Cranial Nerves

Total Page:16

File Type:pdf, Size:1020Kb

Cranial Nerves Cranial Nerves (1,5,7,8,9,10,11 and 12) Slides not included 9th and 10th Cranial 11th and 12th Cranial 8th Cranial Nerve 5th and 7th Cranial 1st Cranial Nerve Nerves Nerves Nerves (3,7,11,12,13,21,23,24) - (10,16) (12,23) Slides included: (14 to 17) *Slides that are not included mostly are slides of summaries or pictures. Nouf Alabdulkarim. Med 435 Olfactory Nerve [The 1st Cranial Nerve] Special Sensory Olfactory pathway 1st order neuron Receptors Axons of 1st order Neurons Olfactory receptors are specialized, ciliated nerve cells The axons of these bipolar cells 12 -20 fibers form the that lie in the olfactory epithelium. true olfactory nerve fibers. Which passes through the cribriform plate of ethmoid → They join the olfactory bulb Preliminary processing of olfactory information It is within the olfactory bulb, which contains interneurones and large Mitral cells; axons from the latter leave the bulb to form the olfactory tract. nd 2 order neuron • It is formed by the Mitral cells of olfactory bulb. • The axons of these cells form the olfactory tract. • Each tract divides into 2 roots at the anterior perforated substance: Lateral root Medial root Carries olfactory fibers to end in cortex of the Uncus & • crosses midline through anterior commissure adjacent part of Hippocampal gyrus (center of smell). and joins the uncrossed lateral root of opposite side. • It connects olfactory centers of 2 cerebral hemispheres. • So each olfactory center receives smell sensation from both halves of nasal cavity. NB. Olfactory pathway is the only sensory pathway which reaches the cerebral cortex without passing through the Thalamus . Trigeminal Nerve [The 5th Cranial Nerve] Mixed Nuclei Trigeminal Branches Ganglion The 5th nerve emerges from the middle of the ventral surface of the pons by 2 roots (Large Lateral sensory root & small medial motor root). Divides into 3 divisions (dendrites of trigeminal ganglion): Principal 1. Ophthalmic Mesenceph (main) Spinal (Pure Sensory) 2. Maxillary Motor nucleus 3. Mandibular alic nucleus sensory nucleus Site: Axons of cells of motor (Pure Sensory) (Mixed) nucleus -Occupies a nucleus join only the Supplies: depression in mandibular division. the middle 1. Upper 2. Face: Motor Sensory cranial fossa. teeth, gums (zygomaticofa Branche 3. Branches: -Importance: & maxillary cial & s: 2. Nasocilia Contains cell 1. air sinus: infraorbital Lacrimal: ry: (midbrain (pons): (pons, (pons): bodies: 1. Frontal: (posterior, nerves). 1. Lingual: supplies supplies &pons): receives medulla & supplies: Whose supplies middle & receives General dendrites carry skin of skin of anterior sensations from receives touch fibers upper 2-3 -Four Muscles skin of superior anterior 2/3 the propriocepti from face & cervical of mastication sensations from face & face, to 8 face & alveolar of tongue. ve fibers scalp segments of (temporalis, the face. lacrimal nasal muscles scalp. nerves). 2. Inferior from spinal masseter, 2. Whose axons gland. cavity & alveolar: (4 muscles of cord): medial & form the eyeball. supplies Lower muscles mastication. receives lateral sensory root of teeth, gums & of pain & pterygoid). trigeminal face. masticat 3. Buccal: ion & temperatur -Other four nerve. supplies Face other 4 e sensations muscles (cheek on upper muscles) from face & (Anterior belly They pass through superior jaw) . 