MOZART ETKİSİ

Yıl 2021, Cilt: 4 Sayı: 1, 17 - 23, 31.01.2021

Hilal Adil , Güler Öztürk

https://doi.org/10.48124/husagbilder.799929

Cited By: 1

Öz

Müzik birtakım duygu ve düşünceleri belli kurallar çerçevesinde uyumlu seslerle anlatma sanatıdır. Müziğin canlılar üzerindeki etkisinin sadece duygudurumlarında değişiklik yaratmak ya da sanatsal haz vermekle sınırlı olmadığı; aynı zamanda bir takım rahatsızlıklara da iyi gelebileceği düşünülmüştür. Bu düşünce bazı araştırmacıları müziğin deney hayvanları ve insanlar üzerindeki etkilerini incelemeye yöneltmiştir. Mozart etkisi, müzik dinleyen canlıların uzamsal öğrenme ve belleklerinde artış olmasını ifade eder. Mozart etkisi üzerine yapılan çalışmalar bilimde ve popüler medyada büyük bir ses getirmiştir. Çeşitli araştırmacılar bu etkiyi kendi laboratuvarlarında gözlemlemeye çalışmış, ancak bir kısmı başarılı olamamıştır. Bu derlemede amacımız Mozart etkisi üzerine yapılan insan ve hayvan çalışmalarını gözden geçirerek müziğin uzamsal öğrenme ve bellek üzerine etkisini incelemektir. Çalışmamızda müzik dinlemenin uzamsal öğrenme ve belleği artırdığı, fakat bu artışın gözlenebilmesinin deney koşullarının iyi tasarlanmasına bağlı olduğu sonucuna varılmıştır. Mozart etkisinin görülme koşulları netleştirildiği takdirde ucuz, kolay erişilebilir, kolay uygulanabilir ve yan etkisiz olan müzik ile terapi yöntemlerinin eğitim ve sağlık alanında kullanılmasının önü açılabilir.

