Long-term recovery from hippocampal-related behavioral and biochemical abnormalities induced by noise exposure during brain development. Evaluation of auditory pathway integrity

International Journal of Developmental Neuroscience

Volumn 37, Issue , 2014, Pages 41-51

  Uran, S L ^a   Gomez Casati M E ^b,c   Guelman, L R ^a  

^a Centre de Estudios Farmacologicos y Botanicos   (Argentina)

^b INSTITUTO DE INVESTIGACIONES EN INGENIERÍA GENÉTICA Y BIOLOGÍA MOLECULAR   (Argentina)

^c UNIVERSIDAD DE BUENOS AIRES   (Argentina)

Author keywords

Auditory pathway; Developing CNS; Hippocampus; Noise

Indexed keywords

CATALASE; REACTIVE OXYGEN METABOLITE; SUPEROXIDE DISMUTASE; ARABIDOPSIS PROTEIN; NUCLEAR PROTEIN; TIC PROTEIN, ARABIDOPSIS;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ANXIETY; ARTICLE; ASSOCIATIVE MEMORY; AUDITORY NERVOUS SYSTEM; AUDITORY THRESHOLD; BEHAVIOR CHANGE; BRAIN DEVELOPMENT; CHEMICAL ANALYSIS; COCHLEA POTENTIAL; ENZYME ACTIVITY; FEMALE; HABITUATION; HEARING TEST; HIPPOCAMPUS; LONG TERM EXPOSURE; MALE; NOISE; NOISE MEASUREMENT; NONHUMAN; PERINATAL PERIOD; PRIORITY JOURNAL; RAT; RECOGNITION; TASK PERFORMANCE; ADVERSE EFFECTS; AGE; ANIMAL; AUDITORY STIMULATION; AVOIDANCE BEHAVIOR; BRAIN; EXPLORATORY BEHAVIOR; GROWTH, DEVELOPMENT AND AGING; MAZE TEST; METABOLISM; NEWBORN; PHYSIOLOGY; TIME; WISTAR RAT;

ACOUSTIC STIMULATION; AGE FACTORS; ANIMALS; ANIMALS, NEWBORN; ARABIDOPSIS PROTEINS; AUDITORY PATHWAYS; AVOIDANCE LEARNING; BRAIN; CATALASE; EXPLORATORY BEHAVIOR; FEMALE; HEARING TESTS; MALE; MAZE LEARNING; NOISE; NUCLEAR PROTEINS; RATS; RATS, WISTAR; REACTIVE OXYGEN SPECIES; RECOGNITION (PSYCHOLOGY); SUPEROXIDE DISMUTASE; TIME FACTORS;

EID: 84903842587     PISSN: 07365748     EISSN: 1873474X     Source Type: Journal    
DOI: 10.1016/j.ijdevneu.2014.06.002     Document Type: Article

References (62)

