Kohl F V
Zentrum für Innere Medizin der Philipps-Universität Marburg.
Z Hautkr. 1988;63 Suppl 4:21-5.
Effects of histamine on bronchial mucosal permeability, mucus secretion and smooth muscle cells change the airway geometry to bronchoconstriction. Histamine is also involved in the underlying early and late asthmatic response, chronic inflammation and increased airway responsiveness. The actions of histamine enhancing bronchial obstruction arise from its interaction with specific H1-receptors. In contrast to the bronchoconstrictive potency of histamine, antagonists do not lower bronchial resistance. Therefore they are without any therapeutic effect in acute asthmatic attacks. However, histamine H1-antagonists produce significant protection against bronchospasms which are induced experimentally by a variety of conditions in asthmatic patients. The protective actions of modern histamine H1-antagonists are caused mainly by the capacity to inhibit synthesis or release of mediators which are implicated in airway inflammation and hyperresponsiveness. Anti-inflammatory properties and restoration of desensitize beta-adrenoceptor responsiveness account for the possibility to reduce treatment with glucocorticoids and other drugs at least in some cases. In summary, modern H1-antagonists are useful in longterm control of moderate forms of primarily allergic asthma.
组胺对支气管黏膜通透性、黏液分泌和平滑肌细胞的影响会改变气道几何形状,导致支气管收缩。组胺还参与潜在的早期和晚期哮喘反应、慢性炎症以及气道反应性增加。组胺增强支气管阻塞的作用源于其与特定H1受体的相互作用。与组胺的支气管收缩效力相反,拮抗剂不会降低支气管阻力。因此,它们对急性哮喘发作没有任何治疗作用。然而,组胺H1拮抗剂对哮喘患者在各种实验条件下诱发的支气管痉挛具有显著的保护作用。现代组胺H1拮抗剂的保护作用主要是由于其抑制与气道炎症和高反应性有关的介质合成或释放的能力。抗炎特性和脱敏β-肾上腺素能受体反应性的恢复至少在某些情况下说明了减少使用糖皮质激素和其他药物治疗的可能性。总之,现代H1拮抗剂对中度原发性过敏性哮喘的长期控制有用。