Softening of the Brain Medical Term
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S18. Experimental Studies in Cerebrovascular Disease : Echoencephalographic, Electroencephalographic and Histologic Observations
S17. Experimental Study on intracerebral Hemorrhage Mitsuo TsURU, Kenzoh YADA and Minoru TSUNODA Dept. of Neurosurgery, Hokkaido University School of Medicine Using a physiological pressure transducer, prolonged supratentorial intra- cranial pressure was recorded in cats with experimentally produced intracerebral hematoms, together with recordings of electroencephalogram, arterial and venous pressure, pulse rate, respiration rate, and electrocardiogram. Except for these which die right after the introduction of intracerebral hematoma due to respiratory arrest, the intracranial pressure soon starts to de- cline and continues to decline until it reaches close to normal range. In this stage, although resting intracranial pressure is fairly close to normal, it can extremely easily be elevated by various factors such as minor change of respira- tion, straining etc. We offer to call this appearing normal, but very unstable state of intracranial condition as "latent intracranial hypertension". This im- portant finding gives us warning not to give unnecessary manipulations to the patients with intracranial hematomas even in case they do not seem to have extremely high intracranial pressure. S18. Experimental Studies in Cerebrovascular Disease : Echoencephalographic, Electroencephalographic and Histologic Observations Hajime NAGAI,Kazumi SAKURAI,Masayuki HAYASHI,Kazuhiro FURUSE, Kazuhiko OKAMURA,A. SHINTANI,and T. KOBAYASHI 2nd Dept. of Surgery,School of Medicine,Nagoya University Recent advances in neurosurgery for hypertensive intracerebral hemorrhage have made possible to improve patients suffering from cerebrovascular disease. It is difficult problem, however, to differentiate cerebral hemorrhage from cerebral softening in practice. The purpose of the present paper is to estimate differentiation in both diseases, using echoencephalography and electroencephalography in dogs with experimental- ly produced intracerebral hematoma and cerebral infarction. -
The Baseline Structure of the Enteric Nervous System and Its Role in Parkinson’S Disease
life Review The Baseline Structure of the Enteric Nervous System and Its Role in Parkinson’s Disease Gianfranco Natale 1,2,* , Larisa Ryskalin 1 , Gabriele Morucci 1 , Gloria Lazzeri 1, Alessandro Frati 3,4 and Francesco Fornai 1,4 1 Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56126 Pisa, Italy; [email protected] (L.R.); [email protected] (G.M.); [email protected] (G.L.); [email protected] (F.F.) 2 Museum of Human Anatomy “Filippo Civinini”, University of Pisa, 56126 Pisa, Italy 3 Neurosurgery Division, Human Neurosciences Department, Sapienza University of Rome, 00135 Rome, Italy; [email protected] 4 Istituto di Ricovero e Cura a Carattere Scientifico (I.R.C.C.S.) Neuromed, 86077 Pozzilli, Italy * Correspondence: [email protected] Abstract: The gastrointestinal (GI) tract is provided with a peculiar nervous network, known as the enteric nervous system (ENS), which is dedicated to the fine control of digestive functions. This forms a complex network, which includes several types of neurons, as well as glial cells. Despite extensive studies, a comprehensive classification of these neurons is still lacking. The complexity of ENS is magnified by a multiple control of the central nervous system, and bidirectional communication between various central nervous areas and the gut occurs. This lends substance to the complexity of the microbiota–gut–brain axis, which represents the network governing homeostasis through nervous, endocrine, immune, and metabolic pathways. The present manuscript is dedicated to Citation: Natale, G.; Ryskalin, L.; identifying various neuronal cytotypes belonging to ENS in baseline conditions. -
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 -
Student Academic Learning Services Nervous System Quiz
Student Academic Learning Services Page 1 of 8 Nervous System Quiz 1. The term central nervous system refers to the: A) autonomic and peripheral nervous systems B) brain, spinal cord, and cranial nerves C) brain and cranial nerves D) spinal cord and spinal nerves E) brain and spinal cord 2. The peripheral nervous system consists of: A) spinal nerves only B) the brain only C) cranial nerves only D) the brain and spinal cord E) the spinal and cranial nerves 3. Which of these cells are not a type of neuroglia found in the CNS: A) astrocytes B) microglia C) Schwann cells D) ependymal cells E) oligodendrocytes 4. The Schwann cells form a myelin sheath around the: A) dendrites B) cell body C) nucleus D) axon E) nodes of Ranvier 5. The neuron processes that normally receives incoming stimuli are called: A) axons B) dendrites C) neurolemmas D) Schwann cells E) satellite cells www.durhamcollege.ca/sals Student Services Building (SSB), Room 204 905.721.2000 ext. 2491 This document last updated: 7/29/2011 Student Academic Learning Services Page 2 of 8 6. Collections of nerve cell bodies inside the PNS are called: A) ganglia B) tracts C) nerves D) nuclei E) tracts or ganglia 7. Which of the following best describes the waxy-appearing material called myelin: A) an outermembrane on a neuroglial cell B) a lipid-protein (lipoprotein) cell membrane on the outside of axons C) a mass of white lipid material that surrounds the cell body of a neuron D) a mass of white lipid material that insulates the axon of a neuron E) a mass of white lipid material that surrounds the dendrites of a neuron 8. -
