Lecture 13: Insect Nerve System (NS)
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Chapter 2 Test Review
Unit III, Modules 9-13 Test Review • See also the Unit III notes and pages 76-122 • About 45 m.c., plus two essays; one on brain functioning, the other review concepts from previous units. • Some practice questions are embedded in this presentation • Other practice questions are available at the textbook website and in the textbook after each module. Neuron Order of a transmission: dendrite, cell body, axon, synapse (see arrow below) Neural Communication Neurons, 80 Neural Communication • (a)Dendrite – the bushy, branching extensions of a neuron that receive messages and conduct impulses toward the (b)cell body • (c)Axon – the extension of a neuron, ending in branching terminal fibers, through which messages are sent to other neurons or to muscles or glands • Myelin [MY-uh-lin] Sheath – a layer of fatty cells segmentally encasing the fibers of many neurons – makes possible vastly greater transmission speed of neutral impulses, – Damage to can lead to Multiple sclerosis Neural Communication • Action Potential – a neural impulse; a brief electrical charge that travels down an axon; DEPOLARIZED – generated by the movement of positively charges atoms in and out of channels in the axon’s membrane • Threshold – the level of stimulation required to trigger a neural impulse Action Potential A neural impulse. A brief electrical charge that travels down an axon and is generated by the movement of positively charged atoms in and out of channels in the axon’s membrane. Practice question • Multiple sclerosis is a disease that is most directly associated with the degeneration of: a. the myelin sheath. b. the pituitary gland. -
Crayfish Escape Behavior and Central Synapses
Crayfish Escape Behavior and Central Synapses. III. Electrical Junctions and Dendrite Spikes in Fast Flexor Motoneurons ROBERT S. ZUCKER Department of Biological Sciences and Program in the Neurological Sciences, Stanford University, Stanford, California 94305 THE LATERAL giant fiber is the decision fiber and fast flexor motoneurons are located in for a behavioral response in crayfish in- the dorsal neuropil of each abdominal gan- volving rapid tail flexion in response to glion. Dye injections and anatomical recon- abdominal tactile stimulation (27). Each structions of ‘identified motoneurons reveal lateral giant impulse is followed by a rapid that only those motoneurons which have tail flexion or tail flip, and when the giant dentritic branches in contact with a giant fiber does not fire in response to such stim- fiber are activated by that giant fiber (12, uli, the movement does not occur. 21). All of tl ie fast flexor motoneurons are The afferent limb of the reflex exciting excited by the ipsilateral giant; all but F4, the lateral giant has been described (28), F5 and F7 are also excited by the contra- and the habituation of the behavior has latkral giant (21 a). been explained in terms of the properties The excitation of these motoneurons, of this part of the neural circuit (29). seen as depolarizing potentials in their The properties of the neuromuscular somata, does not always reach threshold for junctions between the fast flexor motoneu- generating a spike which propagates out the rons and the phasic flexor muscles have also axon to the periphery (14). Indeed, only t,he been described (13). -
Signaling by Sensory Receptors
Signaling by Sensory Receptors David Julius1 and Jeremy Nathans2 1Department of Physiology, University of California School of Medicine, San Francisco, California 94158 2Department of Molecular Biology and Genetics, Johns Hopkins Medical School, Baltimore, Maryland 21205 Correspondence: [email protected] and [email protected] SUMMARY Sensory systems detect small molecules, mechanical perturbations, or radiation via the activa- tion of receptor proteins and downstream signaling cascades in specialized sensory cells. In vertebrates, the two principal categories of sensory receptors are ion channels, which mediate mechanosensation, thermosensation, and acid and salt taste; and G-protein-coupled recep- tors (GPCRs), which mediate vision, olfaction, and sweet, bitter, and umami tastes. GPCR- based signaling in rods and cones illustrates the fundamental principles of rapid activation and inactivation, signal amplification, and gain control. Channel-based sensory systems illus- trate the integration of diverse modulatory signals at the receptor, as seen in the thermosen- sory/pain system, and the rapid response kinetics that are possible with direct mechanical gating of a channel. Comparisons of sensory receptor gene sequences reveal numerous exam- ples in which gene duplication and sequence divergence have created novel sensory specific- ities. This is the evolutionary basis for the observed diversity in temperature- and ligand- dependent gating among thermosensory channels, spectral tuning among visual pigments, and odorant binding among olfactory receptors. The coding of complex external stimuli by a limited number of sensory receptor types has led to the evolution of modality-specific and species-specific patterns of retention or loss of sensory information, a filtering operation that selectively emphasizes features in the stimulus that enhance survival in a particular ecological niche. -
