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复方苦参注射液通过途径促进血小板活化因子的产生诱导速发型超敏反应。

Compound Kushen Injection Induces Immediate Hypersensitivity Reaction Through Promoting the Production of Platelet-Activating Factor via Pathway.

作者信息

Gao Yuan, Hai Lina, Kang Yuan, Qin Wenjie, Liu Fang, Cai Runlan, Yang Xiuwei, Qi Yun

机构信息

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

Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, China.

出版信息

Front Pharmacol. 2021 Oct 8;12:768643. doi: 10.3389/fphar.2021.768643. eCollection 2021.

Abstract

Compound Kushen Injection (CKI) is a herbal formulation extracted from Kushen (Radix Sophorae Flavescentis) and Baituling (Rhizoma Heterosmilacis Yunnanensis). Clinically, it is used as the adjuvant treatment of cancer. However, with the increased application, the cases of immediate hypersensitivity reactions (IHRs) also gradually rise. In this study, we investigated the underlying mechanism(s) and active constituent(s) for CKI-induced IHRs in experimental models. The obtained results showed that CKI did not elevate serum total IgE (tIgE) and mouse mast cell protease 1 (MMCP1) after consecutive immunization for 5 weeks, but could induce Evans blue extravasation (local) and cause obvious hypothermia (systemic) after a single injection. Further study showed that alkaloids in Kushen, especially matrine, were responsible for CKI-induced IHRs. Mechanism study showed that various platelet-activating factor (PAF) receptor antagonists could significantly counter CKI-induced IHRs locally or systemically. In cell system, CKI was able to promote PAF production in a non-cell-selective manner. In cell lysate, the effect of CKI on PAF production became stronger and could be abolished by blocking pathway. In conclusion, our study identifies, for the first time, that CKI is a PAF inducer. It causes non-immunologic IHRs, rather than IgE-dependent IHRs, by promoting PAF production through pathway. Alkaloids in Kushen, especially matrine, are the prime culprits for IHRs. Our findings may provide a potential approach for preventing and treating CKI-induced IHRs.

摘要

复方苦参注射液(CKI)是一种从苦参(苦参根)和白土苓(云南土茯苓根茎)中提取的草药制剂。临床上,它被用作癌症的辅助治疗药物。然而,随着应用的增加,速发型过敏反应(IHRs)的病例也逐渐增多。在本研究中,我们在实验模型中研究了CKI诱导IHRs的潜在机制和活性成分。所得结果表明,连续免疫5周后,CKI并未升高血清总IgE(tIgE)和小鼠肥大细胞蛋白酶1(MMCP1),但单次注射后可诱导伊文思蓝外渗(局部)并导致明显体温过低(全身)。进一步研究表明,苦参中的生物碱,尤其是苦参碱,是CKI诱导IHRs的原因。机制研究表明,各种血小板活化因子(PAF)受体拮抗剂可显著局部或全身对抗CKI诱导的IHRs。在细胞系统中,CKI能够以非细胞选择性方式促进PAF的产生。在细胞裂解物中,CKI对PAF产生的作用更强,并且可以通过阻断 途径消除。总之,我们的研究首次确定CKI是一种PAF诱导剂。它通过 途径促进PAF的产生,从而导致非免疫性IHRs,而不是IgE依赖性IHRs。苦参中的生物碱,尤其是苦参碱,是IHRs的主要罪魁祸首。我们的发现可能为预防和治疗CKI诱导的IHRs提供一种潜在方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cca4/8531113/010320a813e4/fphar-12-768643-g001.jpg

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