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清开灵注射液诱导速发型超敏反应及过敏毒素C3的激活。

Qing-Kai-Ling Injection Induces Immediate Hypersensitivity Reaction the Activation of Anaphylatoxin C3.

作者信息

Gao Yuan, Qi Ruijuan, Zhang Xiaoyu, Xu Xudong, Han Yixin, Fei Qiaoling, Wang Xiaojing, Cai Runlan, Sun Guibo, Qi Yun

机构信息

Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Front Pharmacol. 2020 Jan 9;10:1524. doi: 10.3389/fphar.2019.01524. eCollection 2019.

Abstract

Qing-Kai-Ling (QKL) is derived from a famous ancient Chinese patent medicine Angong Niuhuang pills (ANP) which has been used across Asia, especially in China, for the treatment of "febrile disease," such as stroke, encephalitis and meningitis for hundreds of years. As an extract of ANP without heavy metal, the clinical applicability of QKL is more intensive, of which its injection is commonly used in acute and serious diseases. This study aims to clarify the potential mechanisms of immediate hypersensitivity reaction (IHR) induced by QKL injection (QKLI). β-hexosaminidase release assay was performed on the human mast cell line LAD2 and mouse peritoneal mast cells. T helper 2 (Th2) immunity-amplified mice were prepared by aluminum adjuvant. Anaphylactic shock was detected by measuring rectal thermometry in propranolol-pretreated mice. For evaluating microvascular permeability, Evans Blue extravasation assay was used. Serum total IgE (tIgE) and the activated complement-derived anaphylatoxin C3 (C3a) levels were measured by ELISA. QKLI was unable to elevate serum tIgE level in the Th2 immunity-amplified mice, but can increase vasopermeability and trigger anaphylaxis after the first injection. By screening seven fractions of QKLI, only the extract of Isatidis Radix () induced hindpaw Evans Blue extravasation, which was disappeared in Isatidis Radix-free QKLI. Mechanism study indicated that QKLI or Isatidis Radix-caused IHR could be blocked by the antagonists for histamine or C3a, rather than PAF or C5a. Consistently, QKLI and Isatidis Radix could also directly activate human serum complement-derived anaphylatoxin 3 (C3) with the half effective concentration values of 0.69% and 218.6 μg/ml, respectively. QKLI-IHR is complement activation-related pseudoallergy, rather than an IgE-mediated allergy. QKLI activates C3 and might consequently provoke mast cells to release histamine, which is a principal effector of its IHR. The pseudoallergic reaction induced by QKLI was attributed to the extract of Isatidis Radix. This study suggests a potential therapeutic strategy for the prophylaxis and treatment of QKLI-IHR.

摘要

清开灵(QKL)源自著名的古代中成药安宫牛黄丸(ANP),数百年来,安宫牛黄丸在亚洲尤其是中国一直用于治疗“热病”,如中风、脑炎和脑膜炎等。作为不含重金属的安宫牛黄丸提取物,清开灵的临床适用性更强,其注射剂常用于急性和重症疾病。本研究旨在阐明清开灵注射液(QKLI)诱导速发型超敏反应(IHR)的潜在机制。对人肥大细胞系LAD2和小鼠腹腔肥大细胞进行了β-己糖胺酶释放试验。用铝佐剂制备辅助性T细胞2(Th2)免疫增强小鼠。通过测量普萘洛尔预处理小鼠的直肠温度来检测过敏性休克。采用伊文思蓝外渗试验评估微血管通透性。用酶联免疫吸附测定法检测血清总IgE(tIgE)和活化补体衍生的过敏毒素C3(C3a)水平。QKLI在Th2免疫增强小鼠中不能提高血清tIgE水平,但在首次注射后可增加血管通透性并引发过敏反应。通过筛选QKLI的七个组分,只有板蓝根提取物可诱导后爪伊文思蓝外渗,在不含板蓝根的QKLI中这种现象消失。机制研究表明,QKLI或板蓝根引起的IHR可被组胺或C3a拮抗剂阻断,而非血小板活化因子或C5a拮抗剂。一致地,QKLI和板蓝根也可直接激活人血清补体衍生的过敏毒素3(C3),其半数有效浓度分别为0.69%和218.6μg/ml。QKLI-IHR是补体激活相关的假过敏反应,而非IgE介导的过敏反应。QKLI激活C3,可能进而促使肥大细胞释放组胺,这是其IHR的主要效应因子。QKLI诱导的假过敏反应归因于板蓝根提取物。本研究提示了预防和治疗QKLI-IHR的潜在治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e32d/6962097/e966e6858a40/fphar-10-01524-g001.jpg

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