Sutbeyaz Y, Yakan B, Ozdemir H, Karasen M, Doner F, Kufrevioglu I
Department of Otolaryngology, School of Medicine, Ataturk University, Erzurum, Turkey.
Ann Otol Rhinol Laryngol. 1996 Jun;105(6):476-80. doi: 10.1177/000348949610500611.
Arachidonic acid metabolites such as prostaglandins and leukotrienes have been shown to play an important role in the pathogenesis of otitis media (OM). Among these mediators, leukotriene B4 (LTB4) is one of the most potent inducers of inflammatory processes. SC-41930 has been shown to be a specific LTB4 receptor antagonist both in vitro and in vivo. In this study, anti-inflammatory effects of SC-41930 were investigated in a guinea pig model of OM induced by middle ear (ME) inoculation of killed Staphylococcus aureus. Outcome of treatment was determined by measurement of myeloperoxidase activity in the samples of ME mucosa, evaluation of temporal bone histopathology, and presence of ME fluids. Myeloperoxidase activity in the SC-41930-treated group was found to be significantly lower than that in the control group. Histopathology of temporal bones indicated decreased inflammation in the treated group as compared to the controls. In addition, ME fluids were absent in four out of six treated animals. These results demonstrate that SC-41930 can produce significant anti-inflammatory effects in this model of OM.
花生四烯酸代谢产物如前列腺素和白三烯已被证明在中耳炎(OM)的发病机制中起重要作用。在这些介质中,白三烯B4(LTB4)是炎症过程中最有效的诱导剂之一。SC-41930在体外和体内均已被证明是一种特异性LTB4受体拮抗剂。在本研究中,在通过中耳(ME)接种灭活金黄色葡萄球菌诱导的豚鼠中耳炎模型中研究了SC-41930的抗炎作用。通过测量ME黏膜样本中的髓过氧化物酶活性、评估颞骨组织病理学以及ME积液的存在来确定治疗结果。发现SC-41930治疗组的髓过氧化物酶活性明显低于对照组。颞骨组织病理学表明,与对照组相比,治疗组的炎症减轻。此外,在六只接受治疗的动物中,有四只没有ME积液。这些结果表明,SC-41930在该中耳炎模型中可产生显著的抗炎作用。