1. Lateral View of Lobes in Left Hemisphere TOPOGRAPHY

Total Page:16

File Type:pdf, Size:1020Kb

1. Lateral View of Lobes in Left Hemisphere TOPOGRAPHY TOPOGRAPHY T1 Division of Cerebral Cortex into Lobes 1. Lateral View of Lobes in Left Hemisphere 2. Medial View of Lobes in Right Hemisphere PARIETAL PARIETAL LIMBIC FRONTAL FRONTAL INSULAR: buried OCCIPITAL OCCIPITAL in lateral fissure TEMPORAL TEMPORAL 3. Dorsal View of Lobes 4. Ventral View of Lobes PARIETAL TEMPORAL LIMBIC FRONTAL OCCIPITAL FRONTAL OCCIPITAL Comment: The cerebral lobes are arbitrary divisions of the cerebrum, taking their names, for the most part, from overlying bones. They are not functional subdivisions of the brain, but serve as a reference for locating specific functions within them. The anterior (rostral) end of the frontal lobe is referred to as the frontal pole. Similarly, the anterior end of the temporal lobe is the temporal pole, and the posterior end of the occipital lobe the occipital pole. TOPOGRAPHY T2 central sulcus central sulcus parietal frontal occipital lateral temporal lateral sulcus sulcus SUMMARY CARTOON: LOBES SUMMARY CARTOON: GYRI Lateral View of Left Hemisphere central sulcus postcentral superior parietal superior precentral gyrus gyrus lobule frontal intraparietal sulcus gyrus inferior parietal lobule: supramarginal and angular gyri middle frontal parieto-occipital sulcus gyrus incision for close-up below OP T preoccipital O notch inferior frontal cerebellum gyrus: O-orbital lateral T-triangular sulcus superior, middle and inferior temporal gyri OP-opercular Lateral View of Insula central sulcus cut surface corresponding to incision in above figure insula superior temporal gyrus Comment: Insula (insular gyri) exposed by removal of overlying opercula (“lids” of frontal and parietal cortex). TOPOGRAPHY T3 Language sites and arcuate fasciculus. MRI reconstruction from a volunteer. central sulcus supramarginal site (posterior Wernicke’s) Language sites (squares) approximated from electrical stimulation sites in patients undergoing operations for epilepsy or tumor removal (Ojeman and Berger). Broca’s site superior temporal site (anterior Wernicke’s) corpus callosum arcuate fasciculus supramarginal site (posterior Wernicke’s) superior temporal site (anterior Wernicke’s) Broca’s site Dissection of arcuate fasciculus transverse central sulcus arcuate fasciculus temporal gyrus visual radiation caudate Broca’s site arcuate fasciculus Broca’s region supramarginal site (posterior Wernicke’s) superior temporal gyrus TOPOGRAPHY T4 Lateral Dissections central sulcus cut surface of middle supramarginal gyrus frontal gyrus lateral fissure putamen middle temporal gyrus pons medulla external capsule spinal cord pyramidal cell in central sulcus corona radiata precentral gyrus internal capsule fiber in cerebral peduncle fiber in base of pons fiber in pyramid pyramidal decussation TOPOGRAPHY T5 Dorsal View of Brain LEFT HEMISPHERE RIGHT HEMISPHERE superior frontal gyrus longitudinal fissure middle frontal gyrus superior frontal sulcus precentral sulcus central sulcus precentral gyrus postcentral sulcus postcentral gyrus superior parietal lobule intraparietal sulcus parieto-occipital fissure occipital lobe Posterior View of Brain longitudinal fissure falx lies between the cerebral hemi- parieto-occipital spheres in the longitu- sulcus dinal fissure occipital lobe tentorium lies between occipital lobes and cerebellum cerebellum medulla T6 TOPOGRAPHY B B parieto- central sulcus occipital fissure A A lateral fissure A corpus callosum FRONTAL LOBE longitudinal caudate fissure nucleus thalamus central sulcus lateral fissure intraparietal lateral sulcus ventricle: posterior- horn parieto- occipital parieto- fissure OCCIPITAL LOBE occipital fissure B corpus callosum caudate parieto- nucleus occipital fissure thalamus lateral occipital fissure pole lateral ventricle: inferior cerebellum horn TOPOGRAPHY T7 Dorsal View of Brain LEFT RIGHT frontal lobe genu of corpus