Anterior Peri-Insular Quadrantotomy: a Cadaveric White Matter Dissection Study
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Combined Structural and Diffusion Tensor Imaging Detection of Ischemic Injury in Moyamoya Disease: Relation to Disease Advancement and Cerebral Hypoperfusion
CLINICAL ARTICLE Combined structural and diffusion tensor imaging detection of ischemic injury in moyamoya disease: relation to disease advancement and cerebral hypoperfusion Ken Kazumata, MD, PhD,1 Kikutaro Tokairin, MD,1 Masaki Ito, MD, PhD,1 Haruto Uchino, MD, PhD,1 Taku Sugiyama, MD, PhD,1 Masahito Kawabori, MD, PhD,1 Toshiya Osanai, MD, PhD,1 Khin Khin Tha, MD, PhD,2 and Kiyohiro Houkin, MD, PhD1 1Department of Neurosurgery, Hokkaido University Graduate School of Medicine; and 2Clinical Research and Medical Innovation Center, Hokkaido University Hospital, Sapporo, Japan OBJECTIVE The microstructural integrity of gray and white matter is decreased in adult moyamoya disease, suggesting covert ischemic injury as a mechanism of cognitive dysfunction. Establishing a microstructural brain imaging marker is critical for monitoring cognitive outcomes following surgical interventions. The authors of the present study determined the pathophysiological basis of altered microstructural brain injury in relation to advanced arterial occlusion, cerebral hypoperfusion, and cognitive function. METHODS The authors examined 58 patients without apparent brain lesions and 30 healthy controls by using structural MRI, as well as diffusion tensor imaging (DTI). Arterial occlusion in each hemisphere was classified as early or ad- vanced stage based on MRA and posterior cerebral artery (PCA) involvement. Regional cerebral blood flow (rCBF) was measured with N-isopropyl-p-[123I]-iodoamphetamine SPECT. Furthermore, cognitive performance was examined using the Wechsler Adult Intelligence Scale, Third Edition and the Trail Making Test (TMT). Both voxel- and region of inter- est–based analyses were performed for groupwise comparisons, as well as correlation analysis, using parameters such as cognitive test scores; gray matter volume; fractional anisotropy (FA) of association fiber tracts, including the inferior frontooccipital fasciculus (IFOF) and superior longitudinal fasciculus (SLF); PCA involvement; and rCBF. -
Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia
brain sciences Review Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper Motor Neuron Dominant Amyotrophic Lateral Sclerosis, and Hereditary Spastic Paraplegia Timothy Fullam and Jeffrey Statland * Department of Neurology, University of Kansas Medical Center, Kansas, KS 66160, USA; [email protected] * Correspondence: [email protected] Abstract: Following the exclusion of potentially reversible causes, the differential for those patients presenting with a predominant upper motor neuron syndrome includes primary lateral sclerosis (PLS), hereditary spastic paraplegia (HSP), or upper motor neuron dominant ALS (UMNdALS). Differentiation of these disorders in the early phases of disease remains challenging. While no single clinical or diagnostic tests is specific, there are several developing biomarkers and neuroimaging technologies which may help distinguish PLS from HSP and UMNdALS. Recent consensus diagnostic criteria and use of evolving technologies will allow more precise delineation of PLS from other upper motor neuron disorders and aid in the targeting of potentially disease-modifying therapeutics. Keywords: primary lateral sclerosis; amyotrophic lateral sclerosis; hereditary spastic paraplegia Citation: Fullam, T.; Statland, J. Upper Motor Neuron Disorders: Primary Lateral Sclerosis, Upper 1. Introduction Motor Neuron Dominant Jean-Martin Charcot (1825–1893) and Wilhelm Erb (1840–1921) are credited with first Amyotrophic Lateral Sclerosis, and describing a distinct clinical syndrome of upper motor neuron (UMN) tract degeneration in Hereditary Spastic Paraplegia. Brain isolation with symptoms including spasticity, hyperreflexia, and mild weakness [1,2]. Many Sci. 2021, 11, 611. https:// of the earliest described cases included cases of hereditary spastic paraplegia, amyotrophic doi.org/10.3390/brainsci11050611 lateral sclerosis, and underrecognized structural, infectious, or inflammatory etiologies for upper motor neuron dysfunction which have since become routinely diagnosed with the Academic Editors: P. -
Long-Term Microstructure and Cerebral Blood Flow Changes in Patients Recovered from COVID-19 Without Neurological Manifestations