1. Barros D., Amaral O.B., Izquierdo I., Geracitano L., do Carmo Bassols Raseira M., Henriques A.T., Ramirez M.R. Behavioral and genoprotective effects of Vaccinium berries intake in mice. Pharmacol. Biochem. Behav. 2006, 84(2):229-234.
2. Beers R.F., Sizer I.W. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem. 1952, 195(1):133-140.
3. Bevins R.A., Besheer J. Object recognition in rats and mice: a one-trial non-matching-to-sample learning task to study 'recognition memory'. Nat. Protoc. 2006, 1(3):1306-1311.
4. Bohne B.A. Growth of cochlear damage with increasing severity of exposure. Trans. Sect. Otolaryngol. Am. Acad. Ophthalmol. Otolaryngol. 1977, 84(2):420-421.
5. Brenes J.C., Padilla M., Fornaguera J. A detailed analysis of open-field habituation and behavioral and neurochemical antidepressant-like effects in postweaning enriched rats. Behav. Brain Res. 2009, 197(1):125-137.
6. Campeau S., Dolan D., Akil H., Watson S.J. c-fos mRNA induction in acute and chronic audiogenic stress: possible role of the orbitofrontal cortex in habituation. Stress 2002, 5(2):121-130.
7. Chang E.F., Merzenich M.M. Environmental noise retards auditory cortical development. Science 2003, 300:498-502.
8. Chen F.Q., Zheng H.W., Hill K., Sha S.H. Traumatic noise activates Rho-family GTPases through transient cellular energy depletion. J. Neurosci. 2012, 32(36):12421-12430.
9. Chengzhi C., Yan T., Xuejun J., Xiang L., Youbin Q., Baijie T. Recovery of chronic noise exposure induced spatial learning and memory deficits in young male Sprague-Dawley rats. J. Occup. Health 2011, 53(3):157-163.
10. Clark R.E., Zola S.M., Squire L.R. Impaired recognition memory in rats after damage to the hippocampus. J. Neurosci. 2000, 20(23):8853-8860.
11. Costalupes J.A., Young E.D., Gibson D.J. Effects of continuous noise backgrounds on rate response of auditory nerve fibers in cat. J. Neurophysiol. 1984, 51(6):1326-1344.
12. Cui B., Wu M., She X. Effects of chronic noise exposure on spatial learning and memory of rats in relation to neurotransmitters and NMDAR2B alteration in the hippocampus?. J. Occup. Health 2009, 51(2):152-158.
13. Cui B., Wu M.Q., Zhu L.X., She X.J., Ma Q., Liu H.T. Effect of chronic noise exposure on expression of N-methyl-d-aspartic acid receptor 2B and Tau phosphorylation in hippocampus of rats?. Biomed. Environ. Sci. 2013, 26(3):163-168.
14. Driver A.S., Kodavanti P.R., Mundy W.R. Age-related changes in reactive oxygen species production in rat brain homogenates. Neurotoxicol. Teratol. 2000, 22(2):175-181.
15. Ennaceur A., Delacour J. A new one-trial test for neurobiological studies of memory in rats. 1. Behavioral data. Behav. Brain Res. 1988, 31(1):47-59.
16. Fonseca J., Martins dos Santos J., Oliveira P., Laranjeira N., Castelo Branco N.A. Noise-induced duodenal lesions: a light and electron microscopy study of the lesions of the rat duodenal mucosa exposed to low frequency noise. Clin. Res. Hepatol. Gastroenterol. 2012, 36(1):72-77.
17. Furman A.C., Kujawa S.G., Liberman M.C. Noise-induced cochlear neuropathy is selective for fibers with low spontaneous rates. J. Neurophysiol. 2013, 110(3):577-586.
18. Goble T.J., Møller A.R., Thompson L.T. Acute high-intensity sound exposure alters responses of place cells in hippocampus. Hear. Res. 2009, 253(1-2):52-59.
19. Hamernik R.P., Turrentine G., Roberto M., Salvi R., Henderson D. Anatomical correlates of impulse noise-induced mechanical damage in the cochlea. Hear. Res. 1984, 13(3):229-247.
20. Heldt S.A., Stanek L., Chhatwal J.P., Ressler K.J. Hippocampus-specific deletion of BDNF in adult mice impairs spatial memory and extinction of aversive memories. Mol. Psychiatry 2007, 12(7):656-670.
21. Hu B.H., Zheng G.L. Membrane disruption: an early event of hair cell apoptosis induced by exposure to intense noise. Brain Res. 2008, 239:107-118.
