Diencephalon Diencephalon

Total Page:16

File Type:pdf, Size:1020Kb

Diencephalon Diencephalon Diencephalon Diencephalon • Thalamus dorsal thalamus • Hypothalamus pituitary gland • Epithalamus habenular nucleus and commissure pineal gland • Subthalamus ventral thalamus subthalamic nucleus (STN) field of Forel Diencephalon dorsal surface Diencephalon ventral surface Diencephalon Medial Surface THALAMUS Function of the Thalamus • Sensory relay – ALL sensory information (except smell) • Motor integration – Input from cortex, cerebellum and basal ganglia • Arousal – Part of reticular activating system • Pain modulation – All nociceptive information • Memory & behavior – Lesions are disruptive Classification of Thalamic Nuclei I. Lateral Nuclear Group II. Medial Nuclear Group III. Anterior Nuclear Group IV. Posterior Nuclear Group V. Metathalamic Nuclear Group VI. Intralaminar Nuclear Group VII. Thalamic Reticular Nucleus Classification of Thalamic Nuclei LATERAL NUCLEAR GROUP Ventral Nuclear Group Ventral Posterior Nucleus (VP) ventral posterolateral nucleus (VPL) ventral posteromedial nucleus (VPM) Input to the Thalamus Sensory relay - Ventral posterior group all sensation from body and head, including pain Projections from the Thalamus Sensory relay Ventral posterior group all sensation from body and head, including pain LATERAL NUCLEAR GROUP Ventral Lateral Nucleus Ventral Anterior Nucleus Input to the Thalamus Motor control and integration Projections from the Thalamus Motor control and integration LATERAL NUCLEAR GROUP Prefrontal SMA MI, PM SI Ventral Nuclear Group SNr TTT GPi Cbll ML, STT Lateral Dorsal Nuclear Group Lateral Dorsal Nucleus Lateral Posterior Nucleus Pulvinar LATERAL NUCLEAR GROUP cingulate gyrus, Somesthetic precuneus Association Visual Area Association area HF SC, Pretectal MEDIAL NUCLEAR GROUP Dorsomedial Nucleus (MD) - pars magnocellularis - pars parvocellularis Midline Nuclear Group Input to the Thalamus Behavior and emotion connection with hypothalamus Projections from the Thalamus Behavior and emotion connection with hypothalamus MEDIAL & ANTERIOR NUCLEAR GROUP Prefrontal Frontal MB, HF Cortex Eye Field Medial Frontal Gyrus cingulate gyrus Basal forebrain SNr, SC, RF METATHALAMIC NUCLEAR GROUP Medial Geniculate Nucleus (MG) ventral nucleus dorsal nucleus medial nucleus Lateral Geniculate Nucleus (LG) dorsal nucleus ventral nucleus Input to the Thalamus Metathalamus Vision and Hearing Projections from the Thalamus Metathalamus Vision and Hearing INTRALAMINAR NUCLEAR GROUP Rostral Intralaminar Nuclei central lateral nucleus, central medial nucleus, paracentral nucleus, Caudal Intralaminar Nuclei centro-median nucleus THALAMIC RETICULAR NUCLEUS Cerebral Cortex Thalamic Thalamocortical Reticular Neuron Nucleus Subcortical Structure Summary of Thalamic Connectivity I. Sensory Input general sensation special sensation taste, equilibrium, hearing, vision II. Motor Input cerebellum, basal ganglia III. Reticular Formation IV. Limbic System mammillary nucleus hippocampal formation Sensory Input (1) General Sensation 1. Medial lemniscus - VPL 2. Spinothalamic tract - VPL 3. Trigeminothalamic tract – VPM (2) Taste sensation - VPM (3) Sense of equilibrium - VPL (4) Auditory sensation - MG (5) Vision - LG Motor Input (1) Cerebellum VL, VPL, (2) Basal ganglia 1. GPi 2. SNr Reticular Formation & Limbic System Reticular formation rostral intralaminar nuclei thalamic reticular nucleus Limbic System Mammillary Body - AN Hippocampal Formation - AN Clinical Syndromes of the Thalamus Posterolateral thalamic syndromes sensory disorders Thalamic (Dejerine-Roussy) syndrome ----- VP nucleus - pain Medial thalamic syndromes disorders of consciousness thalamic neglect, thalamic amnesia, akinetic mutism Anterolateral thalamic syndromes motor disorders paresis, ataxia, motor incoordination, dysphagia Thalamic (Dejerine-Roussy) Syndrome Joseph Jules Dejerine Gustave Roussy (1849-1917) (1874-1948) Epithalamus Limbic System Habenular Nucleus Medial Habenular Nucleus Lateral Habenular Nucleus Habenular Commissure Pineal Gland Epithalamus Corpus pineale Trigonum & commissura habenulae Stria medullaris thalami Commissura posterior Tela choroidea & plexus choroideus of 3rd ventricle Epithalamus 1. Trigonum habenulae Small nuclei habenulae, above commissura posterior. 