Insampaedok-San Extract Exerts an Immune-Enhancing Effect through NF-κB p65 Pathway Activation

被引:0
|
作者
Huh, Gyuwon [1 ,2 ]
Oh, Youngse [3 ]
Jeon, Youngsic [1 ]
Kang, Ki Sung [4 ]
Kim, Su Nam [1 ]
Jung, Sang Hoon [1 ,2 ]
Kim, Seung Hyun [3 ]
Kim, Young-Joo [1 ]
机构
[1] Korea Inst Sci & Technol, Nat Prod Res Ctr, Kangnung 25451, South Korea
[2] Univ Sci & Technol, Div Biomed Sci & Technol, Daejeon 34113, South Korea
[3] Yonsei Univ, Yonsei Inst Pharmaceut Sci, Coll Pharm, Incheon 21983, South Korea
[4] Gachon Univ, Coll Korean Med, Seongnam 13120, South Korea
关键词
D O I
10.1155/2023/5458504
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Insampaedok-san (IS) has traditionally been prescribed as a medication for cold-related symptoms in Northeast Asia, including Korea and China. In this study, we focused on elucidating the molecular mechanism underlying the immunomodulatory activity of IS water extract (ISE) in macrophages. ISE significantly enhanced the levels of nitric oxide (NO) and prostaglandin E2 (PGE2) by increasing the expression of inducible NO synthase and cyclooxygenase-2 (COX-2) in a dose-dependent manner. ISE, which consists of many herbs, contains a large number of active compounds whose pharmacological targets and mechanisms are complicated. Therefore, network pharmacology analysis was used to predict the potential key components, targets, and mechanisms of ISE as immunomodulators. Subsequently, the network pharmacology results were validated experimentally. Seven key components were identified through HPLC-QTOF-MS. As predicted by the network pharmacology analysis, ISE increased the mRNA expression of Tnf and Il6. Furthermore, ISE increased the phosphorylation, nuclear translocation, and transcriptional activity of the p65 subunit of the nuclear factor-kappa B (NF-kappa B) signaling pathway. In contrast, rapamycin, an NF-kappa B inhibitor, suppressed the ISE-induced mRNA expression of Tnf and Il6. In conclusion, ISE is an immune activator that can elevate the production of NO, PGE2, and proinflammatory cytokines mediated by NF-kappa B signaling.
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页数:13
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