KAUDAT NUKLEUS BAĞLANTI YOLLARI MİKROCERRAHİ ANATOMİSİ’NİN PSİKOŞİRÜRJİKAL ÖNEMİ: ÖZGÜN KADAVRA ARAŞTIRMA ÇALIŞMASI

Amaç Nükleus kaudatus bazı nörolojik ve psikiyatrik hastalıkların tedavisinde bir hedef olabilir mi diye tartışılmaktadır. Mikrocerrahi girişimler ve stereotaksik yaklaşımlar için kaudat nükleus bağlantılarının daha açık bir şekilde tanımlanması gerekmektedir. Bu çalışmamızda nükleus kaudatus mikrocerrahi anatomisini ve bağlantı yollarını fiber diseksiyon tekniği kullanarak ortaya koymayı ve bunun psikoşirürjikal önemini orrtaya koymayı amaçladık. Gereç ve Yöntem Dört adet formalinle fikse edilmiş insan beyni (8 hemisfer) detaylı şekilde incelendi. Tüm örnekler Klingler’ in tekniğine göre -16 °C'de en az 15 gün donduruldu ve birkaç saat boyunca su altında çözülmeleri sağlandı. X6 ila x40 mikroskopik büyütme altında ak madde lif diseksiyonu gerçekleştirildi. Tüm beyin hemisferleri, lateralden mediale doğru kaudat nükleusun başı ve gövdesi ortaya çıkana kadar olarak disseke edildi. Ayrıca, adım adım iki ve üç boyutlu fotoğraflar çekildi. Bulgular Nükleus kaudatus etrafındaki tüm yapılar kademeli olarak diseke edildi. Bu yapı ile iletişim halinde olan ve fiziksel olarak temas eden tüm kortikal alanlar gözden geçirildi. Frontokaudat ve frontotemporal bağlantıların mikrocerrahi anatomisi ayrıntılı ortaya konuldu. Sonuç Psikoşirürji, medikal tedavilerin henüz gelişmediği dönemlerde, depresyon tedavisinde öncelikli olarak kullanılmıştır. Kaudat nükleusa yönelik yapılan derin beyin stimülasyonu klinik pratikte standart bir tedavi yöntemi değildir ama Parkinson hastalığı, obsesif kompülsif hastalık ve majör depresyonda alternatif tedavi olabilir.

MICROSURGICAL ANATOMY OF THE CONNECTIONS OF CAUDATE NUCLEUS AND PSYCHOSURGICAL CONSIDERATIONS : A UNIQUE CADAVER STUDY

ObjectiveCaudate nucleus has been discussed as a target fornew treatments of neurologic and psychiatric diseases but the connectivity remains unclear for both microsurgical procedures and stereotactic interventionsdespite the basic neuroanatomical knowledge. Weaim to reveal the anatomic features of the caudatenucleus in psychiatric diseases using fiber dissectiontechnique.Material and MethodsFour brain specimens (8 Hemispheres) were frozen for 15 days at -16 °C according to Klingler’s Technique. The freezing process facilitates the dissectionof the fiber tracts. After completion of the freezing process, all of the hemispheres were dissected and thedissections were stepwise performed from lateral tomedial, under x6 to x40 magnification using a surgicalmicroscope, two and three-dimensional anatomic pictures were obtained.ResultsStepwise microsurgical fiber dissection of the caudate nucleus and adjacent areas were dissected. Thecortical areas communicating with and overlying thecaudate nucleus are reviewed. Frontocaudate connection fibers and temporocaudate fibers were intenseand the microsurgical anatomy of the area were revealed. Two and three dimetional pictures were takenstep by step.ConclusionPsychosurgery has been used primarily in treatmentof depression when medical treatments were notadequate. Deep brain stimulation of caudate nucleusis not a standard method in clinical practice. Deepbrain stimulation of caudate nucleus is not a standardmethod in clinical practice but it could be an alternatetreatment for Parkinson's disease, obsessive compulsive disorder and major depression.

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  • 1. Ribas EC, Yagmurlu K, de Oliveira E, Ribas GC, Rhoton A, Jr. Microsurgical anatomy of the central core of the brain. J Neurosurg. 2017:1-18.
