Clinical and experimental studies of Bell's palsy.
Clinical and experimental studies of Bell's palsy.
批准号:
11671696
负责人:
MURAKANI Shingo
金额:
$2.43万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000
中文摘要
1型单纯疱疹是贝尔氏麻痹最可能的病因。我们证实了从贝尔氏麻痹患者获得的神经内膜液和耳肌中存在HSV-1 DNA,并阐明了HSV-1感染与贝尔氏麻痹的发病直接相关。我们还成功地制造了急性和短暂性面瘫,模拟贝尔麻痹,通过接种HSV到老鼠的耳廓。本研究通过动物模型和贝尔麻痹对面神经麻痹的发病机制进行了研究。小鼠模型的组织病理学表现为严重的神经肿胀、炎性细胞浸润和面神经空泡变性。完整的、脱髓鞘的和退化的神经混杂在面神经干中。电生理研究表明,眨眼反射测试中R1潜伏期的时间过程与面神经麻痹的恢复具有良好的平行性,而ENoG的恢复则比面神经麻痹的恢复有延迟的趋势;这些反应通常出现在贝尔氏麻痹中。部分贝尔麻痹患者面神经血流量有不同程度的减少。然而,没有面瘫的胆脂瘤患者的血流量也有同样的减少。提示单纯疱疹病毒1型感染是贝尔麻痹患者面瘫的主要原因,神经缺血是继发于病毒感染。回顾性分析69例Bell患者应用阿昔洛韦-强的松治疗的疗效。总回收率为95.7%。在发病后3天内开始这种治疗的患者的比率为100%。这些结果表明,早期治疗是有效的阿昔洛韦-强的松治疗贝尔麻痹的必要条件。
英文摘要
Herpes simplex type 1 is the most probable cause of Bell's palsy. We have demonstrated the presence of HSV-1 DNA in the endoneural fluid and auricular muscle obtained from patients with Bell's palsy, and clarified that HSV-1infection is directly related to the pathogenesis of Bell's palsy. We have also succeeded in producing an acute and transient facial paralysis, simulating Bell's palsy, by inoculating HSV into the auricle of mice. In the present study, we have studied pathomechanism of facial palsy by using animal model and Bell's palsy. Histopathology of the mouse model demonstrated severe nerve swelling, inflammatory cell infiltration and vacuolar degeneration in the affected facial nerve. Intact, demyelinated, and degenerated nerves were intermingled in the facial nerve trunk. Electro physiological study has demonstrated that the time course of R1 latency in the blink reflex tests paralleled the recovery of the facial nerve paralysis well, whereas ENoG recovery tended to be delayed, compared to that of the paralysis ; these responses are usually seen in Bell's palsy. The blood flow in the facial nerve was decreased to some extent in some patients with Bell's palsy. However, the same decrease of blood flow was noted in patients with cholesteatoma without facial paralysis. These results suggested that viral infection of HSV-1 was the primary cause of facial palsy in Bell's palsy and ischemia of the nerve was secondary to the viral infection. The effect of acyclovir-prednisone treatment was analyzed retrospectively in 69 Bell's patients. The overall recovery rate was 95.7 %. The rate in patients who started this treatment within 3 days after onset was 100 %. These results suggest that early treatment is necessary for effective acylovir-prednisone therapy in Bell's palsy.
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脇坂浩之,木崎久喜,高橋宏尚,本多伸光,村上信五,暁清文: "HSV-1初感染顔面神経麻痺モデルの麻痺治癒後の組織学的検討"Facial N Res Jpn. 20. 46-48 (2000)
Hiroyuki Wakisaka、Hisaki Kizaki、Hironao Takahashi、Nobumitsu Honda、Shingo Murakami、Kiyofumi Akira:“原发性 HSV-1 感染的面神经麻痹模型麻痹愈合后的组织学研究” Facial N Res Jpn. 20. 46-48 ( 2000)
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高橋宏尚, 本多伸光, 木崎久喜, 脇坂浩之, 羽藤直人, 暁 清文, 村上信五: "単純ヘルペスウイルス1型の再活性化によるマウス顔面神経麻痺モデルの研究"Facial N Res Jpn. 20. 49-51 (2000)
Hironaka Takahashi、Nobumitsu Honda、Hisaki Kizaki、Hiroyuki Wakisaka、Naoto Hato、Kiyofumi Akatsuki、Shingo Murakami:“由于单纯疱疹病毒 1 型再激活引起的小鼠面瘫模型的研究” Facial N Res Jpn. 20. 49 -51 (2000) )
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木崎久喜, 高橋宏尚, 脇坂浩之, 本多伸光, 羽藤直人, 暁清文, 村上信五: "D4+,CD8+T細胞の抑制によるHSV-1再活性化顔面神経麻痺発現に関する検討"Facial N Res Jpn. 20. 58-60 (2000)
Hisaki Kizaki、Hironaka Takahashi、Hiroyuki Wakisaka、Nobumitsu Honda、Naoto Hato、Kiyofumi Akatsuki、Shingo Murakami:“通过抑制 D4+、CD8+ T 细胞而导致 HSV-1 重新激活引起的面瘫表达的研究”Facial N Res Jpn 20。 58-60(2000)
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村上信五, 宮本直哉, 渡邊暢浩, 松田太志: "日本臨床58(4)"αヘルペス感染の臨床、耳鼻咽喉科領域 -αヘルペスウイルスによる顔面神経麻痺. 5 (2000)
Shingo Murakami、Naoya Miyamoto、Nobuhiro Watanabe、Futoshi Matsuda:“日本临床58(4)”α疱疹感染的临床实践,耳鼻喉科-α疱疹病毒引起的面神经麻痹5(2000)。
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