TY - JOUR
T1 - Leocarpinolide B attenuates LPS-induced inflammation on RAW264.7 macrophages by mediating NF-κB and Nrf2 pathways
AU - Linghu, Ke Gang
AU - Ma, Qiu Shuo
AU - Zhao, Guan Ding
AU - Xiong, Wei
AU - Lin, Ligen
AU - Zhang, Qing Wen
AU - Bian, Zhaoxiang
AU - Wang, Yitao
AU - Yu, Hua
N1 - Funding Information:
This work was supported by grants from the National Natural Science Foundation of China [NSFC, No. 81470170 ], the Science and Technology Development Fund , Macau SAR [File No. 0096/2019/A2 ] and the Research Committee of the University of Macau [ MYRG2017-00178-ICMS and MYRG2018-00043-ICMS ].
PY - 2020/2/5
Y1 - 2020/2/5
N2 - Macrophages-mediated inflammation is involved in the regulation of rheumatoid arthritis (RA). Sigesbeckiae Herba (SH) has been traditionally used for rheumatism. However, the bioactive ingredients of SH are still unclear. Recently, we isolated a compound (Leocarpinolide B, LB) from SH and identified its potent anti-inflammatory and antioxidant effects on RAW264.7 macrophages for the first time. LB effectively inhibited excessive production of nitric oxide (NO), prostaglandin E2 (PGE2), cytokines (IL-6, TNF-α and MCP-1), and the expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthases (iNOS) in lipopolysaccharide (LPS)-induced RAW264.7 cells. LB blocked the degradation of inhibitor of kappa B (IκBα) and translocation of nuclear factor kappa B (NF-κB) p65. Additionally, LB reduced the intracellular reactive oxygen species, and increased the expression of heme oxygenase-1 (HO-1) and the translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) in the presence or absence of LPS. The results suggested that LB might be one of the bioactive components of SH, and be potential for the treatment of RA and valuable to be further investigated.
AB - Macrophages-mediated inflammation is involved in the regulation of rheumatoid arthritis (RA). Sigesbeckiae Herba (SH) has been traditionally used for rheumatism. However, the bioactive ingredients of SH are still unclear. Recently, we isolated a compound (Leocarpinolide B, LB) from SH and identified its potent anti-inflammatory and antioxidant effects on RAW264.7 macrophages for the first time. LB effectively inhibited excessive production of nitric oxide (NO), prostaglandin E2 (PGE2), cytokines (IL-6, TNF-α and MCP-1), and the expression of cyclooxygenase-2 (COX-2) and inducible nitric oxide synthases (iNOS) in lipopolysaccharide (LPS)-induced RAW264.7 cells. LB blocked the degradation of inhibitor of kappa B (IκBα) and translocation of nuclear factor kappa B (NF-κB) p65. Additionally, LB reduced the intracellular reactive oxygen species, and increased the expression of heme oxygenase-1 (HO-1) and the translocation of nuclear factor erythroid 2-related factor 2 (Nrf2) in the presence or absence of LPS. The results suggested that LB might be one of the bioactive components of SH, and be potential for the treatment of RA and valuable to be further investigated.
KW - Leocarpinolide B
KW - Nuclear factor erythroid 2-related factor 2 (Nrf2)
KW - Nuclear transcription factor-kappa B (NF-κB)
KW - Rheumatoid arthritis (RA)
KW - Sigesbeckiae herba (SH)
UR - http://www.scopus.com/inward/record.url?scp=85076434802&partnerID=8YFLogxK
U2 - 10.1016/j.ejphar.2019.172854
DO - 10.1016/j.ejphar.2019.172854
M3 - Journal article
C2 - 31837308
AN - SCOPUS:85076434802
SN - 0014-2999
VL - 868
JO - European Journal of Pharmacology
JF - European Journal of Pharmacology
M1 - 172854
ER -