  • 2. Baydin S, Yagmurlu K, Tanriover N, Gungor A, Rhoton AL, Jr. Microsurgical and Fiber Tract Anatomy of the Nucleus Accumbens. Oper Neurosurg (Hagerstown). 2016;12(3):269-88.
  • 3. Yagmurlu K, Vlasak AL, Rhoton AL, Jr. Three-dimensional topographic fiber tract anatomy of the cerebrum. Neurosurgery. 2015;11 Suppl 2:274-305; discussion
  • 4. Fernandez-Miranda JC, Rhoton AL, Jr., Alvarez-Linera J, Kakizawa Y, Choi C, de Oliveira EP. Three-dimensional microsurgical and tractographic anatomy of the white matter of the human brain. Neurosurgery. 2008;62(6 Suppl 3):989-1026; discussion -8.
  • 5. Yeterian EH, Pandya DN. Corticostriatal connections of extrastriate visual areas in rhesus monkeys. J Comp Neurol. 1995;352(3):436-57.
  • 6. Miller CH, Hamilton JP, Sacchet MD, Gotlib IH. Meta-analysis of Functional Neuroimaging of Major Depressive Disorder in Youth. JAMA Psychiatry. 2015;72(10):1045-53.
  • 7. Chen JJ, Liu Z, Zhu D, Li Q, Zhang H, Huang H, et al. Bilateral vs. unilateral repetitive transcranial magnetic stimulation in treating major depression: a meta-analysis of randomized controlled trials. Psychiatry Res. 2014;219(1):51-7.
  • 8. Graham J, Salimi-Khorshidi G, Hagan C, Walsh N, Goodyer I, Lennox B, et al. Meta-analytic evidence for neuroimaging models of depression: state or trait? J Affect Disord. 2013;151(2):423-31.
  • 9. Butters MA, Aizenstein HJ, Hayashi KM, Meltzer CC, Seaman J, Reynolds CF, 3rd, et al. Three-dimensional surface mapping of the caudate nucleus in late-life depression. Am J Geriatr Psychiatry. 2009;17(1):4-12.
  • 10. Tymofiyeva O, Connolly CG, Ho TC, Sacchet MD, Henje Blom E, LeWinn KZ, et al. DTI-based connectome analysis of adolescents with major depressive disorder reveals hypoconnectivity of the right caudate. J Affect Disord. 2017;207:18-25.
  • 11. Forbes EE, Dahl RE. Research Review: altered reward function in adolescent depression: what, when and how? J Child Psychol Psychiatry. 2012;53(1):3-15.
  • 12. Haber SN. The primate basal ganglia: parallel and integrative networks. J Chem Neuroanat. 2003;26(4):317-30.
  • 13. Kier EL, Staib LH, Davis LM, Bronen RA. Anatomic dissection tractography: a new method for precise MR localization of white matter tracts. AJNR Am J Neuroradiol. 2004;25(5):670-6.
  • 14. Burks JD, Conner AK, Bonney PA, Glenn CA, Baker CM, Boettcher LB, et al. Anatomy and white matter connections of the orbitofrontal gyrus. J Neurosurg. 2018;128(6):1865-72.
  • 15. Choi CY, Han SR, Yee GT, Lee CH. Central core of the cerebrum. J Neurosurg. 2011;114(2):463-9.
  • 16. Grahn JA, Parkinson JA, Owen AM. The cognitive functions of the caudate nucleus. Prog Neurobiol. 2008;86(3):141-55.
  • 17. Ding L. Distinct dynamics of ramping activity in the frontal cortex and caudate nucleus in monkeys. J Neurophysiol. 2015;114(3):1850-61.
  • 18. Haber SN. Corticostriatal circuitry. Dialogues Clin Neurosci. 2016;18(1):7-21.
  • 19. Schiff ND, Fins JJ. Deep brain stimulation and cognition: moving from animal to patient. Curr Opin Neurol. 2007;20(6):638- 42.
  • 20. Molina V, Lubeiro A, Blanco J, Blanco JA, Rodriguez M, Rodriguez-Campos A, et al. Parkinsonism is associated to fronto-caudate disconnectivity and cognition in schizophrenia. Psychiatry Res Neuroimaging. 2018;277:1-6.