callosum body of corpus callosum genu of corpus callosum caudate nucleus occipital lobe splenium of corpus callosum internal capsule thalamus transverse temporal gyrus choroid plexus posterior horn of lateral ventricle splenium of corpus callosum TOPOGRAPHY T8 Dorsal View anterior horn of lateral ventricle caudate nucleus internal capsule thalamus amygdala inferior horn of lateral ventricle hippocampus fimbria corpus callosum internal capsule fornix caudate nucleus amygdala thalamus fornix inferior horn fimbria of lateral ventricle hippocampus posterior horn of lateral ventricle TOPOGRAPHY T9 Medial View of Right Hemisphere central sulcus cingulate gyrus parieto-occipital fissure corpus callosum: cuneus (cuneate gyrus ) calcarine body splenium fissure fornix septum genu pellucidum thalamus cerebellar midbrain vermis lingual gyrus pons subcallosal gyrus medulla superior and anterior commissure interventricular cerebral aqueduct and inferior colliculi optic chiasm foramen and fourth ventricle hypothalamus Medial View of Right Hemisphere: Brain Stem and Septum Pellucidum Removed cingulate gyrus corpus callosum fornix caudate isthmus of cingulate gyrus subcallosal gyrus part of thalamus remaining after removal of brainstem uncus fimbria at edge of hippocam- anterior pus (not seen) commissure parahippocampal gyrus lamina terminalis optic chiasm column of fornix entering dissected hypothalamus TOPOGRAPHY T10 Magnetic Resonance Scan: midline septum pellucidum corpus callosum cingulate gyrus parieto-occipital fissure calcarine fissure superior and inferior fornix colliculi third ventricle cerebral aqueduct midbrain optic nerve pituitary fossa cerebellar vermis pons medulla spinal cord fourth ventricle TOPOGRAPHY T11 1. Septum Pellucidum, Hypothalamus & Most of Thalamus Removed parieto-occipital fissure fornix body of corpus callosum cingulate gyrus calcarine sulcus head of caudate nucleus anterior commissure vermis pons 2. Remaining Thalamus & Fornix Removed cingulate gyrus head of caudate thalamus uncus cerebral peduncle nucleus genu of corpus callosum parieto-occipital fissure calcarine sulcus internal capsule vermis pons 3. Caudate Removed anterior commissure splenium of cingulum cingulate gyrus corpus substantia cerebral callosum nigra peduncle uncus body of corpus callosum internal capsule anterior commissure vermis pons uncus substantia cerebral peduncle nigra TOPOGRAPHY OF THE CNS T12 Ventral View of Brain frontal pole olfactory bulb and olfactory tract orbital gyri lateral sulcus FRONTAL LOBE optic nerve, optic chiasm and optic tract temporal pole inferior temporal gyrus collateral sulcus TEMPORAL LOBE floor of hypothalamus lateral and medial (tuber cinereum) occipitotemporal gyri mammillary body of hypothalamus BASE OF cerebral PONS peduncle parahippocampal gyrus trigeminal nerve flocculus MEDULLA (part of cerebellum) olive CEREBELLUM tonsil pyramid (part of cerebellum) occipital pole Comment: The ventral surface of the brain is especially important. It is here that the blood supply to the brain enters. The brain stem and many of the cranial nerves are visible. In addition, one can see the cerebellum, portions of the frontal, temporal and occipital lobes, and the floor of the diencephalon. And it is also here that the pituitary gland (not shown) is attached to the hypothalamus by the small infundibulum (posterior to the optic chiasm). TOPOGRAPHY T13 Cranial Nerves: Numbers and Names orbital gyri I . Olfactory bulb: olfactory nerves (in the nasal epithelium) terminate in the bulb. Olfactory tract straight (rectus) gyrus II. Optic nerve: The cell bodies of origin are in the retina. Half the axons cross (optic chiasm) to the opposite optic tract, half continuing to help form the optic tract of the same side. infundibulum and Optic chiasm and optic tract tuber cinereum mammillary III. Oculomotor nerve body (nucleus) cerebral IV. Trochlear nerve peduncle pons middle cerebellar V. Trigeminal nerve peduncle VI. Abducens nerve VII. Facial