全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS ONE  2012 

Macrostructural Alterations of Subcortical Grey Matter in Psychogenic Erectile Dysfunction

DOI: 10.1371/journal.pone.0039118

Full-Text   Cite this paper   Add to My Lib

Abstract:

Psychogenic erectile dysfunction (ED) has been defined as the persistent inability to attain and maintain an erection sufficient to permit sexual performance. It shows a high incidence and prevalence among men, with a significant impact on the quality of life. Few neuroimaging studies have investigated the cerebral basis of erectile dysfunctions observing the role played by prefrontal, cingulate, and parietal cortices during erotic stimulation. In spite of the well-known involvement of subcortical regions such as hypothalamus and caudate nucleus in male sexual response, and the key role of nucleus accumbens in pleasure and reward, poor attention was paid to their role in male sexual dysfunction. In this study, we determined the presence of grey matter (GM) atrophy patterns in subcortical structures such as amygdala, hippocampus, nucleus accumbens, caudate nucleus, putamen, pallidum, thalamus, and hypothalamus in patients with psychogenic ED and healthy men. After Rigiscan evaluation, urological, general medical, metabolic and hormonal, psychological and psychiatric assessment, 17 outpatients with psychogenic ED and 25 healthy controls were recruited for structural MRI session. Significant GM atrophy of nucleus accumbens was observed bilaterally in patients with respect to controls. Shape analysis showed that this atrophy was located in the left medial-anterior and posterior portion of accumbens. Left nucleus accumbens volumes in patients correlated with low erectile functioning as measured by IIEF-5 (International Index of Erectile Function). In addition, a GM atrophy of left hypothalamus was also observed. Our results suggest that atrophy of nucleus accumbens plays an important role in psychogenic erectile dysfunction. We believe that this change can influence the motivation-related component of sexual behavior. Our findings help to elucidate a neural basis of psychogenic erectile dysfunction.

