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NS201C Anatomy 1: Sensory and Motor Systems
NS201C Anatomy 1: Sensory and Motor Systems 25th January 2017 Peter Ohara Department of Anatomy [email protected] The Subdivisions and Components of the Central Nervous System Axes and Anatomical Planes of Sections of the Human and Rat Brain Development of the neural tube 1 Dorsal and ventral cell groups Dermatomes and myotomes Neural crest derivatives: 1 Neural crest derivatives: 2 Development of the neural tube 2 Timing of development of the neural tube and its derivatives Timing of development of the neural tube and its derivatives Gestational Crown-rump Structure(s) age (Weeks) length (mm) 3 3 cerebral vesicles 4 4 Optic cup, otic placode (future internal ear) 5 6 cerebral vesicles, cranial nerve nuclei 6 12 Cranial and cervical flexures, rhombic lips (future cerebellum) 7 17 Thalamus, hypothalamus, internal capsule, basal ganglia Hippocampus, fornix, olfactory bulb, longitudinal fissure that 8 30 separates the hemispheres 10 53 First callosal fibers cross the midline, early cerebellum 12 80 Major expansion of the cerebral cortex 16 134 Olfactory connections established 20 185 Gyral and sulcul patterns of the cerebral cortex established Clinical case A 68 year old woman with hypertension and diabetes develops abrupt onset numbness and tingling on the right half of the face and head and the entire right hemitrunk, right arm and right leg. She does not experience any weakness or incoordination. Physical Examination: Vitals: T 37.0° C; BP 168/87; P 86; RR 16 Cardiovascular, pulmonary, and abdominal exam are within normal limits. Neurological Examination: Mental Status: Alert and oriented x 3, 3/3 recall in 3 minutes, language fluent. -
Spinal Tracts.Pdf
Spinal Tracts Andreas Talgø Lie Illustrations by: Peder Olai Skjeflo Holman Previous material: Maja Solbakken Definitions to bring home Nerve Ganglion Neuron Nucleus Tract Collection neurons Collection of nerve A single cell Collection of Collection of axons that transmits cell bodies in the transmitting nerve cell bodies in traveling up or sensation or motor PNS, typically linked electrical impluses. the CNS, typically down the spinal impulses depending by synapses. linked by synapses. cord, depending on the function and Location: both on function destination. Location: PNS Location: CNS and destination. Location: PNS Location: CNS - does it matter? Tract - highway to pass anatomy exam? • Highway = Tract • Lane = Neuron • Car = Signal Slow... Fast!! Just to make sure... • Ipsilateral or contralateral • Ventral = anterior • Dorsal = posterior High yield points to understand • What does the tract transmit - Motor or sensory? If sensory: which sensation? • Where does the neurones synapse - 1.st, 2nd and 3rd order neron? Which ganglion/nuclei? • Where there are decussations - If there are any decussations at all? ASCENDING / SENSORY TRACTS Sensations * Temperature NOT transmitted by the tracts: * Pressure * Visualization * Pain * Audition * Fine touch * Olfaction * Crude touch * Gustation * Proprioception * Vibration Sensations Precise sensation Primitive sensation Fine touch Crude touch Pressure Pain Vibration Temperature Proprioception Other: sexual, itching, tickling Ascending tracts / Sensory tracts Dorsal coulmn Lat. Spinothalamic Ant. -
Basal Ganglia & Cerebellum
1/2/2019 This power point is made available as an educational resource or study aid for your use only. This presentation may not be duplicated for others and should not be redistributed or posted anywhere on the internet or on any personal websites. Your use of this resource is with the acknowledgment and acceptance of those restrictions. Basal Ganglia & Cerebellum – a quick overview MHD-Neuroanatomy – Neuroscience Block Gregory Gruener, MD, MBA, MHPE Vice Dean for Education, SSOM Professor, Department of Neurology LUHS a member of Trinity Health Outcomes you want to accomplish Basal ganglia review Define and identify the major divisions of the basal ganglia List the major basal ganglia functional loops and roles List the components of the basal ganglia functional “circuitry” and associated neurotransmitters Describe the direct and indirect motor pathways and relevance/role of the substantia nigra compacta 1 1/2/2019 Basal Ganglia Terminology Striatum Caudate nucleus Nucleus accumbens Putamen Globus pallidus (pallidum) internal segment (GPi) external segment (GPe) Subthalamic nucleus Substantia nigra compact part (SNc) reticular part (SNr) Basal ganglia “circuitry” • BG have no major outputs to LMNs – Influence LMNs via the cerebral cortex • Input to striatum from cortex is excitatory – Glutamate is the neurotransmitter • Principal output from BG is via GPi + SNr – Output to thalamus, GABA is the neurotransmitter • Thalamocortical projections are excitatory – Concerned with motor “intention” • Balance of excitatory & inhibitory inputs to striatum, determine whether thalamus is suppressed BG circuits are parallel loops • Motor loop – Concerned with learned movements • Cognitive loop – Concerned with motor “intention” • Limbic loop – Emotional aspects of movements • Oculomotor loop – Concerned with voluntary saccades (fast eye-movements) 2 1/2/2019 Basal ganglia “circuitry” Cortex Striatum Thalamus GPi + SNr Nolte. -
