Pattern of Autonomic Innervation
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METHODICAL GUIDANCE for the Lecture Academic Subject Human
Ministry of Public Health of Ukraine Ukrainian Medical Stomatological Academy "Approved" at the meeting of the Department of Human Anatomy «29» 08 2020 Minutes № Head of the Department Professor O.O. Sherstjuk ________________________ METHODICAL GUIDANCE for the lecture Academic subject Human Anatomy Module No 3 "The heart. Vessels and nerves of the head, the neck, the trunk, extremities" Lecture No 15 Review of the autonomic nervous system, its central departments. The principles of the autonomic innervation of the organs Year of study ІI Faculty Foreign students' training faculty, specialty «Medicine» Number of 2 academic hours Poltava – 2020 1. Educational basis of the topic The autonomic division of peripheral nervous system regulates physiological processes of the human organism like blood circulation, respiration, digestion, excretion and general metabolism; also, it regulates tissue trophic processes. The autonomic division acts relatively independently from the cerebral cortex and the organs supplied act involuntarily as well. It is quite clear that that distinguishing of the somatic and the autonomic compartments is conditional and exact delimitation is not possible. Such impossibility appears due to common regulatory centers for both divisions and tight morphological and functional associations featured by them. The somatic neurons and the interneurons of PNS like those of CNS feature topographical and synaptic associations so a reflex arc may comprise both somatic (e.g. afferent) and autonomic neurons. Summarizing the aforesaid, the term ’autonomic nervous system’ will be applied to a specific compartment of PNS but not for a separate nervous system. 2. Learning objectives of the lecture: . to familiarize students with the autonomic division of CNS; . -
Autonomic Nerve Activity and Cardiac Arrhythmias
ACORP Complete (with appendices) Last Name of PI► Protocol No. Assigned by the IACUC►02002 Official Date of Approval► 1. Caging needs. Complete the table below to describe the housing that will have to be accommodated by the housing sites for this protocol: d. Is this housing e. Estimated c. Number of consistent with the maximum number a. Species b. Type of housing* individuals per Guide and USDA of housing units housing unit** regulations? needed at any one (yes/no***) time Chain link run, 3x6 Canines 1 no 7 and 4x10 feet cage *See ACORP Instructions, for guidance on describing the type of housing needed. If animals are to be housed according to a local Standard Operating Procedure (SOP), enter “standard (see SOP)” here, and enter the SOP into the table in Item Y. If the local standard housing is not described in a SOP, enter “standard, see below” in the table and describe the standard housing here: Chain link run, 3x6 feet cages ** The Guide states that social animals should generally be housed in stable pairs or groups. Provide a justification if any animals will be housed singly (if species is not considered “social”, then so note) Dogs are housed singly in chain link runs but can socialize with one another since each room has two to five dog runs. In addition, while their runs are being cleaned on a daily basis, pairs of dogs are allowed to exercise and play together in a designated "romper room". Animals are fitted with DSI transmitters and need to be housed singly in a cage for which DSI receivers are installed to receive signals from the transmitters. -
Autonomic Nervous System
AUTONOMIC NERVOUS SYSTEM PAGE 1 AUTONOMIC NERVOUS SYSTEM PAGE 2 AUTONOMIC NERVOUS SYSTEM PAGE 3 AUTONOMIC NERVOUS SYSTEM PAGE 4 AUTONOMIC NERVOUS SYSTEM PAGE 5 AUTONOMIC NERVOUS SYSTEM PAGE 6 AUTONOMIC NERVOUS SYSTEM PAGE 7 AUTONOMIC NERVOUS SYSTEM PAGE 8 AUTONOMIC NERVOUS SYSTEM PAGE 9 REVIEW QUESTIONS 1. The autonomic nervous system controls the activity of _?_. (a) smooth muscle (b) cardiac muscle (c) glands (d) all of these (e) none of these 2. All preganglionic and postganglionic autonomic neurons are _?_ neurons. (a) somatic efferent (b) visceral efferent (c) somatic afferent (d) visceral afferent (e) association neurons 3. Which neurotransmitter is released at the synapses between preganglionic and postganglionic autonomic neurons ? (a) epinephrine (b) norepinephrine (c) acetylcholine (d) serotonin (e) oxytocin 4. All preganglionic sympathetic neurons are located in: (a) the lateral horn of the spinal cord of spinal cord segments T1-L2 (b) brainstem nuclei (c) intramural (terminal) ganglia (d) paravertebral ganglia of the sympathetic chains (e) prevertebral ganglia 5. All preganglionic parasympathetic neurons are located in _?