nach oben

Erschienen in:

01.01.2013 | Original Article

Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study

verfasst von: Juan Martino, Philip C. De Witt Hamer, Mitchel S. Berger, Michael T. Lawton, Christine M. Arnold, Enrique Marco de Lucas, Hugues Duffau

Erschienen in: Brain Structure and Function | Ausgabe 1/2013

Einloggen, um Zugang zu erhalten

Abstract

The anatomy of the perisylvian component of the superior longitudinal fasciculus (SLF) has recently been reviewed by numerous diffusion tensor imaging tractography (DTI) studies. However, little is known about the exact cortical terminations of this tract. The aim of the present work is to isolate the different subcomponents of this tract with fiber dissection and DTI tractography, and to identify the exact cortical connections. Twelve postmortem human hemispheres (6 right and 6 left) were dissected using the cortex-sparing fiber dissection. In addition, three healthy brains were analyzed using DTI-based tractography software. The different components of the perisylvian SLF were isolated and the fibers were followed until the cortical terminations. Three segments of the perisylvian SLF were identified: (1) anterior segment, connecting the supramarginal gyrus and superior temporal gyrus with the precentral gyrus, (2) posterior segment, connecting the posterior portion of the middle temporal gyrus with the angular gyrus, and (3) long segment of the arcuate fasciculus that connects the middle and inferior temporal gyri with the precentral gyrus and posterior portion of the inferior and middle frontal gyri. In the present study, three different components of the perisylvian SLF were identified. For the first time, our dissections revealed that each component was connected to a specific cortical area within the frontal, parietal and temporal lobes. By accurately depicting not only the trajectory but also cortical connections of this bundle, it is possible to develop new insights into the putative functional role of this tract.

Aminoff MJ, Greenberg DA, Simon RP (2005) Clinical neurology. McGraw-Hill, New York

Axer H, Beck S, Axer M, Schuchardt F, Heepe J, Flucken A, Axer M, Prescher A, Witte OW (2011) Microstructural analysis of human white matter architecture using polarized light imaging: views from neuroanatomy. Front Neuroinform 5:28PubMed

Baddeley A (2003) Working memory: looking back and looking forward. Nat Rev Neurosci 4:829–839PubMedCrossRef

Barrick TR, Lawes IN, Mackay CE, Clark CA (2007) White matter pathway asymmetry underlies functional lateralization. Cereb Cortex 17:591–598PubMedCrossRef

Bernal B, Altman N (2010) The connectivity of the superior longitudinal fasciculus: a tractography DTI study. Magn Reson Imaging 28:217–225PubMedCrossRef

Bernal B, Ardila A (2009) The role of the arcuate fasciculus in conduction aphasia. Brain 132:2309–2316PubMedCrossRef

Catani M, de Thiebaut SM (2008) A diffusion tensor imaging tractography atlas for virtual in vivo dissections. Cortex 44:1105–1132PubMedCrossRef

Catani M, Howard RJ, Pajevic S, Jones DK (2002) Virtual in vivo interactive dissection of white matter fasciculi in the human brain. Neuroimage 17:77–94PubMedCrossRef

Catani M, Jones DK, Donato R, Ffytche DH (2003) Occipito-temporal connections in the human brain. Brain 129:2093–2107CrossRef

Catani M, Jones DK, Ffytche DH (2005) Perisylvian language networks of the human brain. Ann Neurol 57:8–16PubMedCrossRef

Catani M, Allin MP, Husain M, Pugliese L, Mesulam MM, Murray RM, Jones DK (2007) Symmetries in human brain language pathways correlate with verbal recall. Proc Natl Acad Sci USA 104:17163–17168PubMedCrossRef

Choi C, Rubino PA, Fernandez-Miranda JC, Abe H, Rhoton AL Jr (2006) Meyer’s loop and the optic radiations in the transylvian approach to the mediobasal temporal lobe. Neurosurgery 59:ONS228–ONS235

Croxson PL, Johansen-Berg H, Behrens TE, Robson MD, Pinsk MA, Gross CG, Richter W, Richter MC, Kastner S, Rushworth MF (2005) Quantitative investigation of connections of the prefrontal cortex in the human and macaque using probabilistic diffusion tractography. J Neurosci 25:8854–8866PubMedCrossRef

