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DOI 10.1016/j.ijporl.2014.10.017

Медицинская библиотека · International journal of pediatric otorhinolaryngology · 2014

Mucosal trauma induced apoptosis in guinea pig middle ear: comparision of hemostatic agents.

Eren Erdem, Başoğlu Mehmet Sinan, Kulduk Erkan, Şimsek Fatma, İnan Sevinç

Сравнительное исследованиеСтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

The aim of this study is to compare the effects of the absorbable gelatin sponge (AGS), microporous polysaccharide hemospheres (MPH), and Ankaferd on wound healing after middle ear trauma and to evaluate their ototoxicity in an experimental guinea pig model.

METHODS

Middle ear mucosal trauma was created in 21 healthy adult guinea pigs. MPH, Ankaferd, and AGS were applied into the right tympanic bulla of the guinea pigs (7 ears for each treatment modality). The left ears of the seven animals were used as the sham group. At the fourth postoperative week (28-30 days), the guinea pigs were decapitated. Apoptosis was investigated, and the expression of Bcl-xl, Apaf, p53, cytochrome 3, and caspase 3 were evaluated.

RESULTS

The Ankaferd and AGS groups demonstrated significantly lower epithelial thickness, inflammation, and capillary dilatation than did the control group (p<0.001, <0.001, /0.001, <0.001/, 0.005, and 0.005, respectively). A statistically significant decrease in Bcl-xl staining was observed in the middle ears of animals treated with MPH (p=0.003). There was significantly higher caspase 3 expression in the Ankaferd and AGS groups than in the control group (p<0.001 and p=0.002, respectively).

CONCLUSION

Light microscopy indicates that Ankaferd and AGS create less inflammation and increased caspase expression, which seems to induce inflammatory cell apoptosis. Ankaferd seems to be a promising hemostatic agent in otology.

Для цитирования: Eren Erdem, Başoğlu Mehmet Sinan, Kulduk Erkan, Şimsek Fatma, İnan Sevinç. Mucosal trauma induced apoptosis in guinea pig middle ear: comparision of hemostatic agents.. International journal of pediatric otorhinolaryngology. 2014. DOI: 10.1016/j.ijporl.2014.10.017.

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