3 connections: – Stria medullaris thalami – afferents to nuclei habenulae mainly from area septalis – Commissura habenularum – btwn trigonum habenulae – Tractus habenulointerpeduncularis (fasciculus retroflexus) – efferents to nucl. interpeduncularis, RF, substantia grisea centralis 2. Functions of nuclei habenulae Vague. Supposed to mediate olfactory stimuli and feeding behavior. Connect olfactory brain, hypothalamus and limbic system with brain stem. 3. Corpus pineale Produces melatonin and serotonin. Controls circadian rhythms, reprductive cycles and maturation (puberty) Subthalamus Basal Ganglia Subthalamic nucleus zona incerta Field of Forel H ansa lenticularis H1 thalamic fasciculus H2 lenticular fasciculus .
Recommended publications
  • Cortex and Thalamus Lecture.Pptx
    Cerebral Cortex and Thalamus Hyperbrain Ch 2 Monica Vetter, PhD January 24, 2013 Learning Objectives: • Anatomy of the lobes of the cortex • Relationship of thalamus to cortex • Layers and connectivity of the cortex • Vascular supply to cortex • Understand the location and function of hypothalamus and pituitary • Anatomy of the basal ganglia • Primary functions of the different lobes/ cortical regions – neurological findings 1 Types of Cortex • Sensory (Primary) • Motor (Primary) • Unimodal association • Multimodal association - necessary for language, reason, plan, imagine, create Note: • Gyri • Sulci • Fissures • Lobes 2 The Thalamus is highly interconnected with the cerebral cortex, and handles most information traveling to or from the cortex. “Specific thalamic Ignore nuclei” – have well- names of defined sensory or thalamic nuclei for motor functions now - A few Other nuclei have will more distributed reappear later function 3 Thalamus Midbrain Pons Limbic lobe = cingulate gyrus Structure of Neocortex (6 layers) white matter gray matter Pyramidal cells 4 Connectivity of neurons in different cortical layers Afferents = inputs Efferents = outputs (reciprocal) brainstem etc Eg. Motor – Eg. Sensory – more efferent more afferent output input Cortico- cortical From Thalamus To spinal cord, brainstem etc. To Thalamus Afferent and efferent connections to different ….Depending on whether they have more layers of cortex afferent or efferent connections 5 Different areas of cortex were defined by differences in layer thickness, and size and
    [Show full text]
  • Clones in the Chick Diencephalon Contain Multiple Cell Types and Siblings Are Widely Dispersed
    Development 122, 65-78 (1996) 65 Printed in Great Britain © The Company of Biologists Limited 1996 DEV8292 Clones in the chick diencephalon contain multiple cell types and siblings are widely dispersed Jeffrey A. Golden1,2 and Constance L. Cepko1,3 1Department of Genetics, Harvard Medical School, 2Department of Pathology, Brigham and Women’s Hospital, and 3Howard Hughes Medical Institute, 200 Longwood Avenue, Boston, MA 02115, USA SUMMARY The thalamus, hypothalamus and epithalamus of the ver- clones dispersed in all directions, resulting in sibling cells tebrate central nervous system are derived from the populating multiple nuclei within the diencephalon. In embryonic diencephalon. These regions of the nervous addition, several distinctive patterns of dispersion were system function as major relays between the telencephalon observed. These included clones with siblings distributed and more caudal regions of the brain. Early in develop- bilaterally across the third ventricle, clones that originated ment, the diencephalon morphologically comprises distinct in the lateral ventricle, clones that crossed neuromeric units known as neuromeres or prosomeres. As development boundaries, and clones that crossed major boundaries of proceeds, multiple nuclei, the functional and anatomical the developing nervous system, such as the diencephalon units of the diencephalon, derive from the neuromeres. It and mesencephalon. These findings demonstrate that prog- was of interest to determine whether progenitors in the enitor cells in the diencephalon are multipotent and that diencephalon give rise to daughters that cross nuclear or their daughters can become widely dispersed. neuromeric boundaries. To this end, a highly complex retroviral library was used to infect diencephalic progeni- tors. Retrovirally marked clones were found to contain Key words: cell lineage, central nervous system, diencephalon, neurons, glia and occasionally radial glia.