The Journal of Clinical Investigation CLINICAL MEDICINE Long-term microstructure and cerebral blood flow changes in patients recovered from COVID-19 without neurological manifestations Yuanyuan Qin,1 Jinfeng Wu,2 Tao Chen,3 Jia Li,1 Guiling Zhang,1 Di Wu,1 Yiran Zhou,1 Ning Zheng,2 Aoling Cai,2 Qin Ning,3 Anne Manyande,4 Fuqiang Xu,2,5 Jie Wang,2,5 and Wenzhen Zhu1 1Department of Radiology, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China. 2State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Key Laboratory of Magnetic Resonance in Biological Systems, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan, Hubei, China. 3Institute and Department of Infectious Disease, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China. 4School of Human and Social Sciences, University of West London, Middlesex, United Kingdom. 5University of Chinese Academy of Sciences, Beijing, China. BACKGROUND. The coronavirus disease 2019 (COVID-19) rapidly progressed to a global pandemic. Although some patients totally recover from COVID-19 pneumonia, the disease’s long-term effects on the brain still need to be explored. METHODS. We recruited 51 patients with 2 subtypes of COVID-19 (19 mild and 32 severe) with no specific neurological manifestations at the acute stage and no obvious lesions on the conventional MRI 3 months after discharge. Changes in gray matter morphometry, cerebral blood flow (CBF), and white matter (WM) microstructure were investigated using MRI. The relationship between brain imaging measurements and inflammation markers was further analyzed. -
Connectivity and Neurochemistry of the Commissura Anterior of the Pigeon (Columba Livia)
RESEARCH ARTICLE Connectivity and Neurochemistry of the Commissura Anterior of the Pigeon (Columba livia) Sara Letzner,* Annika Simon, and Onur Gunt€ urk€ un€ Department of Biopsychology, Institute of Cognitive Neuroscience, Faculty of Psychology, Ruhr-University Bochum, Bochum, Germany ABSTRACT pallial and amygdaloid projections were reciprocally The anterior commissure (AC) and the much smaller organized, and all AC projections originated within a hippocampal commissure constitute the only interhemi- rather small area of the arcopallium and the PoA. The spheric pathways at the telencephalic level in birds. commissural neurons were not GABA-positive, and thus Since the degeneration study from Zeier and Karten possibly not of an inhibitory nature. In sum, our neuroa- (1973), no detailed description of the topographic orga- natomical study demonstrates that a small group of nization of the AC has been performed. This information arcopallial and amygdaloid neurons constitute a wide is not only necessary for a better understanding of range of contralateral projections to sensorimotor and interhemispheric transfer in birds, but also for a com- limbic structures. Different from mammals, in birds the parative analysis of the evolution of commissural sys- neurons that project via the AC constitute mostly heter- tems in the vertebrate classes. We therefore examined otopically organized and unidirectional connections. In the fiber connections of the AC by using choleratoxin addition, the great majority of pallial areas do not par- subunit B (CTB) and biotinylated dextran amine (BDA). ticipate by themselves in interhemispheric exchange in Injections into subareas of the arcopallium and poste- birds. Instead, commissural exchange rests on a rather rior amygdala (PoA) demonstrated contralateral projec- small arcopallial and amygdaloid cluster of neurons. -
Handbook on White Matter: Structure, Function and Changes
Neuroanatomy Research at the Leading Edge HANDBOOK ON WHITE MATTER: STRUCTURE, FUNCTION AND CHANGES No part of this digital document may be reproduced, stored in a retrieval system or transmitted in any form or by any means. The publisher has taken reasonable care in the preparation of this digital document, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. No liability is assumed for incidental or consequential damages in connection with or arising out of information contained herein. This digital document is sold with the clear understanding that the publisher is not engaged in rendering legal, medical or any other professional services. NEUROANATOMY RESEARCH AT THE LEADING EDGE Handbook on White Matter: Structure, Function and Changes Timothy B. Westland and Robert N. Calton 2009 ISBN: 978-1-60692-375-7 