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减少抗组胺药在过敏性疾病管理中引起的中枢神经系统不良反应:策略与进展

Reduction of the central nervous system adverse effects associated with antihistamines in the management of allergic disorders: strategies and progress.

作者信息

Gengo F M

机构信息

Department of Neurology and Pharmacy, School of Medicine, State University of New York at Buffalo, USA.

出版信息

J Allergy Clin Immunol. 1996 Dec;98(6 Pt 3):S319-25.

PMID:8977543
Abstract

To reduce the risks associated with the treatment of allergic disorders, physicians should understand the benefits and risks of drugs in the antihistamine class. The risk of central nervous system adverse effects associated with antihistamine use is significant with the use of first-generation antihistamines, which show pharmacologic activity in serotonergic, alpha-adrenergic, dopaminergic, and muscarinic-cholinergic pathways. Adverse effects reported with the use of first-generation antihistamines most often include drowsiness, fatigue, and an inability to concentrate; these effects may result in decreased compliance with therapy. The second-generation antihistamines have the property of low lipid solubility, which slows access across the blood-brain barrier. The low sedative profile of these new drugs may also be linked to a more pronounced binding to peripheral rather than brain histamine H1-receptors. The use of antihistamines with lower lipid solubility and greater specificity can provide an effective alternative for the relief of allergic symptoms, can improve compliance, and can reduce neurologic side effects. Because of the differences now recognized in the side effects of drugs of this class, an individualized approach to selection of antihistamine therapy is required.

摘要

为降低与过敏性疾病治疗相关的风险,医生应了解抗组胺类药物的益处和风险。使用第一代抗组胺药时,与抗组胺药使用相关的中枢神经系统不良反应风险很大,第一代抗组胺药在血清素能、α-肾上腺素能、多巴胺能和毒蕈碱-胆碱能途径中表现出药理活性。使用第一代抗组胺药报告的不良反应最常见的包括嗜睡、疲劳和注意力不集中;这些效应可能导致治疗依从性下降。第二代抗组胺药具有低脂溶性的特性,这减缓了其穿过血脑屏障的速度。这些新药的低镇静作用也可能与其对外周而非脑组胺H1受体的更显著结合有关。使用脂溶性较低且特异性更高的抗组胺药可为缓解过敏症状提供有效的替代方法,可提高依从性,并可减少神经副作用。由于现已认识到该类药物副作用的差异,需要采用个体化方法选择抗组胺治疗。

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