    [Show full text]
  • MRI Atlas of the Human Deep Brain Jean-Jacques Lemaire
    MRI Atlas of the Human Deep Brain Jean-Jacques Lemaire To cite this version: Jean-Jacques Lemaire. MRI Atlas of the Human Deep Brain. 2019. hal-02116633 HAL Id: hal-02116633 https://hal.uca.fr/hal-02116633 Preprint submitted on 1 May 2019 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. Distributed under a Creative Commons Attribution - NonCommercial - NoDerivatives| 4.0 International License MRI ATLAS of the HUMAN DEEP BRAIN Jean-Jacques Lemaire, MD, PhD, neurosurgeon, University Hospital of Clermont-Ferrand, Université Clermont Auvergne, CNRS, SIGMA, France This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ or send a letter to Creative Commons, PO Box 1866, Mountain View, CA 94042, USA. Terminologia Foundational Model Terminologia MRI Deep Brain Atlas NeuroNames (ID) neuroanatomica usages, classical and french terminologies of Anatomy (ID) Anatomica 1998 (ID) 2017 http://fipat.library.dal.ca In
    [Show full text]
  • Lecture 12 Notes
    Somatic regions Limbic regions These functionally distinct regions continue rostrally into the ‘tweenbrain. Fig 11-4 Courtesy of MIT Press. Used with permission. Schneider, G. E. Brain structure and its Origins: In the Development and in Evolution of Behavior and the Mind. MIT Press, 2014. ISBN: 9780262026734. 1 Chapter 11, questions about the somatic regions: 4) There are motor neurons located in the midbrain. What movements do those motor neurons control? (These direct outputs of the midbrain are not a subject of much discussion in the chapter.) 5) At the base of the midbrain (ventral side) one finds a fiber bundle that shows great differences in relative size in different species. Give examples. What are the fibers called and where do they originate? 8) A decussating group of axons called the brachium conjunctivum also varies greatly in size in different species. It is largest in species with the largest neocortex but does not come from the neocortex. From which structure does it come? Where does it terminate? (Try to guess before you look it up.) 2 Motor neurons of the midbrain that control somatic muscles: the oculomotor nuclei of cranial nerves III and IV. At this level, the oculomotor nucleus of nerve III is present. Fibers from retina to Superior Colliculus Brachium of Inferior Colliculus (auditory pathway to thalamus, also to SC) Oculomotor nucleus Spinothalamic tract (somatosensory; some fibers terminate in SC) Medial lemniscus Cerebral peduncle: contains Red corticospinal + corticopontine fibers, + cortex to hindbrain fibers nucleus (n. ruber) Tectospinal tract Rubrospinal tract Courtesy of MIT Press. Used with permission. Schneider, G.
    [Show full text]
  • Neuromodulation in Eating Disorders and Obesity: a Promising Way of Treatment?
