共 43 条
Anti-inflammatory potential of low-molecular-weight and high-sulfation-degree sulfated polysaccharides extracted from Antrodia cinnamomea
被引:1
|作者:
Qiu, Wei-Lun
[1
]
Chao, Chi-Hsein
[1
]
Hsu, Yu-Chi
[1
]
Lu, Mei-Kuang
[1
,2
,3
,4
,5
]
机构:
[1] Minist Hlth & Welf, Natl Res Inst Chinese Med, 155-1 Li-Nung St,Sec.2, Taipei 155, Taiwan
[2] Taipei Med Univ, Grad Inst Pharmacognosy, 252 Wu-Hsing St, Taipei 110, Taiwan
[3] Natl Yang Ming Chiao Tung Univ, Inst Tradit Med, 155 Li Nung St,7 Sec 2, Taipei 112, Taiwan
[4] Natl Yang Ming Chiao Tung Univ, Dept Chinese Med, Taipei, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Tradit Chinese Med Glyc Res Ctr, Taipei, Taiwan
关键词:
Antrodia cinnamomea;
Sulfated polysaccharide;
Anti-inflammation;
KAPPA-B;
INFLAMMATION;
CELLS;
GALACTOGLUCAN;
ACTIVATION;
CYTOKINES;
D O I:
10.1016/j.ijbiomac.2024.134360
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Two novel sulfated polysaccharides (SPs), N10 and K5 were isolated from ammonium sulfate or potassium sulfate at concentrations of 10 mM and 5 mM in liquid cultures of Antrodia cinnamomea, respectively. N10 and K5 were galactoglucans with a galactose:glucose molar ratio of approximately 1:3. In lipopolysaccharide (LPS)-stimulated RAW264.7 cells, N10 and K5 exhibited strong anti-inflammatory potential, of 56% and 23 % maximal inhibition of IL-6 and TNF-alpha production, respectively. Mechanical analysis revealed differences between N10 and K5, with N10 inhibiting the LPS-stimulated phosphorylation of ERK and p38 in RAW264.7 cells. K5 inhibited the LPSstimulated phosphorylation of AKT and TGF beta R-II. N10 and K5 were fragmented into F1, F2, and F3, the molecular weights of which were 455, 24, 0.9, and 327, 36, 1.9 kDa, respectively. K5 F2 and K5 F3 exhibited high degrees of sulfation of 1:3 and 1:8, resulting in strong anti-inflammation, of 83 % and 37 % highest inhibition of IL-6 and TNF-alpha production, respectively. Therefore, low-molecular-weight and high-sulfation-degree SPs exhibited strong anti-inflammatory activity. Specifically, K5 F2 inhibited the phosphorylation of p38, and K5 F3 suppressed the signaling pathway of p38/JNK. Overall, the sulfation degree of SPs is concluded to affect the antiinflammatory responses.
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