Novel rat model of tympanostomy tube otorrhea.

Novel rat model of tympanostomy tube otorrhea.
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DOI:
10.1016/j.ijporl.2011.11.001
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发表时间:
2012-02
影响因子:
1.5
通讯作者:
Hebda, Patricia A.
Hebda, Patricia A.
中科院分区:
医学4区
文献类型:
--
作者:
Silva, Rodrigo C.;Dohar, Joseph E.;Hebda, Patricia A.

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鼓膜造口置管术最常见的并发症是鼓膜造口置管术后中耳炎(TTO)。没有研究描述了TTO的可重现动物模型。我们的目的是建立一种大鼠TTO模型,该模型可用于检测整个感染过程中TNF-α和IL-1β的水平。用牙胶堵塞55只雄性Sprague-Dawley白化病大鼠的左咽鼓管(ETO=咽鼓管堵塞)。通过每周一次的耳显微镜检查确定中耳(ME)积液。在3周时,双侧放置鼓膜造口管,并通过管用肺炎链球菌双侧接种ME。将大鼠随机分配至两种每日耳局部治疗之一:环丙沙星/地塞米松(CDX)或安慰剂。将两个给药组中的动物进一步分为接受1、2、5或7天给药。治疗结束后处死大鼠。观察两组中耳炎发生率、中耳培养阳性率及中耳液中TNF-α、IL-1β水平。左ETO,然后ME接种S。肺炎和安慰剂治疗导致持续感染(10天时100%培养阳性ME液)和耳炎(85.7%)。左耳持续感染伴IL-1β和TNF-α水平显著升高。CDX治疗的耳在所有时间点的耳畸形发生率均较低,IL-1β和TNF-α水平也较低。本研究首次描述了急性TTO的可重复动物模型。手术阻塞ET,然后放置TT和ME接种S。肺炎引起持续性耳炎和感染。IL-1β和TNF-α可能是持续性中耳感染的潜在标志物。这种新的模型可能用于TTO的发病机制和治疗的未来研究。
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-α and IL-1β through the course of the infection. The left Eustachian tubes of 55 male Sprague-Dawley albino rats were occluded with gutta-percha (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-α and IL-1β in the ME fluid were measured. 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-1β and TNF-α. Ears treated with CDX had lower rates of otorrhea at all time points and lower levels of IL-1β and TNF-α. 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-1β and TNF-α 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.
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