Key Laboratory of Beijing for Identification and Safety Evaluation of Chinese Medicine, Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing, China.
J Ethnopharmacol. 2023 Jun 12;309:116357. doi: 10.1016/j.jep.2023.116357. Epub 2023 Mar 9.
Adverse reactions to traditional Chinese medicine injections involve pseudo-allergic reactions (PARs). However, in clinical practice, "immediate allergic reactions" and PARs in response to these injections are not often differentiated.
This study aimed to clarify the type of reactions produced by Shengmai injections (SMI) and elucidate the possible mechanism.
A mouse model was used to evaluate vascular permeability. Metabolomic and arachidonic acid metabolite (AAM) analyses were performed using UPLC-MS/MS, and the p38 MAPK/cPLA2 pathway was detected by western blotting.
The first exposure to intravenous SMI rapidly and dose-dependently induced edema and exudative reactions in the ears and lungs. These reactions were not IgE-dependent and were likely to be PARs. Metabolomic analysis showed that endogenous substances were perturbed in SMI-treated mice, in which the arachidonic acid (AA) metabolic pathway was the most affected. SMI substantially increased the levels of AAMs in lung, including prostaglandins (PGs), leukotrienes (LTs), and hydroxy-eicosatetraenoic acids (HETEs). The p38 MAPK/cPLA2 signaling pathway was activated after a single SMI dose. Inhibitors of cyclooxygenase-2 and 5-lipoxygenase enzymes reduced exudation and inflammation in the ears and lungs of mice.
Production of inflammatory factors that increase vascular permeability may result in SMI-induced PARs, and p38 MAPK/cPLA2 signaling pathway and downstream AA metabolic pathway are involved in the reactions.
中药注射液不良反应涉及假性过敏反应(PAR)。然而,在临床实践中,这些注射剂引起的“即刻过敏反应”和 PAR 通常没有得到区分。
本研究旨在阐明参麦注射液(SMI)引起的反应类型,并阐明可能的机制。
采用小鼠模型评估血管通透性。使用 UPLC-MS/MS 进行代谢组学和花生四烯酸代谢物(AAM)分析,并通过 Western blot 检测 p38 MAPK/cPLA2 通路。
首次静脉注射 SMI 可快速且剂量依赖性地诱导耳和肺部的水肿和渗出反应。这些反应不是 IgE 依赖性的,可能是 PAR。代谢组学分析表明,SMI 处理的小鼠内源性物质受到干扰,其中花生四烯酸(AA)代谢途径受影响最大。SMI 显著增加了肺中的 AAMs 水平,包括前列腺素(PGs)、白三烯(LTs)和羟基二十碳四烯酸(HETEs)。单次 SMI 剂量后,p38 MAPK/cPLA2 信号通路被激活。环加氧酶-2 和 5-脂氧合酶抑制剂可减少小鼠耳部和肺部的渗出和炎症。
增加血管通透性的炎症因子的产生可能导致 SMI 引起的 PAR,p38 MAPK/cPLA2 信号通路和下游 AA 代谢途径参与了这些反应。