A Brief Introduction Into the Peripheral Nervous System
A Brief Introduction into the Peripheral Nervous System Bianca Flores, PhD Candidate, Neuroscience Tuesday, October 15th, 2019 Brief overview: • What are you hoping to learn? • Subdivisions of the peripheral nervous system (PNS) • Physiology • Diseases associated with PNS • Special topics (current research at Vanderbilt) Brief question- • Is there a location in our body that does not have neurons (signals being sent to move or sense)? The body’s nervous system is made up of two parts: The Peripheral Nervous System (PNS) is divided into two parts PNS: Sensory components: • Nociception • Proprioception • Mechanoreception • Thermoception Parasympathetic vs Sympathetic PNS • Includes everything outside of the brain and spinal cord • Is divided into motor and sensory subsets • Controls the “rest and relax” and “flight or fight” responses PNS: Physiology & Anatomy Dorsal Root ganglion are sensory body of the PNS Anatomy of the PNS- Dorsal Root Ganglion How the PNS sends signals to the CNS Nerve impulses carry electrical signals Myelin sheath on surrounds to the nerve to contribute to signal propagation Myelin sheath on surrounds to the nerve to contribute to signal propagation Nerve impulses carry electrical signals PNS Physiology and Anatomy • Dorsal root ganglion are the sensory bodies of the PNS • The Ventral root is responsible for motor movement • Myelin Sheath is imperative to proper nerve function Diseases associated with the PNS: Peripheral Neuropathy What is peripheral neuropathy? Peripheral Neuropathy: -Damage to peripheral nerves -
The Enteric Nervous System: a Second Brain
The Enteric Nervous System: A Second Brain MICHAEL D. GERSHON Columbia University Once dismissed as a simple collection of relay ganglia, the enteric nervous system is now recognized as a complex, integrative brain in its own right. Although we still are unable to relate complex behaviors such as gut motility and secretion to the activity of individual neurons, work in that area is proceeding briskly--and will lead to rapid advances in the management of functional bowel disease. Dr. Gershon is Professor and Chair, Department of Anatomy and Cell Biology, Columbia University College of Physicians and Surgeons, New York. In addition to numerous scientific publications, he is the author of The Second Brain (Harper Collins, New York, 1998). Structurally and neurochemically, the enteric nervous system (ENS) is a brain unto itself. Within those yards of tubing lies a complex web of microcircuitry driven by more neurotransmitters and neuromodulators than can be found anywhere else in the peripheral nervous system. These allow the ENS to perform many of its tasks in the absence of central nervous system (CNS) control--a unique endowment that has permitted enteric neurobiologists to investigate nerve cell ontogeny and chemical mediation of reflex behavior in a laboratory setting. Recognition of the importance of this work as a basis for developing effective therapies for functional bowel disease, coupled with the recent, unexpected discovery of major enteric defects following the knockout of murine genes not previously known to affect the gut, has produced a groundswell of interest that has attracted some of the best investigators to the field. Add to this that the ENS provides the closest thing we have to a window on the brain, and one begins to understand why the bowel--the second brain--is finally receiving the attention it deserves. -
The Peripheral Nervous System
The Peripheral Nervous System Dr. Ali Ebneshahidi Peripheral Nervous System (PNS) – Consists of 12 pairs of cranial nerves and 31 pairs of spinal nerves. – Serves as a critical link between the body and the central nervous system. – peripheral nerves contain an outermost layer of fibrous connective tissue called epineurium which surrounds a thinner layer of fibrous connective tissue called perineurium (surrounds the bundles of nerve or fascicles). Individual nerve fibers within the nerve are surrounded by loose connective tissue called endoneurium. Cranial Nerves Cranial nerves are direct extensions of the brain. Only Nerve I (olfactory) originates from the cerebrum, the remaining 11 pairs originate from the brain stem. Nerve I (Olfactory)- for the sense of smell (sensory). Nerve II (Optic)- for the sense of vision (sensory). Nerve III (Oculomotor)- for controlling muscles and accessory structures of the eyes ( primarily motor). Nerve IV (Trochlear)- for controlling muscles of the eyes (primarily motor). Nerve