nerve nerve VIII. Vestibulocochlear nerve pyramid XII. Hypoglossal nerve rootlets olive X. Vagus nerve rootlets IX. Glossopharyngeal and XI. Accessory (cranial) nerve rootlets are too small to see here: position is rostral and caudal to the vagus in the same line TOPOGRAPHY T14 Ventral View Dissections olfactory tract frontal pole optic chiasm hypothalamus temporal pole mammillary nucleus (body) amygdala optic tract hippocampus uncus cerebral peduncle parahippocampal gyrus substantia cerebral aqueduct nigra splenium of corpus callosum occipital pole olfactory bulb infundibulum amygdala optic tract inferior horn of lateral uncus ventricle hippocampus parahippocampal gyrus mammillary body cerebral peduncle midbrain posterior horn splenium of of lateral ventricle corpus callosum TOPOGRAPHY T15 Ventral Dissection: Optic Radiation RIGHT LEFT optic nerve, chiasm and tract olfactory bulb and tract middle cerebral artery infundibulum and hypothalamus hypothalamus dura oculomotor cerebral peduncle nerve optic radiation: substantia temporal (Meyer’s) nigra loop lateral geniculate medial geniculate parahippocampal gyrus pulvinar optic radiation splenium of corpus callosum midbrain dissected lower bank of calcarine fissure TOPOGRAPHY T16 BRAINSTEM 1. Medial view of right hemisphere corpus callosum septum fornix pellucidum pineal anterior thalamus commissure superior & midbrain cerebellar inferior vermis colliculus hypothalamus pons cerebral aqueduct optic medulla chiasm mammillary body fourth ventricle 3. Posterior view: cerebellum removed 2. Anterior view superior colliculus internal capsule inferior colliculus optic chiasm striatum and tract cerebral peduncle superior cerebellar hypothalamus cerebral peduncle peduncle pons cerebellar middle cerebellar hemisphere peduncle VIII flocculus inferior floor of inferior cerebellar olive tonsil medulla 4th ventricle peduncle pyramid 4. Lateral view from left side cerebral peduncle cerebellar hemisphere optic trigeminal tract nerve (V) flocculus hypothalamus pons tonsil pyramid inferior olive medulla.
Recommended publications
  • The Neural Correlates of Visual Imagery: a Co-Ordinate-Based Meta-Analysis
    cortex 105 (2018) 4e25 Available online at www.sciencedirect.com ScienceDirect Journal homepage: www.elsevier.com/locate/cortex Special issue: Research report The neural correlates of visual imagery: A co-ordinate-based meta-analysis * Crawford I.P. Winlove a, , Fraser Milton b, Jake Ranson c, Jon Fulford a, Matthew MacKisack a, Fiona Macpherson d and Adam Zeman a a Medical School, University of Exeter, UK b School of Psychology, University of Exeter, UK c St George's Medical School, London, UK d Department of Philosophy, University of Glasgow, UK article info abstract Article history: Visual imagery is a form of sensory imagination, involving subjective experiences typi- Received 4 August 2017 cally described as similar to perception, but which occur in the absence of corresponding Reviewed 2 October 2017 external stimuli. We used the Activation Likelihood Estimation algorithm (ALE) to iden- Revised 11 December 2017 tify regions consistently activated by visual imagery across 40 neuroimaging studies, the Accepted 18 December 2017 first such meta-analysis. We also employed a recently developed multi-modal parcella- Published online 2 January 2018 tion of the human brain to attribute stereotactic co-ordinates to one of 180 anatomical regions, the first time this approach has been combined with the ALE algorithm. We Keywords: identified a total 634 foci, based on measurements from 464 participants. Our overall fMRI comparison identified activation in the superior parietal lobule, particularly in the left Neuroimaging hemisphere, consistent with the proposed ‘top-down’ role for this brain region in im- Imagery agery. Inferior premotor areas and the inferior frontal sulcus were reliably activated, a Imagination finding consistent with the prominent semantic demands made by many visual imagery ALE tasks.