De Renzi E (1989) Agnosia. Recenti Prog Med 80:633–637PubMed

Dell’acqua F, Scifo P, Rizzo G, Catani M, Simmons A, Scotti G, Fazio F (2010) A modified damped Richardson-Lucy algorithm to reduce isotropic background effects in spherical deconvolution. Neuroimage 49:1446–1458PubMedCrossRef

Dronkers NF, Wilkins DP, Van VR Jr, Redfern BB, Jaeger JJ (2004) Lesion analysis of the brain areas involved in language comprehension. Cognition 92:145–177PubMedCrossRef

Duffau H (2011) The “frontal syndrome” revisited: lessons from electrostimulation mapping studies. Cortex (Epub ahead of print)

Duffau H, Capelle L, Sichez N, Denvil D, Lopes M, Sichez JP, Bitar A, Fohanno D (2002) Intraoperative mapping of the subcortical language pathways using direct stimulations. An anatomo-functional study. Brain 125:199–214PubMedCrossRef

Duffau H, Capelle L, Denvil D, Gatignol P, Sichez N, Lopes M, Sichez JP, Van ER (2003a) The role of dominant premotor cortex in language: a study using intraoperative functional mapping in awake patients. Neuroimage 20:1903–1914PubMedCrossRef

Duffau H, Gatignol P, Denvil D, Lopes M, Capelle L (2003b) The articulatory loop: study of the subcortical connectivity by electrostimulation. Neuroreport 14:2005–2008PubMedCrossRef

Duffau H, Gatignol P, Mandonnet E, Capelle L, Taillandier L (2008) Intraoperative subcortical stimulation mapping of language pathways in a consecutive series of 115 patients with Grade II glioma in the left dominant hemisphere. J Neurosurg 109:461–471PubMedCrossRef

Fernandez-Miranda JC, Rhoton AL Jr, Kakizawa Y, Choi C, varez-Linera J (2008a) The claustrum and its projection system in the human brain: a microsurgical and tractographic anatomical study. J Neurosurg 108:764–774PubMedCrossRef

Fernandez-Miranda JC, Rhoton AL Jr, varez-Linera J, Kakizawa Y, Choi C, de Oliveira EP (2008b) Three-dimensional microsurgical and tractographic anatomy of the white matter of the human brain. Neurosurgery 62:989–1026PubMedCrossRef

Gharabaghi A, Kunath F, Erb M, Saur R, Heckl S, Tatagiba M, Grodd W, Karnath HO (2009) Perisylvian white matter connectivity in the human right hemisphere. BMC Neurosci 10:15PubMedCrossRef

Giolli RA, Gregory KM, Suzuki DA, Blanks RH, Lui F, Betelak KF (2001) Cortical and subcortical afferents to the nucleus reticularis tegmenti pontis and basal pontine nuclei in the macaque monkey. Vis Neurosci 18:725–740PubMedCrossRef

Glasser MF, Rilling JK (2008) DTI tractography of the human brain’s language pathways. Cereb Cortex 18:2471–2482PubMedCrossRef

Hagmann P, Thiran JP, Jonasson L, Vandergheynst P, Clarke S, Maeder P, Meuli R (2003) DTI mapping of human brain connectivity: statistical fibre tracking and virtual dissection. Neuroimage 19:545–554PubMedCrossRef

Henry RG, Berman JI, Nagarajan SS, Mukherjee P, Berger MS (2004) Subcortical pathways serving cortical language sites: initial experience with diffusion tensor imaging fiber tracking combined with intraoperative language mapping. Neuroimage 21:616–622PubMedCrossRef

Hickok G, Poeppel D (2004) Dorsal and ventral streams: a framework for understanding aspects of the functional anatomy of language. Cognition 92:67–99PubMedCrossRef

Ingham RJ, Fox PT, Ingham JC, Xiong J, Zamarripa F, Hardies LJ, Lancaster JL (2004) Brain correlates of stuttering and syllable production: gender comparison and replication. J Speech Lang Hear Res 47:321–341PubMedCrossRef

Kaplan E, Naeser MA, Martin PI, Ho M, Wang Y, Baker E, Pascual-Leone A (2010) Horizontal portion of arcuate fasciculus fibers track to pars opercularis, not pars triangularis, in right and left hemispheres: a DTI study. Neuroimage 52:436–444PubMedCrossRef

