Giannoulaki Vassiliki, Papathanassiou Miltiades, Sitaras Nikolaos M, Tiligada Ekaterini
Department of Experimental Pharmacology, Medical School, University of Athens, M. Asias 75, GR-11527 Athens, Greece.
Eur J Pharmacol. 2003 Nov 14;481(1):119-24. doi: 10.1016/j.ejphar.2003.08.080.
This study sought to investigate the effects of nadroparine on an in vivo experimental model of type I hypersensitivity response in the rat conjunctiva. Following drug application onto the eye, either before or after challenge with the mast cell degranulator, basic polyamine compound 48/80, the conjunctival histamine content and the nitrite levels in the conjunctival lavage fluid were quantified fluorometrically and spectrophotometrically, respectively. Instillation into the eye of nadroparine inhibited the C48/80-induced decreases in conjunctival histamine and the delayed increases in nitrite levels, without influencing basal mediator levels. Protamine did not induce histamine release and only partially reversed the effects of nadroparine post-challenge, yet it had no effect on the protective action of the drug when administered prior to degranulation. The results showed that nadroparine was equally effective in attenuating the effects of compound 48/80 in the eye when administered topically either before or after challenge.
本研究旨在探讨那屈肝素对大鼠结膜Ⅰ型超敏反应体内实验模型的影响。在使用肥大细胞脱颗粒剂碱性多胺化合物48/80攻击之前或之后,将药物滴入眼内,分别采用荧光法和分光光度法对结膜组织中的组胺含量以及结膜灌洗液中的亚硝酸盐水平进行定量分析。那屈肝素滴入眼内可抑制C48/80诱导的结膜组胺含量降低以及亚硝酸盐水平的延迟升高,且不影响基础介质水平。鱼精蛋白不会诱导组胺释放,仅能部分逆转攻击后那屈肝素的作用,但在脱颗粒前给药时,对该药物的保护作用无影响。结果表明,在攻击前或攻击后局部给予那屈肝素,其减轻化合物48/80在眼内作用的效果相同。