Neuroanatomy Research at the Leading Edge HANDBOOK ON WHITE MATTER: STRUCTURE, FUNCTION AND CHANGES TIMOTHY B. WESTLAND AND ROBERT N. CALTON EDITORS Nova Science Publishers, Inc. New York Copyright © 2009 by Nova Science Publishers, Inc. All rights reserved. No part of this book may be reproduced, stored in a retrieval system or transmitted in any form or by any means: electronic, electrostatic, magnetic, tape, mechanical photocopying, recording or otherwise without the written permission of the Publisher. For permission to use material from this book please contact us: Telephone 631-231-7269; Fax 631-231-8175 Web Site: http://www.novapublishers.com NOTICE TO THE READER The Publisher has taken reasonable care in the preparation of this book, but makes no expressed or implied warranty of any kind and assumes no responsibility for any errors or omissions. -
Glutamate Transporter Mrna Expression in Proliferative Zones of the Developing and Adult Murine CNS
The Journal of Neuroscience, April 1, 1996, 76(7):2191-2207 Glutamate Transporter mRNA Expression in Proliferative Zones of the Developing and Adult Murine CNS Margaret L. Sutherland,is2 Tracy A. Delaney,’ and Jeffrey L. Noebels’s2 1Division of Neuroscience, “Developmental Neurogenetics Laboratory, Department of Neurology, Baylor College of Medicine, Houston, Texas 77030 Neuronal migration, differentiation, and synapse formation are transcript expression continued in the subventricular zone developmental processes within the CNS significantly influ- postnatally and persisted in this proliferative zone in the adult enced by ionotropic and metabotropic glutamate receptor ac- brain. From PO onward, mEAAT1 mRNA was present predom- tivity. Extracellular glutamate concentrations mediating this ac- inantly in the cerebellar Purkinje cell layer and at a much lower tivity are regulated by transport proteins localized in neuronal abundance in the cortex, hippocampus, basal nuclei, and sep- and glial cell membranes. We have used in situ hybridization tum, whereas from P7 onward, mEAAT2 mRNA expression analysis with subtype-specific antisense-oligonucleotides to increased throughout most of the neuraxis. Postnatally, tran- study the distribution of glia-specific excitatory amino acid scripts for mEAAT1 and mEAAT2 were found in cell bodies, transporter (mEAAT1 and mEAAT2) mRNAs during the later processes, and commissural white matter tracts of the CNS. stages of embryogenesis and postnatal CNS development. The divergent temporal and spatial expression -
Quantitative Analysis of Axon Collaterals of Single Pyramidal Cells
Yang et al. BMC Neurosci (2017) 18:25 DOI 10.1186/s12868-017-0342-7 BMC Neuroscience RESEARCH ARTICLE Open Access Quantitative analysis of axon collaterals of single pyramidal cells of the anterior piriform cortex of the guinea pig Junli Yang1,2*, Gerhard Litscher1,3* , Zhongren Sun1*, Qiang Tang1, Kiyoshi Kishi2, Satoko Oda2, Masaaki Takayanagi2, Zemin Sheng1,4, Yang Liu1, Wenhai Guo1, Ting Zhang1, Lu Wang1,3, Ingrid Gaischek3, Daniela Litscher3, Irmgard Th. Lippe5 and Masaru Kuroda2 Abstract Background: The role of the piriform cortex (PC) in olfactory information processing remains largely unknown. The anterior part of the piriform cortex (APC) has been the focus of cortical-level studies of olfactory coding, and asso- ciative processes have attracted considerable attention as an important part in odor discrimination and olfactory information processing. Associational connections of pyramidal cells in the guinea pig APC were studied by direct visualization of axons stained and quantitatively analyzed by intracellular biocytin injection in vivo. Results: The observations illustrated that axon collaterals of the individual cells were widely and spatially distrib- uted within the PC, and sometimes also showed a long associational projection to the olfactory bulb (OB). The data showed that long associational axons were both rostrally and caudally directed throughout the PC, and the intrinsic associational fibers of pyramidal cells in the APC are omnidirectional connections in the PC. Within the PC, associa- tional axons typically followed rather linear trajectories and irregular bouton distributions. Quantitative data of the axon collaterals of two pyramidal cells in the APC showed that the average length of axonal collaterals was 101 mm, out of which 79 mm (78% of total length) were distributed in the PC. -
Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans Ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai
Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai To cite this version: Hans ten Donkelaar, Nathalie Tzourio-Mazoyer, Jürgen Mai. Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex. Frontiers in Neuroanatomy, Frontiers, 2018, 12, pp.93. 10.3389/fnana.2018.00093. hal-01929541 HAL Id: hal-01929541 https://hal.archives-ouvertes.fr/hal-01929541 Submitted on 21 Nov 2018 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. REVIEW published: 19 November 2018 doi: 10.3389/fnana.2018.00093 Toward a Common Terminology for the Gyri and Sulci of the Human Cerebral Cortex Hans J. ten Donkelaar 1*†, Nathalie Tzourio-Mazoyer 2† and Jürgen K. Mai 3† 1 Department of Neurology, Donders Center for Medical Neuroscience, Radboud University Medical Center, Nijmegen, Netherlands, 2 IMN Institut des Maladies Neurodégénératives UMR 5293, Université de Bordeaux, Bordeaux, France, 3 Institute for Anatomy, Heinrich Heine University, Düsseldorf, Germany The gyri and sulci of the human brain were defined by pioneers such as Louis-Pierre Gratiolet and Alexander Ecker, and extensified by, among others, Dejerine (1895) and von Economo and Koskinas (1925). -
01 05 Lateral Surface of the Brain-NOTES.Pdf
Lateral Surface of the Brain Medical Neuroscience | Tutorial Notes Lateral Surface of the Brain 1 MAP TO NEUROSCIENCE CORE CONCEPTS NCC1. The brain is the body's most complex organ. LEARNING OBJECTIVES After study of the assigned learning materials, the student will: 1. Demonstrate the four paired lobes of the cerebral cortex and describe the boundaries of each. 2. Sketch the major features of each cerebral lobe, as seen from the lateral view, identifying major gyri and sulci that characterize each lobe. NARRATIVE by Leonard E. WHITE and Nell B. CANT Duke Institute for Brain Sciences Department of Neurobiology Duke University School of Medicine Overview When you view the lateral aspect of a human brain specimen (see Figures A3A and A102), three structures are usually visible: the cerebral hemispheres, the cerebellum, and part of the brainstem (although the brainstem is not visible in the specimen photographed in lateral view for Fig. 1 below). The spinal cord has usually been severed (but we’ll consider the spinal cord later), and the rest of the subdivisions are hidden from lateral view by the hemispheres. The diencephalon and the rest of the brainstem are visible on the medial surface of a brain that has been cut in the midsagittal plane. Parts of all of the subdivisions are also visible from the ventral surface of the whole brain. Over the next several tutorials, you will find video demonstrations (from the brain anatomy lab) and photographs (in the tutorial notes) of these brain surfaces, and sufficient detail in the narrative to appreciate the overall organization of the parts of the brain that are visible from each perspective. -
A Fiber, 9, 10, 66, 67 Abdomen, 221 Visceral Afferent, 222 Absolute
INDEX A fiber, 9, 10, 66, 67 all-or-none law, 62 Abdomen, 221 current during propagation, 62, 63 visceral afferent, 222 current loop, 64 Absolute temperature, 26 definition, 40 Acceleration depolarization phase, 38 angular, 183 duration, 38 linear, 183, 184 effect on contraction, 144 negative, 184 frequency, 50 positive, 184 generation, 88, 89 Accommodation, excitability, 60 inactivation, 48 Acetic acid, 74, 78 inhibition, 96 Acetylenoline ion current, 42, 43 cycle, 78 ion shift, 40, 42, 43 end plate, 74, 75 kinetics, 44-52 fate, 77, 78 mechanism of propagation, 62 intestinal muscle, 237 membrane conductance, 49 membrane receptor, 77-79 muscle, 129 muscarinergic transmission, 223, 225 overshoot, 38 nicotinergic transmission, 223, 225 peak, 38 quanta, 82 phase, 38 receptor, 78, 79 potassium conductance, 41 Renshaw cell, 100 propagation, 61-68 smooth muscle, 230, 231 refractory period, 50 transmitter function, 100, 101 refractory phase, 49, 50 Acetylcholinesterase, 101 repolarization, 38 ACh, 74, 75, s.a. acetylcholine rising phase, 38 Acid, fatty, 225 saltatory conduction, 64-66 Actin, 131-133, 139, 147 smooth muscle, 230, 231 Actinomycin, '312 sodium conductance, 41, 42 Action potential, 37-43 sodium deficiency, 43 Action potential tetrodotoxin, 52 after-potential, 39 threshold, 39 327 328 Index Action potential (cont.) Anion, 21 time course, 37, 38 Anococcygeal muscle, 233 trigger, 39 Anoce,58 triphasic current, 64 Antagonist inhibition, 109, 212 upstroke, 38 Anterior pens, micturition center, 241 velocity of conduction, 61 Anticholinergic substance, 313 Active transport Antidiuretic hormone, 259 membrane, 32 Aphagia, 264 sodium, 35 Aphasia Activity clock, 288 motor, 305 Adaptation, hormonal, 259 sensory, 305 Adenohypophysis Apoplexy, 196, 310 feedback system, 259 ARAS,295 hormone control, 257-259 Areflexia, 170 hypothalamus, 254 Arousal, 295 Adenosine triphosphate, 132-134, 147, 226 Arterial pressure, 247, s.a. -
