Mitochondrial Dysfunction and Therapeutic Targets in Auditory Neuropathy

被引:6
|
作者
Feng, Baoyi [1 ,2 ,3 ]
Jin, Chenxi [1 ,2 ,3 ]
Cheng, Zhenzhe [1 ,2 ,3 ]
Zhao, Xingle [1 ,2 ,3 ]
Sun, Zhuoer [1 ,2 ,3 ]
Zheng, Xiaofei [1 ,2 ,3 ]
Li, Xiang [1 ,2 ,3 ]
Dong, Tingting [4 ]
Tao, Yong [1 ,2 ,3 ]
Wu, Hao [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Otolaryngol Head & Neck Surg, 639 Zhizaoju Rd, Shanghai 200011, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Med, Ear Inst, 115 Jinzun Rd, Shanghai 200011, Peoples R China
[3] Shanghai Key Lab Translat Med Ear & Nose Dis, 115 Jinzun Rd, Shanghai 200011, Peoples R China
[4] Shanghai Jiao Tong Univ, Sch Med, Biobank Peoples Hosp 9, 115 Jinzun Rd, Shanghai 200011, Peoples R China
基金
中国国家自然科学基金;
关键词
SENSORINEURAL HEARING-LOSS; SPIRAL GANGLION NEURONS; OXIDATIVE STRESS; ENDOPLASMIC-RETICULUM; CALORIE RESTRICTION; MOUSE MODEL; HAIR-CELLS; COCHLEAR; DEGENERATION; ANTIOXIDANT;
D O I
10.1155/2020/8843485
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sensorineural hearing loss (SNHL) becomes an inevitable worldwide public health issue, and deafness treatment is urgently imperative; yet their current curative therapy is limited. Auditory neuropathies (AN) were proved to play a substantial role in SNHL recently, and spiral ganglion neuron (SGN) dysfunction is a dominant pathogenesis of AN. Auditory pathway is a high energy consumption system, and SGNs required sufficient mitochondria. Mitochondria are known treatment target of SNHL, but mitochondrion mechanism and pathology in SGNs are not valued. Mitochondrial dysfunction and pharmacological therapy were studied in neurodegeneration, providing new insights in mitochondrion-targeted treatment of AN. In this review, we summarized mitochondrial biological functions related to SGNs and discussed interaction between mitochondrial dysfunction and AN, as well as existing mitochondrion treatment for SNHL. Pharmaceutical exploration to protect mitochondrion dysfunction is a feasible and effective therapeutics for AN.
引用
收藏
页数:10
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