Noise-induced changes in expression levels of NADPH oxidases in the cochlea

Hearing Research

Volumn 304, Issue , 2013, Pages 145-152

  Vlajkovic, Srdjan M ^a   Lin, Shelly Ching yu ^a   Wong, Ann Chi Yan ^b   Wackrow, Brad ^a   Thorne, Peter R ^a  

^a UNIVERSITY OF AUCKLAND   (New Zealand)

^b UNIVERSITY OF NEW SOUTH WALES   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

DIPHENYLIODONIUM SALT; DUOX2 PROTEIN; ISOENZYME; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE 1; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE 3; UNCLASSIFIED DRUG;

ADULT ANIMAL; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; COCHLEA; COCHLEA INJURY; CONTROLLED STUDY; CORTI ORGAN; DOWN REGULATION; ENZYME INHIBITION; EVOKED BRAIN STEM AUDITORY RESPONSE; IMMUNOHISTOCHEMISTRY; MALE; NERVE CELL; NOISE; NOISE INJURY; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FAMILY; PROTEIN LOCALIZATION; RAT; REGULATORY MECHANISM; SENSORY NERVE CELL; SPIRAL GANGLION; SPIRAL GANGLION NERVE CELL; UPREGULATION;

ABR; AUDITORY BRAINSTEM RESPONSE; BOVINE SERUM ALBUMIN; BSA; DIPHENYLENEIODONIUM; DPI; DUAL DOMAIN OXIDASE; DUOX; EDTA; ETHYLENDIAMINTETRAACETATE; NADPH; NDS; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; NIHL; NOISE-INDUCED HEARING LOSS; NORMAL DONKEY SERUM; PARAFORMALDEHYDE; PBS; PFA; PHOSPHATE BUFFER SALINE; REACTIVE NITROGEN SPECIES; REACTIVE OXYGEN SPECIES; REGION OF INTEREST; RNS; ROI; ROS; ROUND WINDOW MEMBRANE; RWM;

ANIMALS; AUDITORY THRESHOLD; COCHLEA; DISEASE MODELS, ANIMAL; ENZYME INHIBITORS; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; GENE EXPRESSION; HEARING LOSS, NOISE-INDUCED; ISOENZYMES; MALE; NADPH OXIDASE; NOISE; ONIUM COMPOUNDS; ORGAN OF CORTI; RATS; RATS, WISTAR; RNA, MESSENGER;

EID: 84881494693     PISSN: 03785955     EISSN: 18785891     Source Type: Journal    
DOI: 10.1016/j.heares.2013.07.012     Document Type: Article

References (31)