_. (a) prevertebral ganglia (b) the lateral horn of spinal cord segments T1-L2 (c) sympathetic chain ganglia (d) intramural ganglia (e) brainstem nuclei and spinal cord segments S2-S4 6. Prevertebral and paravertebral ganglia contain _?_. (a) preganglionic sympathetic neurons (b) preganglionic parasympathetic neurons (c) postganglionic sympathetic neurons (d) postganglionic parasympathetic neurons (e) all of these 7. The otic, ciliary, submandibular and pterygopalatine ganglia are located in the head region and contain _?_. (a) preganglionic sympathetic neurons (b) preganglionic parasympathetic neurons (c) postganglionic sympathetic neurons (d) postganglionic parasympathetic neurons (e) none of these 8. -
MINIREVIEW Posterior Gut Development in Drosophila: a Model System for Identifying Genes Controlling Epithelial Morphogen- Esis
Cell Research (1998), 8, 273-284 MINIREVIEW Posterior gut development in Drosophila: a model system for identifying genes controlling epithelial morphogen- esis LENGYEL JUDITH A* , XUE JUN LIU Department of Molecular, Cell and Developmental Biology University of California at Los Angeles, Los Angeles, CA USA, 90095-1606 USA ABSTRACT The posterior gut of the Drosophila embryo, consist- ing of hindgut and Malpighian tubules, provides a simple, well-defined system where it is possible to use a genetic approach to define components essential for epithelial mor- phogenesis. We review here the advantages of Drosophila as a model genetic organism, the morphogenesis of the ep- ithelial structures of the posterior gut, and what is known about the genetic requirements to form these structures. In overview, primordia are patterned by expression of hi- erarchies of transcription factors; this leads to localized expression of cell signaling molecules, and finally, to the least understood step: modulation of cell adhesion and cell shape. We describe approaches to identify additional genes that are required for morphogenesis of these simple epithelia, particularly those that might play a structural role by affecting cell adhesion and cell shape. Key words: Organogenesis, cell rearrangement, con- vergent extension, hindgut, Malpighian tubule. Advantages of Drosophila Work on Drosophila genetics began 90 years ago, when Thomas Hunt Morgan * Corresponding author: [email protected] Drosophila gut epithelial morphogenesis genes (who later received the Nobel Prize for his work) began studying inheritance in the fruit fly. At that time, the advantage of working with this small organism was that it reproduced rapidly in the laboratory, requiring only a simple growth medium, no special attention, and little expense. -
Thesis Comprises Only My Original Work Towards the Doctor of Philosophy Except Where Indicated in the Preface;
Development, prevalence and treatment of blood pressure abnormalities in spinal cord injury Min Yin Goh ORCID: 0000-0003-2517-7745 Doctor of Philosophy August 2019 Department of Medicine, Austin Health Faculty of Medicine, Dentistry and Health Sciences The University of Melbourne Submitted in total fulfilment of the requirements of the degree of Doctor of Philosophy Abstract Disorders of blood pressure control arise from disruption of the autonomic nervous system and result in symptomatic orthostatic hypotension and large fluctuations in blood pressure. Ambulatory blood pressure monitoring is used in the general population for assessment of blood pressure control and to detect episodes of hypotension. In spinal cord injury (SCI), impaired control of the sympathetic nervous system leads to orthostatic intolerance and autonomic dysreflexia. Smaller studies in restricted populations have examined ambulatory pressures in SCI and observed abnormalities in diurnal blood pressure variation in complete cervical SCI. Altered diurnal blood pressure is associated with abnormalities in diurnal urine production and orthostatic intolerance in autonomic failure. This triad may also occur in SCI to explain the orthostatic intolerance. A retrospective examination of ambulatory pressures of patients with SCI referred for clinically significant blood pressure disorders revealed a high prevalence of abnormalities in diurnal blood pressure and urine production in acute and chronic tetraplegia and in acute paraplegia. To characterise the course of diurnal blood pressure, urine production and orthostatic symptoms in SCI, two prospective studies were performed. First, consecutive patients admitted with acute SCI were screened for recruitment, and consenting volunteers were compared with immobilised and mobilising controls. In the second study, people with chronic SCI (>1 year) living in the community were compared with mobilising controls. -