4. scalp. of digastric, orbital fissure to the orbit mylohyoid, Auriculotemporal: tensor palati & supplies auricle, temple, parotid gland & TMJ. Facial Nerve [The 7th Cranial Nerve] Mixed Nuclei Course Branches Nerve Lesions tensor Special General Special tympani). In facial canal: visceral visceral Damage of the visceral 1.Greater petrosal 3.Nerve to efferent: efferent: 2.Chorda tympani facial nerve results afferent: nerve stapedius motor nucleus superior in paralysis of (nucleus carries: of facial salivatory muscles of facial solitarius): a) preganglionic expressions: nerve: nucleus carries parasympathetic control the sends Facial (Bell’s) supplies: preganglionic fibers to amplitude of preganglionic palsy; lower motor muscles of -Emerges from the cerebellopontine parasympathetic submandibular & sound waves parasympathet neuron lesion face, posterior fibers to lacrimal, sublingual from the external ic secretory angle by 2 roots: nasal & palatine glands. environment to (whole face receives taste belly of fibers to 1. Medial motor root: contains motor glands. b) taste fibers the inner ear. affected) from the digastric, sublingual, fibers. from anterior 2/3 anterior 2/3 stylohyoid, submandibula 2. Lateral root (nervous of tongue. • NB. In upper of tongue platysma, r, lacrimal, intermedius): contains Geniculate ganglion: contains cell bodies of neurones; its motor neuron stapedius, and nasal & fibres carrying taste sensations from anterior 2/3 of tongue; lesion (upper face occipitofrontal parasympathetic & taste fibers. palatine -Passes through internal auditory ending in solitary nucleus in M.O. is intact). is. glands. meatus to inner ear where it runs in Lies in internal acoustic meatus. Just as it emerges from the stylomastoid -Face is distorted: Fibers facial canal. - Drooping of foramen it gives: Then emerges from the stylomastoid lower eyelid, 1.Posterior auricular 2.Muscular branches Special Special General foramen & enters the parotid gland - Sagging of to occipitofrontalis visceral visceral visceral where it ends. to posterior belly of mouth angle, muscle. afferent efferent efferent digastric & stylohyoid. - Dribbling of saliva, supplying - Loss of facial parasympathet carrying supplying expressions, ic secretory Inside parotid gland: taste muscles - Loss of chewing, fibers to gives 5 terminal motor branches: Temporal, sensation developed - Loss of blowing, submandibula from from the 2nd Zygomatic, Buccal, Mandibular & Cervical - Loss of sucking, r, sublingual, anterior 2/3 pharyngeal To the muscles of the face. - Unable to show lacrimal, nasal of the tongue. arch. teeth or close the & palatine eye on that side. glands Vestibulo-Cochlear [The 8th Cranial Nerve] Special sensory Vestibular Nerve Cochlear Nerve Vestibular & cochlear parts leave the ventral surface of brain stem through the ponto-medullary sulcus ‘at crebello-pontine angle’ (lateral to facial nerve), run laterally in posterior cranial fossa and enter the internal acoustic meatus along with 7th nerve. Vestibular nuclei belong to special somatic afferent column in brain stem. Cochlear nuclei belong to special somatic afferent column in brain stem. Medial Vestibulospina Vestibular Auditory Pathway Other Functions Afferent Efferent Longitudinal Afferent *Check the picture in the slides it l Tracts Cortex Fasciculus helps. of some nuclei The cell bodies Function: Extends through •Vestibulospinal The cell bodies From the cochlear nuclei, 2nd order • Superior olivary (1st order 1. control of out the brain fibers influence (1st order neurons) neurons, fibers ascend into the pons, nucleus sends olivocochlear neurons) are posture stem and formed the activity of are located in the where: fibers to end in organ of located in the 2. maintenance of of both spinal motor spiral ganglion 1- Most fibers cross the midline in Corti through the vestibular equilibrium descending & neurons trapezoid body and terminate in the within the cochlea vestibulocochlear nerve. ganglion within 3. co-ordination ascending fibers • concerned nucleus of trapezoid body or in the (organ of Corti in These fibers are inhibitory in the internal of head Projects with the Located in contralateral superior olivary nucleus. inner ear). function and serve to auditory meatus. 