Facial Sensory Symptoms in Medullary Infarcts
Arq Neuropsiquiatr 2005;63(4):946-950 FACIAL SENSORY SYMPTOMS IN MEDULLARY INFARCTS Adriana Bastos Conforto1, Fábio Iuji Yamamoto1, Cláudia da Costa Leite2, Milberto Scaff1, Suely Kazue Nagahashi Marie1 ABSTRACT - Objective: To investigate the correlation between facial sensory abnormalities and lesional topography in eight patients with lateral medullary infarcts (LMIs). Method: We reviewed eight sequen- tial cases of LMIs admitted to the Neurology Division of Hospital das Clínicas/ São Paulo University between J u l y, 2001 and August, 2002 except for one patient who had admitted in 1996 and was still followed in 2002. All patients were submitted to conventional brain MRI including axial T1-, T2-weighted and Fluid attenuated inversion-re c o v e ry (FLAIR) sequences. MRIs were evaluated blindly to clinical features to deter- mine extension of the infarct to presumed topographies of the ventral trigeminothalamic (VTT), lateral spinothalamic, spinal trigeminal tracts and spinal trigeminal nucleus. Results:S e n s o ry symptoms or signs w e re ipsilateral to the bulbar infarct in 3 patients, contralateral in 4 and bilateral in 1. In all of our cases with exclusive contralateral facial sensory symptoms, infarcts had medial extensions that included the VTT t o p o g r a p h y. In cases with exclusive ipsilateral facial sensory abnormalities, infarcts affected lateral and posterior bulbar portions, with slight or no medial extension. The only patient who presented bilateral facial symptoms had an infarct that covered both medial and lateral, in addition to the posterior re g i o n of the medulla. Conclusion: Our results show a correlation between medial extension of LMIs and pres- ence of contralateral facial sensory symptoms. -
The Brain Stem Medulla Oblongata
Chapter 14 The Brain Stem Medulla Oblongata Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Central sulcus Parietal lobe • embryonic myelencephalon becomes Cingulate gyrus leaves medulla oblongata Corpus callosum Parieto–occipital sulcus Frontal lobe Occipital lobe • begins at foramen magnum of the skull Thalamus Habenula Anterior Epithalamus commissure Pineal gland • extends for about 3 cm rostrally and ends Hypothalamus Posterior commissure at a groove between the medulla and Optic chiasm Mammillary body pons Cerebral aqueduct Pituitary gland Fourth ventricle Temporal lobe • slightly wider than spinal cord Cerebellum Midbrain • pyramids – pair of external ridges on Pons Medulla anterior surface oblongata – resembles side-by-side baseball bats (a) • olive – a prominent bulge lateral to each pyramid • posteriorly, gracile and cuneate fasciculi of the spinal cord continue as two pair of ridges on the medulla • all nerve fibers connecting the brain to the spinal cord pass through the medulla • four pairs of cranial nerves begin or end in medulla - IX, X, XI, XII Medulla Oblongata Associated Functions • cardiac center – adjusts rate and force of heart • vasomotor center – adjusts blood vessel diameter • respiratory centers – control rate and depth of breathing • reflex centers – for coughing, sneezing, gagging, swallowing, vomiting, salivation, sweating, movements of tongue and head Medulla Oblongata Nucleus of hypoglossal nerve Fourth ventricle Gracile nucleus Nucleus of Cuneate nucleus vagus -
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. -
Interneuronal Activity in Reflex Pathways from Group II Muscle Afferents Is Monitored by Dorsal Spinocerebellar Tract Neurons in the Cat
The Journal of Neuroscience, April 2, 2008 • 28(14):3615–3622 • 3615 Behavioral/Systems/Cognitive Interneuronal Activity in Reflex Pathways from Group II Muscle Afferents Is Monitored by Dorsal Spinocerebellar Tract Neurons in the Cat Elzbieta Jankowska and Anna Puczynska Department of Physiology, Sahlgrenska Academy, Go¨teborg University, 405 30 Go¨teborg, Sweden The main aim of the study was to investigate whether group II muscle afferents contribute to the inhibition of dorsal spinocerebellar tract (DSCT) neurons and thereby modulate information provided by these neurons in the cat. In intracellular recordings, we found disynaptic IPSPs from group II afferents in the majority of DSCT neurons, most often in parallel with IPSPs evoked from group I afferents. In an attempt to identify interneurons that mediate these IPSPs, the second aim of the study, laminas IV–VII in midlumbar segments were searched for interneurons antidromically activated by stimuli applied within Clarke’s column. Such interneurons were found in regions in which focal field potentials were evoked by group I and II afferents, or ventral to them, and most were coexcited by these afferents. The input to these interneurons and their location indicate that they belonged to the previously identified population of premotor interneu- rons in disynaptic pathways between group I and II afferents and hindlimb motoneurons. The study leads thus to the conclusion that inhibitory actions of group II afferents on DSCT neurons are collateral to actions on motoneurons and that DSCT neurons monitor inhibitory actions of group II afferents on motoneurons as closely as they monitor actions of group I afferents. -
