DR. Sanaa Alshaarawy
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Section of Neurosurgery, Department of Surgery, University of Michigan Hospital, Ann Arbor, Michigan
ANATOMIC PATHWAYS RELATED TO PAIN IN FACE AND NECK* JAMES A. TAREN, M.D., AND EDGAR A. KAHN, M.D. Section of Neurosurgery, Department of Surgery, University of Michigan Hospital, Ann Arbor, Michigan (Received for publication May 19, 1961) HE remarkable ability of the higher V is most dorsal in the tract. Fig. 4 is a dia- portions of the central nervous system gram of the medulla 6 mm. below the obex T to readjust to surgical lesions presup- which we believe to be the optimal level for poses the existence of alternate pathways. tractotomy. The operation is done with the This hypothesis has been tested with regard patient in the sitting position to facilitate to a specific localized sensory input, pain exposure. The medullary incision, 4-5 mm. from the face. in depth, extends from the bulbar accessory Our method has been to study the degen- rootlet to a line extrapolated from the pos- eration of nerve fibers by Weil and Marchi terior rootlets of the ~ud cervical nerve root. techniques following various surgical lesions An adequate incision results in complete in man and monkey. The lesions have con- analgesia of all 8 divisions as well as analgesia sisted of total and selective retrogasserian in the distribution of VII, IX, and X except rhizotomy in 3 humans and 3 monkeys, for sparing of the vermilion border of the lips medullary tractotomy in ~ humans and (Fig. 5). A degree of ataxia of the ipsilateral monkeys, and extirpation of the cervical upper extremity usually accompanies effec- portion of the nucleus of the descending tract tive tractotomy and is caused by compromise of V in ~ monkeys. -
The Superior and Inferior Colliculi of the Mole (Scalopus Aquaticus Machxinus)
THE SUPERIOR AND INFERIOR COLLICULI OF THE MOLE (SCALOPUS AQUATICUS MACHXINUS) THOMAS N. JOHNSON' Laboratory of Comparative Neurology, Departmmt of Amtomy, Un&versity of hfiehigan, Ann Arbor INTRODUCTION This investigation is a study of the afferent and efferent connections of the tectum of the midbrain in the mole (Scalo- pus aquaticus machrinus). An attempt is made to correlate these findings with the known habits of the animal. A subterranean animal of the middle western portion of the United States, Scalopus aquaticus machrinus is the largest of the genus Scalopus and its habits have been more thor- oughly studied than those of others of this genus according to Jackson ('15) and Hamilton ('43). This animal prefers a well-drained, loose soil. It usually frequents open fields and pastures but also is found in thin woods and meadows. Following a rain, new superficial burrows just below the surface of the ground are pushed in all directions to facili- tate the capture of worms and other soil life. Ten inches or more below the surface the regular permanent highway is constructed; the mole retreats here during long periods of dry weather or when frost is in the ground. The principal food is earthworms although, under some circumstances, larvae and adult insects are the more usual fare. It has been demonstrated conclusively that, under normal conditions, moles will eat vegetable matter. It seems not improbable that they may take considerable quantities of it at times. A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the University of Michigan. -
Circuits in the Rodent Brainstem That Control Whisking in Concert with Other Orofacial Motor Actions