References

[1]  Stoléru S, Grégoire MC, Gérard D, Decety J, Lafarge E, et al. (1999) Neuroanatomical correlates of visually evoked sexual arousal in human males. Arc Sex Behav 28: 1–21.
[2]  Redouté J, Stoléru S, Grégoire MC, Costes N, Cinotti L, et al. (2000) Brain processing of visual sexual stimuli in human males. Hum Brain Mapping 11: 162–177.
[3]  Arnow BA, Desmond JE, Banner LL, Glover GH, Solomon A, et al. (2002) Brain activation and sexual arousal in healthy, heterosexual males. Brain 125: 1014–1023.
[4]  Ferretti A, Caulo M, Del Gratta C, Di Matteo R, Merla A, et al. (2005) Dynamics of male sexual arousal: distinct components of brain activation revealed by fMRI. Neuroimage 26: 1086–1096.
[5]  Georgiadis JR, Farrell MJ, Boessen R, Denton DA, Gavrilescu M, et al. (2010) Dynamic subcortical blood flow during male sexual activity with ecological validity: a perfusion fMRI study. Neuroimage 50: 208–216.
[6]  Montorsi F, Perani D, Anchisi D, Salonia A, Scifo P, et al. (2003) Apomorphine-induced brain modulation during sexual stimulation: a new look at central phenomena related to erectile dysfunction Int J Impot Res. 15(3): 203–9.
[7]  Montorsi F, Perani D, Anchisi D, Salonia A, Scifo P, et al. (2003) Brain activation patterns during video sexual stimulation following the administration of apomorphine: results of placebo-controlled study. Eur Urol 43: 405–411.
[8]  Redouté J, Stoléru S, Pugeat M, Costes N, Lavenne F, et al. (2005) Brain processing of visual sexual stimuli in treated and untreated hypogonadal patients. Psychoneuroend 30: 461–482.
[9]  Giuliano F, Rampin O (2004) Neural control of erection. Physiology & Behavior 83: 189–201.
[10]  Kondo Y, Sachs BD, Sakuma Y (1998) Importance of the medial amygdala in rat penile erection evoked by remote stimuli from estrous females. Behav Brain Res 91: 215–222.
[11]  Dominiguez JM, Hull EM (2005) Dopamine, the medial preoptic area, and male sexual behavior. Physiology & Behavior 86: 356–368.
[12]  Argiolas A, Melis MR (2004) The role of oxytocin and the paraventricular nucleus in the sexual behaviour of male mammals. Physiology & Behavior 83: 309–317.
[13]  West CHK, Clancy AN, Michael RP (1992) Enhanced responses of nucleus accumbens neurons in male rats to novel odors associated with sexually receptive females. Brain Res. 585: 49–55.
[14]  Becker JB, Rudick CN, Jenkins WJ (2001) The role of dopamine in the nucleus accumbens and striatum during sexual behavior in the female rat. J Neurosci. 21(9): 3236–3241.
[15]  Koch M, Schmid A, Schnitzler HU (1996) Pleasure-attenuation of startle is disrupted by lesions of the nucleus accumbens. Neuroreport 7(8): 1442–1446.
[16]  Knutson B, Adams CM, Fong GW, Hommer D (2001) Anticipation of increasing monetary reward selectively recruits nucleus accumbens. J Neurosci. 21(16): RC159.
[17]  Rosen RC, Beck JG (1988) Concerns involving human subjects in sexual psychophysiology. In: Rosen RC, Beck JG, editors. New York: Guilford.
[18]  Wespes E, Amar E, Hatzichristou D, Hatzimouratidis K, Montorsi F (2005) Guidelines on Erectile Dysfunction. (European Association of Urology).
[19]  Harte C, Meston CM (2008) Acute effects of nicotine on physiological and subjective sexual arousal in nonsmoking men: a randomized, double-blind, placebo-controlled trial. J Sex Med 5: 110–21.
[20]  Sheehan DV, Lecrubier Y, Sheehan KH, Amorim P, Janavs J, et al. (1998) The Mini-International Neuropsychiatric Interview (M.I.N.I.): the development and validation of a structured diagnostic psychiatric interview for DSM-IV and ICD-10. J Clin Psychiatry 29: 22–33.
[21]  Rosen RC, Riley A, Wagner G, Osterloh IH, Kirkpatrick J, et al. (1997) The international Index of Erectile Function (IIEF): a multidimensional scale for assessment of erectile dysfunction. Urology 49: 822–830.
[22]  Hoon EF, Hoon PW, Wincze JP (1976) An inventory for the measurement of female sexual arousability. Arc Sex Behav 5: 291–300.
[23]  Derogatis LR (1977) The SCL-90R Manual. I. Scoring, Administration and Procedures for the SCL-90R. Baltimore, MD: Clinical Psychometrics.
[24]  Spielberg C, Gorsuch RL, Lushene RE (1970) The state–trait anxiety inventory. Palo Alto, CA: Consulting Psychologists Press.
[25]  Carver CS, White T (1994) Behavioral inhibition, behavioral activation, and affective responses to impending reward and punishment: the BIS/BAS scales. J. Pers and Soc Psychology 67: 319–333.