The Nervous System: Sensory and Motor Tracts of the Spinal Cord
15 The Nervous System: Sensory and Motor Tracts of the Spinal Cord PowerPoint® Lecture Presentations prepared by Steven Bassett Southeast Community College Lincoln, Nebraska © 2012 Pearson Education, Inc. Introduction • Millions of sensory neurons are delivering information to the CNS all the time • Millions of motor neurons are causing the body to respond in a variety of ways • Sensory and motor neurons travel by different tracts within the spinal cord © 2012 Pearson Education, Inc. Sensory and Motor Tracts • Communication to and from the brain involves tracts • Ascending tracts are sensory • Deliver information to the brain • Descending tracts are motor • Deliver information to the periphery © 2012 Pearson Education, Inc. Sensory and Motor Tracts • Naming the tracts • If the tract name begins with “spino” (as in spinocerebellar), the tract is a sensory tract delivering information from the spinal cord to the cerebellum (in this case) • If the tract name ends with “spinal” (as in vestibulospinal), the tract is a motor tract that delivers information from the vestibular apparatus (in this case) to the spinal cord © 2012 Pearson Education, Inc. Sensory and Motor Tracts • There are three major sensory tracts • The posterior column tract • The spinothalamic tract • The spinocerebellar tract © 2012 Pearson Education, Inc. Sensory and Motor Tracts • The three major sensory tracts involve chains of neurons • First-order neuron • Delivers sensations to the CNS • The cell body is in the dorsal or cranial root ganglion • Second-order neuron • An interneuron with the cell body in the spinal cord or brain • Third-order neuron • Transmits information from the thalamus to the cerebral cortex © 2012 Pearson Education, Inc. -
Spinal Tracts Summary Tables.P
1.Spinothalamic 2.Dorsal Column/Medial Leminscal 3.Spinocerebellar Name Function Origin Ending Location in Cord Spinothalamic Sharp pain, Skin 1st order terminates in Ventral and Tract crude touch and Dorsal Gray Column, Lateral Column temperature 2nd order decussates in spinal cord close to entry level and projects to contralateral VPL nucleus of thalamus, 3rd order projects to sensorimotor cortex Dorsal Fine touch, Skin, 1st order ascends spine Dorsal Column Column/Medial conscious joints, on ipsilateral side and Lemniscal proprioception, tendons terminates in two point brainstem nuclei, 2nd discrimination order decussate and project to the VPL of thalamus, 3rd order neurons project to sensorimotor cortex System Function Origin Ending Location in Cord Spinocerebellar Unconscious Muscle spindle 1st order neurons Lateral Tract proprioception cells, Golgi tendon synapse in spinal Column organs, touch and cord, 2nd order pressure receptors neurons ascend on the ipsilateral side and project to the cerebellar cortex 1.Corticospinal 2.Extrapyramidal System Function Origin Ending Location in Cord Lateral Fine motor Motor and pre- Motor neurons Lateral column Corticospinal function (distal motor cortex of ventral grey Decussates in Tract musculature) column pyramids of medulla Anterior Gross and Motor and pre- Motor neurons Anterior column Corticospinal postural motor motor cortex of ventral grey Decussates after Tract function column the fibres has (proximal and descended axial musculature) System Function Origin Ending Location in Cord Rubrospinal -
The Role of Neuromodulation Techniques for Management Of
Research Article iMedPub Journals 2018 www.imedpub.com Journal of Anaesthesiology and Critical Care Vol.1 No.2:9 The Role of Neuromodulation Techniques Enrique Latorre Marques* for Management of Back Pain Based on Department of Anesthesiology, "Miguel Servet" Hospital, School of Medicine, Scientific Evidence University of Zaragoza, Spain *Corresponding author: Enrique Latorre Marques Abstract Background: Low back pain (LBP) is characterized for its prevalence, great [email protected] [email protected] variability, high rates of disability and costs. Chronic Low Back Pain (CLBP) has excessive rate of surgery. Evidence based studies demonstrates only few Head of Pain Clinic, Department of techniques are cost-effective and many others dangerous. CLBP may originate in Anesthesiology, "Miguel Servet" Hospital, dysfunctional nociceptive processing within the central