Long-term white noise exposure-induced mtDNA deletion in the auditory system

Acta Oto-Laryngologica

Volumn 128, Issue 3, 2008, Pages 309-313

  Han, Weiju ^a   Shi, Yongbing ^b   Yang, Weiyan ^a   Han, Dongyi ^a  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

DNA deletion; Hearing loss; Mitochondrial DNA; Noise exposure

Indexed keywords

MITOCHONDRIAL DNA;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; AUDITORY SYSTEM; AUDITORY THRESHOLD SHIFT; COCHLEA; COCHLEAR NUCLEUS; CONTROLLED STUDY; DNA EXTRACTION; ENVIRONMENTAL EXPOSURE; EVOKED BRAIN STEM AUDITORY RESPONSE; FEMALE; GENE AMPLIFICATION; HEARING; HEARING LOSS; MALE; NONHUMAN; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RAT; TEMPORAL LOBE; WHITE NOISE; WISTAR RAT;

ALLELES; ANIMALS; AUDITORY PATHWAYS; CHROMOSOME DELETION; COCHLEA; COCHLEAR NUCLEUS; DNA, MITOCHONDRIAL; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FEMALE; HEARING LOSS, NOISE-INDUCED; MALE; POLYMERASE CHAIN REACTION; RATS; RATS, WISTAR; SEQUENCE ANALYSIS, DNA; TEMPORAL LOBE;

EID: 39349107669     PISSN: 00016489     EISSN: 16512553     Source Type: Journal    
DOI: 10.1080/00016480601126994     Document Type: Article

References (16)

1. Kujoth GC, Hiona A, Pugh TD, Someya S, Panzer K, Wohlgemuth SE, et al. Mitochondrial DNA mutations, oxidative stress, and apoptosis in mammalian aging. Science 2005;309:481-4.
2. 4977 deletions associated with human presbycusis.] Zhonghua Er Bi Yan Hou Ke Za Zhi 2000;35:416-19 (in Chinese).
3. Dai P, Jiang S, Gu R. [Cochlear hypoxia and mtDNA deletion: possible correlated factors to cause presbycusis.] Zhonghua Yi Xue Za Zhi 2000;80:897-900 (in Chinese).
4. Seidman MD, Bai U, Khan MJ, Murphy MJ, Quirk WS, Castora FL, et al. The association of mitochondrial DNA deletions and cochlear pathology: a molecular biologic tool. Laryngoscope 1996;106:777-83.
5. Quirk WS, Seidman MD. Cochlear vascular changes in response to loud noise. Am J Otol 1995;16:322-5.
6. Nuttall AL. Sound-induced cochlear ischemia/hypoxia as a mechanism of hearing loss. Noise Health 1999;5:17-31.
7. Yamamoto H, Makimoto K. Sensitivity of the endocochlear potential level to cochlear blood flow during hypoventilation. Ann Otol Rhinol Laryngol 2000;109:945-51.
8. Gadaleta G, Pepe G, De Candia G, Quagliariello C, Cbisa E, Saccone C. The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome, cryptic signals revealed by comparative analysis between verrebrates. J Mol Evol 1989;28:497-516.
9. Richter C. Reactive oxygen and DNA damage in mitochondria. Mutat Res 1992;275:249-55.
10. Tritschler H-J, Medori R. Mitochondrial DNA alterations as a source of human disorders. Neurology 1993;43:280-8.
11. Wallace DC. Diseases of the mitochondrial DNA. Annu Rev Biochem 1992;61:1175-212.
12. Shigenaga MK, Hagen TM, Ames BN. Oxidative damage and mitochondrial decay in aging. Proc Natl Acad Sci U S A 1994;91:10771-8.
13. Johnsson LG, Hawkins JE Jr. Vascular changes in the human inner ear associated with aging. Ann Otol Rhinol Laryngol 1972;81:361-5.
14. Leibovitz BE, Siegl BV. Aspects of free radical reactions in biological systems: ageing. J Gerontol 1980;35:45-56.
15. Han W, Shi X, Nuttall AL. AIF and EndoG translocation in noise exposure induced hair cell death. Hear Res 2006;211:85-95.
16. Yang WP, Henderson D, Hu BH, Nicotera TM. Quantitative analysis of apoptotic and necrotic outer hair cells after exposure to different levels of continuous noise. Hear Res 2004;196:69-76.