V (Trigeminal)- for controlling muscles of the eyes, upper and lower jaws and tear glands (mixed). Nerve VI (Abducens)- for controlling muscles that move the eye (primarily motor). Nerve VII (Facial) – for the sense of taste and controlling facial muscles, tear glands and salivary glands (mixed). Nerve VIII (Vestibulocochlear)- for the senses of hearing and equilibrium (sensory). Nerve IX (Glossopharyngeal)- for controlling muscles in the pharynx and to control salivary glands (mixed). Nerve X (Vagus)- for controlling muscles used in speech, swallowing, and the digestive tract, and controls cardiac and smooth muscles (mixed). Nerve XI (Accessory)- for controlling muscles of soft palate, pharynx and larynx (primarily motor). Nerve XII (Hypoglossal) for controlling muscles that move the tongue ( primarily motor). -
The Remarkable, Yet Not Extraordinary, Human Brain As a Scaled-Up Primate Brain and Its Associated Cost
The remarkable, yet not extraordinary, human brain as a scaled-up primate brain and its associated cost Suzana Herculano-Houzel1 Instituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, 21941-902, Rio de Janeiro, Brazil; and Instituto Nacional de Neurociência Translacional, Instituto Nacional de Ciência e Tecnologia/Ministério de Ciência e Tecnologia, 04023-900, Sao Paulo, Brazil Edited by Francisco J. Ayala, University of California, Irvine, CA, and approved April 12, 2012 (received for review February 29, 2012) Neuroscientists have become used to a number of “facts” about the The incongruity between our extraordinary cognitive abilities human brain: It has 100 billion neurons and 10- to 50-fold more glial and our not-that-extraordinary brain size has been the major cells; it is the largest-than-expected for its body among primates driving factor behind the idea that the human brain is an outlier, and mammals in general, and therefore the most cognitively able; an exception to the rules that have applied to the evolution of all it consumes an outstanding 20% of the total body energy budget other animals and brains. A largely accepted alternative expla- despite representing only 2% of body mass because of an increased nation for our cognitive superiority over other mammals has been metabolic need of its neurons; and it is endowed with an overde- our extraordinary brain size compared with our body size, that is, veloped cerebral cortex, the largest compared with brain size. our large encephalization quotient (8). Compared -
Are Astrocytes Executive Cells Within the Central Nervous System? ¿Son Los Astrocitos Células Ejecutivas Dentro Del Sistema Nervioso Central? Roberto E
DOI: 10.1590/0004-282X20160101 VIEW AND REVIEW Are astrocytes executive cells within the central nervous system? ¿Son los astrocitos células ejecutivas dentro del Sistema Nervioso Central? Roberto E. Sica1, Roberto Caccuri1, Cecilia Quarracino1, Francisco Capani1 ABSTRACT Experimental evidence suggests that astrocytes play a crucial role in the physiology of the central nervous system (CNS) by modulating synaptic activity and plasticity. Based on what is currently known we postulate that astrocytes are fundamental, along with neurons, for the information processing that takes place within the CNS. On the other hand, experimental findings and human observations signal that some of the primary degenerative diseases of the CNS, like frontotemporal dementia, Parkinson’s disease, Alzheimer’s dementia, Huntington’s dementia, primary cerebellar ataxias and amyotrophic lateral sclerosis, all of which affect the human species exclusively, may be due to astroglial dysfunction. This hypothesis is supported by observations that demonstrated that the killing of neurons by non-neural cells plays a major role in the pathogenesis of those diseases, at both their onset and their progression. Furthermore, recent findings suggest that astrocytes might be involved in the pathogenesis of some psychiatric disorders as well. Keywords: astrocytes; physiology; central nervous system; neurodegenerative diseases. RESUMEN Evidencias experimentales sugieren que los astrocitos desempeñan un rol crucial en la fisiología del sistema nervioso central (SNC) modulando la actividad y plasticidad sináptica. En base a lo actualmente conocido creemos que los astrocitos participan, en pie de igualdad con las neuronas, en los procesos de información del SNC. Además, observaciones experimentales y humanas encontraron que algunas de las enfermedades degenerativas primarias del SNC: la demencia fronto-temporal; las enfermedades de Parkinson, de Alzheimer, y de Huntington, las ataxias cerebelosas primarias y la esclerosis lateral amiotrófica, que afectan solo a los humanos, pueden deberse a astroglíopatía. -
Appendix A: Glossary for Section 2.1 (PDF)
