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C21-steroidal pregnane sapogenins and their derivatives as anti-inflammatory agents.
Huang, Lie-Jun; Chen, Shao-Ru; Yuan, Chun-Mao; Gu, Wei; Guo, Bao-Jian; Wang, Yi-Tao; Wang, Ying; Hao, Xiao-Jiang.
Afiliação
  • Huang LJ; State Key Laboratory of Functions and Applications of Medicinal Plants, Guiyang 550002, People's Republic of China; Center for Research and Development of Fine Chemicals, Guizhou University, Guiyang 550025, People's Republic of China.
  • Chen SR; State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China.
  • Yuan CM; State Key Laboratory of Functions and Applications of Medicinal Plants, Guiyang 550002, People's Republic of China.
  • Gu W; State Key Laboratory of Functions and Applications of Medicinal Plants, Guiyang 550002, People's Republic of China.
  • Guo BJ; State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China.
  • Wang YT; State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China.
  • Wang Y; State Key Laboratory of Quality Research in Chinese Medicine and Institute of Chinese Medical Sciences, University of Macau, Avenida da Universidade, Taipa, Macao SAR, China. Electronic address: emilyywang@umac.mo.
  • Hao XJ; State Key Laboratory of Functions and Applications of Medicinal Plants, Guiyang 550002, People's Republic of China. Electronic address: haoxj@mail.kib.ac.cn.
Bioorg Med Chem ; 25(13): 3512-3524, 2017 07 01.
Article em En | MEDLINE | ID: mdl-28506585
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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sapogeninas / Citocinas / Anti-Inflamatórios Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sapogeninas / Citocinas / Anti-Inflamatórios Idioma: En Ano de publicação: 2017 Tipo de documento: Article