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采用大鼠嗜碱性白血病 2H3 细胞和变应性疾病实验室 2 双混合/细胞膜色谱模型同时鉴定中药注射液中的类过敏成分。

Simultaneous identification of the anaphylactoid components from traditional Chinese medicine injections using rat basophilic leukemia 2H3 and laboratory of allergic disease 2 dual-mixed/cell membrane chromatography model.

机构信息

School of Pharmacy, Xi'an Jiaotong University, Xi'an, P. R. China.

School of Pharmacy and Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.

出版信息

Electrophoresis. 2018 May;39(9-10):1181-1189. doi: 10.1002/elps.201700457. Epub 2018 Feb 6.

DOI:10.1002/elps.201700457
PMID:29359345
Abstract

Traditional Chinese medicine (TCM) has been used for prevention and treatment of various diseases for many decades. TCM injection is a new dosage form, with incidence of anaphylactoid reactions increasing every year. In this study, the rat basophilic leukemia 2H3 (RBL-2H3) and laboratory of allergic disease 2 (LAD2) dual-mixed/CMC was established and was coupled with an HPLC-ESI-IT-TOF-MS system to identify the potential allergenic components in Haqing injection. Cinobufagin, piperine, osthole, praeruptorin A, and schizandrin A were screened from Haqing injection via this coupled system. Competitive binding assay showed piperine, praeruptorin A, and schizandrin A acting on MrgprX2 and cinobufagin and osthole act on the IgE receptor. The release of mediators of anaphylaxis results showed cinobufagin and osthole can cause anaphylactoid reactions by triggering the release of β-hexosaminidase and histamine via IgE-R. Praeruptorin A and schizandrin A could promote the release of β-hexosaminidase and histamine via MrgprX2 receptor. In summary, the dual-mixed/CMC model can significantly improve the efficiency of target component identification from a complex sample. When combined with competitive binding assay and validation of biological activities, this model enables accurate determination of the dual-target components, offering improved methods for quality control of TCM injections.

摘要

中药(TCM)几十年来一直用于预防和治疗各种疾病。中药注射液是一种新的剂型,其过敏性反应的发生率逐年增加。在本研究中,建立了大鼠嗜碱性白血病 2H3(RBL-2H3)和过敏性疾病实验室 2(LAD2)双混合/CMC,并与 HPLC-ESI-IT-TOF-MS 系统相结合,以鉴定海清注射液中的潜在过敏原成分。通过该偶联系统从海清注射液中筛选出华蟾酥毒基、胡椒碱、蛇床子素、前胡素 A 和五味子 A。竞争结合测定表明,胡椒碱、前胡素 A 和五味子 A 通过 MrgprX2 作用于 IgE 受体,华蟾酥毒基和蛇床子素作用于 IgE 受体。过敏反应介质释放结果表明,华蟾酥毒基和蛇床子素通过 IgE-R 触发β-己糖胺酶和组胺的释放,引起过敏样反应。前胡素 A 和五味子 A 可通过 MrgprX2 受体促进β-己糖胺酶和组胺的释放。总之,双混合/CMC 模型可以显著提高从复杂样品中鉴定目标成分的效率。当与竞争结合测定和生物活性验证相结合时,该模型可以准确确定双靶成分,为中药注射液的质量控制提供了改进的方法。

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