de Graaf-in 't Veld T, Garrelds I M, van Toorenenbergen A W, Mulder P G, Gerth van Wijk R, Boegheim J P
Department of Allergology, University Hospital Rotterdam-Dijkzigt, The Netherlands.
Ann Allergy Asthma Immunol. 1995 Sep;75(3):261-6.
It has been demonstrated that some oral antihistamines reduce nasal nonspecific reactivity and that topical levocabastine reduces cellular influx after nasal allergen challenge. This suggests that antihistamines possess other properties besides classical H1-receptor antagonism.
To evaluate the effect of 1 week's treatment with topical levocabastine on the nasal clinical response, inflammatory mediators, and nasal hyperreactivity.
In a double-blind, placebo-controlled, 2-period, 2-treatment, crossover study, 21 rhinitic patients allergic to house dust mite participated. After each treatment period patients were challenged with house dust mite extract. Symptom scores and nasal lavages were collected for nine and one-half hours after challenge. Allergen-induced nasal hyperreactivity was determined by nasal methacholine challenge 24 hours after allergen challenge. A nasal histamine challenge was performed as well.
Patients showed only an immediate nasal response. Levocabastine significantly reduced the symptom score after 100 (P = .0063), 1000 (P = .0035), and 10,000 biological units (BU)/mL (P = .0013) of house dust mite extract. Albumin influx and tryptase release were not significantly reduced by levocabastine. No release of histamine and eosinophil cationic protein was seen. Levocabastine did not reduce nasal response to methacholine. Active treatment significantly reduced histamine-induced nasal secretion (P = .0009) and the number of sneezes (P = .0001).
A significant effect of levocabastine was shown on the immediate clinical response to house dust mite and to histamine challenge only. Our findings suggest that levocabastine is an effective H1-receptor antagonist without anti-inflammatory properties.
已证实某些口服抗组胺药可降低鼻非特异性反应性,且局部用左卡巴斯汀可减少鼻过敏原激发后的细胞内流。这表明抗组胺药除具有经典的H1受体拮抗作用外,还具有其他特性。
评估局部用左卡巴斯汀治疗1周对鼻临床反应、炎症介质和鼻高反应性的影响。
在一项双盲、安慰剂对照、2期、2治疗、交叉研究中,21名对屋尘螨过敏的鼻炎患者参与。每个治疗期后,患者接受屋尘螨提取物激发。激发后9个半小时收集症状评分和鼻灌洗液。在过敏原激发后24小时通过鼻用乙酰甲胆碱激发测定过敏原诱导的鼻高反应性。同时进行鼻组胺激发试验。
患者仅表现出即刻鼻反应。左卡巴斯汀在100(P = 0.0063)、1000(P = 0.0035)和10,000生物单位(BU)/mL(P = 0.0013)的屋尘螨提取物作用后显著降低症状评分。左卡巴斯汀未显著降低白蛋白内流和类胰蛋白酶释放。未见组胺和嗜酸性粒细胞阳离子蛋白释放。左卡巴斯汀未降低鼻对乙酰甲胆碱的反应。积极治疗显著降低组胺诱导的鼻分泌物(P = 0.0009)和喷嚏次数(P = 0.0001)。
左卡巴斯汀仅对屋尘螨和组胺激发的即刻临床反应有显著作用。我们的研究结果表明左卡巴斯汀是一种有效的H1受体拮抗剂,无抗炎特性。