    [Show full text]
  • BONY FISHES 602 Bony Fishes
    click for previous page BONY FISHES 602 Bony Fishes GENERAL REMARKS by K.E. Carpenter, Old Dominion University, Virginia, USA ony fishes constitute the bulk, by far, of both the diversity and total landings of marine organisms encoun- Btered in fisheries of the Western Central Atlantic.They are found in all macrofaunal marine and estuarine habitats and exhibit a lavish array of adaptations to these environments. This extreme diversity of form and taxa presents an exceptional challenge for identification. There are 30 orders and 269 families of bony fishes presented in this guide, representing all families known from the area. Each order and family presents a unique suite of taxonomic problems and relevant characters. The purpose of this preliminary section on technical terms and guide to orders and families is to serve as an introduction and initial identification guide to this taxonomic diversity. It should also serve as a general reference for those features most commonly used in identification of bony fishes throughout the remaining volumes. However, I cannot begin to introduce the many facets of fish biology relevant to understanding the diversity of fishes in a few pages. For this, the reader is directed to one of the several general texts on fish biology such as the ones by Bond (1996), Moyle and Cech (1996), and Helfman et al.(1997) listed below. A general introduction to the fisheries of bony fishes in this region is given in the introduction to these volumes. Taxonomic details relevant to a specific family are explained under each of the appropriate family sections. The classification of bony fishes continues to transform as our knowledge of their evolutionary relationships improves.
    [Show full text]
  • FUS-Mediated Functional Neuromodulation for Neurophysiologic Assessment in a Large Animal Model Wonhye Lee1*, Hyungmin Kim2, Stephanie D
    Lee et al. Journal of Therapeutic Ultrasound 2015, 3(Suppl 1):O23 http://www.jtultrasound.com/content/3/S1/O23 ORALPRESENTATION Open Access FUS-mediated functional neuromodulation for neurophysiologic assessment in a large animal model Wonhye Lee1*, Hyungmin Kim2, Stephanie D. Lee1, Michael Y. Park1, Seung-Schik Yoo1 From Current and Future Applications of Focused Ultrasound 2014. 4th International Symposium Washington, D.C, USA. 12-16 October 2014 Background/introduction element FUS transducer with radius-of-curvature of Focused ultrasound (FUS) is gaining momentum as a 7 cm) was transcranially delivered to the unilateral sen- new modality of non-invasive neuromodulation of regio- sorimotor cortex, the optic radiation (WM tract) as well as nal brain activity, with both stimulatory and suppressive the visual cortex. An acoustic intensity of 1.4–15.5 W/cm2 potentials. The utilization of the method has largely Isppa, tone-burst-duration of 1 ms, pulse-repetition fre- been demonstrated in small animals. Considering the quency of 500 Hz (i.e. duty cycle of 50%), sonication dura- small size of the acoustic focus, having a diameter of tion of 300 ms, were used for the stimulation. A batch of only a few millimeters, FUS insonification to a larger continuous sonication ranging from 50 to 150 ms in dura- animal’s brain is conducive to examining the region- tion were also given. Evoked electromyogram responses specific neuromodulatory effects on discrete anatomical from the hind legs and electroencephalogram from the Fz areas, including the white matter (WM) tracts. The and Oz-equivalent sites were measured. The histology of study involving large animals would also establish preli- the extracted brain tissue (within one week and 2 months minary safety data prior to its translational research in post-sonication) was obtained.
    [Show full text]
  • Brain Sulci and Gyri: a Practical Anatomical Review
    Journal of Clinical Neuroscience 21 (2014) 2219–2225 Contents lists available at ScienceDirect Journal of Clinical Neuroscience journal homepage: www.elsevier.com/locate/jocn Neuroanatomical study Brain sulci and gyri: A practical anatomical review ⇑ Alvaro Campero a,b, , Pablo Ajler c, Juan Emmerich d, Ezequiel Goldschmidt c, Carolina Martins b, Albert Rhoton b a Department of Neurological Surgery, Hospital Padilla, Tucumán, Argentina b Department of Neurological Surgery, University of Florida, Gainesville, FL, USA c Department of Neurological Surgery, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina d Department of Anatomy, Universidad de la Plata, La Plata, Argentina article info abstract Article history: Despite technological advances, such as intraoperative MRI, intraoperative sensory and motor monitor- Received 26 December 2013 ing, and awake brain surgery, brain anatomy and its relationship with cranial landmarks still remains Accepted 23 February 2014 the basis of neurosurgery. Our objective is to describe the utility of anatomical knowledge of brain sulci and gyri in neurosurgery. This study was performed on 10 human adult cadaveric heads fixed in formalin and injected with colored silicone rubber. Additionally, using procedures done by the authors between Keywords: June 2006 and June 2011, we describe anatomical knowledge of brain sulci and gyri used to manage brain Anatomy lesions. Knowledge of the brain sulci and gyri can be used (a) to localize the craniotomy procedure, (b) to Brain recognize eloquent areas of the brain, and (c) to identify any given sulcus for access to deep areas of the Gyri Sulci brain. Despite technological advances, anatomical knowledge of brain sulci and gyri remains essential to Surgery perform brain surgery safely and effectively.
