Ventricles of Brain ▪ Ventricles Are Cavities Or Expansions Within the Brain That Are Derived from the Lumen of the Embryonic Neural Tube
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The Connexions of the Amygdala
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.28.2.137 on 1 April 1965. Downloaded from J. Neurol. Neurosurg. Psychiat., 1965, 28, 137 The connexions of the amygdala W. M. COWAN, G. RAISMAN, AND T. P. S. POWELL From the Department of Human Anatomy, University of Oxford The amygdaloid nuclei have been the subject of con- to what is known of the efferent connexions of the siderable interest in recent years and have been amygdala. studied with a variety of experimental techniques (cf. Gloor, 1960). From the anatomical point of view MATERIAL AND METHODS attention has been paid mainly to the efferent connexions of these nuclei (Adey and Meyer, 1952; The brains of 26 rats in which a variety of stereotactic or Lammers and Lohman, 1957; Hall, 1960; Nauta, surgical lesions had been placed in the diencephalon and and it is now that there basal forebrain areas were used in this study. Following 1961), generally accepted survival periods of five to seven days the animals were are two main efferent pathways from the amygdala, perfused with 10 % formol-saline and after further the well-known stria terminalis and a more diffuse fixation the brains were either embedded in paraffin wax ventral pathway, a component of the longitudinal or sectioned on a freezing microtome. All the brains were association bundle of the amygdala. It has not cut in the coronal plane, and from each a regularly spaced generally been recognized, however, that in studying series was stained, the paraffin sections according to the Protected by copyright. the efferent connexions of the amygdala it is essential original Nauta and Gygax (1951) technique and the frozen first to exclude a contribution to these pathways sections with the conventional Nauta (1957) method. -
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. -
Anatomical Specificity of Septal Projections in Active and Passive Avoidance Behavior in Rats
MATOMICAL SPECIFICITY OF SEPTAL PROJECTIONS IN ACTIVE AND PASSIVE AVOIDANCE BEHAVIOR IN RATS by GARY W. VAN HOESEN B. A., Humboldt State College 1965 A MASTER'S THESIS submitted in partial fulfillment of the requirements for the degree MASTER OF SCIENCE Department of Psychology KANSAS STATE UNIVERSITY Manhattan, Kansas 1968 Approved by: Ma/or Professor 7'/ 'VS^^^ 1'^^^ 0^ CONTENTS ACKNOWLEDGEMENTS iii INTRODUCTION 1 METHOD 2 Subjects 2 Apparatus 2 Surgery and Histology 3 Procedure Passive Avoidance I4 Active Avoidance 5 Retention 5 Massed Extinction 5 RESULTS 5 Histology 5 Passive Avoidance 20 Active Avoidance Retention Massed Extinction 28 DISCUSSION 21 BIBLIOGRAPHY 28 Ill ACraOVJLEDGEMNTS This research was conducted while the author was a National Aeronautics and Space Administration Pre-Doctorate Trainee. Additional support was pro- vided by an NIGMS Training Grant, GM I362 awarded to the Kansas State Univer- sity Departments of Psychology, Zoology, and Physiology. I thank Dr. James C. Mitchell for his generous contributions of his time and guidance in the preparation of this work, and Dr. Charles P. Thompson and Dr. Robert C. Haygood for their interest and helpful criticisms. Additionally I would like to thank Mr. Jim MacDougall for his aid in the execution and prepara- tion of this research. The beha.vicral effects of septal lesions have been intensely investigated in recent years. Experiments encompassing wide ranges of test conditions and laboratory species have implicated the septum in a broad spectrum of psycho- logical and physiological phenomena. The lesion induced effects, as reviewed by KcCleary (1966), incl.ude hyperirritabllity or hypersensitivity, enhanced performance on active avoidance, and decrements on passive avoidance, timdng, alternation, and position reversal. -
Auditory and Vestibular Systems Objective • to Learn the Functional
Auditory and Vestibular Systems Objective • To learn the functional organization of the auditory and vestibular systems • To understand how one can use changes in auditory function following injury to localize the site of a lesion • To begin to learn the vestibular pathways, as a prelude to studying motor pathways controlling balance in a later lab. Ch 7 Key Figs: 7-1; 7-2; 7-4; 7-5 Clinical Case #2 Hearing loss and dizziness; CC4-1 Self evaluation • Be able to identify all structures listed in key terms and describe briefly their principal functions • Use neuroanatomy on the web to test your understanding ************************************************************************************** List of media F-5 Vestibular efferent connections The first order neurons of the vestibular