1. 2. A) Explain the Compositions of White Matter and Gray
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Neural Control of Movement: Motor Neuron Subtypes, Proprioception and Recurrent Inhibition
List of Papers This thesis is based on the following papers, which are referred to in the text by their Roman numerals. I Enjin A, Rabe N, Nakanishi ST, Vallstedt A, Gezelius H, Mem- ic F, Lind M, Hjalt T, Tourtellotte WG, Bruder C, Eichele G, Whelan PJ, Kullander K (2010) Identification of novel spinal cholinergic genetic subtypes disclose Chodl and Pitx2 as mark- ers for fast motor neurons and partition cells. J Comp Neurol 518:2284-2304. II Wootz H, Enjin A, Wallen-Mackenzie Å, Lindholm D, Kul- lander K (2010) Reduced VGLUT2 expression increases motor neuron viability in Sod1G93A mice. Neurobiol Dis 37:58-66 III Enjin A, Leao KE, Mikulovic S, Le Merre P, Tourtellotte WG, Kullander K. 5-ht1d marks gamma motor neurons and regulates development of sensorimotor connections Manuscript IV Enjin A, Leao KE, Eriksson A, Larhammar M, Gezelius H, Lamotte d’Incamps B, Nagaraja C, Kullander K. Development of spinal motor circuits in the absence of VIAAT-mediated Renshaw cell signaling Manuscript Reprints were made with permission from the respective publishers. Cover illustration Carousel by Sasha Svensson Contents Introduction.....................................................................................................9 Background...................................................................................................11 Neural control of movement.....................................................................11 The motor neuron.....................................................................................12 Organization -
Innovations Present in the Primate Interneuron Repertoire
Article Innovations present in the primate interneuron repertoire https://doi.org/10.1038/s41586-020-2781-z Fenna M. Krienen1,2 ✉, Melissa Goldman1,2, Qiangge Zhang2,3, Ricardo C. H. del Rosario2, Marta Florio1,2, Robert Machold4, Arpiar Saunders1,2, Kirsten Levandowski2,3, Heather Zaniewski2,3, Received: 19 July 2019 Benjamin Schuman4, Carolyn Wu3, Alyssa Lutservitz1,2, Christopher D. Mullally1,2, Nora Reed1,2, Accepted: 1 July 2020 Elizabeth Bien1,2, Laura Bortolin1,2, Marian Fernandez-Otero2,5, Jessica D. Lin2, Alec Wysoker2, James Nemesh2, David Kulp2, Monika Burns5, Victor Tkachev6,7,8, Richard Smith9,10, Published online: xx xx xxxx Christopher A. Walsh9,10, Jordane Dimidschstein2, Bernardo Rudy4,11, Leslie S. Kean6,7,8, Check for updates Sabina Berretta5,12,13, Gord Fishell2,14, Guoping Feng2,3 & Steven A. McCarroll1,2 ✉ Primates and rodents, which descended from a common ancestor around 90 million years ago1, exhibit profound diferences in behaviour and cognitive capacity; the cellular basis for these diferences is unknown. Here we use single-nucleus RNA sequencing to profle RNA expression in 188,776 individual interneurons across homologous brain regions from three primates (human, macaque and marmoset), a rodent (mouse) and a weasel (ferret). Homologous interneuron types—which were readily identifed by their RNA-expression patterns—varied in abundance and RNA expression among ferrets, mice and primates, but varied less among primates. Only a modest fraction of the genes identifed as ‘markers’ of specifc interneuron subtypes in any one species had this property in another species. In the primate neocortex, dozens of genes showed spatial expression gradients among interneurons of the same type, which suggests that regional variation in cortical contexts shapes the RNA expression patterns of adult neocortical interneurons. -
Spinal Cord Organization
Lecture 4 Spinal Cord Organization The spinal cord . Afferent tract • connects with spinal nerves, through afferent BRAIN neuron & efferent axons in spinal roots; reflex receptor interneuron • communicates with the brain, by means of cell ascending and descending pathways that body form tracts in spinal white matter; and white matter muscle • gives rise to spinal reflexes, pre-determined gray matter Efferent neuron by interneuronal circuits. Spinal Cord Section Gross anatomy of the spinal cord: The spinal cord is a cylinder of CNS. The spinal cord exhibits subtle cervical and lumbar (lumbosacral) enlargements produced by extra neurons in segments that innervate limbs. The region of spinal cord caudal to the lumbar enlargement is conus medullaris. Caudal to this, a terminal filament of (nonfunctional) glial tissue extends into the tail. terminal filament lumbar enlargement conus medullaris cervical enlargement A spinal cord segment = a portion of spinal cord that spinal ganglion gives rise to a pair (right & left) of spinal nerves. Each spinal dorsal nerve is attached to the spinal cord by means of dorsal and spinal ventral roots composed of rootlets. Spinal segments, spinal root (rootlets) nerve roots, and spinal nerves are all identified numerically by th region, e.g., 6 cervical (C6) spinal segment. ventral Sacral and caudal spinal roots (surrounding the conus root medullaris and terminal filament and streaming caudally to (rootlets) reach corresponding intervertebral foramina) collectively constitute the cauda equina. Both the spinal cord (CNS) and spinal roots (PNS) are enveloped by meninges within the vertebral canal. Spinal nerves (which are formed in intervertebral foramina) are covered by connective tissue (epineurium, perineurium, & endoneurium) rather than meninges. -
