吸入肝素及相关糖胺聚糖对豚鼠变应原诱导的嗜酸性粒细胞浸润的影响

E.A.M. Seeds, A.P. Horne, D.J. Tyrrell, C.P. Page
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引用次数: 36

摘要

摘要:在160和1600 U/ml剂量下,雾化未分离肝素GM1060可显著抑制豚鼠气道中过敏原诱导的嗜酸性粒细胞浸润(通过组织学和支气管肺泡灌洗或BAL进行评估)。与雾化未分离肝素类似,在1000u /ml、2000u /ml和5000 U/ml时,Multiparin可有效降低BAL液中的嗜酸性粒细胞水平,但这种降低仅在使用最高剂量时具有统计学意义。此外,Fragmin(一种低分子量肝素)在500 U/ml剂量下显著抑制变应原诱导的嗜酸性粒细胞向BAL液的浸润,在1000和2000 U/ml较高剂量下,这种作用消失。过敏原诱导的嗜酸性粒细胞浸润不受皮肤硫酸盐的影响。然而,糖胺聚糖硫酸软骨素A、硫酸软骨素C和硫酸肝素能够影响变应原诱导的嗜酸性粒细胞浸润BAL液的程度。这些结果表明,肝素和一些相关的糖胺聚糖直接给药可抑制过敏原诱导的嗜酸性粒细胞浸润。
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The Effect of Inhaled Heparin and Related Glycosaminoglycans on Allergen-induced Eosinophil Infiltration in Guinea-Pigs

Summary: Aerosolized unfractionated heparin GM1060 significantly inhibited allergen-induced eosinophil infiltration into the airways of guinea-pigs (as assessed both histologically and by bronchoalveolar lavage, or BAL) at doses of 160 and 1600 U/ml. Similarly aerosolized unfractionated heparin, Multiparin was effective at reducing eosinophil levels in the BAL fluid at 1000, 2000 and 5000 U/ml, but this reduction was statistically significant only at the highest dose used.

Additionally, Fragmin (a low molecular weight heparin) significantly inhibited allergen-induced eosinophil infiltration into BAL fluid at a dose of 500 U/ml, an effect that was lost at the higher doses of 1000 and 2000 U/ml.

Allergen-induced eosinophil infiltration was unaffected by dermatan sulphate. However, the glycosaminoglycans chondroitin sulphate A, chondroitin sulphate C and heparan sulphate were able to influence the extent of allergen-induced eosinophil infiltration into BAL fluid.

These results suggest that heparin and some related glycosaminoglycans can inhibit allergen-induced eosinophil infiltration when administered directly to the airways.

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