Neuronal Types and Their Specification Dynamics in the Autonomic Nervous System
From the Department of Medical Biochemistry and Biophysics Karolinska Institutet, Stockholm, Sweden NEURONAL TYPES AND THEIR SPECIFICATION DYNAMICS IN THE AUTONOMIC NERVOUS SYSTEM Alessandro Furlan Stockholm 2016 All previously published papers were reproduced with permission from the publisher. Published by Karolinska Institutet. Printed by E-Print AB © Alessandro Furlan, 2016 ISBN 978-91-7676-419-0 On the cover: abstract illustration of sympathetic neurons extending their axons Credits: Gioele La Manno NEURONAL TYPES AND THEIR SPECIFICATION DYNAMICS IN THE AUTONOMIC NERVOUS SYSTEM THESIS FOR DOCTORAL DEGREE (Ph.D.) By Alessandro Furlan Principal Supervisor: Opponent: Prof. Patrik Ernfors Prof. Hermann Rohrer Karolinska Institutet Max Planck Institute for Brain Research Department of Medical Biochemistry and Research Group Developmental Neurobiology Biophysics Division of Molecular Neurobiology Examination Board: Prof. Jonas Muhr Co-supervisor(s): Karolinska Institutet Prof. Ola Hermansson Department of Cell and Molecular Biology Karolinska Institutet Department of Neuroscience Prof. Tomas Hökfelt Karolinska Institutet Assistant Prof. Francois Lallemend Department of Neuroscience Karolinska Institutet Division of Chemical Neurotransmission Department of Neuroscience Prof. Ted Ebedal Uppsala University Department of Neuroscience Division of Developmental Neuroscience To my parents ABSTRACT The autonomic nervous system is formed by a sympathetic and a parasympathetic division that have complementary roles in the maintenance of body homeostasis. Autonomic neurons, also known as visceral motor neurons, are tonically active and innervate virtually every organ in our body. For instance, cardiac outflow, thermoregulation and even the focusing of our eyes are just some of the plethora of physiological functions under the control of this system. Consequently, perturbation of autonomic nervous system activity can lead to a broad spectrum of disorders collectively known as dysautonomia and other diseases such as hypertension. -
Dear Subscribers! This Issue of Our Magazine Is Devoted to Cooperation of Our Editorial Board with Ukrainian Medical Scientists
Deutscher Wissenschaftsherold • German Science Herald, N 4/2016 Dear subscribers! This issue of our magazine is devoted to cooperation of our editorial board with Ukrainian medical scientists. We present you the results of their researches. UDC: 611.831.1:611.216-018.73 Boichuk O.M. Higher State Educational Institution of Ukraine “Bukovinian State Medical University”, M.H. Turkevych Department of Human Anatomy, Chernivtsi, Ukraine, [email protected] Kryvetska I.I. Higher State Educational Institution of Ukraine “Bukovinian State Medical University”, S.M. Savenko Department of Neurology, Psychiatry and Medical Psychology Chernivtsi, Ukraine Bambuliak A.V. Higher State Educational Institution of Ukraine “Bukovinian State Medical University”, Department of Surgical and Pediatric Dentistry, Chernivtsi, Ukraine, [email protected] Sapunkov O.D. Higher State Educational Institution of Ukraine “Bukovinian State Medical University”, Department of Pediatric Surgery and Otolaryngology, Chernivtsi, Ukraine STRUCTURAL COMPONENTS OF AUTONOMIC INNERVATION OF MUCOSA OF NASAL CAVITY AND PARANASAL SINUSES Abstract. Autonomic innervation of mucosa of the nasal cavity and paranasal sinuses has been studied using complex morphological methods. It was determined that autonomic innervation of the nasal cavity and paranasal sinuses mostly occurs due to the branches of the pterygopalatine ganglion Keywords: nasal cavity, paranasal sinuses, innervation, pterygopalatine ganglion, mucosa, anatomy. Introduction. Mucosa of nasal cavity is peripheral element of olfactory analyzer functionally large receptor surface with a very consists of highly specialized epithelium of the complex and various reflex connections. It is upper nasal passage, short dendrites, which equipped with lots of blood and lymphatic ends with receptors, and axons form olfactory vessels, which are surrounded with numerous filaments that enter the olfactory bulb where nerve endings. -
