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首页> 外文期刊>Journal of child neurology >Neuroprotective effects of brain-derived neurotrophic factor (BDNF) on hearing in experimental pneumococcal meningitis.
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Neuroprotective effects of brain-derived neurotrophic factor (BDNF) on hearing in experimental pneumococcal meningitis.

机译:在实验性肺炎球菌性脑膜炎中,脑源性神经营养因子(BDNF)对听力的神经保护作用。

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Bacterial meningitis is still one of the most common causes of acquired profound sensorineural deafness in children despite antibiotic treatment. We investigated the neuroprotective effects of brain-derived neurotrophic factor on hearing function in experimental bacterial meningitis. We implanted stainless steel tubes into both cerebral ventricles of Sprague-Dawley rats aged 21 days. Bacterial meningitis was induced by inoculating a strain of serotype III Streptococcus pneumoniae into the cisterna magna. Six micrograms per day of brain-derived neurotrophic factor (groups 1 and 3) or albumin (groups 2 and 4) was injected into the cerebral ventricles 24 hours after or before infection, respectively, for a duration of 7 days. Additionally, all rats received antibiotic subcutaneous treatment starting 24 hours after infection for 7 days. Brainstem auditory evoked potentials were recorded 24 hours before and 24 hours after infection and after 7 days of treatment with brain-derived neurotrophic factor or placebo and antibiotics, respectively, to determine hearing threshold. Our results showed that the hearing thresholds of animals in each group increased significantly 24 hours after infection compared with the results recorded 24 hours before infection (P < .01). After 7 days of treatment with brain-derived neurotrophic factor, brainstem auditory evoked potential responses recurred in 16 ears when stimulated at 75 dB hearing level in groups 1 and 3. Their hearing thresholds significantly decreased compared with the control group 2 (P < .05) and group 4 (P < .01). However, 13 of 14 ears absent brainstem auditory evoked potential responses could still not be identified at 75 dB hearing level in control groups 2 and 4. The improvement of the hearing thresholds in group 3 (treated before infection) was greater than that of group 1 (treated after infection) (P < .05), but there was no significant difference found between the control groups before and after infection (P > .05). Our study supports the hypothesis that the administration of exogenous brain-derived neurotrophic factor can be effective in preventing or treating hearing loss following bacterial meningitis.
机译:尽管进行了抗生素治疗,但细菌性脑膜炎仍然是儿童后天性严重感音神经性耳聋的最常见原因之一。我们调查了实验性细菌性脑膜炎中脑源性神经营养因子对听力功能的神经保护作用。我们将不锈钢管植入21天大的Sprague-Dawley大鼠的两个脑室。细菌性脑膜炎是通过将一种血清型III型肺炎链球菌接种到巨大的水罐中而诱发的。感染后24小时或之前,每天将六微克的脑源性神经营养因子(第1组和第3组)或白蛋白(第2组和第4组)注射至脑室,持续7天。此外,所有大鼠在感染后24小时开始接受抗生素皮下治疗7天。分别在感染前24小时和感染后24小时以及分别用脑源性神经营养因子或安慰剂和抗生素治疗7天后记录脑干听觉诱发电位,以确定听力阈值。我们的结果表明,与感染前24小时记录的结果相比,感染后24小时每组动物的听力阈值均显着提高(P <.01)。在用脑源性神经营养因子治疗7天后,在第1组和第3组中,以75 dB的听力水平进行刺激时,在16耳中出现了脑干听觉诱发电位反应,与对照组2相比,其听力阈值显着降低(P <.05 )和第4组(P <.01)。然而,在对照组2和4的75 dB听力水平下,仍未鉴定出14耳中没有脑干听觉诱发电位的潜在反应。组3(感染前接受治疗)的听力阈值改善程度大于组1。 (感染后治疗)(P <.05),但对照组感染前后没有显着差异(P> .05)。我们的研究支持以下假设:外源性脑源性神经营养因子的给药可以有效预防或治疗细菌性脑膜炎后的听力丧失。

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