22. Izquierdo I., Medina J.H. Memory formation: the sequence of biochemical events in the hippocampus and its connection to activity in other brain structures. Neurobiol. Learn. Mem. 1997, 68(3):285-316.
23. Jáuregui-Huerta F., García-Estrada J., Ruvalcaba-Delgadillo Y., Trujillo X., Huerta M., Feria-Velasco A., Gonzalez-Perez O., Luquín S. Chronic exposure of juvenile rats to environmental noise impairs hippocampal cell proliferation in adulthood. Noise Health 2011, 13(53):286-291.
24. Kraus K.S., Canlon B. Neuronal connectivity and interactions between the auditory and limbic systems. Effects of noise and tinnitus. Hear. Res. 2012, 2288(1-2):34-46.
25. Kraus K.S., Mitra S., Jimenez Z., Hinduja S., Ding D., Jiang H., Gray L., Lobarinas E., Sun W., Salvi R.J. Noise trauma impairs neurogenesis in the rat hippocampus. Neuroscience 2010, 167(4):1216-1226.
26. Krebs H., Macht M., Weyers P., Weijers H.G., Janke W. Effects of stressful noise on eating and non-eating behavior in rats. Appetite 1996, 26(2):193-202.
27. Kujawa S.G., Liberman M.C. Acceleration of age-related hearing loss by early noise exposure: evidence of a misspent youth. J. Neurosci. 2006, 26(7):2115-2123.
28. Kujawa S.G., Liberman M.C. Adding insult to injury: cochlear nerve degeneration after temporary noise-induced hearing loss. J. Neurosci. 2009, 29(45):14077-14085.
29. Liberman L.D., Wang H., Liberman M.C. Opposing gradients of ribbon size and AMPA receptor expression underlie sensitivity differences among cochlear-nerve/hair-cell synapses. J. Neurosci. 2011, 31(3):801-808.
30. Lin H.W., Furman A.C., Kujawa S.G., Liberman M.C. Primary neural degeneration in the Guinea pig cochlea after reversible noise-induced threshold shift. J. Assoc. Res. Otolaryngol. 2011, 12:605-616.
31. Lukashkin A.N., Lukashkina V.A., Russell I.J. One source for distortion product otoacoustic emissions generated by low- and high-level primaries. J. Acoust. Soc. Am. 2002, 111(6):2740-2748.
32. Maison S.F., Usubuchi H., Liberman M.C. Efferent feedback minimizes cochlear neuropathy from moderate noise exposure. J. Neurosci. 2013, 33(13):5542-5552.
33. Manikandan S., Padmab M.K., Srikumar R., Parthasarathy N.J., Muthuvel A., Sheela Devi R. Effects of chronic noise stress on spatial memory of rats in relation to neuronal dendritic alteration and free radical-imbalance in hippocampus and medial prefrontal cortex. Neurosci. Lett. 2006, 399:17-22.
34. McCord J.M., Fridovich I. Superoxide dismutase: an enzymic function for erythrocuprein (hemocuprein). J. Biol. Chem. 1969, 244:6049-6055.
35. Melcher J.R., Kiang N.Y. Generators of the brainstem auditory evoked potential in cat. III. Identified cell populations. Hear. Res. 1996, 93(1-2):52-71.
36. Munoz-Lopez M.M., Mohedano-Moriano A., Insausti R. Anatomical pathways for auditory memory in primates. Front. Neuroanat. 2010, 4:129.
37. National Institute for Occupational Safety and Health (NIOSH), 1998. Criteria for a Recommended Standard: Occupational Noise Exposure, NIOSH Publication No. 98-126.
38. Pereira M., Dombrowski P.A., Losso E.M., Chioca L.R., Da Cunha C., Andreatini R. Memory impairment induced by sodium fluoride is associated with changes in brain monoamine levels. Neurotox. Res. 2011, 9(1):55-62.
39. Pienkowski M., Eggermont J.J. Reversible long-term changes in auditory processing in mature auditory cortex in the absence of hearing loss induced by passive, moderate-level sound exposure. Ear Hear. 2012, 33(3):305-314.
40. Pietraforte D., Malorni W. Focusing at the double-edged sword of redox imbalance: signals for cell survival or for cell death?. Antioxid. Redox Signal. 2014, 21(1):52-55.
41. Popa-Wagner A., Mitran S., Sivanesan S., Chang E., Buga A.M. ROS and brain diseases: the good, the bad, and the ugly. Oxid. Med. Cell. Longev. 2013, 2013:963520.
