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Time-Course Analysis of the Neuroanatomical Correlates of Sexual Arousal Evoked by Erotic Video Stimuli in Healthy Males

  • Sundaram, Thirunavukkarasu (Department of Biomedical Engineering, Chonnam National University Hospital, Chonnam National University Medical School) ;
  • Jeong, Gwang-Woo (Department of Biomedical Engineering, Chonnam National University Hospital, Chonnam National University Medical School) ;
  • Kim, Tae-Hoon (Department of Biomedical Engineering, Chonnam National University Hospital, Chonnam National University Medical School) ;
  • Kim, Gwang-Won (Department of Biomedical Engineering, Chonnam National University Hospital, Chonnam National University Medical School) ;
  • Baek, Han-Su (Department of Biomedical Engineering, Chonnam National University Hospital, Chonnam National University Medical School) ;
  • Kang, Heoung-Keun (Department of Radiology, Chonnam National University Hospital, Chonnam National University Medical School)
  • 투고 : 2009.09.23
  • 심사 : 2010.01.04
  • 발행 : 2010.06.01

초록

Objective: To assess the dynamic activations of the key brain areas associated with the time-course of the sexual arousal evoked by visual sexual stimuli in healthy male subjects. Materials and Methods: Fourteen right-handed heterosexual male volunteers participated in this study. Alternatively combined rest period and erotic video visual stimulation were used according to the standard block design. In order to illustrate and quantify the spatiotemporal activation patterns of the key brain regions, the activation period was divided into three different stages as the EARLY, MID and LATE stages. Results: For the group result (p < 0.05), when comparing the MID stage with the EARLY stage, a significant increase of the brain activation was observed in the areas that included the inferior frontal gyrus, the supplementary motor area, the hippocampus, the head of the caudate nucleus, the midbrain, the superior occipital gyrus and the fusiform gyrus. At the same time, when comparing the EARLY stage with the MID stage, the putamen, the globus pallidus, the pons, the thalamus, the hypothalamus, the lingual gyrus and the cuneus yielded significantly increased activations. When comparing the LATE stage with the MID stage, all the above mentioned brain regions showed elevated activations except the hippocampus. Conclusion: Our results illustrate the spatiotemporal activation patterns of the key brain regions across the three stages of visual sexual arousal.

키워드

과제정보

연구 과제 주관 기관 : Korea Research Foundation, Korea Science and Engineering Foundation

