Andersson M, Nolte H, Olsson M, Skov P S, Pipkorn U
Department of Oto-Rhino-Laryngology, University Hospital of Lund, Sweden.
J Allergy Clin Immunol. 1990 Nov;86(5):815-20. doi: 10.1016/s0091-6749(05)80188-5.
The determination of histamine in nasal secretions and nasal lavage fluid may be of importance to monitor activation of histamine containing cells in the nasal cavity. However, such studies have been besieged by controversy, specifically to findings of changes in histamine levels in relation to allergenic stimulation. This controversy may be due to the specificity and accuracy of the various methods used to determine histamine in the nasal fluid. We have therefore applied and compared three new methods to determine histamine in nasal lavage fluids obtained before and after allergen challenge in normal subjects and patients with allergic rhinitis. We used a fluorometric glass fiber-based histamine method (FHR) and two RIAs, I and II. The FHR (detection limit, 7.0 nmol) and the RIA II (detection limit, 0.2 nmol) are specific for histamine itself, whereas the RIA I (detection limit, 18.0 nmol) measures mainly methylhistamine and cross-reacts to some extent with histamine. The histamine levels in the nasal lavage fluids from the nasal challenges demonstrated histamine values between 100 and 2000 nmol/L of histamine with significantly higher levels in the postallergen challenges for the allergic subjects as compared to the normal control subjects. The FHR correlated well with the RIA I and RIA II methods with correlation coefficients of 0.77 to 0.88 (p less than 0.001), respectively. However, the RIA I (methylhistamine antibody) always demonstrated absolute histamine values 5% to 20% of values measured by the RIA II (at the level of cross-reactivity to histamine).(ABSTRACT TRUNCATED AT 250 WORDS)
测定鼻分泌物和鼻腔灌洗液中的组胺,对于监测鼻腔中含组胺细胞的激活情况可能具有重要意义。然而,此类研究一直饱受争议,尤其是在组胺水平与变应原刺激相关变化的研究结果方面。这种争议可能归因于用于测定鼻液中组胺的各种方法的特异性和准确性。因此,我们应用并比较了三种新方法,以测定正常受试者和变应性鼻炎患者在变应原激发前后获得的鼻腔灌洗液中的组胺。我们使用了一种基于荧光玻璃纤维的组胺方法(FHR)和两种放射免疫分析法(RIA),即I法和II法。FHR(检测限为7.0 nmol)和RIA II(检测限为0.2 nmol)对组胺本身具有特异性,而RIA I(检测限为18.0 nmol)主要检测甲基组胺,并在一定程度上与组胺发生交叉反应。鼻腔激发后鼻腔灌洗液中的组胺水平显示,组胺值在100至2000 nmol/L之间,变应性受试者变应原激发后的组胺水平明显高于正常对照受试者。FHR与RIA I和RIA II方法的相关性良好,相关系数分别为0.77至0.88(p小于0.001)。然而,RIA I(甲基组胺抗体)所显示的组胺绝对数值始终是RIA II所测数值的5%至20%(在与组胺的交叉反应水平上)。(摘要截短于250字)