White Matter Tracts - Brain A143 (1)
WHITE MATTER TRACTS - BRAIN A143 (1) White Matter Tracts Last updated: August 8, 2020 CORTICOSPINAL TRACT .......................................................................................................................... 1 ANATOMY .............................................................................................................................................. 1 FUNCTION ............................................................................................................................................. 1 UNCINATE FASCICULUS ........................................................................................................................... 1 ANATOMY .............................................................................................................................................. 1 DTI PROTOCOL ...................................................................................................................................... 4 FUNCTION .............................................................................................................................................. 4 DEVELOPMENT ....................................................................................................................................... 4 CLINICAL SIGNIFICANCE ........................................................................................................................ 4 ARTICLES .............................................................................................................................................. -
Memory Loss from a Subcortical White Matter Infarct
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.51.6.866 on 1 June 1988. Downloaded from Journal of Neurology, Neurosurgery, and Psychiatry 1988;51:866-869 Short report Memory loss from a subcortical white matter infarct CAROL A KOOISTRA, KENNETH M HEILMAN From the Department ofNeurology, College ofMedicine, University ofFlorida, and the Research Service, Veterans Administration Medical Center, Gainesville, FL, USA SUMMARY Clinical disorders of memory are believed to occur from the dysfunction of either the mesial temporal lobe, the mesial thalamus, or the basal forebrain. Fibre tract damage at the level of the fornix has only inconsistently produced amnesia. A patient is reported who suffered a cerebro- vascular accident involving the posterior limb of the left internal capsule that resulted in a persistent and severe disorder of verbal memory. The inferior extent of the lesion effectively disconnected the mesial thalamus from the amygdala and the frontal cortex by disrupting the ventral amygdalofugal and thalamic-frontal pathways as they course through the diencephalon. This case demonstrates that an isolated lesion may cause memory loss without involvement of traditional structures associated with memory and may explain memory disturbances in other white matter disease such as multiple sclerosis and lacunar state. Protected by copyright. Memory loss is currently believed to reflect grey day of his illness the patient was transferred to Shands matter damage of either the mesial temporal lobe,' -4 Teaching Hospital at the University of Florida for further the mesial or the basal forebrain.'0 l evaluation. thalamus,5-9 Examination at that time showed the patient to be awake, Cerebrovascular accidents resulting in memory dys- alert, attentive and fully oriented. -
White Matter Dissection and Structural Connectivity of the Human Vertical
www.nature.com/scientificreports OPEN White matter dissection and structural connectivity of the human vertical occipital fasciculus to link vision-associated brain cortex Tatsuya Jitsuishi1, Seiichiro Hirono2, Tatsuya Yamamoto1,3, Keiko Kitajo1, Yasuo Iwadate2 & Atsushi Yamaguchi1* The vertical occipital fasciculus (VOF) is an association fber tract coursing vertically at the posterolateral corner of the brain. It is re-evaluated as a major fber tract to link the dorsal and ventral visual stream. Although previous tractography studies showed the VOF’s cortical projections fall in the dorsal and ventral visual areas, the post-mortem dissection study for the validation remains limited. First, to validate the previous tractography data, we here performed the white matter dissection in post-mortem brains and demonstrated the VOF’s fber bundles coursing between the V3A/B areas and the posterior fusiform gyrus. Secondly, we analyzed the VOF’s structural connectivity with difusion tractography to link vision-associated cortical areas of the HCP MMP1.0 atlas, an updated map of the human cerebral cortex. Based on the criteria the VOF courses laterally to the inferior longitudinal fasciculus (ILF) and craniocaudally at the posterolateral corner of the brain, we reconstructed the VOF’s fber tracts and found the widespread projections to the visual cortex. These fndings could suggest a crucial role of VOF in integrating visual information to link the broad visual cortex as well as in connecting the dual visual stream. Te VOF is the fber tract that courses vertically at the posterolateral corner of the brain. Te VOF was histori- cally described in monkey by Wernicke1 and then in human by Obersteiner2. -