    [Show full text]
  • Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection
    Distance Learning Program Anatomy of the Human Brain/Sheep Brain Dissection This guide is for middle and high school students participating in AIMS Anatomy of the Human Brain and Sheep Brain Dissections. Programs will be presented by an AIMS Anatomy Specialist. In this activity students will become more familiar with the anatomical structures of the human brain by observing, studying, and examining human specimens. The primary focus is on the anatomy, function, and pathology. Those students participating in Sheep Brain Dissections will have the opportunity to dissect and compare anatomical structures. At the end of this document, you will find anatomical diagrams, vocabulary review, and pre/post tests for your students. The following topics will be covered: 1. The neurons and supporting cells of the nervous system 2. Organization of the nervous system (the central and peripheral nervous systems) 4. Protective coverings of the brain 5. Brain Anatomy, including cerebral hemispheres, cerebellum and brain stem 6. Spinal Cord Anatomy 7. Cranial and spinal nerves Objectives: The student will be able to: 1. Define the selected terms associated with the human brain and spinal cord; 2. Identify the protective structures of the brain; 3. Identify the four lobes of the brain; 4. Explain the correlation between brain surface area, structure and brain function. 5. Discuss common neurological disorders and treatments. 6. Describe the effects of drug and alcohol on the brain. 7. Correctly label a diagram of the human brain National Science Education
    [Show full text]
  • Anatomy of the Temporal Lobe
    Hindawi Publishing Corporation Epilepsy Research and Treatment Volume 2012, Article ID 176157, 12 pages doi:10.1155/2012/176157 Review Article AnatomyoftheTemporalLobe J. A. Kiernan Department of Anatomy and Cell Biology, The University of Western Ontario, London, ON, Canada N6A 5C1 Correspondence should be addressed to J. A. Kiernan, [email protected] Received 6 October 2011; Accepted 3 December 2011 Academic Editor: Seyed M. Mirsattari Copyright © 2012 J. A. Kiernan. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Only primates have temporal lobes, which are largest in man, accommodating 17% of the cerebral cortex and including areas with auditory, olfactory, vestibular, visual and linguistic functions. The hippocampal formation, on the medial side of the lobe, includes the parahippocampal gyrus, subiculum, hippocampus, dentate gyrus, and associated white matter, notably the fimbria, whose fibres continue into the fornix. The hippocampus is an inrolled gyrus that bulges into the temporal horn of the lateral ventricle. Association fibres connect all parts of the cerebral cortex with the parahippocampal gyrus and subiculum, which in turn project to the dentate gyrus. The largest efferent projection of the subiculum and hippocampus is through the fornix to the hypothalamus. The choroid fissure, alongside the fimbria, separates the temporal lobe from the optic tract, hypothalamus and midbrain. The amygdala comprises several nuclei on the medial aspect of the temporal lobe, mostly anterior the hippocampus and indenting the tip of the temporal horn. The amygdala receives input from the olfactory bulb and from association cortex for other modalities of sensation.
    [Show full text]
  • Prefrontal and Posterior Parietal Contributions to the Perceptual Awareness of Touch M
    www.nature.com/scientificreports OPEN Prefrontal and posterior parietal contributions to the perceptual awareness of touch M. Rullmann1,2,5, S. Preusser1,5 & B. Pleger1,3,4* Which brain regions contribute to the perceptual awareness of touch remains largely unclear. We collected structural magnetic resonance imaging scans and neurological examination reports of 70 patients with brain injuries or stroke in S1 extending into adjacent parietal, temporal or pre-/frontal regions. We applied voxel-based lesion-symptom mapping to identify brain areas that overlap with an impaired touch perception (i.e., hypoesthesia). As expected, patients with hypoesthesia (n = 43) presented lesions in all Brodmann areas in S1 on postcentral gyrus (BA 1, 2, 3a, 3b). At the anterior border to BA 3b, we additionally identifed motor area BA 4p in association with hypoesthesia, as well as further ventrally the ventral premotor cortex (BA 6, BA 44), assumed to be involved in whole-body perception. At the posterior border to S1, we found hypoesthesia associated efects in attention-related areas such as the inferior parietal lobe and intraparietal sulcus. Downstream to S1, we replicated previously reported lesion-hypoesthesia associations in the parietal operculum and insular cortex (i.e., ventral pathway of somatosensory processing). The present fndings extend this pathway from S1 to the insular cortex by prefrontal and posterior parietal areas involved in multisensory integration and attention processes. Te primary somatosensory cortex (S1) in monkeys can be divided into four Brodmann areas: (BA) 1, 2, 3a, and 3b. Each BA consists of a somatotopically organized map that subserves distinct somatosensory functions1–3.
