期刊
EVIDENCE-BASED COMPLEMENTARY AND ALTERNATIVE MEDICINE
卷 2021, 期 -, 页码 -出版社
HINDAWI LTD
DOI: 10.1155/2021/8879862
关键词
-
资金
- National Natural Science Foundation of China [81900528]
Isatidis Radix, a traditional herb, exhibits anti-inflammatory properties by regulating the phosphorylation of MAPK pathway and NF-κB pathway, ultimately reducing the expression of inflammation-related genes. This mechanism may explain its potential therapeutic effects on conditions like cold, fever, and sore throat.
Isatidis Radix, the dried root of Isatidis indigotica Fort, is a traditional heat-clearing and detoxicating herb, which has the antiviral and anti-inflammatory activity and immune regulation. It has been widely used to treat cold, fever, sore throat, mumps, and tonsillitis in clinics. A previous study demonstrated that the acidic fraction of Isatidis Radix (RIAF) had strong anti-inflammatory activity, but the mechanism of action was not well elucidated. Lipopolysaccharide- (LPS-) induced RAW 264.7 cells were employed to observe the anti-inflammatory activity of RIAF. The level of interleukin-1 beta (IL-1 beta), tumor necrosis factor-alpha (TNF-alpha), nitric oxide (NO), prostaglandin E-2 (PGE(2)), and interleukin-6 (IL-6) was determined by enzyme-linked immunosorbent assay kits. Western blot was performed to quantify the expression of extracellular signal-regulated kinase (ERK) 1/2, c-jun NH2-termianl kinase (JNK), p38, inducible NO synthetase (iNOS), cyclooxygenase (COX)-2, andnudear factor-kappa B (NF-kappa B). Immunofluorescence assay and electrophoretic mobility shift assay (EMSA) were used to quantify the translocation and the binding-DNA activity of NF-kappa B. RIAF could inhibit the secretion of inflammatory cytokines (PGE(2), IL-6, IL-1 beta, and NO, other than TNF-alpha) in a dose-dependent manner. Further investigation showed that the expression of iNOS and COX-2 induced by LPS were downregulated by treatment with RIAF. Meanwhile, data from the signal pathway exhibited that RIAF significantly suppressed the phosphorylation of ERK1/2, JNK, and p38 and reduced the translocation of NF-kappa B from the cytoplasm to nucleus, as well as the binding-DNA activity. The anti-inflammatory mechanism of action of RI AF was to reduce inflammation-associated gene expression (iNOS, COX-2, IL-1 beta, IL-6) by regulating the phosphorylation of the mitogen-activated protein kinases (MAP K) pathway and interventing the activation of the NF-kappa B pathway, which partly illustrated the basis of treatment of Isatidis Radix on cold, fever, sore throat, mumps, and tonsillitis in clinics.
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