참고문헌

  1. Levin R, Riley A. The physiology of human sexual function. Psychiatry 2007;6:90-94 https://doi.org/10.1016/j.mppsy.2007.01.004
  2. Schober JM, Pfaff D. The neurophysiology of sexual arousal. Best Pract Res Clin Endocrinol Metab 2007;21:445-461 https://doi.org/10.1016/j.beem.2007.04.006
  3. Stoleru S, Gregoire MC, Gerard D, Decety J, Lafarge E, Cinotti L, et al. Neuroanatomical correlates of visually evoked sexual arousal in human males. Arch Sex Behav 1999;28:1-21
  4. Redoute J, Stoleru S, Gregoire MC, Costes N, Cinotti L, Lavenne F, et al. Brain processing of visual sexual stimuli in human males. Hum Brain Mapp 2000;11:162-177 https://doi.org/10.1002/1097-0193(200011)11:3<162::AID-HBM30>3.0.CO;2-A
  5. Graziottin A. Sexual arousal: similarities and differences between men and women. J Mens Health Gend 2004;1:215-223 https://doi.org/10.1016/j.jmhg.2004.07.026
  6. Redoute J, Stoleru S, Pugeat M, Costes N, Lavenne F, Le Bars D, et al. Brain processing of visual sexual stimuli in treated and untreated hypogonadal patients. Psychoneuroendocrinology 2005;30:461-482 https://doi.org/10.1016/j.psyneuen.2004.12.003
  7. Stoleru S, Redoute J, Costes N, Lavenne F, Bars DL, Dechaud H, et al. Brain processing of visual sexual stimuli in men with hypoactive sexual desire disorder. Psychiatry Res 2003;124:67- 86 https://doi.org/10.1016/S0925-4927(03)00068-4
  8. Bocher M, Chisin R, Parag Y, Freedman N, Meir Weil Y, Lester H, et al. Cerebral activation associated with sexual arousal in response to a pornographic clip: a 150-H2O PET study in heterosexual men. Neuroimage 2001;14:105-117 https://doi.org/10.1006/nimg.2001.0794
  9. Arnow BA, Desmond JE, Banner LL, Glover GH, Solomon A, Polan ML, et al. Brain activation and sexual arousal in healthy, heterosexual males. Brain 2002;125:1014-1023 https://doi.org/10.1093/brain/awf108
  10. Ferretti A, Caulo M, Del Gratta C, Di Matteo R, Merla A, Montorsi F, et al. Dynamics of male sexual arousal: distinct components of brain activation revealed by fMRI. Neuroimage 2005;26:1086-1096 https://doi.org/10.1016/j.neuroimage.2005.03.025
  11. Moulier V, Mouras H, Pelegrini-Issac M, Glutron D, Rouxel R, Grandjean B, et al. Neuroanatomical correlates of penile erection evoked by photographic stimuli in human males. Neuroimage 2006;33:689-699 https://doi.org/10.1016/j.neuroimage.2006.06.037
  12. Park K, Seo JJ, Kang HK, Ryu SB, Kim HJ, Jeong GW. A new potential of blood oxygenation level dependent (BOLD) functional MRI for evaluating cerebral centers of penile erection. Int J Impot Res 2001;13:73-81 https://doi.org/10.1038/sj.ijir.3900649
  13. Karama S, Lecours AR, Leroux JM, Bourgouin P, Beaudoin G, Joubert S, et al. Areas of brain activation in males and females during viewing of erotic film excerpts. Hum Brain Mapp 2002;16:1-13 https://doi.org/10.1002/hbm.10014
  14. Mouras H, Stoleru S, Bittoun J, Glutron D, Pelegrini-Issac M, Paradis AL, et al. Brain processing of visual sexual stimuli in healthy men: a functional magnetic resonance imaging study. Neuroimage 2003;20:855-869 https://doi.org/10.1016/S1053-8119(03)00408-7
  15. Hamann S, Herman RA, Nolan CL, Wallen K. Men and women differ in amygdala response to visual sexual stimuli. Nat Neurosci 2004;7:411-416 https://doi.org/10.1038/nn1208
  16. Yang JC, Jeong GW, Lee MS, Kang HK, Eun SJ, Kim YK, et al. Functional MR imaging of psychogenic amnesia: a case report. Korean J Radiol 2005;6:196-199 https://doi.org/10.3348/kjr.2005.6.3.196
  17. Yang JC. Functional neuroanatomy in depressed patients with sexual dysfunction: blood oxygenation level dependent functional MR imaging. Korean J Radiol 2004;5:87-95 https://doi.org/10.3348/kjr.2004.5.2.87
  18. Maravilla KR, Yang CC. Sex and the brain: the role of fMRI for assessment of sexual function and response. Int J Impot Res 2007;19:25-29 https://doi.org/10.1038/sj.ijir.3901493
  19. Friston KJ, Ashburner J, Frith CD, Poline J-B, Heather JD, Frackowiak RSJ. Spatial registration and normalisation of images. Hum Brain Mapp 1995;2:165-189
  20. Friston KJ, Holmes AP, Poline J-B, Grasby PJ, Williams SCR, Frackowiak RSJ, et al. Analysis of fMRI time-series revisited. Neuroimage 1995;2:45-53 https://doi.org/10.1006/nimg.1995.1007
  21. Friston KJ, Holmes AP, Worsley KJ, Poline J-P, Frith CD, Frackowiak RSJ. Statistical parametric maps in functional imaging: a general linear approach. Hum Brain Mapp 1995;2:189-210
  22. Friston KJ, Williams S, Howard R, Frackowiak RS, Turner R. Movement-related effects in fMRI time-series. Magn Reson Med 1996;35:346-355 https://doi.org/10.1002/mrm.1910350312
  23. Hajnal JV, Myers R, Oatridge A, Schwieso JE, Young IR, Bydder GM. Artifacts due to stimulus correlated motion in functional imaging of the brain. Magn Reson Med 1994;31:283- 291 https://doi.org/10.1002/mrm.1910310307
  24. Lee JM, Jeong GW, Kim HJ, Cho SH, Kang HK, Seo JJ, et al. Qualitative and quantitative measurement of human brain activity using pixel subtraction algorithm. J Korean Radiol Soc 2004;51:165-177 [Korean] https://doi.org/10.3348/jkrs.2004.51.2.165
  25. Janssen E, Everaerd W, Spiering M, Janssen J. Automatic processes and the appraisal of sexual stimuli: toward an information processing model of sexual arousal. J Sex Res 2000;37:8-23 https://doi.org/10.1080/00224490009552016
  26. Kapp B, Cain M. The neural basis of arousal. In: Smelser N, Baltes P, eds. The international encyclopedia of social and behavioral sciences. Oxford: Elsevier Science Ltd, 2001:1463- 1466
  27. Giuliano F, Allard J. Dopamine and sexual function. Int J Impot Res 2001;13:S18-S28 https://doi.org/10.1038/sj.ijir.3900719
  28. MacLean PD, Ploog DW. Cerebral presentation of penile erection. J Neurophysiol 1962;25:29-55 https://doi.org/10.1152/jn.1962.25.1.29
  29. MacLean PD, Denniston RH, Dua S. Further studies on cerebral representation of penile erection: caudal thalamus, midbrain, and pons. J Neurophysiol 1963;26:273-293 https://doi.org/10.1152/jn.1963.26.2.273
  30. Michael RP, Clancy AN, Zumpe D. Effects of mating on c-fos expression in the brains of male macaques. Physiol Behav 1999;66:591-597 https://doi.org/10.1016/S0031-9384(98)00329-1
  31. Ferris CF, Snowdon CT, King JA, Sullivan JM Jr, Ziegler TE, Olson DP, et al. Activation of neural pathways associated with sexual arousal in non-human primates. J Magn Reson Imaging 2004;19:168-175 https://doi.org/10.1002/jmri.10456
  32. Perachio AA, Marr LD, Alexander M. Sexual behavior in male rhesus monkeys elicited by electrical stimulation of preoptic and hypothalamic areas. Brain Res 1979;177:127-144 https://doi.org/10.1016/0006-8993(79)90923-5
  33. Robinson BW, Mishkin M. Penile erection evoked from forebrain structures in Macaca mulatta. Arch Neurol 1968;19:184-198 https://doi.org/10.1001/archneur.1968.00480020070007
  34. Liu YC, Salamone JD, Sachs BD. Lesions in medial preoptic area and bed nucleus of stria terminalis: differential effects on copulatory behavior and noncontact erection in male rats. J Neurosci 1997;17:5245-5253
  35. Georgiadis JR, Holstege G. Human brain activation during sexual stimulation of the penis. J Comp Neurol 2005;493:33-38 https://doi.org/10.1002/cne.20735

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