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豚鼠光化学诱导的局灶性耳蜗损伤:II. 透射电子显微镜研究。

Photochemically induced focal cochlear lesions in the guinea pig: II. A transmission electron microscope study.

作者信息

Miyashita H, Iwasaki S, Hoshino T

机构信息

Department of Otolaryngology, Hamamatsu University School of Medicine, Japan.

出版信息

Microsc Res Tech. 1998 May 15;41(4):334-40. doi: 10.1002/(SICI)1097-0029(19980515)41:4<334::AID-JEMT6>3.0.CO;2-Q.

Abstract

Photochemically induced focal lesions in guinea pig cochleas were studied by light microscopy and transmission electron microscopy. The lesions were induced in the second cochlear turns of 35 adult guinea pigs by illumination for 10 minutes with a focused green light immediately after a rose bengal solution was injected into the jugular vein. The cochlear lateral wall and organ of Corti were examined 5, 10, 20, 30, and 90 minutes, 12 and 24 hours, and 3, 7, and 30 days after the procedure. Aggregations of platelets and red blood cells were found in strial capillaries at 5 minutes after illumination. After 30 minutes, marginal cell surfaces protruded into the endolymphatic space; surface membranes were ruptured and the cytoplasm was expelled into the space. In outer hair cells, disruption of the cellular membrane was found near the cuticular plate 12 hours after the procedure. All cellular elements of the lateral wall and organ of Corti were markedly degenerated in the 30-day specimens. Histological changes found in the stria vascularis were consistent with cell damage caused by active oxygen species. It is likely that the stria vascularis is more sensitive to the photochemical reaction than other parts of the cochlea. Cell damage in other parts of the cochlea seemed to have been caused by local microvascular ischemia in addition to the action of active oxygen species induced by the photochemical reaction.

摘要

通过光学显微镜和透射电子显微镜研究了豚鼠耳蜗光化学诱导的局灶性病变。在将孟加拉玫瑰红溶液注入颈静脉后,立即用聚焦绿光照射35只成年豚鼠的第二耳蜗转,诱导病变。在手术后5、10、20、30和90分钟、12和24小时以及3、7和30天检查耳蜗外侧壁和柯蒂氏器。光照后5分钟,在血管纹毛细血管中发现血小板和红细胞聚集。30分钟后,边缘细胞表面突入内淋巴间隙;表面膜破裂,细胞质被排入该间隙。在手术后12小时,在外毛细胞中,靠近角质板处发现细胞膜破坏。在30天的标本中,外侧壁和柯蒂氏器的所有细胞成分均明显退化。在血管纹中发现的组织学变化与活性氧引起的细胞损伤一致。血管纹可能比耳蜗的其他部分对光化学反应更敏感。除了光化学反应诱导的活性氧的作用外,耳蜗其他部位的细胞损伤似乎是由局部微血管缺血引起的。

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