Reinero Carol R, Decile Kendra C, Byerly Jenni R, Berghaus Roy D, Walby William E, Berghaus Londa J, Hyde Dallas M, Schelegle Edward S, Gershwin Laurel J
Departments of Pathology, Microbiology, and Immunology, School of Veterinary Medicine, University of California, Davis, CA 95616-8734, USA.
Am J Vet Res. 2005 Jul;66(7):1121-7. doi: 10.2460/ajvr.2005.66.1121.
To compare the effects of an orally administered corticosteroid (prednisone), an inhaled corticosteroid (flunisolide), a leukotriene-receptor antagonist (zafirlukast), an antiserotonergic drug (cyproheptadine), and a control substance on the asthmatic phenotype in cats with experimentally induced asthma.
6 cats with asthma experimentally induced by the use of Bermuda grass allergen (BGA).
A randomized, crossover design was used to assess changes in the percentage of eosinophils in bronchoalveolar lavage fluid (BALF); airway hyperresponsiveness; blood lymphocyte phenotype determined by use of flow cytometry; and serum and BALF content of BGA-specific IgE, IgG, and IgA determined by use of ELISAs.
Mean +/- SE eosinophil percentages in BALF when cats were administered prednisone (5.0 +/- 2.3%) and flunisolide (2.5 +/- 1.7%) were significantly lower than for the control treatment (33.7 +/- 11.1%). We did not detect significant differences in airway hyperresponsiveness or lymphocyte surface markers among treatments. Content of BGA-specific IgE in serum was significantly lower when cats were treated with prednisone (25.5 +/- 5.4%), compared with values for the control treatment (63.6 +/- 12.9%); no other significant differences were observed in content of BGA-specific immunoglobulins among treatments.
Orally administered and inhaled corticosteroids decreased eosinophilic inflammation in airways of cats with experimentally induced asthma. Only oral administration of prednisone decreased the content of BGA-specific IgE in serum; no other significant local or systemic immunologic effects were detected among treatments. Inhaled corticosteroids can be considered as an alternate method for decreasing airway inflammation in cats with asthma.
比较口服皮质类固醇(泼尼松)、吸入皮质类固醇(氟尼缩松)、白三烯受体拮抗剂(扎鲁司特)、抗5-羟色胺能药物(赛庚啶)及一种对照物质对实验性诱发哮喘猫的哮喘表型的影响。
6只通过使用百慕大草过敏原(BGA)实验性诱发哮喘的猫。
采用随机交叉设计,以评估支气管肺泡灌洗液(BALF)中嗜酸性粒细胞百分比的变化;气道高反应性;通过流式细胞术测定的血液淋巴细胞表型;以及使用酶联免疫吸附测定法(ELISA)测定的BGA特异性IgE、IgG和IgA的血清及BALF含量。
给猫服用泼尼松(5.0±2.3%)和氟尼缩松(2.5±1.7%)时,BALF中嗜酸性粒细胞的平均±标准误百分比显著低于对照处理(33.7±11.1%)。我们未检测到各处理之间在气道高反应性或淋巴细胞表面标志物方面存在显著差异。与对照处理值(63.6±12.9%)相比,猫用泼尼松治疗时血清中BGA特异性IgE的含量显著降低(25.5±5.4%);各处理之间在BGA特异性免疫球蛋白含量方面未观察到其他显著差异。
口服和吸入皮质类固醇可减轻实验性诱发哮喘猫气道中的嗜酸性粒细胞炎症。仅口服泼尼松可降低血清中BGA特异性IgE的含量;各处理之间未检测到其他显著的局部或全身免疫效应。吸入皮质类固醇可被视为减轻哮喘猫气道炎症的一种替代方法。