Facsimile Del Frontespizio Della Tesi Di Dottorato
Allma Mater Studiiorum – Uniiversiità dii Bollogna DOTTORATO DI RICERCA IN SCIENZE MEDICHE VETERINARIE Ciclo XXIX° Settore Concorsuale di afferenza: 07/H1 Settore Scientifico disciplinare: VET 01 The nervous system of Delphinidae: neurochemical studies on different central and peripheral regions Presentata da: Anna Maria Rambaldi Coordinatore Dottorato Relatore Chiar.mo Prof. Arcangelo Gentile Chiar.mo Prof. Cristiano Bombardi Esame finale anno 2017 The nervous system of Delphinidae: neurochemical studies on different central and peripheral regions INDEX ABSTRACT 1 INTRODUCTION 7 1 Cetaceans and general adaptations to aquatic environment 8 2 The nervous system of cetaceans 11 2.1 Evolution 11 2.2 The central nervous system 14 2.3 The peripheral nervous system 23 EXPERIMENTAL STUDIES 25 3 Distribution of calretinin immunoreactivity in the lateral nucleus of the 26 bottlenose dolphin (Tursiops truncatus) amygdala 4 Calcitonin gene-related peptide (CGRP) expression in the spinal cord and 41 spinal ganglia of the bottlenose dolphin (Tursiops truncatus) 5 Nitrergic and substance P immunoreactive neurons in the enteric nervous 58 system of the bottlenose dolphin (Tursiops truncatus) intestine 6 Preliminary study on the expression of calcium binding proteins and 72 neuronal nitric oxide synthase (nNOS) in different brain regions of striped dolphins (Stenella Coeruleoalba) affected by morbillivirus CONCLUSIONS 91 REFERENCES 94 ABSTRACT During the evolutionary path, Cetaceans experienced a return to waters and hence had to adapt many of their anatomical and physiological features to this new life. Many organs and systems present several modifications and specialisations, which make these mammals different from their mainland ancestors. The nervous system either displays peculiar features like an extremely large brain, in terms of both absolute and relative mass, a very high level of gyrification, a minimization, or in some cases a complete lack, of olfactory structures, and a poorly developed corpus callosum. -
Thesis Rests with the Author
University of Bath PHD Studies on the alpha-bungarotoxin binding component in human brain. Whyte, J. Award date: 1985 Awarding institution: University of Bath Link to publication Alternative formats If you require this document in an alternative format, please contact: [email protected] General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. • Users may download and print one copy of any publication from the public portal for the purpose of private study or research. • You may not further distribute the material or use it for any profit-making activity or commercial gain • You may freely distribute the URL identifying the publication in the public portal ? Take down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Download date: 10. Oct. 2021 i Ta \ D'--- V ^ STUDIES ON THE a-BUNGAROTOXIN BINDING COMPONENT IN HUMAN BRAIN submitted by J. Whyte for the degree of Ph.D. of the University of Bath 1985 COPYRIGHT Attention is drawn to the fact that the copyright of this thesis rests with the author. This copy of the thesis has been supplied on condition that anyone who consults it is under stood to recognize that its copyright rests with the author and that no quotation from the thesis and no information derived from it may be published without the prior written consent of the author. -
The Sacral Autonomic Outflow Is Sympathetic