Morphological Evidence for the Sprouting of Inhibitory Commissural Fibers in Response to the Lesion of the Excitatory Entorhinal Input to the Rat Dentate Gyrus
The Journal of Neuroscience, October 1995, 75(10): 6868-6878 Morphological Evidence for the Sprouting of Inhibitory Commissural Fibers in Response to the Lesion of the Excitatory Entorhinal Input to the Rat Dentate Gyrus T. Deller,’ M. Frotscher,’ and R. Nitsch2 ‘Institute of Anatomy, University of Freiburg, D-79001 Freiburg, Germany and ‘Institute of Anatomy, Humboldt University Berlin (Charitb), D-l 0098 Berlin, Germany Recently a commissural fiber projection that terminates in missural and associational fibers to the inner molecular layer the outer molecular layer of the fascia dentata was de- expand their termination zone (e.g., Lynch et al., 1973, 1976; scribed in normal rats (Deller et al., 1995). In the present Zimmer et al., 1973; Goldowitz and Cotman, 1980; Lynch et article, Phaseolus vu/g&s leucoagglutinin (PHAL) tracing al., 1982; West et al., 1984); (2) septohippocampal fibers, known was used to analyze the contribution of this previously un- to terminate throughout the molecular layer of the dentate gyms, known projection to the commissural sprouting response form a dense fiber plexus in the denervated zone (Lynch et al., after entorhinal cortex lesion. Rats 4-9 weeks after unilat- 1972; Nadler et al., 1977; Nyakas et al., 1988); and (3) axons eral entorhinal lesion received a single PHAL deposit into of the crossed temporo-dentate pathway participate in the rein- the hilus of the fascia dentata contralateral to the lesion nervation of the denervated septal portion of the hippocampal side. Unlesioned control animals received a similar PHAL formation (Steward et al., 1974; Goldowitz et al., 1975; Deller deposit. The degree of axonal arborization and the bouton et al., 1995b). -
Features of the Cerebral Vascular Pattern That Predict Vulnerability to Perfusion Or Oxygenation Deficiency: an Anatomic Study
431 Features of the Cerebral Vascular Pattern That Predict Vulnerability to Perfusion or Oxygenation Deficiency: An Anatomic Study D. M. Moody1 In an ongoing study of brain microvasculature in humans at autopsy, we had the 1 2 M.A. Bell · opportunity to analyze the overall scheme of this vascular supply. The native endothelial V. R. Challa3 membrane enzyme, alkaline phosphatase, is used to precipitate black lead sulfide salt in the vessel wall, rendering the brain microvasculature visible by both light microscopy and microradiography. There are six distinct patterns of intraparenchymal afferent blood supply to the supratentorial brain: short arterioles from a single source (e.g., those in the cortex); short- to intermediate-length arterioles, single source (anterior two-thirds of the corpus callosum); short- to intermediate-length arterioles and arteries, dual source (subcortical U fibers); intermediate-length arterioles and arteries, triple source (extreme/ external capsule and claustrum); long arteries and arterioles, single source (centrum semiovale); and large, long muscular arteries, single source (thalamus and basal ganglia). The nature of this arrangement offers some protection to certain regions of the cerebrum from circulatory challenges such as hypotension, while leaving other areas vulnerable. The distal arterioles supplying two of these protected regions, the U-fiber area and the extreme/external capsule and claustrum area, also exhibit the feature of interdigitation, which can offer additional collateral potential from one arteriolar territory to the next. Aging, hypertension, diabetes mellitus, and atherosclerosis can have a significant impact on brain microcirculation. The way in which vascular patterns dictate the distribution of these effects is discussed. The ability to stain the cerebral microvessels and demonstrate the finer points of their patterns in sections and microradiographs has enabled us to resolve some long-standing questions about vascular connections and directions.