[26]  Smith SM, Jenkinson M, Woolrich MW, Beckmann CF, Behrens TE, et al. (2004) Advances in functional and structural MR image analysis and implementation as FSL. NeuroImage 23: 208–219.
[27]  Jenkinson M, Beckmann CF, Behrens TE, Woolrich MW, Smith SM (2012) FSL. Neuroimage. In press.
[28]  Jenkinson M, Smith SM (2001) A global optimisation method for robust affine registration of brain images. Medical Image Analysis 5: 143–156.
[29]  Jenkinson M, Bannister PR, Brady JM, Smith SM (2002) Improved optimisation for the robust and accurate linear registration and motion correction of brain images. NeuroImage 17: 825–841.
[30]  Patenaude B, Smith SM, Kennedy D, Jenkinson MA (2011) Bayesian Model of Shape and Appearance for Subcortical Brain. Neuroimage;1 56(3): 907–22.
[31]  Zarei M, Patenaude B, Damoiseaux J, Morgese C, Smith S, et al. (2010) Combining shape and connectivity analysis: an MRI study of thalamic degeneration in Alzheimer’s disease. Neuroimage 49: 1–8.
[32]  Zhang Y, Brady M, Smith S (2001) Segmentation of brain MR images through a hidden Markov random field model and the expectation maximization algorithm. IEEE Trans. on Medical Imaging. 20: 45–57.
[33]  Holle D, Naegel S, Krebs S, Gaul C, Gizewski E, et al. (2011) Hypothalamic gray matter volume loss in hypnic headache. Ann Neurol. 69: 533–9.
[34]  Baroncini M, Jissendi P, Balland E, Besson P, Pruvo JP, et al. (2012) MRI atlas of the human hypothalamus. Neuroimage 59: 168–80.
[35]  Ashburner J, Friston K (2000) Voxel-based morphometry-The methods. NeuroImage 11: 805–821.
[36]  Good C, Johnsrude I, Ashburner J, Henson R, Friston K, et al. (2001) A voxel-based morphometric study of ageing in 465 normal adult human brains. NeuroImage 14: 21–36.
[37]  Smith SM (2002) Fast robust automated brain extraction. Human Brain Mapping 2002 17: 143–155.
[38]  Andersson JLR, Jenkinson M, Smith S (2007) Non-linear optimisation. FMRIB technical report TR07JA1. Accessed 2012 May 29.
[39]  Andersson JLR, Jenkinson M, Smith S (2007) Non-linear registration, aka Spatial normalisation FMRIB technical report TR07JA2. Accessed 2012 May 29.
[40]  Everitt BJ (1990) Sexual motivation:a neural and behavioral analysis of the mechanisms underlying appetitive copulatory responses of male rats. Neurosci Biobehav Rev 14: 217–32.
[41]  Zahm DS (2000) An integrative neuroanatomical perspective on some subcortical substrates of adaptive responding with emphasis on the nucleus accumbens. Neuroscience and Biobehavioral Reviews 24: 85–105.
[42]  Sabatinelli D, Bradley MM, Lang PJ, Costa VD, Versace F (2007) Pleasure rather than salience activates human nucleus accumbens and medial prefrontal cortex. J Neurophysiol 98: 1374–9.
[43]  Berridge KC (2007) The debate over dopamine’s role in reward: the case for incentive salience. Psychopharm 191: 391–431.
[44]  Salamone JD, Correa M, Farrar A, Mingote SM (2007) Effort-related functions of nucleus accumbens dopamine and associated forebrain circuits. Psychopharm 191: 461–482.
[45]  Ambroggi F, Ghazizadeh A, Nicola SM, Fields HL (2011) Roles of nucleus accumbens core and shell in incentive-cue responding and behavioral inhibition. J Neurosci 31: 6820–30.
[46]  Paredes RG, Baum MJ (1997) Role of the medial preoptic area/anterior hypothalamus in the control of masculine sexual behavior. Annu Rev Sex Res 8: 68–101.
[47]  Lloyd SA, Dixson AF (1998) Effects of hypothalamic lesions upon the sexual and social behaviour of the male common marmoset (Callithrix jacchus). Brain Res 463: 317–329.
[48]  Paredes RG, Tzschentke T, Nakach N (1998) Lesions of the medial preoptic area/anterior hypothalamus (MPOA/AH) modify partner preference in male rats. Brain Res. 813: 1–8.
[49]  Hurtazo HA, Paredes RG, Agmo A (2008) Inactivation of the medial preoptic area/anterior hypothalamus by lidocaine reduces male sexual behavior and sexual incentive motivation in male rats. Neuroscience 152: 331–337.
[50]  Swanson LW (1987) The hypothalamus. In: Bjorklund A, Hokfelt T, Swanson LW, editors. pp 1–124.
[51]  de Jong LW, van der Hiele K, Veer IM, Houwing JJ, Westendorp RG, et al. (2008) Strongly reduced volumes of putamen and thalamus in Alzheimer’s disease: an MRI study. Brain 131: 3277–85.
[52]  Bookstein FL (2001) ‘Voxel-based morphometry’ should not be used with imperfectly registered images. Neuroimage14: 1454–1462.
[53]  Frisoni GB, Whitwell JL (2008) How fast will it go, doc? New tools for an old question from patients with Alzheimer disease. Neurology 70: 2194–2195.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133