Anahtar Kelimeler

MÜZİK, MOZART ETKİSİ, ÖĞRENME, BELLEK

Kaynakça

• 1. Bunt L, Brynjulf S. Music Therapy: An Art Beyond Words. 2nd ed. New York: Routledge; 2014.
• 2. Kühlmann AY, de Rooij A, Hunink MG, De Zeeuw CI, Jeekel J. Music Affects Rodents: A Systematic Review of Experimental Research. Front Behav Neurosci. 2018;12:301.
• 3. Hetland L. Listening to music enhances spatial-temporal reasoning: Evidence for the "Mozart Effect". Journal of Aesthetic Education 2000;34(3/4):105-48.
• 4. Johnson J, Cotman C, Tasaki C, Shaw G. Enhancement of spatial-temporal reasoning after a Mozart listening condition in Alzheimer’s disease: a case study. Neurol Res. 1998;20(8):666-72.
• 5. Johnson JK, Shaw GL, Vuong M, Vuong S, Cotman CW. Short-term improvement on a spatial-task after music listening in Alzheimer disease: A group study. Activ Adapt Aging 2002;26(3):37-50.
• 6. Hughes JR, Daaboul Y, Fino JJ, Shaw GL. The “Mozart effect” on epileptiform activity. Clinical Electroencephalography 1998;29(3):109-119.
• 7. Hughes JR, John JF, Michelle AM. Is there a chronic change of the “Mozart effect” on epileptiform activity? A case study. Clin Electroencephalogr. 1999;30(2):44-45.
• 8. Hughes JR. The Mozart effect: additional data. Epilepsy Behav. 2002;3(2):182-4.
• 9. He H, Yang M, Duan M, Chen X, Lai Y, Xia Y, et al. Music intervention leads to increased insular connectivity and improved clinical symptoms in schizophrenia. Front Neurosci. 2018;11:744.
• 10. Shih YN, Chen CS, Chiang HY, Liu CH. Influence of background music on work attention in clients with chronic schizophrenia. Work. 2015;51(1):153-8.
• 11. Geretsegger M, Mössler KA, Bieleninik Ł, Chen XJ, Heldal TO, Gold C. Music therapy for people with schizophrenia and schizophrenia-like disorders. Cochrane Database Syst Rev. 2017;5.
• 12. Vinayak. The efficacy of music interventions on pain in cancer patients undergoing therapeutic treatment. International Journal of Current Research. 2017.
• 13. Jenkins JS. The Mozart effect. J R Soc Med. 2001;94(4):170-2.
• 14. Knox RA. Mozart makes you smarter, Calif. Researchers suggest. Boston Globe 1993:1.
• 15. Rauscher FH, Gordon LS, Catherine NK. Music and spatial task performance. Nature. 1993;365(6447):611.
• 16. Shaw GL, Silverman DJ, Pearson JC. Model of cortical organization embodying a basis for a theory of information processing and memory recall. Proc Natl Acad Sci. 1985;82(8):2364-8.
• 17. Shaw GL. Keeping Mozart in mind. 2nd ed. California: Elsevier; 2003.
• 18. Rauscher FH, Shaw GL. Key components of the Mozart effect. Percept Mot Skills. 1998;86(3):835-41.
• 19. Rauscher F, Shaw G, Levine L, Wright E, Dennis W, Newcomb R. Music training causes long-term enhancement of preschool children’s spatial–temporal reasoning. Neurol Res. 1997;19(1):2-8.
• 20. Rauscher F, Robinson D, Jens J. Improved maze learning through early music exposure in rats. Neurol Res. 1998;20(5):427-32.
• 21. Steele KM. Do rats show a Mozart effect? Music Percept. 2003;21(2):251-65.
• 22. Xu J, Yu L, Cai R, Zhang J, Sun X. Early auditory enrichment with music enhances auditory discrimination learning and alters NR2B protein expression in rat auditory cortex. Behav Brain Res. 2009;196(1):49-54.
• 23. Rideout BE, Fairchild RA, Urban GE. The ‘Mozart Effect’ and Skin Conductance. Eastern Psychological Association. 1998.
• 24. Steele KM, Bass KE, Crook MD. The mystery of the Mozart effect: Failure to replicate. Psychol Sci. 1999;10(4):366-9.
• 25. Nantais KM, Schellenberg EG. The Mozart effect: An artifact of preference. Psychol Sci. 1999;10(4):370-3.
• 26. Xing Y, Xia Y, Kendrick K, Liu X, Wang M, Wu D. Mozart, mozart rhythm and retrograde mozart effects: evidences from behaviours and neurobiology bases. Sci Rep. 2016;6:18744.
• 27. Rauscher FH, Hinton SC. The Mozart effect: Music listening is not music instruction. Educ Psychol. 2006;41(4):233-8.
• 28. Hughes JR, Fino JJ. The Mozart effect: distinctive aspects of the music—a clue to brain coding? Clin Electroencephalogr. 2000;31(2):94-103.
• 29. Sarnthein J, VonStein A, Rappelsberger P, Petsche H, Rauscher F, Shaw G. Persistent patterns of brain activity: an EEG coherence study of the positive effect of music on spatial-temporal reasoning. Neurol Res. 1997;19(2):107-16.
• 30. Bodner M, Muftuler LT, Nalcioglu O, Shaw GL. FMRI study relevant to the Mozart effect: brain areas involved in spatial–temporal reasoning. Neurol Res. 2001;23(7):683-90.
• 31. Warren JD. Variations on the musical brain. J R Soc Med. 1999;92(11):571-575.
• 32. Platel H, Price C, Baron JC, Wise R, Lambert J, Frackowiak RS et al. The structural components of music perception. A functional anatomical study. Brain. 1997;120(2):229-43.
• 33. Liégeois-Chauvel C, Peretz I, Babaï M, Laguitton V, Chauvel P. Contribution of different cortical areas in the temporal lobes to music processing. Brain. 1998;121(10):1853-67.
• 34. Mellet E, Tzourio N, Crivello F, Joliot M, Denis M, Mazoyer B. Functional anatomy of spatial mental imagery generated from verbal instructions. J Neurosci. 1996;16(20):6504-6512.
• 35. Kim H, Lee MH, Chang HK, Lee TH, Lee HH, Shin MC et al. Influence of prenatal noise and music on the spatial memory and neurogenesis in the hippocampus of developing rats. Brain Dev. 2006;28(2): 109-14.
• 36. Kim CH, Lee SC, Shin JW, Chung KJ, Lee SH, Shin MS et al. Exposure to music and noise during pregnancy influences neurogenesis and thickness in motor and somatosensory cortex of rat pups. Int Neurourol J. 2013;17(3):107.
