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首页> 外文期刊>Neurobiology of Aging: Experimental and Clinical Research >Caloric restriction suppresses apoptotic cell death in the mammalian cochlea and leads to prevention of presbycusis.
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Caloric restriction suppresses apoptotic cell death in the mammalian cochlea and leads to prevention of presbycusis.

机译:热量限制会抑制哺乳动物耳蜗中凋亡细胞的死亡,并导致预防老年性耳聋。

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摘要

Presbycusis is characterized by an age-related progressive decline of auditory function, and arises mainly from the degeneration of hair cells or spiral ganglion (SG) cells in the cochlea. Here we show that caloric restriction suppresses apoptotic cell death in the mouse cochlea and prevents late onset of presbycusis. Calorie restricted (CR) mice, which maintained body weight at the same level as that of young control (YC) mice, retained normal hearing and showed no cochlear degeneration. CR mice also showed a significant reduction in the number of TUNEL-positive cells and cleaved caspase-3-positive cells relative to middle-age control (MC) mice. Microarray analysis revealed that CR down-regulated the expression of 24 apoptotic genes, including Bak and Bim. Taken together, our findings suggest that loss of critical cells through apoptosis is an important mechanism of presbycusis in mammals, and that CR can retard this process by suppressing apoptosis in the inner ear tissue.
机译:老年性耳聋的特征是与年龄有关的听觉功能逐渐下降,并且主要源于耳蜗中毛细胞或螺旋神经节(SG)细胞的变性。在这里,我们显示热量限制可以抑制小鼠耳蜗中的凋亡细胞死亡,并预防老年性耳聋的发作。热量限制(CR)小鼠的体重保持与年轻对照组(YC)小鼠相同的水平,保持正常听力并且未显示耳蜗变性。与中年对照(MC)小鼠相比,CR小鼠还显示出TUNEL阳性细胞和裂解的caspase-3阳性细胞数量显着减少。基因芯片分析显示CR下调了24个凋亡基因的表达,包括Bak和Bim。综上所述,我们的研究结果表明,通过凋亡导致的关键细胞丢失是哺乳动物老年性耳聋的重要机制,而CR可以通过抑制内耳组织的凋亡来延迟这一过程。

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