4. eye bilaterally control of the lower 2- Some fibers run ipsilaterally and 1-The Peripheral modulate transmission of 1-The movements • Has two body posture part of terminate in the superior olivary nucleus processes: make • From the superior olivary nuclei, sound to the cochlear nerve. Peripheral 5. the conscious components: and balance postcentral dendritic contact ascending fibers comprise the lateral • Superior olivary processes: awareness of 1-The ascending • Two tracts: gyrus with hair cells of lemniscus. containg both crossed (mainly) nucleus & the nucleus of (vestibular nerve vestibular component -Lateral (head the organ of Corti and direct (few) cochlear fibres, which the lateral lemniscus fibers) make stimulation. (vestibulo- arises from area). within the cochlear runs through tegmentum of pons and establish reflex connections dendritic contact They Are: ocular): lateral terminate in the inferior colliculus of the Responsib duct of the inner with motor neurons of with hair cells of 1. To ipsilateral establishes vestibular mdibrain (3rd order neurones). ear. trigeminal and facial motor the membranous flocculonodular connections with (Deiter’s) le for • Some axons within lateral lemniscus 2-The central nuclei mediating contraction labyrinth (inner lobe of the nuclei of the nucleus, conscious terminate in small nucleus of the lateral processes: of tensor tympani and ear). cerebellum Occulomotor, descends awareness lemniscus • The inferior colliculi project (cochlear nerve to medial geniculate nuclei (4th order stapedius muscles as They 2- The central (vestibulocerebell Trochlear & ipsilaterally of fibers) terminate in neurones) of thalamus reduce the amount of sound processes: ar tract) through Abducent nerves -Medial is the vestibular the dorsal and • The axons originating from the medial that gets into the inner ear (form the inferior (motor nuclei for descending sensation. ventral cochlear geniculate nucleus (auditory
Recommended publications
  • The Use of Cholinesterase Techniques to Study Topographical Localization in the Hypoglossal Nucleus of the Rat
    J. Anat. (1971), 110, 2, pp. 203-213 203 With 1O figures Printed in Great Britain The use of cholinesterase techniques to study topographical localization in the hypoglossal nucleus of the rat P. R. LEWIS*, B. A. FLUMERFELTt AND C. C. D. SHUTE* Department ofAnatomy, University of Cambridge (Accepted 4 August 1971) INTRODUCTION The hypoglossal nucleus is perhaps the most suitable motor nucleus for the experi- mental study of the cytological changes occurring in cholinergic neurons following axotomy. The cells are large and the nucleus is easy to find even in a fresh unfixed brain; furthermore, the nucleus is so close to the midline that it is possible to use one side as a control for the other with complete confidence and to view equivalent control and experimental neurons simultaneously at quite high magnifications. An added advantage is that the hypoglossal nerve trunk in the neck region is almost purely motor; the central effects of axotomy are therefore not complicated by any significant loss of sensory fibres. Our interest in the nucleus was heightened by the discovery that in the rat a group of neurons at the caudal end contained a high concentration of an enzyme resembling in its histochemical reactions pseudocholin- esterase (Shute & Lewis, 1963). The enzyme will hydrolyse acetylthiocholine and is inhibited by ethopropazine, but its most characteristic property is a rapid hydrolysis of butyrylthiocholine; BuChE would thus seem an appropriate abbreviation to distinguish it from true cholinesterase (AChE), the enzyme typically present in motor neurons. It was shown originally by Schwarzacher (1958) that there is a marked decrease in AChE activity in hypoglossal neurons during the second and third weeks following axotomy (although he also looked at the response of pseudocholinesterase he did not comment on the specifically staining group of cells).