Kareken DA, Mosnik DM, Doty RL, Dzemidzic M, Hutchins GD (2003) Functional anatomy of human odor sensation, discrimination, and identification in health and aging. Neuropsychology 17:482–495PubMedCrossRef

Kier EL, Staib LH, Davis LM, Bronen RA (2004a) Anatomic dissection tractography: a new method for precise MR localization of white matter tracts. AJNR Am J Neuroradiol 25:670–676PubMed

Kier EL, Staib LH, Davis LM, Bronen RA (2004b) MR imaging of the temporal stem: anatomic dissection tractography of the uncinate fasciculus, inferior occipitofrontal fasciculus, and Meyer’s loop of the optic radiation. AJNR Am J Neuroradiol 25:677–691PubMed

Klingler J (1935) Erleichterung der makroskopischen Praeparation des Gehirns durch den Gefrierprozess. Schweiz Arch Neurol Psychiatr 36:247–256

Klingler J, Gloor P (1960) The connections of the amygdala and of the anterior temporal cortex in the human brain. J Comp Neurol 115:333–369PubMedCrossRef

Lawes IN, Barrick TR, Murugam AB, Spierings N, Evans DR, Song M, Clarke CA (2008) Atlas-based segmentation of white matter tracts of the human brain using diffusion tensor tractography and comparison with classical dissection. Neuroimage 39:79CrossRef

Le BD, Mangin JF, Poupon C, Clark CA, Pappata S, Molko N, Chabriat H (2001) Diffusion tensor imaging: concepts and applications. J Magn Reson Imaging 13:534–546CrossRef

Leclercq D, Duffau H, Delmaire C, Capelle L, Gatignol P, Ducros M, Chiras J, Lehericy S (2010) Comparison of diffusion tensor imaging tractography of language tracts and intraoperative subcortical stimulations. J Neurosurg 112:503–511PubMedCrossRef

Liberman AM, Mattingly IG (1985) The motor theory of speech perception revised. Cognition 21:1–36PubMedCrossRef

Liberman AM, Cooper FS, Shankweiler DP, Studdert-Kennedy M (1967) Perception of the speech code. Psychol Rev 74:431–461PubMedCrossRef

Ludwig E, Klingler J (1956) Atlas Cerebri Humani: Der innere Bau des Gehirns dargestellt auf Grund mackroskopischer Präparate. Brown, Boston

Makris N, Kennedy DN, McInerney S, Sorensen AG, Wang R, Caviness VS Jr, Pandya DN (2005) Segmentation of subcomponents within the superior longitudinal fascicle in humans: a quantitative, in vivo DT-MRI study. Cereb Cortex 15:854–869PubMedCrossRef

Maldonado IL, Moritz-Gasser S, Duffau H (2011) Does the left superior longitudinal fascicle subserve language semantics? A brain electrostimulation study. Brain Struct Funct (In press)

Martino J, Brogna C, Robles SG, Vergani F, Duffau H (2010a) Anatomic dissection of the inferior fronto-occipital fasciculus revisited in the lights of brain stimulation data. Cortex 46:691–699PubMedCrossRef

Martino J, Vergani F, Robles SG, Duffau H (2010b) New insights into the anatomic dissection of the temporal stem with special emphasis on the inferior fronto-occipital fasciculus: implications in surgical approach to left mesiotemporal and temporoinsular structures. Neurosurgery 66:4–12PubMedCrossRef

Martino J, De Witt Hamer PC, Vergani F, Brogna C, de Lucas EM, Vazquez-Barquero A, Garcia-Porrero JA, Duffau H (2011) Cortex-sparing fiber dissection: an improved method for the study of white matter anatomy in the human brain. J Anat 219:531–541. doi:10.1111/j.1469-7580.2011.01414.x (Epub ahead of print)

Mesulam MM (1990) Large-scale neurocognitive networks and distributed processing for attention, language, and memory. Ann Neurol 28:597–613PubMedCrossRef

Mesulam M (2009) Defining neurocognitive networks in the BOLD new world of computed connectivity. Neuron 62:1–3PubMedCrossRef

Mori S, van Zijl PC (2002) Fiber tracking: principles and strategies: a technical review. NMR Biomed 15:468–480PubMedCrossRef