  • 21. Persson K, Bohbot VD, Bogdanovic N, Selbaek G, Braekhus A, Engedal K. Finding of increased caudate nucleus in patients with Alzheimer's disease. Acta Neurol Scand. 2018;137(2):224- 32.
  • 22. Williams NR, Okun MS. Deep brain stimulation (DBS) at the interface of neurology and psychiatry. J Clin Invest. 2013;123(11):4546-56.
  • 23. Fink GR. [Deep brain stimulation in neurology and psychiatry]. Fortschr Neurol Psychiatr. 2010;78(2):69.
  • 24. Aouizerate B, Cuny E, Martin-Guehl C, Guehl D, Amieva H, Benazzouz A, et al. Deep brain stimulation of the ventral caudate nucleus in the treatment of obsessive-compulsive disorder and major depression. Case report. J Neurosurg. 2004;101(4):682- 6.
  • 25. J. K. Erleichterung der makroskopischen Praeparation des Gehirns durch den Gefrierprozess. Schweiz Arch Neurol Psychiatr 1935;36:247–56.
  • 26. Ribas EC, Yagmurlu K, de Oliveira E, Ribas GC, Rhoton A, Jr. Microsurgical anatomy of the central core of the brain. J Neurosurg. 2018;129(3):752-69.
  • 27. Kim MJ, Hamilton JP, Gotlib IH. Reduced caudate gray matter volume in women with major depressive disorder. Psychiatry Res. 2008;164(2):114-22.
  • 28. Kotz SA, Anwander A, Axer H, Knosche TR. Beyond cytoarchitectonics: the internal and external connectivity structure of the caudate nucleus. PLoS One. 2013;8(7):e70141.
  • 29. Im I, Jun JP, Hwang S, Ko MH. Swallowing outcomes in patients with subcortical stroke associated with lesions of the caudate nucleus and insula. J Int Med Res. 2018;46(9):3552-62.
  • 30. Postle BR, D'Esposito M. Spatial working memory activity of the caudate nucleus is sensitive to frame of reference. Cogn Affect Behav Neurosci. 2003;3(2):133-44.
  • 31. Postle BR, D'Esposito M. Dissociation of human caudate nucleus activity in spatial and nonspatial working memory: an event-related fMRI study. Brain Res Cogn Brain Res. 1999;8(2):107-15.
  • 32. White NM. Some highlights of research on the effects of caudate nucleus lesions over the past 200 years. Behav Brain Res. 2009;199(1):3-23.
  • 33. Da Cunha C, Packard MG. Special issue on the role of the basal ganglia in learning and memory. Preface. Behav Brain Res. 2009;199(1):1-2.
  • 34. Foerde K, Shohamy D. The role of the basal ganglia in learning and memory: insight from Parkinson's disease. Neurobiol Learn Mem. 2011;96(4):624-36.
  • 35. Grahn JA, Parkinson JA, Owen AM. The role of the basal ganglia in learning and memory: neuropsychological studies. Behav Brain Res. 2009;199(1):53-60.
  • 36. Elliott R, Newman JL, Longe OA, Deakin JF. Differential response patterns in the striatum and orbitofrontal cortex to financial reward in humans: a parametric functional magnetic resonance imaging study. J Neurosci. 2003;23(1):303-7.
  • 37. Levitt JJ, McCarley RW, Dickey CC, Voglmaier MM, Niznikiewicz MA, Seidman LJ, et al. MRI study of caudate nucleus volume and its cognitive correlates in neuroleptic-naive patients with schizotypal personality disorder. Am J Psychiatry. 2002;159(7):1190-7.
  • 38. McGaugh JL. The amygdala modulates the consolidation of memories of emotionally arousing experiences. Annu Rev Neurosci. 2004;27:1-28.
  • 39. Seger CA, Cincotta CM. The roles of the caudate nucleus in human classification learning. J Neurosci. 2005;25(11):2941-51.
  • 40. Chiu YC, Jiang J, Egner T. The Caudate Nucleus Mediates Learning of Stimulus-Control State Associations. J Neurosci. 2017;37(4):1028-38.
