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衰老加速小鼠中与年龄相关的耳蜗退化

Age-related cochlear degeneration in senescence-accelerated mouse.

作者信息

Saitoh Y, Hosokawa M, Shimada A, Watanabe Y, Yasuda N, Murakami Y, Takeda T

机构信息

Department of Otolaryngology, Kyoto Prefectural University of Medicine, Japan.

出版信息

Neurobiol Aging. 1995 Mar-Apr;16(2):129-36. doi: 10.1016/0197-4580(94)00153-7.

Abstract

Age-related hair cell loss and strial atrophy were investigated in an accelerated senescence-prone strain, SAMP1 mice, and an accelerated senescence-resistant strain, SAMR1 mice. The loss of inner and outer hair cells in SAMP1 progressed more rapidly than that in SAMR1 with age. In both strains, areas of the loss of inner and outer hair cells were located mainly in the apex and base. Atrophy of the stria vascularis was observed in both strains, but in SAMP1 it appeared to increase earlier than in SAMR1. These results reveal that age-related hair cell loss and atrophy of the stria vascularis comparable to that in the human cochlea occur earlier and progress more rapidly in SAMP1 than in SAMR1. Hearing impairment in SAM may be due to a combination of sensory and strial presbycusis as well as to neural presbycusis, as reported previously. The morphological changes in the cochlea observed in SAMP1 and SAMR1 make these strains suitable for the study of the mechanisms of presbycusis.

摘要

在易加速衰老的品系SAMP1小鼠和抗加速衰老的品系SAMR1小鼠中,研究了与年龄相关的毛细胞丢失和血管纹萎缩情况。随着年龄增长,SAMP1小鼠内、外毛细胞的丢失比SAMR1小鼠进展得更快。在这两个品系中,内、外毛细胞丢失的区域主要位于顶端和基部。在两个品系中均观察到血管纹萎缩,但在SAMP1中,其出现似乎比SAMR1更早。这些结果表明,与人类耳蜗中情况类似的与年龄相关的毛细胞丢失和血管纹萎缩在SAMP1中比在SAMR1中出现得更早且进展更快。如先前报道的那样,SAM小鼠的听力障碍可能是由于感觉性和血管纹性老年性聋以及神经性老年性聋共同导致的。在SAMP1和SAMR1中观察到的耳蜗形态学变化使这些品系适合用于研究老年性聋的机制。

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