APPENDIX A GLOSSARY FOR SECTION 2.1 Sources: The Concise Columbia Encyclopedia. 1995. Columbia University Press; Solomon et al. 1993. Biology, Third Edition. Harcourt Brace Publishing astrocyte - a star-shaped cell, especially a neuroglial cell of nervous tissue. axon - the long, tubular extension of the neuron that conducts nerve impulses away from the cell body. blood-brain barrier - system of capillaries that regulates the movement of chemical substances, ions, and fluids in and out of the brain. central nervous system - the portion of the vertebrate nervous system consisting of the brain and spinal cord. cerebellum - the trilobed structure of the brain, lying posterior to the pons and medulla oblongata and inferior to the occipital lobes of the cerebral hemispheres, that is responsible for the regulation and coordination of complex voluntary muscular movement as well as the maintenance of posture and balance. cerebral cortex - the extensive outer layer of gray matter of the cerebral hemispheres, largely responsible for higher brain functions, including sensation, voluntary muscle movement, thought, reasoning, and memory. cerebrum - the large, rounded structure of the brain occupying most of the cranial cavity, divided into two cerebral hemispheres that are joined at the bottom by the corpus callosum. It controls and integrates motor, sensory, and higher mental functions, such as thought, reason, emotion, and memory. cognitive development - various mental tasks and processes (e.g. receiving, processing, storing, and retrieving information) that mediate between stimulus and response and determine problem-solving ability. demyelination - to destroy or remove the myelin sheath of (a nerve fiber), as through disease. dendrite - a branched protoplasmic extension of a nerve cell that conducts impulses from adjacent cells inward toward the cell body. -
Vascular Cognitive Impairment in Clinical Practice
This page intentionally left blank Vascular Cognitive Impairment in Clinical Practice Vascular Cognitive Impairment in Clinical Practice Edited by Lars-Olof Wahlund Timo Erkinjuntti Serge Gauthier CAMBRIDGE UNIVERSITY PRESS Cambridge, New York, Melbourne, Madrid, Cape Town, Singapore, São Paulo Cambridge University Press The Edinburgh Building, Cambridge CB2 8RU, UK Published in the United States of America by Cambridge University Press, New York www.cambridge.org Information on this title: www.cambridge.org/9780521875370 © Cambridge University Press 2009 This publication is in copyright. Subject to statutory exception and to the provision of relevant collective licensing agreements, no reproduction of any part may take place without the written permission of Cambridge University Press. First published in print format 2009 ISBN-13 978-0-511-50680-2 eBook (EBL) ISBN-13 978-0-521-87537-0 hardback Cambridge University Press has no responsibility for the persistence or accuracy of urls for external or third-party internet websites referred to in this publication, and does not guarantee that any content on such websites is, or will remain, accurate or appropriate. Contents List of Contributors page vii Preface xi Section 1: Diagnosis 1 1. Diagnosing vascular cognitive impairment and dementia: concepts and controversies 3 Timo Erkinjuntti and Serge Gauthier 2. Vascular cognitive impairment: prodrome to VaD? 11 Adriane Mayda and Charles DeCarli 3. Clinical evaluation: a systematic but user-friendly approach 32 Oscar L. Lopez and David A. Wolk 4. Cognitive functioning in vascular dementia before and after diagnosis 46 Erika J. Laukka, Sari Karlsson, Stuart W.S. MacDonald and Lars Ba¨ ckman 5. Structural neuroimaging: CT and MRI 58 Wiesje M. -
11 Introduction to the Nervous System and Nervous Tissue
11 Introduction to the Nervous System and Nervous Tissue ou can’t turn on the television or radio, much less go online, without seeing some- 11.1 Overview of the Nervous thing to remind you of the nervous system. From advertisements for medications System 381 Yto treat depression and other psychiatric conditions to stories about celebrities and 11.2 Nervous Tissue 384 their battles with illegal drugs, information about the nervous system is everywhere in 11.3 Electrophysiology our popular culture. And there is good reason for this—the nervous system controls our of Neurons 393 perception and experience of the world. In addition, it directs voluntary movement, and 11.4 Neuronal Synapses 406 is the seat of our consciousness, personality, and learning and memory. Along with the 11.5 Neurotransmitters 413 endocrine system, the nervous system regulates many aspects of homeostasis, including 11.6 Functional Groups respiratory rate, blood pressure, body temperature, the sleep/wake cycle, and blood pH. of Neurons 417 In this chapter we introduce the multitasking nervous system and its basic functions and divisions. We then examine the structure and physiology of the main tissue of the nervous system: nervous tissue. As you read, notice that many of the same principles you discovered in the muscle tissue chapter (see Chapter 10) apply here as well. MODULE 11.1 Overview of the Nervous System Learning Outcomes 1. Describe the major functions of the nervous system. 2. Describe the structures and basic functions of each organ of the central and peripheral nervous systems. 3. Explain the major differences between the two functional divisions of the peripheral nervous system.