nervous system for that School of Medicine, University of Zaragoza, Neuromodulation offers emergent possibilities. Neuromodulation is reversible, Spain. adjustable, less invasive avoiding surgery and providing functional recovery. The cost is significantly lower and Quality of life clearly better than conventional pain Tel: +976 76 53 00 therapy. The International Association for the study of pain (IASP) and the Special Interest Group on Neuromodulation (SIGN) is the leading forum for science to design therapeutic algorithms for back and neuropathic pain. Citation: Marques EL (2018) The Role Objectives: This Comprehensive Review explains concepts, epidemiology, cost, of Neuromodulation Techniques for indications and types of Neuromodulation on management of LBP and radiating Management of Back Pain Based on pain. Scientific Evidence. J Anaesthesiol Crit Care Vol.1 No.2:9 Methods: A comprehensive review of literature: Clinical Guidelines, IASP sources, SIGN policies, focused on chronic low back pain (CLBP) and Failed Back Surgery Syndrome (FBSS). -
Spinal Cord Stimulation: the Use of Neuromodulation for Treatment of Chronic Pain
PAIN MANAGEMENT IN REHABILITATION Spinal Cord Stimulation: The Use of Neuromodulation for Treatment of Chronic Pain ALEX HAN, BA, MD'21; ALEXIOS G. CARAYANNOPOULOS, DO, MPH, FAAPMR, FAAOE, FFSMB 23 26 EN KEYWORDS: neuromodulation, spinal cord stimulation, all neuromodulation treatments. The valuation of the SCS chronic pain, neuropathic pain marketplace was $1.3 billion in 2014.7 Spinal Cord Stimulation and Mechanisms of Action Spinal cord stimulation (SCS) involves the application of electricity to the spinal dorsal columns, which modulate INTRODUCTION pain signals relayed by ascending pain pathways to the Chronic Pain and the Role of Neuromodulation brain. Although precise mechanisms are complex and not Chronic pain, defined as pain persistent for more than 3–6 fully understood, the concept derives from the gate control months, affects 100 million adults in the United States (US) theory, first described by Melzack and Wall.8 This theory and impacts all dimensions of health-related quality of life describes the presence of a “gate” in the dorsal horn, relay- (QOL) and healthcare expenditures.1 Low back pain is the ing neuronal signals from sensory afferent fibers to brain leading cause of disability, with healthcare expenditures centers involved in pain perception. Ab fibers (myelinated) estimated to be as much as $560–$635 billion, more than the carrying non-nociceptive stimuli and C fibers (non-myelin- combined spending on heart disease and diabetes.1 Despite ated) relaying painful stimuli both synapse in the dorsal lack of consistent evidence, rates of spine surgeries have horn with the spinothalamic tract; the gate theory postu- increased, while other forms of chronic pain management, lates that stimulating the faster Ab fibers leads to closure of including narcotics, contribute to both adverse medical side nerve “gates,” blocking the transmission of pain signals by effects and the ongoing opioid epidemic.2 slower C fibers Figure( 1). -
White Matter Anatomy: What the Radiologist Needs to Know
White Matter Anatomy What the Radiologist Needs to Know Victor Wycoco, MBBS, FRANZCRa, Manohar Shroff, MD, DABR, FRCPCa,*, Sniya Sudhakar, MBBS, DNB, MDb, Wayne Lee, MSca KEYWORDS Diffusion tensor imaging (DTI) White matter tracts Projection fibers Association Fibers Commissural fibers KEY POINTS Diffusion tensor imaging (DTI) has emerged as an excellent tool for in vivo demonstration of white matter microstructure and has revolutionized our understanding of the same. Information on normal connectivity and relations of different white matter networks and their role in different disease conditions is still evolving. Evidence is mounting on causal relations of abnormal white matter microstructure and connectivity in a wide range of pediatric neurocognitive and white matter diseases. Hence there is a pressing need for every neuroradiologist to acquire a strong basic knowledge of white matter anatomy and to make an effort to apply this knowledge in routine reporting. INTRODUCTION (Fig. 1). However, the use of specific DTI sequences provides far more detailed and clini- DTI has allowed in vivo demonstration of axonal cally useful information. architecture and connectivity. This technique has set the stage for numerous studies on normal and abnormal connectivity and their role in devel- DIFFUSION TENSOR IMAGING: THE BASICS opmental and acquired disorders. Referencing established white matter anatomy, DTI atlases, Using appropriate magnetic field gradients, and neuroanatomical descriptions, this article diffusion-weighted sequences can be used to summarizes the major white matter anatomy and detect the motion of the water molecules to and related structures relevant to the clinical neurora- from cells. This free movement of the water mole- diologist in daily practice.