Nebivolol hydrochloride and its impurities induce pseudo‐allergic reactions via mast cell activation

IF 2.7 4区 医学 Q3 TOXICOLOGY Journal of Applied Toxicology Pub Date : 2024-09-17 DOI:10.1002/jat.4699
Liju Yu, Yi Shan, Jiayu Lu, Huaizhen He
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Abstract

Nebivolol hydrochloride is a third‐generation β‐blocker commonly used to treat cardiovascular diseases. However, it has been reported to induce allergic reactions in clinical use which deserves much attention. Therefore, this study focused on the ability of two isomers of nebivolol and chiral isomer impurities to induce allergic reactions. Our findings demonstrate that both nebivolol and two isomeric impurities can activate mast cell degranulation in vitro and show significant retention on Mas‐related G‐protein‐coupled receptor X2 (MRGPRX2)‐HEK293 cell membrane chromatography. These effects were further validated in vivo, where nebivolol and impurity IP‐3 were observed to cause toe swelling and mast cell degranulation in mice. Molecular docking studies revealed interactions between these compounds and key amino acids of MRGPRX2, suggesting a mechanism for the induced allergic reactions. This work lays the foundation for improving the clinical safety of nebivolol.
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盐酸奈必洛尔及其杂质通过激活肥大细胞诱发假性过敏反应
盐酸奈必洛尔是第三代β受体阻滞剂,常用于治疗心血管疾病。然而,有报道称它在临床使用中会诱发过敏反应,这一点值得高度重视。因此,本研究重点关注奈必洛尔的两种异构体和手性异构体杂质诱发过敏反应的能力。我们的研究结果表明,奈必洛尔和两种异构体杂质都能在体外激活肥大细胞脱颗粒,并在 Mas 相关 G 蛋白偶联受体 X2(MRGPRX2)-HEK293 细胞膜层析中显示出显著的保留作用。这些作用在体内得到了进一步验证,观察到奈必洛尔和杂质 IP-3 会导致小鼠脚趾肿胀和肥大细胞脱颗粒。分子对接研究揭示了这些化合物与 MRGPRX2 的关键氨基酸之间的相互作用,提示了诱导过敏反应的机制。这项工作为提高奈必洛尔的临床安全性奠定了基础。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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