College of Korean Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea; Korean Medicine-Based Drug Repositioning Cancer Research Center, College of Korean Medicine, Kyung Hee University, Seoul, 02447, Republic of Korea.
Majors in Plant Resource and Environment, College of Agriculture & Life Sciences, SARI, Jeju National University, Jeju, 63243, Republic of Korea.
J Ethnopharmacol. 2022 Mar 1;285:114893. doi: 10.1016/j.jep.2021.114893. Epub 2021 Dec 4.
A mixture (SH003) of Astragalus membranaceus (Fisch.) Bunge, Angelica gigas Nakai, and Trichosanthes Kirilowii (Maxim.) has beneficial effects against several carcinomas. There have been few reports on an immune-enhancing activity of SH003 and its active constituent nodakenin.
This study aimed at identifying the immune-enhancing effect of SH003 and nodakenin.
The immune-enhancing effect was evaluated using RAW264.7 macrophages, mouse primary splenocytes, and a cyclophosphamide (CP)-induced immunosuppression murine model.
The results show that SH003 or nodakenin stimulated the production levels of granulocyte colony-stimulating factor, IL-12, IL-2, IL-6, TNF-α, and nitric oxide (NO) and the expression levels of iNOS in RAW264.7 macrophages. SH003 or nodakenin also enhanced NF-κB p65 activation in RAW264.7 macrophages. SH003 or nodakenin stimulated the production levels of IFN-γ, IL-12, IL-2, TNF-α, and NO and the expression levels of iNOS in splenocytes. SH003 or nodakenin increased the splenic lymphocyte proliferation and splenic NK cell activity. In addition, SH003 or nodakenin increased the levels of IFN-γ, IL-12, IL-2, IL-6, and TNF-α in the serum and spleen of CP-treated mice, alleviating CP-induced immunosuppression.
Taken together, the results of this study show that SH003 improved immunosuppression through the activation of macrophages, splenocytes, and NK cells. These findings suggest that SH003 could be applied as a potential immunostimulatory agent for a variety of diseases caused or exacerbated by immunodeficiency.
黄芪、当归和瓜蒌组成的混合物(SH003)对多种癌有有益作用。关于 SH003 及其活性成分远志酮的免疫增强活性的报道较少。
本研究旨在确定 SH003 和远志酮的免疫增强作用。
采用 RAW264.7 巨噬细胞、小鼠原代脾细胞和环磷酰胺(CP)诱导的免疫抑制小鼠模型评价免疫增强作用。
结果表明,SH003 或远志酮刺激 RAW264.7 巨噬细胞产生粒细胞集落刺激因子、IL-12、IL-2、IL-6、TNF-α 和一氧化氮(NO)的水平,以及诱导型一氧化氮合酶(iNOS)的表达水平。SH003 或远志酮还增强了 RAW264.7 巨噬细胞中 NF-κB p65 的激活。SH003 或远志酮刺激脾细胞产生 IFN-γ、IL-12、IL-2、TNF-α 和 NO 的水平,以及诱导型一氧化氮合酶(iNOS)的表达水平。SH003 或远志酮增加了脾淋巴细胞的增殖和脾 NK 细胞的活性。此外,SH003 或远志酮增加了 CP 处理小鼠血清和脾脏中 IFN-γ、IL-12、IL-2、IL-6 和 TNF-α 的水平,缓解了 CP 诱导的免疫抑制。
综上所述,本研究结果表明,SH003 通过激活巨噬细胞、脾细胞和 NK 细胞改善了免疫抑制。这些发现表明,SH003 可作为一种潜在的免疫刺激剂,用于治疗由免疫缺陷引起或加剧的多种疾病。