    Journal name: Neuropsychiatric Disease and Treatment Article Designation: Review Year: 2018 Volume: 14 Neuropsychiatric Disease and Treatment Dovepress Running head verso: Jáuregui-Lobera and Martínez-Quiñones Running head recto: Neuromodulation in eating disorders and obesity open access to scientific and medical research DOI: 180231 Open Access Full Text Article REVIEW Neuromodulation in eating disorders and obesity: a promising way of treatment? Ignacio Jáuregui-Lobera1 Abstract: Neuromodulation can affect the functioning of the central nervous system (CNS), José V Martínez-Quiñones2 and emotional/eating behavior is an exciting facet of that functioning. Therefore, it would be possible to offer an alternative (or complement) treatment to psychotropic medications and 1Department of Molecular Biology and Biochemical Engineering, different psychological and nutritional approaches to both eating disorders (EDs) and obe- University of Pablo de Olavide of sity. Although there are a number of publications in these areas, a systematic review has not Seville, Seville, Spain; 2Department of Neurosurgery, Mutua de been conducted to date. Abstracts, letters, conference reports, dissertations, and reviews were Accidentes de Zaragoza (Servicio de excluded. Clinical trials and controlled human clinical trials were filtered and included in this Neurocirugía), Zaragoza, Spain study. Articles included were based on the population suffering from anorexia nervosa, bulimia nervosa, binge ED, overweight, and obesity. No restrictions were placed on the sample size. Only trials investigating the effect of neuromodulation by means of deep brain stimulation (DBS), transcranial direct current stimulation (tDCS), and transcranial magnetic stimulation For personal use only. (TMS) were included. The following databases were used to conduct the search: MEDLINE/ PubMed, PsycINFO, PsycArticles, and Cochrane (Search Trials, CENTRAL).
    [Show full text]
  • ON-LINE FIG 1. Selected Images of the Caudal Midbrain (Upper Row
    ON-LINE FIG 1. Selected images of the caudal midbrain (upper row) and middle pons (lower row) from 4 of 13 total postmortem brains illustrate excellent anatomic contrast reproducibility across individual datasets. Subtle variations are present. Note differences in the shape of cerebral peduncles (24), decussation of superior cerebellar peduncles (25), and spinothalamic tract (12) in the midbrain of subject D (top right). These can be attributed to individual anatomic variation, some mild distortion of the brain stem during procurement at postmortem examination, and/or differences in the axial imaging plane not easily discernable during its prescription parallel to the anterior/posterior commissure plane. The numbers in parentheses in the on-line legends refer to structures in the On-line Table. AJNR Am J Neuroradiol ●:●●2019 www.ajnr.org E1 ON-LINE FIG 3. Demonstration of the dentatorubrothalamic tract within the superior cerebellar peduncle (asterisk) and rostral brain stem. A, Axial caudal midbrain image angled 10° anterosuperior to posteroinferior relative to the ACPC plane demonstrates the tract traveling the midbrain to reach the decussation (25). B, Coronal oblique image that is perpendicular to the long axis of the hippocam- pus (structure not shown) at the level of the ventral superior cerebel- lar decussation shows a component of the dentatorubrothalamic tract arising from the cerebellar dentate nucleus (63), ascending via the superior cerebellar peduncle to the decussation (25), and then enveloping the contralateral red nucleus (3). C, Parasagittal image shows the relatively long anteroposterior dimension of this tract, which becomes less compact and distinct as it ascends toward the thalamus. ON-LINE FIG 2.
