Sader Safaa, Cai Jun, Muller Anna C G, Wu Chun
Department Chemistry & Biochemistry and Department of Translational Biomedical Sciences, College of Science and Mathematics, Rowan University, Glassboro, NJ, 08028, USA.
Department Chemistry & Biochemistry and Department of Translational Biomedical Sciences, College of Science and Mathematics, Rowan University, Glassboro, NJ, 08028, USA.
J Mol Graph Model. 2017 Aug;75:106-116. doi: 10.1016/j.jmgm.2017.05.010. Epub 2017 May 17.
Fexofenadine, a potent antagonist to human histamine 1 (H) receptor, is a non-sedative third generation antihistamine that is widely used to treat various human allergic conditions such as allergic rhinitis, conjunctivitis and atopic dermatitis. Encouragingly, it's been successfully used to treat canine atopic dermatitis, this supports the notion that it might have a great potential for treating other canine allergic conditions and other mammal pets such as dog. Regrettably, while there is a myriad of studies conducted on the interactions of antihistamines with human H receptor, the similar studies on non-human pet H are considerably scarce. The published studies using the first and second generation antihistamines drugs have shown that the antihistamine response is varied and unpredictable. Thus, to probe its efficacy on pet, the homology models of dog and cat H receptors were built based on the crystal structure of human H receptor bound to antagonist doxepin (PDB 3RZE) and fexofenadine was subsequently docked to human, dog and cat H receptors. The docked complexes are then subjected to 1000ns molecular dynamics (MD) simulations with explicit membrane. Our calculated MM/GBSA binding energies indicated that fexofenadine binds comparably to the three receptors; and our MD data also showed the binding poses, structural and dynamic features among three receptors are very similar. Therefore, our data supported the application of fexofenadine to the H related allergic conditions of dog and cat. Nonetheless, subtle systemic differences among human, dog and cat H receptors were also identified. Clearly, there is still a space to develop a more selective, potent and safe antihistamine alternatives such as Fexofenadine for dog or cat based on these differences. Our computation approach might provide a fast and economic way to predict if human antihistamine drugs can also be safely and efficaciously administered to animals.
非索非那定是一种强效的人组胺1(H)受体拮抗剂,是一种非镇静性的第三代抗组胺药,广泛用于治疗各种人类过敏病症,如过敏性鼻炎、结膜炎和特应性皮炎。令人鼓舞的是,它已成功用于治疗犬特应性皮炎,这支持了它可能在治疗其他犬类过敏病症以及其他哺乳动物宠物(如狗)方面具有巨大潜力的观点。遗憾的是,虽然有大量关于抗组胺药与人H受体相互作用的研究,但关于非人类宠物H受体的类似研究却相当稀少。使用第一代和第二代抗组胺药的已发表研究表明,抗组胺反应各不相同且不可预测。因此,为了探究其对宠物的疗效,基于与拮抗剂多塞平结合的人H受体的晶体结构(PDB 3RZE)构建了狗和猫H受体的同源模型,随后将非索非那定对接至人、狗和猫的H受体。然后将对接的复合物在有明确膜的情况下进行1000纳秒的分子动力学(MD)模拟。我们计算的MM/GBSA结合能表明,非索非那定与这三种受体的结合相当;我们的MD数据还表明三种受体之间的结合姿势、结构和动力学特征非常相似。因此,我们的数据支持将非索非那定应用于狗和猫的H相关过敏病症。尽管如此,也发现了人、狗和猫H受体之间存在细微的系统差异。显然,基于这些差异,仍有空间开发更具选择性、强效且安全的抗组胺替代品,如用于狗或猫的非索非那定。我们的计算方法可能提供一种快速且经济的方式来预测人类抗组胺药物是否也能安全有效地用于动物。