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University International
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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. -
The Nuclear Pattern of the Non-Tectal Portions of the Midbrain and Isthmus in Primates
THE NUCLEAR PATTERN OF THE NON-TECTAL PORTIONS OF THE MIDBRAIN AND ISTHMUS IN PRIMATES ELIZABETH C. CROSBY AND RUSSELL T. WOODBURNE Department of Anatomy, University of Michigan FOURTEEN PLATES (TWENTY-THREE FIGURES) INTRODUCTION The various nuclear groups in the midbrain of primates show marked resemblances to their homologues in subprimate forms, although certain regions are characterized by a marked increase and others by a definite decrease in development. The literature dealing with special regions is considerable in amount and some of it is of relatively early date. That pertinent to the present consideration of these regions has been reviewed under the account of the general literature placed at the end of this series of papers. Attention is called here to a few contributions that have been particularly helpful in the preparation of the primate descriptions. Among such are the studies of Ziehen on various regions of the midbrain, particularly his account of the periventricular regions, and the descriptive analysis of Ingram and Ranson ('35) of the nucleus of Darkschewitsch and the interstitial nucleus of the medial longitudinal fasciculus, which confirmed Stengel's ( '24) earlier account. There are innumerable figures and descrip- tions of various parts of the oculomotor and trochlear gray in primates. Among these may be mentioned the work of Panegrossi ('04), Ram6n y Cajal ('ll), Brouwer ('18, and elsewhere), Le Gros Clark ( '26) and Mingazzini ( '28). The differences in nomenclature with respect to the periventricular gray of caudal midbrain and isthmus regions are indicated 441 442 G. CARL HUBER ET AL. to some extent on the figures of the human brain as well as considered in the general literature. -
Lecture (6) Internal Structures of the Brainstem.Pdf
Internal structures of the Brainstem Neuroanatomy block-Anatomy-Lecture 6 Editing file Objectives At the end of the lecture, students should be able to: ● Distinguish the internal structure of the components of the brain stem in different levels and the specific criteria of each level. 1. Medulla oblongata (closed, mid and open medulla) 2. Pons (caudal and rostral). 3. Midbrain ( superior and inferior colliculi). Color guide ● Only in boys slides in Green ● Only in girls slides in Purple ● important in Red ● Notes in Grey Medulla oblongata Caudal (Closed) Medulla Traversed by the central canal Motor decussation (decussation of the pyramids) ● Formed by pyramidal fibers, (75-90%) cross to the opposite side ● They descend in the lateral white column of the spinal cord as the lateral corticospinal tract. ● The uncrossed fibers form the ventral corticospinal tract Trigeminal sensory nucleus. ● it is the larger sensory nucleus. ● The Nucleus Extends Through the whole length of the brainstem and its note :All CN V afferent sensory information enters continuation of the substantia gelatinosa of the spinal cord. the brainstem through the nerve itself located in the pons. Thus, to reach the spinal nucleus (which ● It lies in all levels of M.O, medial to the spinal tract of the trigeminal. spans the entire brain stem length) in the Caudal ● It receives pain and temperature from face, forehead. Medulla those fibers have to "descend" in what's known as the Spinal Tract of the Trigeminal ● Its tract present in all levels of M.O. is formed of descending (how its sensory and descend?see the note) fibers that terminate in the trigeminal nucleus. -
NIH Public Access Author Manuscript Neuromodulation