    [Show full text]
  • Hemisus Marmoratum
    Neuroscience Letters 244 (1998) 5–8 Distribution of hypoglossal motor neurons innervating the prehensile tongue of the African pig-nosed frog, Hemisus marmoratum Curtis W. Andersona,*, Kiisa C. Nishikawab, Joyce Keifera aDepartment of Anatomy and Structural Biology, University of South Dakota School of Medicine, Vermillion, SD 57069, USA bDepartment of Biological Sciences, Physiology and Functional Morphology Group, Northern Arizona University, Flagstaff, AZ 86011, USA Received 15 December 1997; received in revised form 28 January 1998; accepted 28 January 1998 Abstract Using retrograde neuronal tracers, a study of the distribution of hypoglossal motor neurons innervating the tongue musculature was performed in the African pig-nosed frog, Hemisus marmoratum. This species is a radically divergent anuran amphibian with a prehensile tongue that can be aimed in three dimensions relative to the head. The results illustrate a unique rostrocaudal distribution of the ventrolateral hypoglossal nucleus and an unusually large number of motor neurons within this cell group. During the evolution of the long, prehensile tongue of Hemisus, the motor neurons innervating the tongue have greatly increased in number and have become more caudally distributed in the brainstem and spinal cord compared to other anurans. These observations have implications for understanding neuronal reconfiguring of motoneurons for novel morphologies requiring new muscle activation patterns. 1998 Elsevier Science Ireland Ltd. Keywords: Anuran amphibian; Hypoglossal nerve; Motor nuclei; Tongue Recent studies of feeding in anurans have revealed a hylidae [12,15]. In hydrostatic elongation, the tongue diversity of tongue morphologies and feeding mechanisms protractor muscle (M. genioglossus) has two types of mus- [1,5,7,8,10,11,15].
    [Show full text]
  • Cranial Nerves 1, 5, 7-12
    Cranial Nerve I Olfactory Nerve Nerve fiber modality: Special sensory afferent Cranial Nerves 1, 5, 7-12 Function: Olfaction Remarkable features: – Peripheral processes act as sensory receptors (the other special sensory nerves have separate Warren L Felton III, MD receptors) Professor and Associate Chair of Clinical – Primary afferent neurons undergo continuous Activities, Department of Neurology replacement throughout life Associate Professor of Ophthalmology – Primary afferent neurons synapse with secondary neurons in the olfactory bulb without synapsing Chair, Division of Neuro-Ophthalmology first in the thalamus (as do all other sensory VCU School of Medicine neurons) – Pathways to cortical areas are entirely ipsilateral 1 2 Crania Nerve I Cranial Nerve I Clinical Testing Pathology Anosmia, hyposmia: loss of or impaired Frequently overlooked in neurologic olfaction examination – 1% of population, 50% of population >60 years Aromatic stimulus placed under each – Note: patients with bilateral anosmia often report nostril with the other nostril occluded, eg impaired taste (ageusia, hypogeusia), though coffee, cloves, or soap taste is normal when tested Note that noxious stimuli such as Dysosmia: disordered olfaction ammonia are not used due to concomitant – Parosmia: distorted olfaction stimulation of CN V – Olfactory hallucination: presence of perceived odor in the absence of odor Quantitative clinical tests are available: • Aura preceding complex partial seizures of eg, University of Pennsylvania Smell temporal lobe origin
    [Show full text]
  • Is Essential for the Development, Survival and Function of Hypoglossal
    © 2019. Published by The Company of Biologists Ltd | Development (2019) 146, dev174045. doi:10.1242/dev.174045 RESEARCH ARTICLE Teashirt 1 (Tshz1) is essential for the development, survival and function of hypoglossal and phrenic motor neurons in mouse Charlotte Chaimowicz1, Pierre-Louis Ruffault1, Cyril Chéret1,*, Andrew Woehler2, NiccolòZampieri3, Gilles Fortin4, Alistair N. Garratt5 and Carmen Birchmeier1,‡ ABSTRACT the phrenic motor column located in the mid-cervical spinal cord. Feeding and breathing are essential motor functions and rely on the The tongue has crucial functions in feeding and is innervated by activity of hypoglossal and phrenic motor neurons that innervate the the hypoglossal motor neurons in the lower brainstem. The activity tongue and diaphragm, respectively. Little is known about the genetic of phrenic and hypoglossal motor neurons has to be tightly programs that control the development of these neuronal subtypes. coordinated to avoid maladaptive outcomes such as the swallowing The transcription factor Tshz1 is strongly and persistently expressed of air or the blockage of airways (Moore et al., 2014). Hence, in developing hypoglossal and phrenic motor neurons. We used hypoglossal and phrenic motor neurons and the circuitry that conditional mutation of Tshz1 in the progenitor zone of motor neurons coordinates their activity are essential for animal survival. (Tshz1MNΔ) to show that Tshz1 is essential for survival and function of Nevertheless, relatively little is known about the formation of the hypoglossal and phrenic motor neurons. Hypoglossal and phrenic motor neurons that relay breathing and feeding commands. motor neurons are born in correct numbers, but many die between All motor neurons that innervate skeletal muscle, i.e.