Neuroscience 368 (2018) 152–170 CIRCUITS IN THE RODENT BRAINSTEM THAT CONTROL WHISKING IN CONCERT WITH OTHER OROFACIAL MOTOR ACTIONS y y LAUREN E. MCELVAIN, a BETH FRIEDMAN, a provides the reset to the relevant premotor oscillators. HARVEY J. KARTEN, b KAREL SVOBODA, c FAN WANG, d Third, direct feedback from somatosensory trigeminal e a,f,g MARTIN DESCHEˆ NES AND DAVID KLEINFELD * nuclei can rapidly alter motion of the sensors. This feed- a Department of Physics, University of California at San Diego, back is disynaptic and can be tuned by high-level inputs. La Jolla, CA 92093, USA A holistic model for the coordination of orofacial motor actions into behaviors will encompass feedback pathways b Department of Neurosciences, University of California at San Diego School of Medicine, La Jolla, CA 92093, USA through the midbrain and forebrain, as well as hindbrain c areas. Howard Hughes Medical Institute, Janelia Research This article is part of a Special Issue entitled: Barrel Campus, Ashburn, VA 20147, USA Cortex. Ó 2017 IBRO. Published by Elsevier Ltd. All rights d Department of Neurobiology, Duke University Medical reserved. Center, Durham, NC 27710, USA e Department of Psychiatry and Neuroscience, Laval University, Que´bec City, G1J 2G3, Canada f Key words: coupled oscillators, facial nucleus, hypoglossal Section of Neurobiology, University of California at San Diego, La Jolla, CA 92093, USA nucleus, licking, orienting, tongue, vibrissa. g Department of Electrical and Computer Engineering, University of California at San Diego, La Jolla, CA 92093, USA Contents Introduction 153 Abstract—The world view of rodents is largely determined Coordination of multiple orofacial motor actions 153 by sensation on two length scales. -
Neuronal Organization in the Inferior Colliculus Revisited with Cell-Type- Dependent Monosynaptic Tracing
This Accepted Manuscript has not been copyedited and formatted. The final version may differ from this version. Research Articles: Systems/Circuits Neuronal organization in the inferior colliculus revisited with cell-type- dependent monosynaptic tracing Chenggang Chen1, Mingxiu Cheng1,2, Tetsufumi Ito3 and Sen Song1 1Tsinghua Laboratory of Brain and Intelligence (THBI) and Department of Biomedical Engineering, Beijing Innovation Center for Future Chip, Center for Brain-Inspired Computing Research, McGovern Institute for Brain Research, Tsinghua University, Beijing, 100084, China 2National Institute of Biological Sciences, Beijing, 102206, China 3Anatomy II, School of Medicine, Kanazawa Medical University, Uchinada, Ishikawa, 920-0293, Japan DOI: 10.1523/JNEUROSCI.2173-17.2018 Received: 31 July 2017 Revised: 2 February 2018 Accepted: 7 February 2018 Published: 24 February 2018 Author contributions: C.C., T.I., and S.S. designed research; C.C. and M.C. performed research; C.C. and T.I. analyzed data; C.C. wrote the first draft of the paper; C.C., T.I., and S.S. edited the paper; C.C., T.I., and S.S. wrote the paper. Conflict of Interest: The authors declare no competing financial interests. This work was supported by funding from the National Natural Science Foundation of China (31571095, 91332122, for S.S.), Special Fund of Suzhou-Tsinghua Innovation Leading Action (for S.S.), Beijing Program on the Study of Brain-Inspired Computing System and Related Core Technologies (for S.S.), Beijing Innovation Center for Future Chip (for S.S.), and Chinese Academy of Sciences Institute of Psychology Key Laboratory of Mental Health Open Research Grant (KLMH2012K02, for S.S.), grants from Ministry of Education, Science, and Culture of Japan (KAKENHI grant, Grant numbers 16K07026 and 16H01501; for T.I.), and Takahashi Industrial and Economic Research Foundation (for T.I.). -
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. -
Brainstem and Its Associated Cranial Nerves
Brainstem and its Associated Cranial Nerves Anatomical and Physiological Review By Sara Alenezy With appreciation to Noura AlTawil’s significant efforts Midbrain (Mesencephalon) External Anatomy of Midbrain 1. Crus Cerebri (Also known as Basis Pedunculi or Cerebral Peduncles): Large column of descending “Upper Motor Neuron” fibers that is responsible for movement coordination, which are: a. Frontopontine fibers b. Corticospinal fibers Ventral Surface c. Corticobulbar fibers d. Temporo-pontine fibers 2. Interpeduncular Fossa: Separates the Crus Cerebri from the middle. 3. Nerve: 3rd Cranial Nerve (Oculomotor) emerges from the Interpeduncular fossa. 1. Superior Colliculus: Involved with visual reflexes. Dorsal Surface 2. Inferior Colliculus: Involved with auditory reflexes. 