Naeser MA, Alexander MP, Helm-Estabrooks N, Levine HL, Laughlin SA, Geschwind N (1982) Aphasia with predominantly subcortical lesion sites: description of three capsular/putaminal aphasia syndromes. Arch Neurol 39:2–14PubMedCrossRef

Naeser MA, Palumbo CL, Helm-Estabrooks N, Stiassny-Eder D, Albert ML (1989) Severe nonfluency in aphasia. Role of the medial subcallosal fasciculus and other white matter pathways in recovery of spontaneous speech. Brain 112(Pt 1):1–38PubMedCrossRef

Nieuwenhuys R, Voogd J, van Huijzen C (1988) The human central nervous system. Springler-Verlag, Berlin

Nucifora PG, Ragini Verma CA, Melhem ER, Gur RE, Gur RC (2005) Lefward asymmetry in relative fiber density of the arcuate fasciculus. Neuroreport 16:791–794PubMedCrossRef

Obler LK, Gjerlow K (1999) Language and the brain. Cambridge University Press, Cambridge

Ono M, Kubik S, Abernathey CD (1990) Atlas of the cerebral sulci. Georg Thieme Verlag, New York

Parker GJ, Luzzi S, Alexander DC, Wheeler-Kingshott CA, Ciccarelli O, Lambon Ralph MA (2005) Lateralization of ventral and dorsal auditory-language pathways in the human brain. Neuroimage 24:656–666PubMedCrossRef

Petrides M, Pandya DN (1984) Projections to the frontal cortex from the posterior parietal region in the rhesus monkey. J Comp Neurol 228:105–116PubMedCrossRef

Petrides M, Pandya DN (2009) Distinct parietal and temporal pathways to the homologues of Broca’s area in the monkey. PLoS Biol 7:e1000170PubMedCrossRef

Peuskens D, van Loon J, Van Calenbergh F, van den Bergh R, Goffin J, Plets C (2004) Anatomy of the anterior temporal lobe and the frontotemporal region demonstrated by fiber dissection. Neurosurgery 55:1174–1184PubMedCrossRef

Powell HW, Parker GJ, Alexander DC, Symms MR, Boulby PA, Wheeler-Kingshott CA, Barker GJ, Noppeney U, Koepp MJ, Duncan JS (2006) Hemispheric asymmetries in language-related pathways: a combined functional MRI and tractography study. Neuroimage 32:388–399PubMedCrossRef

Price CJ (2000) The anatomy of language: contributions from functional neuroimaging. J Anat 197:335–359PubMedCrossRef

Rhoton AL Jr (2002) The cerebrum. Neurosurgery 51:S1–S51PubMed

Rilling JK, Glasser MF, Preuss TM, Ma X, Zhao T, Hu X, Behrens TE (2008) The evolution of the arcuate fasciculus revealed with comparative DTI. Nat Neurosci 11:426–428PubMedCrossRef

Saur D, Kreher BW, Schnell S, Kummerer D, Kellmeyer P, Vry MS, Umarova R, Musso M, Glauche V, Abel S, Huber W, Rijntjes M, Hennig J, Weiller C (2008) Ventral and dorsal pathways for language. Proc Natl Acad Sci USA 105:18035–18040PubMedCrossRef

Schmahmann JD, Pandya DN (2006) Fiber pathways of the brain. Oxford UP, New YorkCrossRef

Schmahmann JD, Rosene DL, Pandya DN (2004) Motor projections to the basis pontis in rhesus monkey. J Comp Neurol 478:248–268PubMedCrossRef

Schmahmann JD, Pandya DN, Wang R, Dai G, D’Arceuil HE, de Crespigny AJ, Wedeen VJ (2007) Association fibre pathways of the brain: parallel observations from diffusion spectrum imaging and autoradiography. Brain 130:630–653PubMedCrossRef

Shuster LI, Lemieux SK (2005) An fMRI investigation of covertly and overtly produced mono- and multisyllabic words. Brain Lang 93:20–31PubMedCrossRef

Sincoff EH, Tan Y, Abdulrauf SI (2004) White matter fiber dissection of the optic radiations of the temporal lobe and implications for surgical approaches to the temporal horn. J Neurosurg 101:739–746PubMedCrossRef

Soria G, De NM, Tudela R, Blasco G, Puig J, Planas AM, Pedraza S, Prats-Galino A (2011) Improved assessment of ex vivo brainstem neuroanatomy with high-resolution MRI and DTI at 7 Tesla. Anat Rec (Hoboken.) 294:1035–1044CrossRef