Cortex Brainstem Spinal Cord Thalamus Cerebellum Basal Ganglia
Harvard-MIT Division of Health Sciences and Technology HST.131: Introduction to Neuroscience Course Director: Dr. David Corey Motor Systems I 1 Emad Eskandar, MD Motor Systems I - Muscles & Spinal Cord Introduction Normal motor function requires the coordination of multiple inter-elated areas of the CNS. Understanding the contributions of these areas to generating movements and the disturbances that arise from their pathology are important challenges for the clinician and the scientist. Despite the importance of diseases that cause disorders of movement, the precise function of many of these areas is not completely clear. The main constituents of the motor system are the cortex, basal ganglia, cerebellum, brainstem, and spinal cord. Cortex Basal Ganglia Cerebellum Thalamus Brainstem Spinal Cord In very broad terms, cortical motor areas initiate voluntary movements. The cortex projects to the spinal cord directly, through the corticospinal tract - also known as the pyramidal tract, or indirectly through relay areas in the brain stem. The cortical output is modified by two parallel but separate re entrant side loops. One loop involves the basal ganglia while the other loop involves the cerebellum. The final outputs for the entire system are the alpha motor neurons of the spinal cord, also called the Lower Motor Neurons. Cortex: Planning and initiation of voluntary movements and integration of inputs from other brain areas. Basal Ganglia: Enforcement of desired movements and suppression of undesired movements. Cerebellum: Timing and precision of fine movements, adjusting ongoing movements, motor learning of skilled tasks Brain Stem: Control of balance and posture, coordination of head, neck and eye movements, motor outflow of cranial nerves Spinal Cord: Spontaneous reflexes, rhythmic movements, motor outflow to body. -
Intersegmental Interneurons Can Control the Gain of Reflexes in Adjacent Segments of the Locust by Their Action on Nonspiking Local Interneurons
The Journal of Neuroscience, September 1989, g(9): 30303039 Intersegmental Interneurons Can Control the Gain of Reflexes in Adjacent Segments of the Locust by Their Action on Nonspiking Local Interneurons Gilles Laurent and Malcolm Burrows Department of Zoology, University of Cambridge, Cambridge CB2 3EJ, England The gain of local reflexes of one leg of a locust can be altered partmentalized, with synaptic inputs and their associated by mechanosensory inputs generated by movements of or conductance changes restricted to particular branches. In tactile inputs to an adjacent leg. Touching the mesothoracic this way, an individual nonspiking neuron could contribute tarsus, for example, increases the number of spikes that are simultaneously to several local circuits. The inputs from dif- produced by the metathoracic slow extensor tibiae motor ferent intersegmental interneurons could then modulate these neuron and enhances the depolarization of flexor tibiae mo- pathways independently. tor neuron in response to imposed movements of the chor- dotonal organ in the ipsilateral hind femur. The sensory in- Nonspiking interneurons in the metathoracic ganglion of the formation from the middle leg is conveyed directly to locust receive direct inputs from mechanosensory afferents on nonspiking interneurons and motor neurons controlling the one hindleg and are essential elements in local reflex movements movements of the hindleg by a population of mesothoracic of that leg (Laurent and Burrows, 1988; Burrows et al., 1988). intersegmental interneurons (Laurent and Burrows, 1989). They also receive direct inputs from intersegmental intemeu- The metathoracic nonspiking interneurons receive direct in- rons that process the mechanosensory inputs from an ipsilateral puts from receptors on a hindleg and are, therefore, a point middle leg (Laurent and Burrows, 1989). -
The Nomenclature of Human White Matter Association Pathways: Proposal for a Systematic Taxonomic Anatomical Classification
The Nomenclature of Human White Matter Association Pathways: Proposal for a Systematic Taxonomic Anatomical Classification Emmanuel Mandonnet, Silvio Sarubbo, Laurent Petit To cite this version: Emmanuel Mandonnet, Silvio Sarubbo, Laurent Petit. The Nomenclature of Human White Matter Association Pathways: Proposal for a Systematic Taxonomic Anatomical Classification. Frontiers in Neuroanatomy, Frontiers, 2018, 12, pp.94. 10.3389/fnana.2018.00094. hal-01929504 HAL Id: hal-01929504 https://hal.archives-ouvertes.fr/hal-01929504 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: 06 November 2018 doi: 10.3389/fnana.2018.00094 The Nomenclature of Human White Matter Association Pathways: Proposal for a Systematic Taxonomic Anatomical Classification Emmanuel Mandonnet 1* †, Silvio Sarubbo 2† and Laurent Petit 3* 1Department of Neurosurgery, Lariboisière Hospital, Paris, France, 2Division of Neurosurgery, Structural and Functional Connectivity Lab, Azienda Provinciale per i Servizi Sanitari (APSS), Trento, Italy, 3Groupe d’Imagerie Neurofonctionnelle, Institut des Maladies Neurodégénératives—UMR 5293, CNRS, CEA University of Bordeaux, Bordeaux, France The heterogeneity and complexity of white matter (WM) pathways of the human brain were discretely described by pioneers such as Willis, Stenon, Malpighi, Vieussens and Vicq d’Azyr up to the beginning of the 19th century. -