    [Show full text]
  • Clinical Anatomy of the Cranial Nerves Clinical Anatomy of the Cranial Nerves
    Clinical Anatomy of the Cranial Nerves Clinical Anatomy of the Cranial Nerves Paul Rea AMSTERDAM • BOSTON • HEIDELBERG • LONDON NEW YORK • OXFORD • PARIS • SAN DIEGO SAN FRANCISCO • SINGAPORE • SYDNEY • TOKYO Academic Press is an imprint of Elsevier Academic Press is an imprint of Elsevier 32 Jamestown Road, London NW1 7BY, UK The Boulevard, Langford Lane, Kidlington, Oxford OX5 1GB, UK Radarweg 29, PO Box 211, 1000 AE Amsterdam, The Netherlands 225 Wyman Street, Waltham, MA 02451, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA First published 2014 Copyright r 2014 Elsevier Inc. All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the publisher. Details on how to seek permission, further information about the Publisher’s permissions policies and our arrangement with organizations such as the Copyright Clearance Center and the Copyright Licensing Agency, can be found at our website: www.elsevier.com/permissions. This book and the individual contributions contained in it are protected under copyright by the Publisher (other than as may be noted herein). Notices Knowledge and best practice in this field are constantly changing. As new research and experience broaden our understanding, changes in research methods, professional practices, or medical treatment may become necessary. Practitioners and researchers must always rely on their own experience and knowledge in evaluating and using any information, methods, compounds, or experiments described herein. In using such information or methods they should be mindful of their own safety and the safety of others, including parties for whom they have a professional responsibility.
    [Show full text]
  • Amygdala Corticofugal Input Shapes Mitral Cell Responses in the Accessory Olfactory Bulb
    New Research Sensory and Motor Systems Amygdala Corticofugal Input Shapes Mitral Cell Responses in the Accessory Olfactory Bulb Livio Oboti,1 Eleonora Russo,2 Tuyen Tran,1 Daniel Durstewitz,2 and Joshua G. Corbin1 DOI:http://dx.doi.org/10.1523/ENEURO.0175-18.2018 1Center for Neuroscience Research, Children’s National Health System, Washington, DC 20010 and 2Department of Theoretical Neuroscience, Bernstein Center for Computational Neuroscience, Central Institute of Mental Health, Medical Faculty Mannheim of Heidelberg University, 68159 Mannheim, Germany Abstract Interconnections between the olfactory bulb and the amygdala are a major pathway for triggering strong behavioral responses to a variety of odorants. However, while this broad mapping has been established, the patterns of amygdala feedback connectivity and the influence on olfactory circuitry remain unknown. Here, using a combination of neuronal tracing approaches, we dissect the connectivity of a cortical amygdala [posteromedial cortical nucleus (PmCo)] feedback circuit innervating the mouse accessory olfactory bulb. Optogenetic activation of PmCo feedback mainly results in feedforward mitral cell (MC) inhibition through direct excitation of GABAergic granule cells. In addition, LED-driven activity of corticofugal afferents increases the gain of MC responses to olfactory nerve stimulation. Thus, through corticofugal pathways, the PmCo likely regulates primary olfactory and social odor processing. Key words: accessory olfactory bulb; amygdala; circuitry; connectivity; mitral cells Significance Statement Olfactory inputs are relayed directly through the amygdala to hypothalamic and limbic system nuclei, regulating essential responses in the context of social behavior. However, it is not clear whether and how amygdala circuits participate in the earlier steps of olfactory processing at the level of the olfactory bulb.
