TY - JOUR
T1 - Medulla Tetrapanacis water extract alleviates inflammation and infection by regulating macrophage polarization through MAPK signaling pathway
AU - Kwok, Carsten Tsun Ka
AU - Chow, Franklin Wang Ngai
AU - Cheung, Karry Yuen Ching
AU - Zhang, Xiao Yi
AU - Mok, Daniel Kam Wah
AU - Kwan, Yiu Wa
AU - Chan, Gabriel Hoi Huen
AU - Leung, George Pak Heng
AU - Cheung, Ka Wang
AU - Lee, Simon Ming Yuen
AU - Wang, Ning
AU - Li, Jing Jing
AU - Seto, Sai Wang
N1 - Publisher Copyright:
© The Author(s), under exclusive licence to Springer Nature Switzerland AG 2023.
PY - 2024/2
Y1 - 2024/2
N2 - Medulla Tetrapanacis (MT) is a commonly used herb to promote lactation and manage mastitis in lactating mothers. However, its anti-inflammatory and anti-bacterial effects are currently unknown. We hypothesized that MT water extract possesses anti-inflammatory and anti-bacterial effects by modulating macrophage polarization to reduce the release of inflammatory mediators and phagocytosis via inactivation of MAPKs pathways. The chemical composition of the MT water extract was analyzed by UPLC-Orbitrap-mass spectrometry. The anti-inflammatory and anti-bacterial properties of the MT water extract were examined using LPS-stimulated inflammation and Staphylococcus aureus infection model in RAW 264.7 cells, respectively. The underlying mechanism of action of the MT water extract was also investigated. We identified eight compounds by UPLC-Orbitrap-mass spectrometry that are abundant within the MT water extract. MT water extract significantly suppressed LPS-induced nitric oxide, TNF-α and IL-6 secretion in RAW 264.7 cells which was accompanied by the promotion of macrophage polarization from pro-inflammatory towards anti-inflammatory phenotypes. MT water extract significantly suppressed the LPS-induced MAPK activation. Finally, MT water extract decreased the phagocytic capacity of the RAW 264.7 cells against S. aureus infection. MT water extract could suppress LPS-induced inflammation by promoting macrophages towards an anti-inflammatory phenotype. In addition, MT also inhibited the growth of S. aureus. Graphical abstract: (Figure presented.)
AB - Medulla Tetrapanacis (MT) is a commonly used herb to promote lactation and manage mastitis in lactating mothers. However, its anti-inflammatory and anti-bacterial effects are currently unknown. We hypothesized that MT water extract possesses anti-inflammatory and anti-bacterial effects by modulating macrophage polarization to reduce the release of inflammatory mediators and phagocytosis via inactivation of MAPKs pathways. The chemical composition of the MT water extract was analyzed by UPLC-Orbitrap-mass spectrometry. The anti-inflammatory and anti-bacterial properties of the MT water extract were examined using LPS-stimulated inflammation and Staphylococcus aureus infection model in RAW 264.7 cells, respectively. The underlying mechanism of action of the MT water extract was also investigated. We identified eight compounds by UPLC-Orbitrap-mass spectrometry that are abundant within the MT water extract. MT water extract significantly suppressed LPS-induced nitric oxide, TNF-α and IL-6 secretion in RAW 264.7 cells which was accompanied by the promotion of macrophage polarization from pro-inflammatory towards anti-inflammatory phenotypes. MT water extract significantly suppressed the LPS-induced MAPK activation. Finally, MT water extract decreased the phagocytic capacity of the RAW 264.7 cells against S. aureus infection. MT water extract could suppress LPS-induced inflammation by promoting macrophages towards an anti-inflammatory phenotype. In addition, MT also inhibited the growth of S. aureus. Graphical abstract: (Figure presented.)
KW - Anti-bacterial
KW - Inflammation
KW - Macrophage polarization
KW - MAPK signaling pathway
KW - Mastitis
KW - Medulla Tetrapanacis
UR - http://www.scopus.com/inward/record.url?scp=85164465932&partnerID=8YFLogxK
U2 - 10.1007/s10787-023-01266-1
DO - 10.1007/s10787-023-01266-1
M3 - Journal article
C2 - 37429999
AN - SCOPUS:85164465932
SN - 0925-4692
VL - 32
SP - 393
EP - 404
JO - Inflammopharmacology
JF - Inflammopharmacology
IS - 1
ER -