• 37. Kirste I, Nicola Z, Kronenberg G, Walker TL, Liu RC, Kempermann G. Is silence golden? Effects of auditory stimuli and their absence on adult hippocampal neurogenesis. Brain Struct Funct. 2015;220(2):1221-8.
• 38. Lee SM, Kim BK, Kim TW, Ji ES, Choi HH. Music application alleviates short-term memory impairments through increasing cell proliferation in the hippocampus of valproic acid-induced autistic rat pups. J Exerc Rehabil. 2016;12(3):148.
• 39. Angelucci F, Fiore M, Ricci E, Padua L, Sabino A, Tonali PA. Investigating the neurobiology of music: brain-derived neurotrophic factor modulation in the hippocampus of young adult mice. Behav Pharmacol. 2007;18(5-6):491-6.
• 40. Angelucci F, Ricci E, Padua L, Sabino A, Tonali PA. Music exposure differentially alters the levels of brain-derived neurotrophic factor and nerve growth factor in the mouse hypothalamus. Neurosci Lett. 2007;429(2-3):152-5.
• 41. Li WJ, Yu H, Yang JM, Gao J, Jiang H, Feng M. Anxiolytic effect of music exposure on BDNFMet/Met transgenic mice. Brain Res. 2010;1347:71-79.
• 42. Marzban M, Shahbazi A, Tondar M, Soleimani M, Bakhshayesh M, Moshkforoush A et al. Effect of Mozart music on hippocampal content of BDNF in postnatal rats. Basic Clin Neurosci. 2011;2(3):21-6.
• 43. Xing Y, Chen W, Wang Y, Jing W, Gao S, Guo D et al. Music exposure improves spatial cognition by enhancing the BDNF level of dorsal hippocampal subregions in the developing rats. Brain Res Bull. 2016;121:131-7.
• 44. Feduccia AA, Christine LD. Auditory stimuli enhance MDMA-conditioned reward and MDMA-induced nucleus accumbens dopamine, serotonin and locomotor responses. Brain Res Bull. 2008;77(4):189-96.
• 45. Tasset I, Quero I, García-Mayórgaz ÁD, Del Río MC, Túnez I, Montilla P. Changes caused by haloperidol are blocked by music in Wistar rat. J Physiol Biochem. 2012;68(2):175-9.
• 46. Xu F, Cai R, Xu J, Zhang J, Sun X. Early music exposure modifies GluR2 protein expression in rat auditory cortex and anterior cingulate cortex. Neurosci Lett. 2007;420(2):179-83.
• 47. Marianowski R, Liao WH, Van Den Abbeele T, Fillit P, Herman P, Frachet B, et al. Expression of NMDA, AMPA and GABAA receptor subunit mRNAs in the rat auditory brainstem. I. Influence of early auditory deprivation. Hear Res. 2000;150(1-2):1-11.
• 48. Bi C, Cui Y, Mao Y, Dong S, Zhang J, Sun X. The effect of early auditory deprivation on the age-dependent expression pattern of NR2B mRNA in rat auditory cortex. Brain Res. 2006;1110(1):30-8.
• 49. Lu J, Cui Y, Cai R, Mao Y, Zhang J, Sun X. Early auditory deprivation alters expression of NMDA receptor subunit NR1 mRNA in the rat auditory cortex. J Neurosci Res. 2008;86(6):1290-6.
• 50. Wu X, Zhang L, Xu J, Xu F, Yang W, Zhang J, Sun X. Early auditory deprivation and experience modify the expression of NMDA receptor subunit NR2B protein in rat auditory cortex. Progress in Biochemistry and Biophysics. 2006;33(11):1080.
• 51. Jiang J, Liu G, Shi S, Li Z. Musical electroacupuncture may be a better choice than electroacupuncture in a mouse model of alzheimer’s disease. Neural Plast. 2016.
• 52. Chikahisa S, Sei H, Morishima M, Sano A, Kitaoka K, Nakaya Y, et al. Exposure to music in the perinatal period enhances learning performance and alters BDNF/TrkB signaling in mice as adults. Behav Brain Res. 2006;169(2):312-9.
• 53. Amagdei A, Balteş FR, Avram J, Miu AC. Perinatal exposure to music protects spatial memory against callosal lesions. Int J Dev Neurosci. 2010;28(1):105-9.
• 54. Yazdani F, Naghshvarian M, Salehi A, Marzban M. Effects of dexamphetamine and music on reversal learning. Iran J Psychiatry Behav Sci. 2016;10(1).
• 55. Aoun P, Jones T, Shaw GL, Bodner M. Long-term enhancement of maze learning in mice via a generalized Mozart effect. Neurol Res. 2005;27(8):791-6.
• 56. Xiong X, Han L, Liu S, Miao J, Luo M, Xue M, et al. Music intervention improves spatial learning and memory and alters serum proteomics profiling in rats. J Neurosci Res. 2018;96(10):1727-36.
• 57. Xing Y, Qin Y, Jing W, Zhang Y, Wang Y, Guo D, et al. Exposure to Mozart music reduces cognitive impairment in pilocarpine-induced status epilepticus rats. Cogn Neurodyn. 2016;10(1):23-30.
• 58. Chikahisa S, Sano A, Kitaoka K, Miyamoto KI, Sei H. Anxiolytic effect of music depends on ovarian steroid in female mice. Behav Brain Res. 2007;179(1):50-59.
• 59. Meng B, Zhu S, Li S, Zeng Q, Mei B. Global view of the mechanisms of improved learning and memory capability in mice with music-exposure by microarray. Brain Res Bull. 2009;80(1-2):36-44.
• 60. Camargo AMD, Lima DDD, Dal Magro DD, Seubert JK, Cruz JND, Cruz JGPD. Adjuvant effects of classical music on simvastatin induced reduction of anxiety but not object recognition memory in rats. Psychol Neurosci. 2013;6(3):403-10.
• 61. Escribano B, Quero I, Feijóo M, Tasset I, Montilla P, Túnez I. Role of noise and music as anxiety modulators: Relationship with ovarian hormones in the rat. Appl Anim Behav Sci. 2014;152:73-82.
• 62. Cruz JN, Lima DD, Dal Magro DD, Cruz JGP. Anxiolytic effect of mozart music over short and long photoperiods as part of environmental enrichment in captive rattus norvegicus (Rodentia: Muridae). Scand. J. Lab. Anim. Sci. 2015;41(7):1-7.
• 63. Pietschnig J, Voracek M, Formann AK. Mozart effect–Shmozart effect: A meta-analysis. Intelligence 2010;38(3):314-23.