  • 41. Gronholm EO, Roll MC, Horne MA, Sundgren PC, Lindgren AG. Predominance of caudate nucleus lesions in acute ischaemic stroke patients with impairment in language and speech. Eur J Neurol. 2016;23(1):148-53.
  • 42. Aron A, Fisher H, Mashek DJ, Strong G, Li H, Brown LL. Reward, motivation, and emotion systems associated with early-stage intense romantic love. J Neurophysiol. 2005;94(1):327-37.
  • 43. Ishizu T, Zeki S. Toward a brain-based theory of beauty. PLoS One. 2011;6(7):e21852.
  • 44. Crinion J, Turner R, Grogan A, Hanakawa T, Noppeney U, Devlin JT, et al. Language control in the bilingual brain. Science. 2006;312(5779):1537-40.
  • 45. Hickie IB, Naismith SL, Ward PB, Scott EM, Mitchell PB, Schofield PR, et al. Serotonin transporter gene status predicts caudate nucleus but not amygdala or hippocampal volumes in older persons with major depression. J Affect Disord. 2007;98(1-2):137-42.
  • 46. Bartres-Faz D, Junque C, Serra-Grabulosa JM, Lopez-Alomar A, Moya A, Bargallo N, et al. Dopamine DRD2 Taq I polymorphism associates with caudate nucleus volume and cognitive performance in memory impaired subjects. Neuroreport. 2002;13(9):1121-5.
  • 47. Nakamura K, Hikosaka O. Role of dopamine in the primate caudate nucleus in reward modulation of saccades. J Neurosci. 2006;26(20):5360-9.
  • 48. Krishna Karthik D, Khardenavis V, Kulkarni S, Deshpande A. Global aphasia in a case of bilateral frontal lobe infarcts involving both caudate nuclei. BMJ Case Rep. 2017;2017.
  • 49. Tang WK, Liang HJ, Chen YK, Chu WC, Abrigo J, Mok VC, et al. Poststroke fatigue is associated with caudate infarcts. J Neurol Sci. 2013;324(1-2):131-5.
  • 50. Pellizzaro Venti M, Paciaroni M, Caso V. Caudate infarcts and hemorrhages. Front Neurol Neurosci. 2012;30:137-40.
  • 51. Bierer J, Wolf A, Lee DH, Rotenberg BW, Duggal N. Bilateral caudate nucleus infarcts: A case report of a rare complication following endoscopic resection of a tuberculum sellae meningioma. Surg Neurol Int. 2017;8:235.
  • 52. Kumral E, Evyapan D, Balkir K. Acute caudate vascular lesions. Stroke. 1999;30(1):100-8.
  • 53. Degos JD, da Fonseca N, Gray F, Cesaro P. Severe frontal syndrome associated with infarcts of the left anterior cingulate gyrus and the head of the right caudate nucleus. A clinico-pathological case. Brain. 1993;116 ( Pt 6):1541-8.
  • 54. Broussolle E, Dentresangle C, Landais P, Garcia-Larrea L, Pollak P, Croisile B, et al. The relation of putamen and caudate nucleus 18F-Dopa uptake to motor and cognitive performances in Parkinson's disease. J Neurol Sci. 1999;166(2):141-51.
  • 55. Owen AM. Cognitive dysfunction in Parkinson's disease: the role of frontostriatal circuitry. Neuroscientist. 2004;10(6):525- 37.
  • 56. Arregui A, Perry EK, Rossor M, Tomlinson BE. Angiotensin converting enzyme in Alzheimer's disease increased activity in caudate nucleus and cortical areas. J Neurochem. 1982;38(5):1490-2.
  • 57. Barber R, McKeith I, Ballard C, O'Brien J. Volumetric MRI study of the caudate nucleus in patients with dementia with Lewy bodies, Alzheimer's disease, and vascular dementia. J Neurol Neurosurg Psychiatry. 2002;72(3):406-7.
  • 58. Robinson D, Wu H, Munne RA, Ashtari M, Alvir JM, Lerner G, et al. Reduced caudate nucleus volume in obsessive-compulsive disorder. Arch Gen Psychiatry. 1995;52(5):393-8.
