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肿瘤坏死因子-α在细菌性脑膜炎后感音神经性听力损失中的作用。

Role of tumor necrosis factor-alpha in sensorineural hearing loss after bacterial meningitis.

作者信息

Aminpour Shervin, Tinling Steven P, Brodie Hilary A

机构信息

Department of Otolaryngology Head and Neck Surgery, University of California, Davis, School of Medicine, Davis, California 95616, USA.

出版信息

Otol Neurotol. 2005 Jul;26(4):602-9. doi: 10.1097/01.mao.0000178121.28365.0d.

Abstract

HYPOTHESIS

Blockade of tumor necrosis factor-alpha with tumor necrosis factor-alpha antibody will reduce the extent of cochlear injury and hearing loss associated with Streptococcus pneumoniae meningitis.

BACKGROUND

Inflammatory mediators play a significant role in the morbidity associated with bacterial meningitis, including hearing loss and labyrinthitis ossificans. Previous studies have shown the attenuation of hearing loss by the nonspecific blockade of such pathways.

METHODS

Fifty Mongolian gerbils were divided into four groups. Auditory brainstem response testing was conducted to measure hearing thresholds. Streptococcus pneumoniae meningitis was induced in Groups 1 and 2. Group 2 was then given a single intraperitoneal injection of tumor necrosis factor-alpha antibody, whereas Group 1 received phosphate-buffered saline. Uninfected animals in Groups 3 and 4 were implanted with osmotic pumps that delivered a continuous 8-day intrathecal flow of either tumor necrosis factor-alpha (Group 4) or phosphate-buffered saline (Group 3). After 6 weeks, auditory brainstem response testing was repeated. The cochleas were harvested and analyzed histomorphometrically.

RESULTS

Group 2 animals with Streptococcus pneumoniae meningitis that also received tumor necrosis factor-alpha antibody developed significantly less hearing loss than Group 1 animals with meningitis alone. The decrease in the average threshold at 4, 8, 16, and 32 kHz was 31, 30, 25, and 28 dB sound pressure level, respectively (p < 0.0092 for each). Furthermore, histomorphometric analysis showed significantly less damage to the organ of Corti, spiral ganglion, spiral ligament, and stria vascularis in Group 2. Conversely, tumor necrosis factor-alpha induced meningitis animals (Group 3) showed increased hearing loss compared with phosphate-buffered saline controls (Group 4), with p < 0.0001 at all frequencies.

CONCLUSION

Tumor necrosis factor-alpha plays an important role in cochlear injury after bacterial meningitis. Blockade of tumor necrosis factor-alpha reduces postmeningitic hearing loss and cochlear injury. Induction of meningitis with intrathecal tumor necrosis factor-alpha also resulted in hearing loss and cochlear injury similar to bacterial meningitis.

摘要

假设

使用肿瘤坏死因子-α抗体阻断肿瘤坏死因子-α将减少与肺炎链球菌性脑膜炎相关的耳蜗损伤程度和听力损失。

背景

炎症介质在细菌性脑膜炎相关的发病过程中起重要作用,包括听力损失和骨化性迷路炎。先前的研究表明,通过对这些途径的非特异性阻断可减轻听力损失。

方法

将50只蒙古沙鼠分为四组。进行听性脑干反应测试以测量听力阈值。在第1组和第2组中诱发肺炎链球菌性脑膜炎。然后给第2组腹腔注射一次肿瘤坏死因子-α抗体,而第1组接受磷酸盐缓冲盐水。第3组和第4组中的未感染动物植入渗透泵,持续8天鞘内输注肿瘤坏死因子-α(第4组)或磷酸盐缓冲盐水(第3组)。6周后,重复进行听性脑干反应测试。收获耳蜗并进行组织形态计量学分析。

结果

患有肺炎链球菌性脑膜炎且接受肿瘤坏死因子-α抗体的第2组动物,其听力损失明显少于仅患有脑膜炎的第1组动物。在4、8、16和32kHz处平均阈值的降低分别为31、30、25和28dB声压级(每个频率p<0.0092)。此外,组织形态计量学分析显示,第2组中柯蒂器、螺旋神经节、螺旋韧带和血管纹的损伤明显较少。相反,与磷酸盐缓冲盐水对照组(第4组)相比,肿瘤坏死因子-α诱发脑膜炎的动物(第3组)听力损失增加,所有频率下p<0.0001。

结论

肿瘤坏死因子-α在细菌性脑膜炎后的耳蜗损伤中起重要作用。阻断肿瘤坏死因子-α可减少脑膜炎后听力损失和耳蜗损伤。鞘内注射肿瘤坏死因子-α诱发脑膜炎也导致与细菌性脑膜炎相似的听力损失和耳蜗损伤。

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