    [Show full text]
  • Lecture 6: Cranial Nerves
    Lecture 6: Cranial Nerves Objective: To understand the organization of cranial nerves with respect to their nuclei within the brain, their course through and exit from the brain, and their functional roles. Olfactory Eye Muscles 3, 4 &6 Cranial Nerves 1-7 I overview Table, Page 49 II Lecture notes Cranial Nerves and their Functions V Trigeminal VII Facial VIII IX X XII XI Cranial Nerves 8-12 Overview sternocephalic I. Factors Responsible for the Complex Internal Organization of the Brain Stem-> leads to altered location of cranial nerve nuclei in adult brain stem 1. Development of the Fourth Ventricle a. Medulla and Pons develop ventral to the 4th ventricle cerebellum b. Alar plate is displaced lateral to basal plate 4 Medulla Developing Neural Tube 2. Cranial nerve nuclei form discontinuous columns Rostral 12 SE Page 48 Notes 3. Some cranial nerve nuclei migrate from their primitive embryonic positions (e.g., nuclei of V and VII) Facial N. Factors responsible for the complex internal organization of the brainstem: 4) Special senses develop in association with the brain stem. Nuclei of special senses 5) Development of the cerebellum and its connections Cerebellum II. Cranial Nerve Nuclei: Nucleus = column of neuron cell bodies. Efferent nuclei are composed of cell bodies of alpha or gamma motor neurons (SE) or preganglionic parasympathetic neurons (VE). III. Motor Efferent Nuclei (Basal Plate Derivatives): 1. SE (Somatic Efferent) Nuclei: SE neurons form two longitudinally oriented but discontinuous columns of cell bodies in the brain stem. Neurons that comprise these columns are responsible for innervating all of the skeletal musculature of the head.
    [Show full text]
  • Cranial Nerves
    Cranial Nerves Cranial nerve evaluation is an important part of a neurologic exam. There are some differences in the assessment of cranial nerves with different species, but the general principles are the same. You should know the names and basic functions of the 12 pairs of cranial nerves. This PowerPage reviews the cranial nerves and basic brain anatomy which may be seen on the VTNE. The 12 Cranial Nerves: CN I – Olfactory Nerve • Mediates the sense of smell, observed when the pet sniffs around its environment CN II – Optic Nerve Carries visual signals from retina to occipital lobe of brain, observed as the pet tracks an object with its eyes. It also causes pupil constriction. The Menace response is the waving of the hand at the dog’s eye to see if it blinks (this nerve provides the vision; the blink is due to cranial nerve VII) CN III – Oculomotor Nerve • Provides motor to most of the extraocular muscles (dorsal, ventral, and medial rectus) and for pupil constriction o Observing pupillary constriction in PLR CN IV – Trochlear Nerve • Provides motor function to the dorsal oblique extraocular muscle and rolls globe medially © 2018 VetTechPrep.com • All rights reserved. 1 Cranial Nerves CN V – Trigeminal Nerve – Maxillary, Mandibular, and Ophthalmic Branches • Provides motor to muscles of mastication (chewing muscles) and sensory to eyelids, cornea, tongue, nasal mucosa and mouth. CN VI- Abducens Nerve • Provides motor function to the lateral rectus extraocular muscle and retractor bulbi • Examined by touching the globe and observing for retraction (also tests V for sensory) Responsible for physiologic nystagmus when turning head (also involves III, IV, and VIII) CN VII – Facial Nerve • Provides motor to muscles of facial expression (eyelids, ears, lips) and sensory to medial pinna (ear flap).