NIH Public Access Author Manuscript Neuromodulation. Author manuscript; available in PMC 2015 June 01. NIH-PA Author ManuscriptPublished NIH-PA Author Manuscript in final edited NIH-PA Author Manuscript form as: Neuromodulation. 2014 June ; 17(4): 312–319. doi:10.1111/ner.12141. Surgical Neuroanatomy and Programming in Deep Brain Stimulation for Obsessive Compulsive Disorder Takashi Morishita, M.D., Ph.D.1, Sarah M. Fayad, M.D.2, Wayne K. Goodman, M.D.3, Kelly D. Foote, M.D.1, Dennis Chen, B.S.2, David A. Peace, M.S., CMI1, Albert L. Rhoton Jr.1, and Michael S. Okun, M.D.1,2 1Department of Neurosurgery, University of Florida College of Medicine/Shands Hospital, Center for Movement Disorders and Neurorestoration, McKnight Brain Institute, Gainesville, FL Corresponding Author: Takashi Morishita, M.D., Ph.D., Department of Neurosurgery, Mcknight Brain Institute Room L2-100, 1149 South Newell Drive, Gainesville, FL 32611, 352-273-9000, 352-392-8413 FAX, [email protected]. Authorship Statement: Drs. Morishita and Okun deigned and conducted the study, including patient recruitment, data collection and data analysis. Drs. Morishita and Fayad prepared the manuscript draft with important intellectual input from Drs. Okun, Rhoton, Goodman and Foote. Mr. Peace provided his illustration into this manuscript. Mr. Chen contributed to collect the data. All authors approved the final manuscript. Author disclosures 1. Takashi Morishita, M.D., Ph.D. Disclosures: Dr. Morishita has received grant support from Nakatomi foundation, St. Luke’s Life Science Institute of Japan, and Japan Society for Promotion of Science in Japan. 2. Sarah M. -
The Three-Dimensional Architecture of the Internal Capsule of the Human Brain Demonstrated by Fiber Dissection Technique
ARS Medica Tomitana - 2014; 3(78): 115 -122 10.2478/arsm-2014-0021 Goga Cristina1,2,3, Brinzaniuc Klara1, Florian I.S.2, Rodriguez Mena R.3 The three-dimensional architecture of the internal capsule of the human brain demonstrated by fiber dissection technique 1. University of Medicine and Pharmacy Tirgu Mures, Tirgu Mures, Romania, Department of Anatomy 2. Cluj County Emergency Hospital, Cluj Napoca, Romania, Department of Neurosurgery 3. Yeditepe University School of Medicine, Istanbul, Turkey, Department of Neurosurgery ABSTRACT Introduction The fiber dissection technique involves peeling away white matter fiber tracts of the brain to display its three-dimensional anatomic arrangement. The intricate three-dimensional configuration and structure of the internal capsule (IC) is not well defined. By using The white matter of the brain consists of the fiber dissection technique, our aim was to expose bundles of myelinated nerve fibers known as and study the IC to achieve a clearer conception of its fascicles or fiber tracts. There are three groups of configuration and relationships with neighboring white nerve fibers: association, connection and projection matter fibers and central nuclei. fibers. Association fibers connect neighboring The lateral and medial aspects of the temporal lobes of and distal cortical region in the same hemisphere. twenty, previously frozen, formalin-fixed human brains Commissural fibers connect homologues regions in were dissected under the operating microscope using the two hemispheres. Projection fibers connect the the fiber dissection technique. The details of the three-dimensional arrangement of the cerebral cortex with subcortical structures such as fibers within the IC were studied and a comprehensive thalamus, basal ganglia, brainstem and spinal cord. -
Esting Resemblances Between the Avian and the Reptilian and the Mam- Malian Nuclear Pattern in This Region
CERTAIN NUCLEAR GROUPS OF THE AVIAX MESENCEPHALON ERWIN JUNGHERR Department of Animal Diseases, Storrs AgI%wltural Experiment Station, Storrs, Connecticut FIVEl PLATJB (TPIN FIGURES) A study of the mesencephalon in the chicken has shown many inter- esting resemblances between the avian and the reptilian and the mam- malian nuclear pattern in this region. The following account attempts to stress those likenesses by an application of mammalian terminology to certain nuclear groups in the avian midbrain. The pertinent litera- ture will be considered in connection with the descriptions of the various areas. TECTAL AND BUBTECTAL REGIONS Superior colliculzls The superior colliculus or optie tectum in the bird is homologous with the similarly designated region in reptiles and mammals. However, in the bird there is a greater degree of layer differentiation than in these other forms. The general pattern of tectal lamination in sub- mammals was first described by Ram& (1896), who differentiated four- teen layers in the lizard. He believed the lamination pattern to be sim- ilar in birds and his observations were confirmed by his brother Ram6n p Cajal ('11). In a restudy of the reptilian optic tectum Huber and Crosby ('33, '33a, '33b, '34) established six fundamental layers, found to be present in a wide range of reptilian forms, which they believed to have phylogenetic as well as functional justification (Huber and Crosby, This study is a partial report on a cooperative project between the U. 8. Regional Poultry Research Laboratory, East Lansing, Mich., and the Storrs (Conn.) Agricultural Experiment Station. It is based upon three Huber ( '27) tolnidin-blue stained sets of serial sections of the brain of the chicken, Gallus domesticus. -
