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Article Publish Status: FREE
Abstract Title:

Ligustrazine Prevents Intervertebral Disc Degeneration via Suppression of Aberrant TGFActivation in Nucleus Pulposus Cells.

Abstract Source:

Biomed Res Int. 2019 ;2019:5601734. Epub 2019 Dec 2. PMID: 31886227

Abstract Author(s):

Shufen Liu, Yuhao Cheng, Yuqi Tan, Jingcheng Dong, Qin Bian

Article Affiliation:

Shufen Liu

Abstract:

Objectives: Aberrant transforming growth factor(TGF) activation is detrimental to both nucleus pulposus (NP) cells and cartilage endplates (CEPs), which can lead to intervertebral disc degeneration (IDD). Ligustrazine (LIG) reduces the expression of inflammatory factors and TGF1 in hypertrophic CEP to prevent IDD. In this study, we investigate the effects of LIG on NP cells and the TGFsignaling.

Design: LIG was injected to the lumbar spinal instability (LSI) mouse model. The effect of LIG was evaluated by intervertebral disc (IVD) score in the LSI mouse model. The expression of activated TGFwas examined using immunostaining with pSmad2/3 antibody. The upright posture (UP) rat model was also treated and evaluated in the same manner to assess the effect of LIG. Instudy, IVDs from four-week old mice were isolated and treated with 10, 10, and 10 M of LIG. We used western blot to detect activated TGFexpression. TGF-treated human nucleus pulposus cells (HNPCs) were cotreated with optimized dose of LIG. Immunofluorescence staining was performed to determine pSmad2/3, connective tissue growth factor (CCN2), and aggrecan (ACAN) expression levels.

Results: IVD score and the percentage of pSmad2/3+ NP cells were low in LIG-treated LSI mice in comparison with LSI mice, but close to the levels in the Sham group. Similarly, LIG reduced the overexpression of TGF1 in NP cells. The inhibitory effect of LIG was dose dependent. A dose of 10 M LIG not only strongly attenuated Smad2/3 phosphorylation in TGF-treated IVDbut also suppressed pSmad2/3, CCN2, and ACAN expression in TGF-treated NP cells.

Conclusions: LIG prevents IDD via suppression of TGFoveractivation in NP cells.

Study Type : Animal Study

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