4.6 Article

Anti-allergic actions of a Chinese patent medicine, huoxiangzhengqi oral liquid, in RBL-2H3 cells and in mice

Journal

PHARMACEUTICAL BIOLOGY
Volume 59, Issue 1, Pages 672-682

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/13880209.2021.1928242

Keywords

IgE-mediated mast cell activation; high-affinity IgE receptor; inflammatory mediators; passive cutaneous anaphylaxis

Funding

  1. Ministry of Science and Technology of the People's Republic of China [2018YFC1707407]

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Huoxiangzhengqi oral liquid (HXZQ-OL) exhibits anti-allergic activity by inhibiting mast cell degranulation, reducing the generation and secretion of cytokines, and modulating the phosphorylation of multiple signaling proteins. HXZQ-OL may serve as an alternative treatment for allergic diseases.
Context Huoxiangzhengqi oral liquid (HXZQ-OL), a traditional Chinese medicine formula, has antibacterial, anti-inflammation and gastrointestinal motility regulation effects. Objective The study investigates the anti-allergic activity and underlying mechanism of HXZQ-OL. Materials and methods IgE/Ag-mediated RBL-2H3 cells were used to evaluate the anti-allergic activity of HXZQ-OL (43.97, 439.7 and 4397 mu g/mL) in vitro. The release of cytokines and eicosanoids were quantified using ELISA. RT-qPCR was used to measure the gene expression of cytokines. The level of intracellular Ca2+ was measured with Fluo 3/AM. Immunoblotting analysis was performed to investigate the mechanism of HXZQ-OL. In the passive cutaneous anaphylaxis (PCA), BALB/c mice (5 mice/group) were orally administrated with HXZQ-OL (263.8, 527.6 and 1055 mg/kg/d) or dexamethasone (5 mg/kg/d, positive control) for seven consecutive days. Results HXZQ-OL not only inhibited degranulation of mast cells (IC50, 123 mu g/mL), but also inhibited the generation and secretion of IL-4 (IC50, 171.4 mu g/mL), TNF-alpha (IC50, 88.4 mu g/mL), LTC4 (IC50, 52.9 mu g/mL) and PGD2 (IC50, 195.8 mu g/mL). Moreover, HXZQ-OL suppressed the expression of IL-4 and TNF-alpha mRNA, as well as the phosphorylation of Fyn, Lyn and multiple downstream signalling proteins including MAPK and PI3K/NF-kappa B pathways. In addition, HXZQ-OL (527.5 mg/kg) attenuated the IgE-mediated PCA with 55% suppression of Evans blue exudation in mice. Conclusions HXZQ-OL attenuated the activation of mast cell and PCA. Therefore, HXZQ-OL might be used as an alternative treatment for allergic diseases.

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