Novel rat model of tympanostomy tube otorrhea

被引:3
|
作者
Silva, Rodrigo C. [1 ]
Dohar, Joseph E. [2 ,3 ,5 ,6 ]
Hebda, Patricia A. [2 ,3 ,4 ,5 ,6 ]
机构
[1] Univ Florida, Dept Otolaryngol, Gainesville, FL 32610 USA
[2] UPMC, Childrens Hosp Pittsburgh, Div Pediat Otolaryngol, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Med, Dept Otolaryngol, Pittsburgh, PA 15260 USA
[4] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15260 USA
[5] Univ Pittsburgh, Sch Hlth & Rehabil Sci, Dept Commun Sci & Disorders, Pittsburgh, PA 15260 USA
[6] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA 15260 USA
关键词
Tympanostomy tube otorrhea; Rat model; Cytokines; ACUTE OTITIS-MEDIA; STREPTOCOCCUS-PNEUMONIAE INFECTION; MIDDLE-EAR EFFUSIONS; TOPICAL CIPROFLOXACIN/DEXAMETHASONE; CHILDREN; OBSTRUCTION; CYTOKINES; SUPERIOR; MICROBIOLOGY; PREVENTION;
D O I
10.1016/j.ijporl.2011.11.001
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: Tympanostomy tube otorrhea (TTO), caused by the presence of pathogenic bacteria in the middle ear, is the most common complication of TT insertion. No studies have described a reproducible animal model of TTO. We aimed to develop a rat model of TTO which, in turn, could be used to assay the levels of TNF-alpha and IL-1 beta through the course of the infection. Methods: The left Eustachian tubes of 55 male Sprague-Dawley albino rats were occluded with guttapercha (ETO = Eustachian Tube Occlusion). Middle ear (ME) effusion was ascertained by weekly otomicroscopy. At 3 weeks tympanostomy tubes were placed bilaterally and the MEs were inoculated bilaterally with Streptococcus pneumoniae through the tubes. The rats were randomly assigned to one of two daily ototopical treatments: ciprofloxacin/dexamethasone (CDX) or placebo. The animals in each of the two treatment groups were further divided to receive 1, 2, 5 or 7 days of treatment. The rats were sacrificed after treatment was finished. The rates of otorrhea, positive middle ear (ME) cultures, and levels of TNF-alpha and IL-1 beta in the ME fluid were measured. Results: Left ETO followed by ME inoculation with S. pneumoniae and treatment with placebo resulted in persistent infection (100% culture-positive ME fluid at 10 days) and otorrhea (85.7%). Persistent infection of the left ear was accompanied by significantly elevated the levels of IL-1 beta and TNF-alpha. Ears treated with CDX had lower rates of otorrhea at all time points and lower levels of IL-1 beta and TNF-alpha. Conclusions: This study is the first to describe a reproducible animal model of acute TTO. Surgical obstruction of the ET, followed by TT placement and ME inoculation with S. pneumoniae induced persistent otorrhea and infection. Both IL-1 beta and TNF-alpha appear to be potential markers of persistent middle ear infection. This novel model may be used in future studies of the pathogenesis and therapy of TTO. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:179 / 182
页数:4
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