Skip to main content
. 2020 Oct 2;11:583171. doi: 10.3389/fphar.2020.583171

Table 5.

The function of Tripterygium ingredients on OC.

Component Models Molecular mechanism Effects Animal disease phenotype Ref.
Cel CIA mice Reduce RANKL levels Inhibiting OC differentiation Alleviate (Wang, 2015)
TP CIA mice Regulating the RANKL/RANK/OPG signaling pathway Inhibiting OC differentiation Alleviate (Liu et al., 2013)
Cel AIA Lewis rats and RANKL induced RAW264.7 Decrease RANKL levels and regulate RANKL/OPG ratio Reduce OC proliferation. Ameliorate bone destruction. Decrease levels of upstream pro-inflammatory cytokine (i.e., IL-6) and downstream effectors (i.e., MMP-9) Alleviate (Nanjundaiah et al., 2012)
Cel IL-1β stimulated MH7A Decrease RANKL levels and increase OPG levels Inhibit OC differentiation and activation NA (Feng et al., 2013)
Cel RANKL induced RAW264.7 and CIA mice Inhibit the protein phosphorylation of RANK downstream signalings, such as NF-κB p65, MAPK (ERK, JNK, p38) and the expression of the relevant transcription factors (i.e., c-Fos, c-Jun, and NFATcl) Inhibit OC differentiation and bone resorption Alleviate (Gan, 2013)
Cel RANKL induced RAW264.7 NA Inhibit OC differentiation and chemokine CCl4 NA (Qian et al., 2015)
TP C57BL/6 mice bone marrow mesenchymal stem cells induced by RANKL, M-CSF, and HMGB1 Reduce the expression of RAGE mRNA to inhibit HMGB1 Inhibit OC differentiation NA (Wang et al., 2017)
TP Co-cultures system of Tregs and BMMs NA Increase the levels of IL-10 and TGF-β1 secreted by Treg to inhibit OC differentiation and bone resorption NA (Xu, 2016; Xu et al., 2016)
TP TNF-Tg mice and spleen cells isolated and induced to differentiate into OCs by M-CSF Down-regulate the cIAP2 Promote OCP apoptosis and OC reduction NA (Wang S. et al., 2019)
TP TNF-Tg mice NA Promote apoptosis rates of OCP and OC. Prohibit the bone erosion Alleviate (Wang et al., 2018)

TP, Triptolide; Cel, Celastrol; RANKL, Nuclear factor kappa B ligand receptor activator; RANK, Nuclear factor receptor activator; OPG, Osteoprotegerin; NF-kappa B, Nuclear factor activated B cell κ light chain enhancer; MAPK, Mitogen activated protein kinase; ERK, Extracellular regulatory protein kinase; JNK, Jun N-terminal kinase; NFATcl, Osteoclast activated T nuclear factor 1; CCl4, C-C motif chemokine ligand 4; HMGB1, High mobility group protein B1; RAGE, Receptor for advanced glycation end products; OC, Osteoclasts.