| Literature DB >> 28506585 |
Lie-Jun Huang1, Shao-Ru Chen2, Chun-Mao Yuan3, Wei Gu3, Bao-Jian Guo2, Yi-Tao Wang2, Ying Wang4, Xiao-Jiang Hao5.
Abstract
During the screening of natural anti-inflammatory agent, we identified some C21-steroidal pregnane sapogenins or the derivatives to inhibit TLR2, TLR3, and TLR4-initiatedinflammatory responses respectively. Treatment with active compounds 10, 2j and 3p failed to impact tumor necrosis factor-α (TNF-α) induced nucleus translocation of NF-κB p65 subunit. However, these compounds regulated distinct canonical or non-canonical NF-κB family members. Ectopic expression of TNF receptor associated factor 6 (TRAF6) abrogated the inhibitory activity of the compounds on production of pro-inflammatory cytokines downstream of TLR4. These results suggested that compounds 10, 2j, and 3p suppressed TLR-initiated innate immunity through TRAF6 with differential regulation of NF-κB family proteins.Entities:
Keywords: Anti-inflammation; C(21)-steroidal pregnane steroids; NF-κB; TLR; TRAF6
Mesh:
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Year: 2017 PMID: 28506585 DOI: 10.1016/j.bmc.2017.04.045
Source DB: PubMed Journal: Bioorg Med Chem ISSN: 0968-0896 Impact factor: 3.641