3. Nerve: 4th Cranial Nerve (Trochlear) emerges caudally to the Inferior Colliculus after decussating in the superior medullary velum. Internal Anatomy of Midbrain 1. Superior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). a. Tectospinal Pathway: turning the head, neck and eyeballs in response to a visual stimuli.1 Level of b. Spinotectal Pathway: turning the head, neck and eyeballs in response to a cutaneous stimuli.2 Superior 2. Oculomotor Nucleus: Situated in the periaqueductal grey matter. Colliculus 3. Red Nucleus: Red mass3 of grey matter situated centrally in the Tegmentum. Involved in motor control (Rubrospinal Tract). 1. Inferior Colliculus: Nucleus of grey matter that is associated with the Tectospinal Tract (descending) and the Spinotectal Tract (ascending). Tectospinal Pathway: turning the head, neck and eyeballs in response to a auditory stimuli. 2. Trochlear Nucleus: Situated in the periaqueductal grey matter. Level of Inferior 3. -
ON-LINE FIG 1. Selected Images of the Caudal Midbrain (Upper Row
ON-LINE FIG 1. Selected images of the caudal midbrain (upper row) and middle pons (lower row) from 4 of 13 total postmortem brains illustrate excellent anatomic contrast reproducibility across individual datasets. Subtle variations are present. Note differences in the shape of cerebral peduncles (24), decussation of superior cerebellar peduncles (25), and spinothalamic tract (12) in the midbrain of subject D (top right). These can be attributed to individual anatomic variation, some mild distortion of the brain stem during procurement at postmortem examination, and/or differences in the axial imaging plane not easily discernable during its prescription parallel to the anterior/posterior commissure plane. The numbers in parentheses in the on-line legends refer to structures in the On-line Table. AJNR Am J Neuroradiol ●:●●2019 www.ajnr.org E1 ON-LINE FIG 3. Demonstration of the dentatorubrothalamic tract within the superior cerebellar peduncle (asterisk) and rostral brain stem. A, Axial caudal midbrain image angled 10° anterosuperior to posteroinferior relative to the ACPC plane demonstrates the tract traveling the midbrain to reach the decussation (25). B, Coronal oblique image that is perpendicular to the long axis of the hippocam- pus (structure not shown) at the level of the ventral superior cerebel- lar decussation shows a component of the dentatorubrothalamic tract arising from the cerebellar dentate nucleus (63), ascending via the superior cerebellar peduncle to the decussation (25), and then enveloping the contralateral red nucleus (3). C, Parasagittal image shows the relatively long anteroposterior dimension of this tract, which becomes less compact and distinct as it ascends toward the thalamus. ON-LINE FIG 2. -
(12) United States Patent (10) Patent No.: US 9,358,393 B1 L0zano (45) Date of Patent: Jun
US00935.8393B1 (12) United States Patent (10) Patent No.: US 9,358,393 B1 L0ZanO (45) Date of Patent: Jun. 7, 2016 (54) STIMULATION METHODS AND SYSTEMS 4,203,440 A 5/1980 Theeuwes FORTREATING AN AUDITORY 4,203.442 A 5/1980 Michaels DYSFUNCTION 4,210,139 A 7/1980 Higuchi (Continued) (76) Inventor: Andres M. Lozano, Toronto (CA) FOREIGN PATENT DOCUMENTS (*) Notice: Subject to any disclaimer, the term of this patent is extended or adjusted under 35 WO WOO1,08617 A1 2/2001 U.S.C. 154(b) by 1826 days. OTHER PUBLICATIONS (21) Appl. No.: 11/271,126 Office action dated Sep. 16, 2009 for related U.S. Appl. No. 1 1/271,688 (Lozano-1), filed Nov. 9, 2005, Inventor: Andres M. (22) Filed: Nov. 9, 2005 Lozano, (14 pages). Related U.S. Application Data (Continued) (60) gynal application No. 60/626,174, filed on Nov. Primary Examiner — Nicole F Lavert s (74) Attorney, Agent, or Firm — Faegre Baker Daniels LLP (51) Int. Cl. A61N L/00 (2006.01) (57) ABSTRACT A6 IB5/02 (2006.01) Methods of treating auditory hallucinations, hyperacusis, A6 IN L/36 (2006.01) Schizophrenia, and/or phonophobia include applying at least A61N L/05 (2006.01) one stimulus to a stimulation site within a patient with an (52) U.S. Cl. implanted stimulator in accordance with one or more stimu CPC .......... A61N I/36132 (2013.01); A61N I/0541 lation parameters. The stimulation site may include, for (2013.01) example, at least one or more of a cochlear nucleus, auditory (58) Field of Classification Search striae, Superior olivary complex, lateral lemniscus, inferior USPC ...................................... -