    [Show full text]
  • Appearance and Transient Expression of Oxytocin Receptors in Fetal, Infant, and Peripubertal -Rat Brain Studied by Autoradiography and Electrophysiology
    The Journal of Neuroscience, May 1969, g(5): 1764-I 773 Appearance and Transient Expression of Oxytocin Receptors in Fetal, Infant, and Peripubertal -Rat Brain Studied by Autoradiography and Electrophysiology Eliane Tribollet,’ Serge Charpak,’ Anne Schmidt,* Michel Dubois-Dauphin,’ and Jean Jacques Dreifussl ‘Department of Physiology, University Medical Center, Geneva, Switzerland, and ‘CNRS-INSERM, Center of Pharmacology-Endocrinology, Montpellier, France The development of oxytocin (OT) receptors in the rat brain The classicalhormonal effects of oxytocin (OT) releasedfrom and spinal cord was studied by in vitro light microscopic the hypothalamoneurohypophyseal axons are well established. autoradiography and by electrophysiology. OT receptors were In addition, OT is also present in axons projecting to various labeled using a monoiodinated OT antagonist in tissue sec- areaswithin the CNS (Sofroniew, 1985), which suggeststhat it tions from animals aged between embryonic day 12 (E12) may play a neurotransmitter or neuromodulator role. Addi- and postnatal day 90 (PN90); the response of ongoing spike tional evidence for such a role includes its releaseunder exper- activity to the addition of OT was assessed in neurons lo- imental conditions in situ and in vitro (Buijs, 1983), its effect cated in the dorsal motor nucleus of the vagus nerve of the on the electrical activity of single neurons in the brain (Mtihle- neonate. thaler et al., 1983, 1984; Charpak et al., 1984), the fact that Specific binding was detected first at El4 in a region that small amounts of OT injected into the brain or the cerebral later differentiated into the dorsal motor nucleus of the vagus ventricles modulate neuroendocrine and autonomic functions nerve.
    [Show full text]
  • Differentiation of the Bulbar Motor Nuclei and the Coincident Develop- Ment of Associated Root Fibers in the Rsbbit
    DIFFERENTIATION OF THE BULBAR MOTOR NUCLEI AND THE COINCIDENT DEVELOP- MENT OF ASSOCIATED ROOT FIBERS IN THE RSBBIT DONALD L. KIMMEL Department of Anatomy, University of Michigan,’ Aim Arbor THIRTY-ONE FIGURES CONTENTS Introduction ........................................................ 83 Material and methods ................................................ 84 General survey of the literature ....................................... 85 Description of material studied ........................................ 86 Somatic efferent component. Its central and peripheral development .... 86 The hypoglossal ............................................. 86 The abdueens ............................................... 96 Visceral efferent component. Its central and peripheral development .... 103 The vago-accessory ........................................... 103 The glossopharyngeal ........................................ 124 The facial .................................................. 129 The trigemiiial .............................................. 137 Geiicrxldisrussion .................................................... 143 INTRODUCTION This present study concerns itself primarily with the onto- genetic development of the nuclear centers of bulbar cranial nerves in the rabbit and with the embryonic and adult distri- butions of their branches. Its purpose is to show that the central development proceeds stage for stage with the pro- A dissertation submitted in partial fulfillment of the requirements for the degree of doctor of philosophy
    [Show full text]
  • Nuclear Architecture in the Medulla Oblongata of the Adult African Giant Pouched Rat (Cricetomys Gambianus, Waterhouse - 1840)