system are bipolar cells whose cell bodies are located in the vestibular ganglion in the internal ear (NTA Fig. 7-3). The distal processes of these cells contact the receptor hair cells located within the ampulae of the semicircular canals and the utricle and saccule. The central processes of the bipolar cells constitute the vestibular portion of the vestibulocochlear (VIIIth cranial) nerve. Most of these primary vestibular afferents enter the ipsilateral brain stem inferior to the inferior cerebellar peduncle to terminate in the vestibular nuclear complex, which is located in the medulla and caudal pons. The vestibular nuclear complex (NTA Figs, 7-2, 7-3), which lies in the floor of the fourth ventricle, contains four nuclei: 1) the superior vestibular nucleus; 2) the inferior vestibular nucleus; 3) the lateral vestibular nucleus; and 4) the medial vestibular nucleus. Vestibular nuclei give rise to secondary fibers that project to the cerebellum, certain motor cranial nerve nuclei, the reticular formation, all spinal levels, and the thalamus. -
Agmatine Modulates Spontaneous Activity in Neurons of the Rat Medial
Weiss et al. Translational Psychiatry (2018) 8:201 DOI 10.1038/s41398-018-0254-z Translational Psychiatry ARTICLE Open Access Agmatine modulates spontaneous activity in neurons of the rat medial habenular complex—a relevant mechanism in the pathophysiology and treatment of depression? Torsten Weiss1,RenéBernard2, Hans-Gert Bernstein3,RüdigerW.Veh1 and Gregor Laube1 Abstract The dorsal diencephalic conduction system connects limbic forebrain structures to monaminergic mesencephalic nuclei via a distinct relay station, the habenular complexes. Both habenular nuclei, the lateral as well as the medial nucleus, are considered to play a prominent role in mental disorders like major depression. Herein, we investigate the effect of the polyamine agmatine on the electrical activity of neurons within the medial habenula in rat. We present evidence that agmatine strongly decreases spontaneous action potential firing of medial habenular neurons by activating I1-type imidazoline receptors. Additionally, we compare the expression patterns of agmatinase, an enzyme capable of inactivating agmatine, in rat and human habenula. In the medial habenula of both species, agmatinase is similarly distributed and observed in neurons and, in particular, in distinct neuropil areas. The putative relevance of 1234567890():,; 1234567890():,; 1234567890():,; 1234567890():,; these findings in the context of depression is discussed. It is concluded that increased activity of the agmatinergic system in the medial habenula may strengthen midbrain dopaminergic activity. Consequently, -
Anatomy of the Superior Olivary Complex.Pdf
Douglas Oliver University of Connecticut Health Center SUPERIOR OLIVE Auditory Pathways Auditory CORTEX GLUT Cortex GABA GLY Medial Geniculate MGB Body Inferior IC Colliculus DLL DLL COCHLEA VLL VLL DCN VCN SOC Auditory Pathways IC Organization of Superior Olivary Complex . Subdivisions and Cytoarchitecture . Neuron types . Inputs . Outputs . Synapses . Basic Circuit Cytoarchitecture of Superior Olivary Complex LSO LSO MSO MSO MNTB D MNTB M (somata & dendrites) (axons & endings) Tsuchitani, 1978, Fig. 10 Comparative anatomy of SOC Tetsufumi Ito & Shig Kuwada Binaural Basic Circuits 8 ‐ 9 Brodal Fig MSO: medial superior olive; LSO: lateral superior olive NTB: nucleus of trapezoid body; IC: inferior colliculus MSO Principle glutamate Cells . Fusiform . Bipolar . Disc‐shaped . Each dendrite innervated by a different side MSO‐In situ hybridization RPO MSO MNTB SPO LSO VGLUT1 VGLUT2 VIAAT NISSL MSO Inputs and Synapses H=high frequency EI - ILD L=low frequency EE - ITD LSO MSO L L B H B B H G LNTB TO LSO MNTB E=Excitation (glutamate) ‐‐‐ I=Inhibition (glycine) ITD CODING Unlike retinal targets, the cochlear nuclei contain maps of frequency, not location. So how does the auditory system know ‘where’ a sound is coming from? T + ITD T By comparing the interaural time differences (ITD) between the ears How is this accomplished?... LSO MSO Right Input A Right Input B C Time Code Time Code E E A A B B C C D D E E Output Output abcde Place Code abcde Place Code Excitation MSO creates a response to Left Input Left Input Inhibition interaural time differences I Time Code E Time Code DEMSO "peak" unit LSO "trough" unit ITD ITD Figure 14.2 Binaural Responses in MSO MSO Summary . -
The Superior Olivary Complex +
