Simons F E, Simons K J
Faculty of Medicine, University of Manitoba, Winnipeg, Canada.
N Engl J Med. 1994 Jun 9;330(23):1663-70. doi: 10.1056/NEJM199406093302307.
The second-generation H1-antagonist drugs are supplanting their predecessors in the treatment of allergic rhinoconjunctivitis and chronic urticaria. Their use can be justified mainly on the basis of a more favorable risk-benefit ratio, because they are less toxic to the central nervous system. Future research into H1 antagonists should include additional dose-response studies in patients with allergic disorders, especially children and the elderly; objective studies of adverse effects; studies of topical mucosal application of H1 antagonists; and studies of H1-antagonist enantiomers and active metabolites. With the cloning of the gene encoding the H1 receptor and increased understanding of the precise structural requirements for H1-receptor activity, H1 antagonists with an even more favorable therapeutic index may be developed.
第二代H1拮抗剂药物正在取代其前代药物用于治疗变应性鼻结膜炎和慢性荨麻疹。它们的使用主要基于更有利的风险效益比,因为它们对中枢神经系统的毒性较小。未来对H1拮抗剂的研究应包括对变应性疾病患者,尤其是儿童和老年人进行更多的剂量反应研究;对不良反应的客观研究;H1拮抗剂局部黏膜应用的研究;以及H1拮抗剂对映体和活性代谢物的研究。随着编码H1受体的基因克隆成功以及对H1受体活性精确结构要求的进一步了解,可能会开发出治疗指数更优的H1拮抗剂。