  • 59. Rigoard P, Buffenoir K, Jaafari N, Giot JP, Houeto JL, Mertens P, et al. The accumbofrontal fasciculus in the human brain: a microsurgical anatomical study. Neurosurgery. 2011;68(4):1102- 11; discussion 11.
  • 60. Rosso IM, Olson EA, Britton JC, Stewart SE, Papadimitriou G, Killgore WD, et al. Brain white matter integrity and association with age at onset in pediatric obsessive-compulsive disorder. Biol Mood Anxiety Disord. 2014;4(1):13.
  • 61. Singh VK, Rivas WH. Prevalence of serum antibodies to caudate nucleus in autistic children. Neurosci Lett. 2004;355(1- 2):53-6.
  • 62. Hoptman MJ, Volavka J, Czobor P, Gerig G, Chakos M, Blocher J, et al. Aggression and quantitative MRI measures of caudate in patients with chronic schizophrenia or schizoaffective disorder. J Neuropsychiatry Clin Neurosci. 2006;18(4):509-15.
  • 63. Benabid AL, Pollak P, Louveau A, Henry S, de Rougemont J. Combined (thalamotomy and stimulation) stereotactic surgery of the VIM thalamic nucleus for bilateral Parkinson disease. Applied neurophysiology. 1987;50(1-6):344-6.
  • 64. Gabriels L. Deep brain stimulation for psychiatric disorders. Psychiatr Danub. 2010;22 Suppl 1:S162.
  • 65. Nuttin BJ, Gabriels L, van Kuyck K, Cosyns P. Electrical stimulation of the anterior limbs of the internal capsules in patients with severe obsessive-compulsive disorder: anecdotal reports. Neurosurgery clinics of North America. 2003;14(2):267-74.
  • 66. Arya S, Filkowski MM, Nanda P, Sheth SA. Deep brain stimulation for obsessive-compulsive disorder. Bull Menninger Clin. 2019;83(1):84-96.
  • 67. Lucas-Jimenez O, Ojeda N, Pena J, Diez-Cirarda M, Cabrera-Zubizarreta A, Gomez-Esteban JC, et al. Altered functional connectivity in the default mode network is associated with cognitive impairment and brain anatomical changes in Parkinson's disease. Parkinsonism Relat Disord. 2016;33:58-64.
  • 68. Costentin G, Derrey S, Gerardin E, Cruypeninck Y, Pressat-Laffouilhere T, Anouar Y, et al. White matter tracts lesions and decline of verbal fluency after deep brain stimulation in Parkinson's disease. Hum Brain Mapp. 2019;40(9):2561-70.
  • 69. Synofzik M, Schlaepfer TE. Electrodes in the brain--ethical criteria for research and treatment with deep brain stimulation for neuropsychiatric disorders. Brain Stimul. 2011;4(1):7-16.
  • 70. Vergani F, Martino J, Morris C, Attems J, Ashkan K, Dell'Acqua F. Anatomic Connections of the Subgenual Cingulate Region. Neurosurgery. 2016;79(3):465-72.
  • 71. Schlapfer T, Volkmann J, Deuschl G. [Deep brain stimulation in neurology and psychiatry]. Nervenarzt. 2014;85(2):135-6.
  • 72. Ashkan K, Shotbolt P, David AS, Samuel M. Deep brain stimulation: a return journey from psychiatry to neurology. Postgrad Med J. 2013;89(1052):323-8.
  • 73. Elliott M, Momin S, Fiddes B, Farooqi F, Sohaib SA. Pacemaker and Defibrillator Implantation and Programming in Patients with Deep Brain Stimulation. Arrhythm Electrophysiol Rev. 2019;8(2):138-42.
  • 74. Casagrande SCB, Cury RG, Alho EJL, Fonoff ET. Deep brain stimulation in Tourette's syndrome: evidence to date. Neuropsychiatr Dis Treat. 2019;15:1061-75.
  • 75. Baylis F. "I Am Who I Am": On the Perceived Threats to Personal Identity from Deep Brain Stimulation. Neuroethics. 2013;6:513-26.
Süleyman Demirel Üniversitesi Tıp Fakültesi Dergisi-Cover
  • ISSN: 1300-7416
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 1994
  • Yayıncı: SDÜ Basımevi / Isparta
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