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. -
Trochlear Nerve Nucleus in Albino Rat
IOSR Journal of Dental and Medical Sciences (IOSR-JDMS) e-ISSN: 2279-0853, p-ISSN: 2279-0861. Volume 5, Issue 5 (Mar.- Apr. 2013), PP 65-68 www.iosrjournals.org Trochlear Nerve Nucleus in Albino rat Singh A., Khanna J. & Bharihoke V. Department of Anatomy, University College of Medical Sciences & Guru Teg Bahadur Hospital, Delhi India Abstract: A study of the trochlear nerve nucleus and its course within the brain is reported based on histological and fluorescent tract tracing techniques. Twenty inbred adult Wistar albino rats weighing between 150 to 250 gm of either sex were taken in the study. The localization of the nucleus giving rise to the nerve supplying the superior oblique muscle was done by using fluorescent dyes, Fast blue and Diamidino yellow. Fast blue was applied to the trochlear nerve of the right side and the Diamidino yellow was applied to the nerve of the left side in each animal. Animals were sacrificed after appropriate survival period. The labeled neurons were localized in the fourth nerve nucleus in the midbrain with the help of a Ziess fluorescence microscope .The majority of the fibers of the trochlear nerve cross to the opposite side and a few fibers remain ipsilateral. Many neurons were labeled with both the dyes indicating bilateral innervation. The nucleus was studied in paraffin sections stained with Kluver Barrera and Marshland, Glees and Erikson’s stain to trace the nerve fibers within the midbrain. Key words: Fluorescent tract tracing techniques, midbrain, superior medullary vellum, trochlear nerve nucleus, Diamidino yellow, Fast blue I. Introduction The basis of origin of the trochlear nerve from the posterior aspect of the midbrain and its crossing before exiting from the brain remains an enigma. -
Cranial Nerves and Their Nuclei
CranialCranial nervesnerves andand theirtheir nucleinuclei 鄭海倫鄭海倫 整理整理 Cranial Nerves Figure 13.4a Location of the cranial nerves • Anterior cranial fossa: C.N. 1–2 • Middle cranial fossa: C.N. 3-6 • Posterior cranial fossa: C.N. 7-12 FunctionalFunctional componentscomponents inin nervesnerves • General Somatic Efferent • Special Visceral Afferent •GSE GSA GVE GVA • (SSE) SSA SVE SVA Neuron columns in the embryonic spinal cord * The floor of the 4th ventricle in the embryonic rhombencephalon Sp: special sensory B:branchial motor Ss: somatic sensory Sm: somataic motor Vi: visceral sensory A: preganglionic autonomic (visceral motor) • STT: spinothalamic tract • CST: corticospinal tract • ML: medial lemniscus Sensory nerve • Olfactory (1) •Optic (2) • Vestibulocochlear (8) Motor nerve • Oculomotor (3) • Trochlear (4) • Abducens (6) • Accessory (11) • Hypoglossal (12) Mixed nerve • Trigeminal (5) • Facial (7) • Glossopharyngeal (9) • Vagus (10) Innervation of branchial muscles • Trigemial • Facial • Glossopharyngeal • Vagus Cranial Nerve I: Olfactory Table 13.2(I) Cranial Nerve II: Optic • Arises from the retina of the eye • Optic nerves pass through the optic canals and converge at the optic chiasm • They continue to the thalamus (lateral geniculate body) where they synapse • From there, the optic radiation fibers run to the visual cortex (area 17) • Functions solely by carrying afferent impulses for vision Cranial Nerve II: Optic Table 13.2(II) Cranial Nerve III: Oculomotor • Fibers extend from the ventral midbrain, pass through the superior orbital fissure, and go to the extrinsic eye muscles • Functions in raising the eyelid, directing the eyeball, constricting the iris, and controlling lens shape Cranial Nerve III: Oculomotor Table 13.2(III) 1.Oculomotor nucleus (GSE) • Motor to ocular muscles: rectus (superior對側, inferior同側and medial同 側),inferior oblique同側, levator palpebrae superioris雙側 2. -