Excitatory and inhibitory transmission in the superior olivary complex. Ian D. Forsythe, Matt Barker, Margaret Barnes-Davies, Brian Billups, Paul Dodson, Fatima Osmani, Steven Owens and Adrian Wong. Department of Cell Physiology and Pharmacology, University of Leicester, Leicester LE1 9HN. UK. The timing and pattern of action potentials propagating into the brainstem from both cochleae contain information about the azimuth location of that sound in auditory space. This binaural information is integrated in the superior olivary complex. This part of the auditory pathway is adapted for fast conduction speeds and the preservation of timing information with several complimentary mechanisms (see Oertel, 1999; Trussell, 1999). There are large diameter axons terminating in giant somatic synapses that activate receptor ion channels with fast kinetics. The resultant postsynaptic potentials generated in the receiving neuron are integrated with a suite of voltage-gated ion channels that determine the action potential threshold, duration and repetitive firing properties. We have studied presynaptic and postsynaptic mechanisms that regulate efficacy, timing and integration of synaptic responses in the medial nucleus of the trapezoid body and the medial and lateral superior olives. Presynaptic calcium currents in the calyx of Held. The calyx of Held is a giant synaptic terminal that forms around the soma of principal cells in the Medial Nucleus of the Trapezoid Body (MNTB) (Forsythe, 1994). Each MNTB neuron receives a single calyx. Action potentials propagating into the synaptic terminal trigger the opening of P-type calcium channels (Forsythe et al. 1998) which in turn trigger the release of glutamate into the synaptic cleft (Borst et al., 1995). -
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. -
Frontal Lobe Anterior Corpora Commissure Quadrigemina Superior Colliculus Optic Chiasm Inferior Colliculus
Chapter 16 The Nervous System The Brain and Cranial Nerves Lecture Presentation by Steven Bassett Southeast Community College © 2015 Pearson Education, Inc. Introduction • The brain is a complex three-dimensional structure that performs a bewildering array of functions • Think of the brain as an organic computer • However, the brain is far more versatile than a computer • The brain is far more complex than the spinal cord • The brain consists of roughly 20 billion neurons © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain • The CNS begins as a neural tube • The lumen of the tube (neurocoel) is filled with fluid • The lumen of the tube will expand thus forming the various ventricles of the brain • In the fourth week of development, the cephalic area of the neural tube enlarges to form: • Prosencephalon • Mesencephalon • Rhombencephalon © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Prosencephalon eventually develops to form: • Telencephalon forms: • Cerebrum • Diencephalon forms: • Epithalamus, thalamus, and hypothalamus. © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Mesencephalon • Does not subdivide • Becomes the midbrain © 2015 Pearson Education, Inc. Table 16.1 Development of the Human Brain © 2015 Pearson Education, Inc. An Introduction to the Organization of the Brain • Embryology of the Brain (continued) • Rhombencephalon • Eventually develops to form: • Metencephalon: forms the pons and cerebellum • Myelencephalon: forms the medulla oblongata © 2015 Pearson Education, Inc. -
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. -
1. 2. A) Explain the Compositions of White Matter and Gray
Tfy-99.2710 Introduction to the Structure and Operation of the Human Brain, fall 2015 Exercise 1 1. 2. a) Explain the compositions of white matter and gray matter. White matter consists of glial cells and myelinated axons. It does not contain the cell bodies of neurons and acts as a signal pathway for the gray matter regions of the central nervous system. Gray matter consists of glial cells and unmyelinated axons. It contains neuronal cell bodies. b) Explain shortly the structure of a neuron. Neurons can be divided into three main parts: the cell body or the soma, the dendrites and the axon. The dendrites act as neuronal antennas in that they receive incoming signals. The cell body functions as the information processing unit of the neuron, and is responsible for sending signals forward. The axon is the signal pathway of the neuron; the signals sent by the cell body are transmitted along the axon to the axon terminals located away from the cell body. Signal transfer is along the axon is aided by the myelin sheath that covers the axon. c) Explain: Tfy-99.2710 Introduction to the Structure and Operation of the Human Brain, fall 2015 Exercise 1 i) myelin Membrane that wraps around axons. Formed from glial support cells: oligodendrogolia in the central nervous system and Schwann cells in the peripheral nervous system. Myelin facilitates signal transfer along axons by allowing action potentials to skip between the nodes of Ranvier (saltatory conduction). ii) receptor Molecule specialized in receiving a chemical signal by binding a specific neurotransmitter.