    [Show full text]
  • Analysis of Evoked Activity Patterns of Human Thalamic Ventrolateral Neurons During Verbally Ordered Voluntary Movements
    Neuroscience Vol. 88, No. 2, pp. 377–392, 1998 Copyright 1998 IBRO. Published by Elsevier Science Ltd Printed in Great Britain. All rights reserved Pergamon PII: S0306-4522(98)00230-9 0306–4522/99 $19.00+0.00 ANALYSIS OF EVOKED ACTIVITY PATTERNS OF HUMAN THALAMIC VENTROLATERAL NEURONS DURING VERBALLY ORDERED VOLUNTARY MOVEMENTS S. RAEVA,* N. VAINBERG, YU. TIKHONOV and I. TSETLIN Laboratory of Human Cell Neurophysiology, Institute of Chemical Physics, Russian Academy of Sciences, 4 Kosygin Street, Moscow 117377, Russia and Burdenko Neurosurgery Institute, Russian Academy of Medical Sciences, Moscow, Russia Abstract––In the human thalamic ventralis lateralis nucleus the responses of 184 single units to verbally ordered voluntary movements and some somatosensory stimulations were studied by microelectrode recording technique during 38 stereotactic operations on parkinsonian patients. The tests were carried out on the same previously examined population of neurons classified into two groups, named A- and B-types according to the functional criteria of their intrinsic structure of spontaneous activity patterns. The evaluation of the responses of these units during functionally different phases of a voluntary movement (preparation, initiation, execution, after-effect) by means of the principal component analysis and correlation techniques confirmed the functional differences between A- and B-types of neurons and their polyvalent convergent nature. Four main conclusions emerge from the studies. (1) The differences of the patterns of A- and B-unit
    [Show full text]
  • Neurophysiological Characterisation of Neurons in the Rostral Nucleus Reuniens in Health and Disease
    Neurophysiological characterisation of neurons in the rostral nucleus reuniens in health and disease. Submitted by Darren Walsh, to the University of Exeter as a thesis for the degree of Doctor of Philosophy in Medical Studies, September 2017. This thesis is available for Library use on the understanding that it is copyright material and that no quotation from the thesis may be published without proper acknowledgement. I certify that all material in this thesis which is not my own work has been identified and that no material has previously been submitted and approved for the award of a degree by this or any other University. (Signature) ……………………………………………………………………………… Word Count = 44,836 1 Abstract Evidence is mounting for a role of the nucleus reuniens (Re) in higher cognitive function. Despite growing interest, very little is known about the intrinsic neurophysiological properties of Re neurons and, to date, no studies have examined if alterations to Re neurons may contribute to cognitive deficits associated with normal aging or dementia. Work presented chapter 3 provides the first detailed description of the intrinsic electrophysiological properties of rostral Re neurons in young adult (~5 months) C57- Bl/6J mice. This includes a number of findings which are highly atypical for thalamic relay neurons including tonic firing in the theta frequency at rest, a paucity of hyperpolarisation-activated cyclic nucleotide–gated (HCN) mediated currents, and a diversity of responses observed in response to depolarising current injections. Additionally this chapter includes a description of a novel form of intrinsic plasticity which alters the functional output of Re neurons. Chapter 4 investigates whether the intrinsic properties of Re neurons are altered in aged (~15 month) C57-Bl/6J mice as compared to a younger control group (~5 months).
    [Show full text]
  • Dorsal “Thalamus”
    Dorsal “Thalamus” Medical Neuroscience Dr. Wiegand The Diencephalon The Diencephalon InterthalamicInterthalamic adhesionadhesion ThalamusThalamus EpithalamusEpithalamus HypothalamusHypothalamus (Pineal(Pineal && Habenula)Habenula) PituitaryPituitary SubthalamusSubthalamus 1 The “Dorsal” Thalamus | Sensory integration nucleus – gateway to the cerebral cortex | Afferents from both rostral and caudal central nervous system structures | Efferents primarily to cerebral cortex via four principal “radiations” | Associated with motor, sensory, limbic and vegetative functions External medullary lamina Anterior n. 3rd Internal capsule Ventricle Medial n. Medial Lateral n. Internal capsule * Reticular n. Internal * Interthalamic adhesion medullary lamina 2 General Organization medialmedial nucleinuclei anterioranterior nuclei nuclei internalinternal medullarymedullary laminalamina laterallateral nuclei nuclei dorsaldorsal tiertier pulvinarpulvinar geniculategeniculate ventralventral tiertier bodiesbodies Frontal Section intralaminarintralaminar nucleinuclei reticularreticular nuclei nuclei 3rd Ventricle externalexternalexternalexternal medullarymedullary laminalamina internalinternal laminalamina medullarymedullary laminalamina 3 Thalamic Nuclei | Anterior | Lateral z Dorsal Tier • lateral dorsal • lateral posterior • pulvinar z Ventral Tier • ventral anterior • ventral lateral • ventral posterior (VLP & VPM) • posterior nucleus Thalamic Nuclei | Medial z medial/medial dorsal z midline nuclei | Pulvinar | Geniculate bodies | Reticular | Intralaminar