Cortical Control of Facial Expression
Review The Journal of Comparative Neurology Research in Systems Neuroscience DOI 10.1002/cne.23908 Topical review Cortical control of facial expression. René M. Müri1,2,3 1Division of Cognitive and Restorative Neurology, Departments of Neurology and Clinical Research, University Hospital Inselspital, Bern, Switzerland 2Gerontechnology and Rehabilitation Group, University of Bern, Bern, Switzerland 3Center for Cognition, Learning, and Memory, University of Bern, Bern, Switzerland Abbreviated title: Cortical control of facial expression Key words: human, facial expression, emotion, facial innervation | downloaded: 13.3.2017 http://boris.unibe.ch/72088/ This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process which may lead to differences between this version and the Version of Record. Please cite this article as an ‘Accepted Article’, doi: 10.1002/cne.23908 source: © 2015 Wiley Periodicals, Inc. Received: Jan 31, 2015; Revised: Sep 19, 2015; Accepted: Sep 25, 2015 This article is protected by copyright. All rights reserved. Journal of Comparative Neurology Page 4 of 23 Abstract The present topical review deals with the motor control of facial expressions in humans. Facial expressions are a central part of human communication. Emotional face expressions have a crucial role in human non-verbal behavior, allowing a rapid transfer of information between individuals. Facial expressions can be both voluntarily or emotionally controlled. Recent studies in non-human primates and humans revealed that the motor control of facial expressions has a distributed neural representation. At least 5 cortical regions on the medial and lateral aspects of each hemisphere are involved: the primary motor cortex, the ventral lateral premotor cortex, the supplementary motor area on the medial wall, and, finally, the rostral and caudal cingulate cortex. -
Commissural Projections of the Nuclei of the Lateral Lemniscus and Keuronal Degeneration Following Midline Transections in the Adult Rat By
Commissural Projections of the Nuclei of the Lateral Lemniscus and Keuronal Degeneration Following Midline Transections in the Adult Rat by Brian Anthony van Adel B .Sc. (Hons) Carleton University, 1995 A thesis subrnitted to the faculty of Graduate Studies and Research in partial fulnllment of the requirements of the degree of Master of Science Specialization in Neuroscience Deparûnent of Biology Ottawa-Carleton Institutes of Biology and Neuroscience Carleton University Ottawa, Ontano May, 1998 O copyright 1998, Brian Anthony van Adel National Library Bibliothèque nationale 1+1 .,nad, du Canada Acquisitions and Acquisitions et Bibliographie Services seMces bibliographiques 395 Wellington Street 395, rue Wellington OttawaON KtAW ûuawaON KtAON4 canada CaMda The author has granted a non- L'auteur a accordé une licence non exclusive licence allowing the exclusive permettant à la National Library of Canada to Bibliothèque nationale du Canada de reproduce, 10- disûiiute or sen reproduire, prêter, distribuer ou copies of this thesis in microform, vendre des copies de cette these sous paper or electronic formats. la forme de microfiche/fïlm, de reproduction sur papier ou sur format électronique. The author retains ownership of the L'auteur conserve la propriété du copyright in this thesis. Neither the droit d'auteur qui protège cette thèse. thesis nor substantial extracts fiom it Ni la thèse ni des extraits substantiels may be printed or otheMrise de celle-ci ne doivent être imprimés reproduced without the author's ou autrement reproduits sans son permission. autorisation. ABSTRACT The normal neuroanatomical organization of the rat's nuclei of the lateral lemniscus (nLL) was investigated (Experiment 1) as a prerequisite for a time course analysis of retrograde changes in commissural projec~glemniscd neurons following midline surgical transection of their axons (Expriment 2). -