Thiebaut de Schotten M, Dell’acqua F, Forkel SJ, Simmons A, Vergani F, Murphy DG, Catani M (2011) A lateralized brain network for visuospatial attention. Nat Neurosci 14:1245–1246PubMedCrossRef

Tomasi D, Volkow ND (2011) Aging and functional brain networks. Mol Psychiatry Jul 5. doi:10.1038/mp.2011.81

Tuch DS, Reese TG, Wiegell MR, Wedeen VJ (2003) Diffusion MRI of complex neural architecture. Neuron 40:885–895PubMedCrossRef

Ture U, Yasargil MG, Pait TG (1997) Is there a superior occipitofrontal fasciculus? A microsurgical anatomic study. Neurosurgery 40:1226–1232PubMedCrossRef

Ture U, Yasargil DC, Al-Mefty O, Yasargil MG (1999) Topographic anatomy of the insular region. J Neurosurg 90:720–733PubMedCrossRef

Ture U, Yasargil MG, Friedman AH, Al-Mefty O (2000) Fiber dissection technique: lateral aspect of the brain. Neurosurgery 47:417–426PubMedCrossRef

Turken AU, Dronkers NF (2011) The neural architecture of the language comprehension network: converging evidence from lesion and connectivity analyses. Front Syst Neurosci 5:1PubMedCrossRef

Wang F, Sun T, Li X-G, Liu N-J (2008) Diffusion tensor tractography of the temporal stem on the inferior limiting sulcus. J Neurosurg 108:775–781PubMedCrossRef

Wedeen VJ, Hagmann P, Tseng WY, Reese TG, Weisskoff RM (2005) Mapping complex tissue architecture with diffusion spectrum magnetic resonance imaging. Magn Reson Med 54:1377–1386PubMedCrossRef

Young P (1997) Basic Clinical Neuroanatomy. Williams and Wilkins, Philadelphia

Titel: Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study
verfasst von: Juan Martino
Philip C. De Witt Hamer
Mitchel S. Berger
Michael T. Lawton
Christine M. Arnold
Enrique Marco de Lucas
Hugues Duffau
Publikationsdatum: 01.01.2013
Verlag: Springer-Verlag
Erschienen in: Brain Structure and Function / Ausgabe 1/2013
Print ISSN: 1863-2653
Elektronische ISSN: 1863-2661
DOI: https://doi.org/10.1007/s00429-012-0386-5

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

^{Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag}

Kostenlos registrieren

Neu im Fachgebiet Neurologie

23.04.2024 | Demenz | Nachrichten

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.

Newsletter bestellen

Springer Medizin

Analysis of the subcomponents and cortical terminations of the perisylvian superior longitudinal fasciculus: a fiber dissection and DTI tractography study

Abstract

Leitlinien kompakt für die Neurologie

Neu im Fachgebiet Neurologie

Demenzkranke durch Antipsychotika vielfach gefährdet

Parkinson-Therapie im Wandel – aktuelle Leitlinie im Fokus

Auf diese Krankheiten bei Geflüchteten sollten Sie vorbereitet sein

Hustenstiller lindert Agitation bei Alzheimer

Update Neurologie

Springer Medizin

Abstract

Bitte loggen Sie sich ein, um Zugang zu diesem Inhalt zu erhalten

Weitere Artikel der Ausgabe 1/2013

A 3-dimensional digital atlas of the ascending sensory and the descending motor systems in the pigeon brain

Cytoarchitectonic mapping of the human dorsal extrastriate cortex

Structure–function relationship of working memory activity with hippocampal and prefrontal cortex volumes

Increased apoptotic neuronal cell death and cognitive impairment at early phase after traumatic brain injury in aged rats

A VBM study demonstrating ‘apparent’ effects of a single dose of medication on T1-weighted MRIs

Aquaporin-4 promotes memory consolidation in Morris water maze

Leitlinien kompakt für die Neurologie

Neu im Fachgebiet Neurologie

Demenzkranke durch Antipsychotika vielfach gefährdet

Parkinson-Therapie im Wandel – aktuelle Leitlinie im Fokus

Auf diese Krankheiten bei Geflüchteten sollten Sie vorbereitet sein

Hustenstiller lindert Agitation bei Alzheimer

Update Neurologie