    [Show full text]
  • Visual Topography of Human Intraparietal Sulcus
    5326 • The Journal of Neuroscience, May 16, 2007 • 27(20):5326–5337 Behavioral/Systems/Cognitive Visual Topography of Human Intraparietal Sulcus Jascha D. Swisher,1 Mark A. Halko,1 Lotfi B. Merabet,1,2 Stephanie A. McMains,1,3 and David C. Somers1,4 1Perceptual Neuroimaging Laboratory, Program in Neuroscience and Department of Psychology, Boston University, Boston, Massachusetts 02215, 2Center for Noninvasive Brain Stimulation, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, 3Neuroscience of Attention and Perception Laboratory, Department of Psychology, Princeton University, Princeton, New Jersey 08544, and 4Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, Massachusetts 02129 Human parietal cortex is implicated in a wide variety of sensory and cognitive functions, yet its precise organization remains unclear. Visual field maps provide a potential structural basis for descriptions of functional organization. Here, we detail the topography of a series of five maps of the contralateral visual hemifield within human posterior parietal cortex. These maps are located along the medial bank of the intraparietal sulcus (IPS) and are revealed by direct visual stimulation during functional magnetic resonance imaging, allowing these parietal regions to be routinely and reliably identified simultaneously with occipital visual areas. Two of these maps (IPS3 and IPS4) are novel, whereas two others (IPS1 and IPS2) have previously been revealed only by higher-order cognitive tasks. Area V7, a previously identified visual map, is observed to lie within posterior IPS and to share a foveal representation with IPS1. These parietal maps are reliably observed across scan sessions; however, their precise topography varies between individuals.
    [Show full text]
  • Quantitative Analysis of Axon Collaterals of Single Pyramidal Cells
    Yang et al. BMC Neurosci (2017) 18:25 DOI 10.1186/s12868-017-0342-7 BMC Neuroscience RESEARCH ARTICLE Open Access Quantitative analysis of axon collaterals of single pyramidal cells of the anterior piriform cortex of the guinea pig Junli Yang1,2*, Gerhard Litscher1,3* , Zhongren Sun1*, Qiang Tang1, Kiyoshi Kishi2, Satoko Oda2, Masaaki Takayanagi2, Zemin Sheng1,4, Yang Liu1, Wenhai Guo1, Ting Zhang1, Lu Wang1,3, Ingrid Gaischek3, Daniela Litscher3, Irmgard Th. Lippe5 and Masaru Kuroda2 Abstract Background: The role of the piriform cortex (PC) in olfactory information processing remains largely unknown. The anterior part of the piriform cortex (APC) has been the focus of cortical-level studies of olfactory coding, and asso- ciative processes have attracted considerable attention as an important part in odor discrimination and olfactory information processing. Associational connections of pyramidal cells in the guinea pig APC were studied by direct visualization of axons stained and quantitatively analyzed by intracellular biocytin injection in vivo. Results: The observations illustrated that axon collaterals of the individual cells were widely and spatially distrib- uted within the PC, and sometimes also showed a long associational projection to the olfactory bulb (OB). The data showed that long associational axons were both rostrally and caudally directed throughout the PC, and the intrinsic associational fibers of pyramidal cells in the APC are omnidirectional connections in the PC. Within the PC, associa- tional axons typically followed rather linear trajectories and irregular bouton distributions. Quantitative data of the axon collaterals of two pyramidal cells in the APC showed that the average length of axonal collaterals was 101 mm, out of which 79 mm (78% of total length) were distributed in the PC.
