • Matrix Metalloproteinase 3