Somatotopic Organization of Perioral Musculature Innervation Within the Pig Facial Motor Nucleus
Original Paper Brain Behav Evol 2005;66:22–34 Received: September 20, 2004 Returned for revision: November 10, 2004 DOI: 10.1159/000085045 Accepted after revision: December 7, 2004 Published online: April 8, 2005 Somatotopic Organization of Perioral Musculature Innervation within the Pig Facial Motor Nucleus Christopher D. Marshall a Ron H. Hsu b Susan W. Herring c aTexas A&M University at Galveston, Galveston, Tex., bDepartment of Pediatric Dentistry, University of North Carolina, Chapel Hill, N.C., and cDepartment of Orthodontics, University of Washington, Seattle, Wash., USA Key Words pools of the lateral 4 of the 7 subnuclei of the facial motor Somatotopy W Innervation W Facial nucleus W Perioral nucleus. The motor neuron pools of the perioral muscles muscles W Orbicularis oris W Buccinator W Mammals were generally segregated from motoneurons innervat- ing other facial muscles of the rostrum. However, motor neuron pools were not confined to single nuclei but Abstract instead spanned across 3–4 subnuclei. Perioral muscle The orbicularis oris and buccinator muscles of mammals motor neuron pools overlapped but were organized so- form an important subset of the facial musculature, the matotopically. Motor neuron pools of portions of the perioral muscles. In many taxa, these muscles form a SOO overlapped greatly with each other but exhibited a robust muscular hydrostat capable of highly manipula- crude somatotopy within the SOO motor neuron pool. tive fine motor movements, likely accompanied by a spe- The large and somatotopically organized SOO motor cialized pattern of innervation. We conducted a retro- neuron pool in pigs suggests that the upper lip might be grade nerve-tracing study of cranial nerve (CN) VII in pigs more richly innervated than the other perioral muscles (Sus scrofa) to: (1) map the motor neuron pool distribu- and functionally divided. -
Impaired Cerebro-Cerebellar White Matter Connectivity and Its
www.nature.com/npjschz ARTICLE OPEN Impaired cerebro-cerebellar white matter connectivity and its associations with cognitive function in patients with schizophrenia ✉ Sung Eun Kim1, Sungcheol Jung2, Gyhye Sung1,3, Minji Bang 1 and Sang-Hyuk Lee1 Schizophrenia is a complex brain disorder of unknown etiology. Based on the notion of “cognitive dysmetria,” we aimed to investigate aberrations in structural white matter (WM) connectivity that links the cerebellum to cognitive dysfunction in patients with schizophrenia. A total of 112 participants (65 patients with schizophrenia and 47 healthy controls [HCs]) were enrolled and underwent diffusion tensor imaging. Between-group voxel-wise comparisons of cerebellar WM regions (superior/middle [MCP]/ inferior cerebellar peduncle and pontine crossing fibers) were performed using Tract-Based Spatial Statistics. Cognitive function was assessed using the Trail Making Test Part A/B (TMT-A/B), Wisconsin Card Sorting Test (WCST), and Rey-Kim Memory Test in 46 participants with schizophrenia. WM connectivity, measured as fractional anisotropy (FA), was significantly lower in the MCP in participants with schizophrenia than in HCs. The mean FAs extracted from the significant MCP cluster were inversely correlated with poorer cognitive performance, particularly longer time to complete the TMB-B (r = 0.559, p < 0.001) and more total errors in the WCST (r = 0.442, p = 0.003). Our findings suggest that aberrant cerebro-cerebellar communication due to disrupted WM connectivity may contribute to cognitive impairments, a core characteristic of schizophrenia. Our results may expand our 1234567890():,; understanding of the neurobiology of schizophrenia based on the cerebro-cerebellar interconnectivity of the brain. npj Schizophrenia (2021) 7:38 ; https://doi.org/10.1038/s41537-021-00169-w INTRODUCTION patients with schizophrenia, implying the possible involvement of Schizophrenia is a complex brain disorder of unknown etiology.