    [Show full text]
  • Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans Ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai
    Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai To cite this version: Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai. Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex. Frontiers in Neuroanatomy, Frontiers, 2018, 12, pp.93. 10.3389/fnana.2018.00093. hal-01929541 HAL Id: hal-01929541 https://hal.archives-ouvertes.fr/hal-01929541 Submitted on 21 Nov 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. REVIEW published: 19 November 2018 doi: 10.3389/fnana.2018.00093 Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans J. ten Donkelaar 1*†, Nathalie Tzourio-Mazoyer 2† and Jürgen K. Mai 3† 1 Department of Neurology, Donders Center for Medical Neuroscience, Radboud University Medical Center, Nijmegen, Netherlands, 2 IMN Institut des Maladies Neurodégénératives UMR 5293, Université de Bordeaux, Bordeaux, France, 3 Institute for Anatomy, Heinrich Heine University, Düsseldorf, Germany The gyri and sulci of the human brain were defined by pioneers such as Louis-Pierre Gratiolet and Alexander Ecker, and extensified by, among others, Dejerine (1895) and von Economo and Koskinas (1925).
    [Show full text]
  • The Role of the Superior Temporal Sulcus and the Mirror Neuron System in Imitation
    r Human Brain Mapping 31:1316–1326 (2010) r The Role of the Superior Temporal Sulcus and the Mirror Neuron System in Imitation Pascal Molenberghs,* Christopher Brander, Jason B. Mattingley, and Ross Cunnington The University of Queensland, Queensland Brain Institute & School of Psychology, St Lucia, Queensland, Australia r r Abstract: It has been suggested that in humans the mirror neuron system provides a neural substrate for imitation behaviour, but the relative contributions of different brain regions to the imitation of manual actions is still a matter of debate. To investigate the role of the mirror neuron system in imita- tion we used fMRI to examine patterns of neural activity under four different conditions: passive ob- servation of a pantomimed action (e.g., hammering a nail); (2) imitation of an observed action; (3) execution of an action in response to a word cue; and (4) self-selected execution of an action. A net- work of cortical areas, including the left supramarginal gyrus, left superior parietal lobule, left dorsal premotor area and bilateral superior temporal sulcus (STS), was significantly active across all four con- ditions. Crucially, within this network the STS bilaterally was the only region in which activity was significantly greater for action imitation than for the passive observation and execution conditions. We suggest that the role of the STS in imitation is not merely to passively register observed biological motion, but rather to actively represent visuomotor correspondences between one’s own actions and the actions of others. Hum Brain Mapp 31:1316–1326, 2010. VC 2010 Wiley-Liss, Inc. Key words: fMRI; imitation; mirror neuron system r r INTRODUCTION ror neurons are visuomotor neurons that fire both when an action is performed and when a similar or identical Motor imitation involves observing the action of another action is passively observed [Rizzolatti and Craighero, individual and matching one’s own movements to those 2004].
    [Show full text]
  • Letters Anterior Part of the Cingulate Gyrus
    J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.51.1.146 on 1 January 1988. Downloaded from Journal of Neurology, Neurosurgery, and Psychiatry 1988;51:146-157 investigate the mesial frontal zone and the Three spontaneous seizures were recorded, Letters anterior part of the cingulate gyrus. Infre- each had the same pattern: diffuse flattening quent spikes occurred in the amygdala and and no in the Orbital frontal epilepsy: a case report paroxysmal discharge sometimes in the mesial frontal cortex. explored sites in the frontal or temporal Sir: Although an orbital frontal origin for A complex partial seizures has been sometimes 12 suggested, few cases have been completely documented.1 2 We report a patient in 23 whom electroclinical correlations were obtained by electroencephalography (EEG) and stereo-EEG recordings. The disap- 3.4 I-w VI,-#a+r - pearance of seizures after a surgical resection limited to the orbital frontal cortex confirmed the localisation of the epileptic 4.5 o I\A-.ViJV "fJ4 WOO focus. A 29 year old male had begun to experi- B ence seizures when 10 years old. The aetiology was unknown. Neurological examination was normal. The seizure pat- terns did not change during the next 19 23 ., years. They were characterised by staring, r by sudden and incomplete loss of contact -- - -. , A- followed by semi-purposeful automatisms, 3-4 v by thrashing movements if he was held, by the shouting of incoherent words and some- times by laughter. Deviation of the head and eyes to either side seemed to mimic natural Protected by copyright.
    [Show full text]