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by UCL Discovery The sacral autonomic outflow is sympathetic Isabel Espinosa-Medina1,†, Orthis Saha1,†, Franck Boismoreau1, Zoubida Chettouh1, Francesca Rossi1, William D. Richardson2 and Jean-François Brunet1* 1 Institut de Biologie de l’ENS (IBENS), INSERM, CNRS, École Normale Supérieure, PSL Research University, Paris, 75005 France. 2 Wolfson Institute for Biomedical Research, University College London, London UK. †These authors contributed equally to this work *Correspondence to [email protected] 1 Abstract In the autonomic nervous system of mammals and birds, sacral preganglionic neurons are considered parasympathetic, as are their targets in the pelvic ganglia that prominently control rectal, bladder and genital functions. The allocation of the sacral autonomic outflow to the parasympathetic nervous system —i.e. as the second tier of a “cranio-sacral outflow”— has an ancient history: rooted in the work of Gaskell 1, formalized by Langley2 and universally accepted ever since (e.g. 3). The rationale lied in several perceived similarities between the sacral and cranial outflows: anatomical —separation from the thoracolumbar, sympathetic outflow by a gap at limb levels 1, a target territory less diffuse than that of the latter and a lack of projections to the paravertebral sympathetic chain 1; physiological —an influence on some organs opposite to that of the thoracolumbar outflow 4; and pharmacological — an overall sensitivity to muscarinic antagonists2. However, cell-phenotypic criteria have been lacking and were never sought. Here we uncover fifteen phenotypic and ontogenetic features that distinguish pre- and postganglionic neurons of the cranial parasympathetic outflow from those of the thoracolumbar sympathetic outflow. -
Sympathetic Tales: Subdivisons of the Autonomic Nervous System and the Impact of Developmental Studies Uwe Ernsberger* and Hermann Rohrer
Ernsberger and Rohrer Neural Development (2018) 13:20 https://doi.org/10.1186/s13064-018-0117-6 REVIEW Open Access Sympathetic tales: subdivisons of the autonomic nervous system and the impact of developmental studies Uwe Ernsberger* and Hermann Rohrer Abstract Remarkable progress in a range of biomedical disciplines has promoted the understanding of the cellular components of the autonomic nervous system and their differentiation during development to a critical level. Characterization of the gene expression fingerprints of individual neurons and identification of the key regulators of autonomic neuron differentiation enables us to comprehend the development of different sets of autonomic neurons. Their individual functional properties emerge as a consequence of differential gene expression initiated by the action of specific developmental regulators. In this review, we delineate the anatomical and physiological observations that led to the subdivision into sympathetic and parasympathetic domains and analyze how the recent molecular insights melt into and challenge the classical description of the autonomic nervous system. Keywords: Sympathetic, Parasympathetic, Transcription factor, Preganglionic, Postganglionic, Autonomic nervous system, Sacral, Pelvic ganglion, Heart Background interplay of nervous and hormonal control in particular The “great sympathetic”... “was the principal means of mediated by the sympathetic nervous system and the ad- bringing about the sympathies of the body”. With these renal gland in adapting the internal -
Autonomic Nervous System
Autonomic nervous System Regulates activity of: Smooth muscle Cardiac muscle certain glands Autonomic- illusory (convenient)-not under direct control Regulated by: hypothalamus Medulla oblongata Divided in to two subdivisions: Sympathetic Parasympathetic Sympathetic: mobilizes all the resources of body in an emergency Parasympathetic: maintains the normal body functions Complimentary to each other. ANS Activity expressed • Regulation of Blood Pressure • Regulation of Body Temperature • Cardio-respiratory rate • Gastro-intestinal motility • Glandular Secretion Sensations • General – Hunger , Thirst , Nausea • Special -- Smell, taste and visceral pain • Location of ANS in CNS: 1. cerebral hemispheres (limbic system) 2. Brain stem (general visceral nuclei of cranial nerves) 3. Spinal cord (intermediate grey column) ANS Anatomy • Pathway: Two motor neurons 1. In CNS -->Axon-->Autonomic ganglion 2. In Autonomic ganglion-->Axon-->effector organ • Anatomy: Preganglionic neuron--->preganglionic fibre (myelinated axon)--->out of CNS as a part of cranial/spinal nerve--->fibres separate & extend to ANS ganglion-->synapse with postganglionic neuron--->postganglionic fibre (nonmyelinated)-- >effector organ Sympathetic system Components • Pair of ganglionic sympathetic trunk • Communicating rami • Branches • Plexuses • Subsidiary ganglia – collateral , terminal ganglia Sympathetic trunk (lateral ganglia) • Paravertebral in position • Extend from base of skull to coccygeal • Both trunk unite to form – ganglion impar Total Ganglia • Cervical-3 • Thoracic-11