1. Ago T., Kitazono T., Ooboshi H., Iyama T., Han Y.H., Takada J., Wakisaka M., Ibayashi S., Utsumi H., Iida M. Nox4 as the major catalytic component of an endothelial NAD(P)H oxidase. Circulation 2004, 109(2):227-233.
2. Banfi B., Malgrange B., Steger K., Dauphin M., Krause K.H. NOX3, a superoxide generating NADPH oxidase of the inner ear. Journal of Biological Chemistry 2004, 279(44):46065-46072.
3. Bedard K., Krause K. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiological Reviews 2007, 87:245-313.
4. Cheng G., Ritsick D., Lambeth J.D. Nox3 regulation by NOXO1, p47phox, and p67phox. Journal of Biological Chemistry 2004, 279(33):34250-34255.
5. Cross R.A., Jones O.T.G. The effect of the inhibitor diphenylene iodonium of the superoxide-generating system of neutrophils. Biochemical Journal 1986, 237:111-116.
6. Forman H.J., Maiorino M., Ursini F. Signaling functions of reactive oxygen species. Biochemistry 2010, 49(5):835-842.
7. Hamernik R.P., Turrentine G., Wright C.G. Surface morphology of the inner sulcus and related epithelial cells of the cochlea following acoustic trauma. Hearing Research 1984, 16(2):143-160.
8. Henderson D., Bielefeld E.C., Harris K.C., Hu B.H. The role of oxidative stress in noise-induced hearing loss. Ear & Hearing 2006, 27(1):1-19.
9. Infanger D.W., Sharma R.V., Davisson R.L. NADPH oxidases of the brain: distribution, regulation, and function. Antioxidants & Redox Signaling 2006, 8(9-10):1583-1596.
10. Irani K. Oxidant signaling in vascular cell growth, death, and survival: a review of the roles of reactive oxygen species in smooth muscle and endothelial cell mitogenic and apoptotic signaling. Circulation Research 2000, 87(3):179-183.
11. Kahles T., Luedike P., Endres M., Galla H.J., Steinmetz H., Busse R., Neumann-Haefelin T., Brandes R.P. NADPH oxidase plays a central role in blood-brain barrier damage in experimental stroke. Stroke 2007, 38(11):3000-3006.
12. Kawahara T., Ritsick D., Cheng G., Lambeth J.D. Point mutations in the proline-rich region of p22phox are dominant inhibitors of Nox1- and Nox2-dependent reactive oxygen generation. Journal of Biological Chemistry 2005, 280(36):31859-31869.
13. Kim H.J., Lee J.H., Kim S.J., Oh G.S., Moon H.D., Kwon K.B., Park C., Park B.H., Lee H.K., Chung S.Y., Park R., So H.S. Roles of NADPH oxidases in cisplatin-induced reactive oxygen species generation and ototoxicity. Journal of Neuroscience 2010, 30(11):3933-3946.
14. Kim J.A., Neupane G.P., Lee E.S., Jeong B.S., Park B.C., Thapa P. NADPH oxidase inhibitors: a patent review. Expert Opinion on Therapeutic Patents 2011, 21(8):1147-1158.
15. Krause K. Tissue distribution and putative physiological function of NOX family NADPH oxidases. Japanese Journal of Infectious Diseases 2004, 57:S28-S29.
16. Le Prell C.G., Yamashita D., Minami S.B., Yamasoba T., Miller J.M. Mechanisms of noise-induced hearing loss indicate multiple methods of prevention. Hearing Research 2007, 226(1-2):22-43.
17. Livak K.J., Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) method. Methods 2001, 25:402-408.
18. Mukherjea D., Whitworth C.A., Nandish S., Dunaway G.A., Rybak L.P., Ramkumar V. Expression of the kidney injury molecule 1 in the rat cochlea and induction by cisplatin. Neuroscience 2006, 139(2):733-740.
19. Mukherjea D., Jajoo S., Kaur T., Sheehan K.E., Ramkumar V., Rybak L.P. Transtympanic administration of short interfering (si)RNA for the NOX3 isoform of NADPH oxidase protects against cisplatin-induced hearing loss in the rat. Antioxidants & Redox Signaling 2010, 13(5):589-598.
20. Nakano Y., Banfi B., Jesaitis A.J., Dinauer M.C., Allen L.A., Nauseef W.M. Critical roles for p22phox in the structural maturation and subcellular targeting of Nox3. Biochemical Journal 2007, 403(1):97-108.
21. Oishi N., Schacht J. Emerging treatments for noise-induced hearing loss. Expert Opinion on Emerging Drugs 2011, 16(2):235-245.
22. Paffenholz R., Bergstrom R.A., Pasutto F., Wabnitz P., Munroe R.J., Jagla W., Heinzmann U., Marquardt A., Bareiss A., Laufs J., Russ A., Stumm G., Schimenti J.C., Bergstrom D.E. Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase. Genes & Development 2004, 18(5):486-491.
23. Rybak L.P., Mukherjea D., Jajoo S., Kaur T., Ramkumar V. siRNA-mediated knock-down of NOX3: therapy for hearing loss?. Cellular and Molecular Life Sciences 2012, 69(14):2429-2434.
24. Schramm A., Matusik P., Osmenda G., Guzik T.J. Targeting NADPH oxidases in vascular pharmacology. Vascular Pharmacology 2012, 56(5-6):216-231.
25. Thorne P.R., Ameratunga S.N., Stewart J., Reid N., Williams W., Purdy S.C., Dodd G., Wallaart J. Epidemiology of noise-induced hearing loss in New Zealand. New Zealand Medical Journal 2008, 121(1280):33-44.
26. Ueno N., Takeya R., Miyano K., Kikuchi H., Sumimoto H. The NADPH oxidase Nox3 constitutively produces superoxide in a p22phox-dependent manner: its regulation by oxidase organizers and activators. Journal of Biological Chemistry 2005, 280(24):23328-23339.
27. + cycling and the endocochlear potential. Hearing Research 2002, 165:1-9.
28. 1 adenosine receptor agonists attenuate noise-induced hearing loss. Hearing Research 2010, 260:81-88.
29. Wong A.C.Y., Velamoor S., Skelton M.R., Thorne P.R., Vlajkovic S.M. Expression and distribution of creatine transporter and creatine kinase (brain isoform) in developing and mature rat cochlear tissues. Histochemistry and Cell Biology 2012, 137:599-613.
30. Yamashita D., Jiang H.-Y., Schacht J., Miller J.M. Delayed production of free radicals following noise exposure. Brain Research 2004, 1019:201-209.
31. Yamashita D., Jiang H.Y., Le Prell C.G., Schacht J., Miller J.M. Post-exposure treatment attenuates noise-induced hearing loss. Neuroscience 2005, 134(2):633-642.