42. Pourova J., Kottova M., Voprsalova M., Pour M. ROS and RNS in physiological processes. Acta Physiol. 2010, 198:15-35.
43. Rabat A., Bouyer J.J., Aran J.M., Courtiere A., Mayo W., Le Moal M. Deleterious effects of an environmental noise on sleep and contribution of its physical components in a rat model. Brain Res. 2004, 1009(1-2):88-97.
44. Rabat A. Extra-auditory effects of noise in laboratory animals: the relationship between noise and sleep. J. Am. Assoc. Lab. Anim. Sci. 2007, 46(1):35-41.
45. Roozendaal B. Stress and memory: opposing effects of glucocorticoids on memory consolidation and memory retrieval. Neurobiol. Learn. Mem. 2002, 78(3):578-595.
46. Sakurai Y. Coding of auditory temporal and pitch information by hippocampal individual cells and cell assemblies in the rat. Neuroscience 2002, 115(4):1153-1163.
47. Säljö A., Bao F., Jingshan S., Hamberger A., Hansson H.A., Haglid K.G. Exposure to short-lasting impulse noise causes neuronal c-Jun expression and induction of apoptosis in the adult rat brain. J. Neurotrauma. 2002, 19(8):985-991.
48. Säljö A., Mayorga M., Bolouri H., Svensson B., Hamberger A. Mechanisms and pathophysiology of the low-level blast brain injury in animal models. Neuroimage 2011, 54(Suppl. 1):S83-S88.
49. Sasse S.K., Greenwood B.N., Masini C.V., Nyhuis T.J., Fleshner M., Day H.E., Campeau S. Chronic voluntary wheel running facilitates corticosterone response habituation to repeated audiogenic stress exposure in male rats. Stress 2008, 11(6):425-437.
50. Saunders J.C., Dear S.P., Schneider M.E. The anatomical consequences of acoustic injury: a review and tutorial. J. Acoust. Soc. Am. 1985, 78(3):833-860.
51. Shera C.A., Guinan J.J. Evoked otoacoustic emissions arise by two fundamentally different mechanisms: a taxonomy for mammalian OAEs. J. Acoust. Soc. Am. 1999, 105(2 Pt 1):782-798.
52. Stankovic K., Rio C., Xia A., Sugawara M., Adams J.C., Liberman M.C., Corfas G. Survival of adult spiral ganglion neurons requires erbB receptor signaling in the inner ear. J. Neurosci. 2004, 24(40):8561-8651.
53. Stansfeld S.A., Matheson M.P. Noise pollution: non-auditory effects on health. Br. Med. Bull. 2003, 68:243-257.
54. Trapanotto M., Benini F., Farina M., Gobber D., Magnavita V., Zacchello F. Behavioural and physiological reactivity to noise in the newborn. J. Paediatr. Child Health 2004, 40:275-281.
55. Uran S.L., Aon-Bertolino L., Caceres L.G., Capani F., Guelman L.R. Rat hippocampal alterations could underlie behavioral abnormalities induced by exposure to moderate noise levels. Brain Res. 2012, 1471:1-12.
56. Uran S.L., Caceres L.G., Guelman L.R. Effects of loud noise on hippocampal and cerebellar-related behaviors. Role of oxidative state. Brain Res. 2010, 1361:102-114.
57. Valko M., Leibfritz D., Moncol J., Cronin M.T.D., Mazur M., Telser J. Free radicals and antioxidants in normal physiological functions and human disease. Int. J. Biochem. Cell Biol. 2007, 39:44-84.
58. Vianna M.R., Alonso M., Viola H., Quevedo J., De-Paris F., Furman M., de Stein M.L., Medina J.H., Izquierdo I. Role of hippocampal signaling pathways in long-term memory formation of nonassociative learning task in the rat. Learn. Mem. 2000, 7:333-340.
59. de Villers-Sidani E., Simpson K.L., Lu Y.F., Lin R.C.S., Merzenich M.M. Manipulating critical period closure across different sectors of the primary auditory cortex. Nat. Neurosci. 2008, 11(8):957-965.
60. Winer J.A., Lee C.C. The distributed auditory cortex. Hear. Res. 2007, 229(1-2):3-13.
61. Xi M.C., Woody C.D., Gruen E. Identification of short latency auditory responsive neurons in the cat dentate nucleus. Neuroreport 1994, 5(13):1567-1570.
62. Zheng W., Knudsen E.I. Gabaergic inhibition antagonizes adaptive adjustment of the owl's auditory space map during the initial phase of plasticity. J. Neurosci. 2001, 21(12):4356-4365.