BRAIN, Hnd CEREBELLAR CENTERS and FIBER TRACTS IS BIRDS1
A CONSIDERATION OF CERTAIN BULBAB, R111)- BRAIN, hND CEREBELLAR CENTERS AND FIBER TRACTS IS BIRDS1 ESTHER ELICK SANDERS Lnboratory of Comparative Xeurology, Department of Anatomy, University of Michigan FIFTEEN FIGURES CONTENTS Introduction . , . 156 Materials and methods . 167 Literature .. ...,..... 157 Description of nuclear . 165 Nuclei aiid root fibers of the eye-muscle nerves . .. .. 163 Oculomotor nuclei aiid root fibers . 166 Trochlear nucleus and root fibers .. , . ,.. ..... .. 168 Abdueens nuclei arid root fibers , ............. 1g9 Fiber connections of the eye-muscle nuclei . , . 171 Tecto-bulbar tract . 173 Dorsal tecto-bulbar tract . , . , . 17.5 Ventral tecto-bulbar tract . ............... 176 Trigemiiial nuclei and root fibers . , . , . 177 Sensory nudei of the trigeminal 177 Motor nuclei of the trigcminal . 179 Cutaneous sensory root of the trigeminal . 183 Mesencephalic and motor roots of the trigeminal . I . 183 Secondary connections of the t.rigemiii 153 Internuclear fibers from sensory trigemiiial nuclci 183 Trigemino-cerebellar connections . , . 183 Secondary ascending trigemiual bundle, (trigemino-mesencephalic tract) ................................................ 186 Quinto-frontal tract . .......... 187 Cerebello-motorius fibers . , . , . , . 189 Nuclei and root fibers of the facial nerve . 189 Sensory nucleus of the facial nerve ........................... 189 Motor nuclei of the facial nerve , , . ._.. 189 Root fibers of the facial nerve . 190 A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the Unirersity of Michigan. 155 THE JOURNAL OF COYPARATIVE NEUROLOGY, VOL. 49, NO. 1 156 ESTHER BLICK SAWDERS Suclear centers and root fibers of the cochlear nerve ................ 190 Nuclear centers of the cochlear nerve ........ ............ 190 194 195 Vestibular nuclei aiid root fibers .... 197 Vestibular nuclei ............................................ 197 Vestibular root fibers ................... .......... 204 Secondary connections of the vestibular nerve .................... -
Ycine As an Inhibitory Neurotransmitter of Vestibular, Reticular, and Prepositus Hypoglossi Neurons That Project to the Cat Abducens Nucleus
The Journal of Neuroscience, August 1989, g(8): 2718-2736 Evidence for G!ycine as an Inhibitory Neurotransmitter of Vestibular, Reticular, and Prepositus Hypoglossi Neurons That Project to the Cat Abducens Nucleus Robert F. Spencer,’ Robert J. Wenthold, and Robert Baker3 ‘Department of Anatomy, Medical College of Virginia, Richmond, Virginia 23298, “Laboratory of Neuro-otolaryngology, National Institute of Neurological and Communicative Disorders and Stroke, National Institutes of Health, Bethesda, Maryland 20892, and 3Department of Physiology and Biophysics, New York University Medical Center, New York, New York 10016 The localization and distribution of brain-stem afferent neu- that were labeled autoradiographically by retrograde trans- rons to the cat abducens nucleus has been examined by port of 3H-glycine from the abducens nucleus. high-affinity uptake and retrograde transport of 3H-glycine. Electrophysiological recordings from abducens motoneu- Injections of 3H-glycine selectively labeled (by autoradiog- rons and internuclear neurons revealed a marked reduction raphy) only neurons located predominantly in the ipsilateral in the slow positivity of the orthodromic extracellular poten- medial vestibular and contralateral prepositus hypoglossi tial elicited by ipsilateral vestibular nerve stimulation follow- nuclei, and in the contralateral dorsomedial reticular for- ing systemic administration of strychnine, an antagonist of mation, the latter corresponding to the location of inhibitory glycine. Intracellular recordings demonstrated that the ves- burst neurons. The specificity of uptake and retrograde tibular-evoked disynaptic inhibitory postsynaptic potentials transport of 3H-glycine was indicated by the absence of la- in abducens neurons were effectively blocked by strychnine beling of the dorsomedial medullary reticular neurons ipsi- but were unaffected by picrotoxin, an antagonist of GABA.