Lin Zhi-Hu, Yeh Hsin, Phan Sang-Nguyen-Cao, Liao Li-Lan, Chen Chien-Chang, Hsu Wei-Hung, Hsu Chung-Hua, Lin Tung-Yi
Institute of Traditional Medicine, National Yang Ming Chiao Tung University, Taipei, Taiwan.
Department of Ophthalmology, Taipei City Hospital, Taipei, Taiwan.
Front Pharmacol. 2025 Aug 6;16:1618488. doi: 10.3389/fphar.2025.1618488. eCollection 2025.
Jing Guan Fang, a formula based on , is commonly used for preventing SARS-CoV-2 infection and alleviating cold-like symptoms. However, the precise immunoregulatory mechanisms underlying its effects remain unclear and warrant investigation. This study aims to investigate the immunomodulatory effects of JGF and further elucidate the underlying mechanisms. The results showed that JGF had minimal impact on the cell viability of RAW264.7 and MH-S. In the absence of LPS stimulation, JGF promoted macrophages to produce NO and pro-inflammatory cytokines in a concentration-dependent manner. However, after LPS treatment, the JGF add-on exhibited contrasting effects, with the half-maximal effective concentrations for reducing macrophage-secreted NO and IL-6 being 80 and 180 μg/mL, respectively. Western blot analysis revealed that the JGF supplement marginally induced the production of iNOS and COX-2 without LPS stimulation. However, in LPS-pretreated cells, JGF demonstrated the opposite effect. JGF monotherapy accelerated phosphorylation in the JNK and JAK2 signaling pathways. In contrast, JGF inhibited LPS-stimulated STAT3 phosphorylation by suppressing JNK1/2 activation. Moreover, JGF reduced LPS-induced expression of IL-6 and TNF-α in the lungs and serum of mice. Collectively, the findings suggest that JGF exhibits immunomodulatory activity and suppresses pro-inflammatory cytokine expression caused by LPS.
荆防方是一种基于……的方剂,常用于预防新型冠状病毒感染和缓解类似感冒的症状。然而,其作用背后的确切免疫调节机制仍不清楚,值得研究。本研究旨在探讨荆防方的免疫调节作用,并进一步阐明其潜在机制。结果表明,荆防方对RAW264.7和MH-S细胞活力的影响极小。在无脂多糖(LPS)刺激的情况下,荆防方以浓度依赖的方式促进巨噬细胞产生一氧化氮(NO)和促炎细胞因子。然而,在LPS处理后,添加荆防方表现出相反的效果,降低巨噬细胞分泌的NO和白细胞介素-6(IL-6)的半数有效浓度分别为80和180μg/mL。蛋白质印迹分析显示,在无LPS刺激时,添加荆防方仅轻微诱导诱导型一氧化氮合酶(iNOS)和环氧化酶-2(COX-2)的产生。然而,在LPS预处理的细胞中,荆防方表现出相反的作用。荆防方单一疗法加速了应激活化蛋白激酶(JNK)和Janus激酶2(JAK2)信号通路中的磷酸化。相反,荆防方通过抑制JNK1/2激活来抑制LPS刺激的信号转导和转录激活因子3(STAT3)磷酸化。此外,荆防方降低了LPS诱导的小鼠肺组织和血清中IL-6和肿瘤坏死因子-α(TNF-α)的表达。总的来说,这些发现表明荆防方具有免疫调节活性,并抑制LPS引起的促炎细胞因子表达。