    [Show full text]
  • Diencephalon Sists of the Midbrain, Pons, and Medulla
    Diencephalon The brain lies within the cranial cavity of the skull and is made up of billions of nerve cells (neu - rons) and supporting cells (glia) . Neuronal cell bodies group together as gray matter, and their processes group together as white matter. The brain can be divided into four main parts: the cerebrum, diencephalon, brain stem, and cere - bellum. • The cerebrum is the largest part of the brain and consists of the four paired lobes with the two cerebral hemispheres, connected by a mass of white matter called the corpus callosum. The cerebrum accounts for about 80% of the brain’s mass and is concerned with higher functions, including perception of sensory impulses, instigation of voluntary movement, memory, thought, and reasoning. There are two layers of the cerebrum: - The cerebral cortex is the thin, wrinkled gray matter covering each hemisphere - The cerebral medulla is a thicker core of white matter • The diencephalon lies beneath the cerebral hemispheres and has two main structures ¾ the thalamus and the hypothalamus. The walnut-sized thalamus is a large mass of gray matter that lies on either side of the third ventricle. The thalamus is a great relay station on the afferent sen - sory pathway to the cerebral cortex. The tiny hypothalamus forms the lower part of the lateral wall and floor of the third ventricle. The hypothalamus exerts an influence on a wide range of body functions. • The cerebellum is attached to the brain and features a highly folded surface. It is important in the control of movement and balance. • The brainstem is the lower extension of the brain where it connects to the spinal cord.
    [Show full text]
  • Motor Systems Basal Ganglia
    Motor systems 409 Basal Ganglia You have just read about the different motor-related cortical areas. Premotor areas are involved in planning, while MI is involved in execution. What you don’t know is that the cortical areas involved in movement control need “help” from other brain circuits in order to smoothly orchestrate motor behaviors. One of these circuits involves a group of structures deep in the brain called the basal ganglia. While their exact motor function is still debated, the basal ganglia clearly regulate movement. Without information from the basal ganglia, the cortex is unable to properly direct motor control, and the deficits seen in Parkinson’s and Huntington’s disease and related movement disorders become apparent. Let’s start with the anatomy of the basal ganglia. The important “players” are identified in the adjacent figure. The caudate and putamen have similar functions, and we will consider them as one in this discussion. Together the caudate and putamen are called the neostriatum or simply striatum. All input to the basal ganglia circuit comes via the striatum. This input comes mainly from motor cortical areas. Notice that the caudate (L. tail) appears twice in many frontal brain sections. This is because the caudate curves around with the lateral ventricle. The head of the caudate is most anterior. It gives rise to a body whose “tail” extends with the ventricle into the temporal lobe (the “ball” at the end of the tail is the amygdala, whose limbic functions you will learn about later). Medial to the putamen is the globus pallidus (GP).
    [Show full text]
  • Thalamus.Pdf
    Thalamus 583 THALAMUS This lecture will focus on the thalamus, a subdivision of the diencephalon. The diencephalon can be divided into four areas, which are interposed between the brain stem and cerebral hemispheres. The four subdivisions include the hypothalamus to be discussed in a separate lecture, the ventral thalamus containing the subthalamic nucleus already discussed, the epithalamus which is made up mostly of the pineal body, and the dorsal thalamus (henceforth referred to as the thalamus) which is the focus of this lecture. Although we will not spend any time in lecture on the pineal body, part of the epithalamus, it does have some interesting features as well as some clinical relevance. The pineal is a small midline mass of glandular tissue that secretes the hormone melatonin. In lower mammals, melatonin plays a central role in control of diurnal rhythms (cycles in body states and hormone levels that follow the day- night cycle). In humans, at least a portion of the control of diurnal rhythms has been taken over by the hypothalamus, but there is increasing evidence that the pineal and melatonin play at least a limited role. Recent investigations have demonstrated a role for melatonin in sleep, tumor reduction and aging. Additionally, based on the observation that tumors of the pineal can induce a precocious puberty in males it has been suggested that the pineal is also involved in timing the onset of puberty. In many individuals the pineal is partially calcified and can serve as a marker for the midline of the brain on x- rays. Pathological processes can sometimes be detected by a shift in its position.
    [Show full text]