    Int. J. Morphol., 29(2):382-388, 2011. Nuclear Architecture in the Medulla Oblongata of the Adult African Giant Pouched Rat (Cricetomys gambianus, Waterhouse - 1840) Arquitectura Nuclear en la Médula Oblonga de la Rata Gigante de Carillos Africana Adulta (Cricetomys gambianus, Waterhouse - 1840) *Ibe, C. S; *Onyeanusi, B. I.; *Hambolu, J. O. & **Ayo, J. O. IBE, C. S.; ONYEANUSI, B. I.; HAMBOLU, J. O. & AYO, J. O. Nuclear architecture in the medulla oblongata of the adult African giant pouched rat (Cricetomys gambianus, Waterhouse - 1840). Int. J. Morphol., 29(2):382-388, 2011. SUMMARY: The architecture of cranial and non-cranial nerve nuclei in the medulla oblongata of the African giant pouched rat was studied by means of light microscopy. Serial sections of the medulla oblongata, in coronal and saggital planes, were stained with the cresyl fast violet and silver stains, respectively. Sections in the saggital plane were used as a guide, while coronal sections were used to identify the nuclei in the rostrocaudal extent of the medulla oblongata. With the obex serving as the landmark, nuclei rostral and caudal to the obex were delineated. Cranial nerve nuclei whose architecture were defined were the motor nucleus of hypoglossal nerve, motor nucleus of vagus nerve, cochlear nucleus, vestibular nucleus and nucleus ambiguus, while non-cranial nerve nuclei identified were the olivary nucleus, solitary tract nucleus, gracile nucleus, cuneate nucleus, spinal nucleus of trigeminal nerve, motor nucleus of corpus trapezoideum, lateral nucleus of reticular formation and gigantocellular nucleus. The olivary nucleus was the most prominent nucleus, while the solitary tract nucleus was faint, and thus, less developed.
    [Show full text]
  • Brainstem Reflexes Herniation Syndromes (CN IX-XII) Lab 7 March 24, 2021 - Dr
    Brainstem Reflexes Herniation Syndromes (CN IX-XII) Lab 7 March 24, 2021 - Dr. Krebs ([email protected]) Objectives: 1. Describe the relationship of the functional anatomy of CN IX - XII and the location of their respective nuclei to a neurological exam which examines the brainstem. 2. Explain the neuroanatomical pathways associated with brainstem reflexes tested in the conscious and unconscious patient. 3. Describe the relationship between the sympathetic and parasympathetic innervation of the eye to the clinical assessment of eye reflexes. 4. Describe the relationship of changes in upper limb posture of unconscious patient to underlying damage to the brainstem. 5. Describe the consequences of herniation syndromes associated with increases in intracranial pressure. Videos for Review: Notes: • For identification of the cranial nerves, use online modules and videos, your atlas and micrographs to locate the nuclei listed. • On the brain and brainstem specimens, locate cranial nerves IX, X, XI and XII. Note the level at which they are attached to the brainstem. ** NOTE: Interactive PDFs are best viewed on desktop/laptop computers - functionality is not reliable on mobile devices ** Design & Artwork: The HIVE (hive.med.ubc.ca) 1 Brainstem Reflexes Herniation Syndromes (CN IX-XII) Lab 7 March 24, 2021 - Dr. Krebs ([email protected]) Glossopharyngeal Nerve (CN IX) Modality Associated Nucleus Function Motor Nucleus ambiguus Motor to stylopharyngeus muscle (SVE) Parasympathetic Inferior salivatory nucleus Stimulation of parotid gland (GVE) Taste Solitary nucleus and tract Taste from posterior 1/3 of tongue (SVA) Somatic Sensory Spinal trigeminal nucleus and General sensation from posterior 1/3 of tongue, (GSA) tract pharynx, external ear/tympanic membrane Visceral Sensory Solitary nucleus and tract Carotid body, gag sensation from oropharynx (GVA) Which foramen does CN IX exit through? Highlight and label the nuclei associated with CN IX in this diagram and show the types of fibres that comprise this peripheral nerve.
    [Show full text]