Neuroanatomy
Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Neuroanatomy W. Jeffrey Wilson Fall 2012 \Without education we are in a horrible and deadly danger of taking educated people seriously." { Gilbert Keith Chesterton [LATEX in use { a Microsoft- & PowerPoint-free presentation] Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Blood-Brain Barrier Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Peripheral Nervous System • Somatic N.S.: skeletal muscles, skin, joints • Autonomic N.S.: internal organs, glands • Sympathetic N.S.: rapid expenditure of energy • Parasympathetic N.S.: restoration of energy Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Spinal Cord Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain | Ventricles Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain Midline Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Brain Midline Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Hindbrain Myelencephalon & Metencephalon Outline Protection Peripheral Nervous System Overview of Brain Hindbrain Midbrain Forebrain Reticular -
Spinal Reflexes
Spinal Reflexes Lu Chen, Ph.D. MCB, UC Berkeley 1 Simple reflexes such as stretch reflex require coordinated contraction and relaxation of different muscle groups Categories of Muscle Based on Direction of Motion Flexors Æ reduce the angle of joints Extensors Æ increase the angle of joints Categories of Muscle Based on Movement Agonist Æmuscle that serves to move the joint in the same direction as the studied muscle Antagonist Æ muscle that moves the joint in the opposite direction 2 1 Muscle Spindles •Small encapsulated sensory receptors that have a Intrafusal muscle spindle-like shape and are located within the fibers fleshy part of the muscle •In parallel with the muscle fibers capsule •Does not contribute to the overall contractile Sensory force endings •Mechanoreceptors are activated by stretch of the central region Afferent axons •Due to stretch of the whole muscle Efferent axons (including intrafusal f.) •Due to contraction of the polar regions of Gamma motor the intrafusal fibers endings 3 Muscle Spindles Organization 2 kinds of intrafusal muscle fibers •Nuclear bag fibers (2-3) •Dynamic •Static •Nuclear chain fibers (~5) •Static 2 types of sensory fibers •Ia (primary) - central region of all intrafusal fibers •II (secondary) - adjacent to the central region of static nuclear bag fibers and nuclear chain fibers Intrafusal fibers stretched Sensory ending stretched, (loading the spindle) increase firing Muscle fibers lengthens Sensory ending stretched, (stretched) increase firing Spindle unloaded, Muscle fiber shortens decrease firing 4 2 Muscle Spindles Organization Gamma motor neurons innervate the intrafusal muscle fibers. Activation of Shortening of the polar regions gamma neurons of the intrafusal fibers Stretches the noncontractile Increase firing of the center regions sensory endings Therefore, the gamma motor neurons provide a mechanism for adjusting the sensitivity of the muscle spindles. -
Retinal Inputs Signal Astrocytes to Recruit Interneurons Into Visual Thalamus
Retinal inputs signal astrocytes to recruit interneurons into visual thalamus Jianmin Sua,1, Naomi E. Charalambakisb,1, Ubadah Sabbagha,c, Rachana D. Somaiyaa,c, Aboozar Monavarfeshania,d, William Guidob,2, and Michael A. Foxa,d,e,2 aCenter for Neurobiology Research, Fralin Biomedical Research Institute at Virginia Tech Carilion, Roanoke, VA 24016; bDepartment of Anatomical Sciences and Neurobiology, University of Louisville School of Medicine, Louisville, KY 40202; cGraduate Program in Translational Biology, Medicine, and Health, Virginia Tech, Blacksburg, VA 24061; dDepartment of Biological Sciences, Virginia Tech, Blacksburg, VA 24061; and eDepartment of Pediatrics, Virginia Tech Carilion School of Medicine, Roanoke, VA 24016 Edited by Carol Ann Mason, Columbia University, New York, NY, and approved December 24, 2019 (received for review July 29, 2019) Inhibitory interneurons comprise a fraction of the total neurons in collection of cell types based on their distribution, gene and the visual thalamus but are essential for sharpening receptive field neurochemical expression, and projection patterns (5–7, 25). properties and improving contrast-gain of retinogeniculate trans- Despite the presence of GABAergic interneurons in the visual mission. During early development, these interneurons undergo thalamus of the adult mouse, these cells are largely absent at long-range migration from germinal zones, a process regulated by birth when RGC axons innervate these nuclei (12). Also lacking the innervation of the visual thalamus by retinal ganglion cells. from the visual thalamus at these early ages are nonretinal inputs Here, using transcriptomic approaches, we identified a motogenic that arise from the neocortex, brainstem, and the thalamic re- cue, fibroblast growth factor 15 (FGF15), whose expression in the ticular nucleus.