Long-Term Adult Human Brain Slice Cultures As a Model System to Study
TOOLS AND RESOURCES Long-term adult human brain slice cultures as a model system to study human CNS circuitry and disease Niklas Schwarz1, Betu¨ l Uysal1, Marc Welzer2,3, Jacqueline C Bahr1, Nikolas Layer1, Heidi Lo¨ ffler1, Kornelijus Stanaitis1, Harshad PA1, Yvonne G Weber1,4, Ulrike BS Hedrich1, Ju¨ rgen B Honegger4, Angelos Skodras2,3, Albert J Becker5, Thomas V Wuttke1,4†*, Henner Koch1†* 1Department of Neurology and Epileptology, Hertie-Institute for Clinical Brain Research, University of Tu¨ bingen, Tu¨ bingen, Germany; 2Department of Cellular Neurology, Hertie-Institute for Clinical Brain Research, University of Tu¨ bingen, Tu¨ bingen, Germany; 3German Center for Neurodegenerative Diseases (DZNE), Tu¨ bingen, Germany; 4Department of Neurosurgery, University of Tu¨ bingen, Tu¨ bingen, Germany; 5Department of Neuropathology, Section for Translational Epilepsy Research, University Bonn Medical Center, Bonn, Germany Abstract Most of our knowledge on human CNS circuitry and related disorders originates from model organisms. How well such data translate to the human CNS remains largely to be determined. Human brain slice cultures derived from neurosurgical resections may offer novel avenues to approach this translational gap. We now demonstrate robust preservation of the complex neuronal cytoarchitecture and electrophysiological properties of human pyramidal neurons *For correspondence: in long-term brain slice cultures. Further experiments delineate the optimal conditions for efficient [email protected] viral transduction of cultures, enabling ‘high throughput’ fluorescence-mediated 3D reconstruction tuebingen.de (TVW); of genetically targeted neurons at comparable quality to state-of-the-art biocytin fillings, and [email protected] demonstrate feasibility of long term live cell imaging of human cells in vitro. -
Specification of Optic Nerve Oligodendrocyte Precursors by Retinal Ganglion Cell Axons
The Journal of Neuroscience, July 19, 2006 • 26(29):7619–7628 • 7619 Cellular/Molecular Specification of Optic Nerve Oligodendrocyte Precursors by Retinal Ganglion Cell Axons Limin Gao and Robert H. Miller Department of Neurosciences, Case Western Reserve University, Cleveland, Ohio 44106 Cell fate commitment in the developing CNS frequently depends on localized cell–cell interactions. In the avian visual system the optic nerve oligodendrocytes are derived from founder cells located at the floor of the third ventricle. Here we show that the induction of these founder cells is directly dependent on signaling from the retinal ganglion cell (RGC) axons. The appearance of oligodendrocyte precursor cells (OPCs) correlates with the projection of RGC axons, and early eye removal dramatically reduces the number of OPCs. In vitro signaling from retinal neurites induces OPCs in responsive tissue. Retinal axon induction of OPCs is dependent on sonic hedgehog (Shh) andneuregulinsignaling,andtheinhibitionofeithersignalreducesOPCinductioninvivoandinvitro.ThedependenceofOPCsonretinal axonal cues appears to be a common phenomenon, because ocular retardation (orJ) mice lacking optic nerve have dramatically reduced OPCs in the midline of the third ventricle. Key words: oligodendrocyte precursors; optic nerve; axon induction; sonic hedgehog; neuregulin; retinal ganglion cells Introduction contributes to the specification of ventral midline cells (Dale et al., During development the oligodendrocytes, the myelinating cells 1997); however, OPCs arise later -
Early Neuronal Processes Interact with Glia to Establish a Scaffold For
bioRxiv preprint doi: https://doi.org/10.1101/754416; this version posted August 31, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Early neuronal processes interact with glia to establish a scaffold for orderly innervation of the cochlea Running Title: Glia and early cochlear wiring N. R. Druckenbrod1, E. B. Hale, O. O. Olukoya, W. E. Shatzer, and L.V. Goodrich* Department of Neurobiology, Harvard Medical School, Boston, MA, 02115 1Current address: Decibel Therapeutics, Boston, Ma, 02215 *correspondence should be addressed to [email protected] Keywords: neuron-glia interactions, axon guidance, spiral ganglion neuron, cochlea Authors’ contributions: This study was conceived of and designed by NRD and LVG. NRD, EBH, OOO, and WES performed experiments and analyzed results. LVG analyzed results and wrote the manuscript. bioRxiv preprint doi: https://doi.org/10.1101/754416; this version posted August 31, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. Summary: Although the basic principles of axon guidance are well established, it remains unclear how axons navigate with high fidelity through the complex cellular terrains that are encountered in vivo. To learn more about the cellular strategies underlying axon guidance in vivo, we analyzed the developing cochlea, where spiral ganglion neurons extend processes through a heterogeneous cellular environment to form tonotopically ordered connections with hair cells. -
Vocabulario De Morfoloxía, Anatomía E Citoloxía Veterinaria
Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) Servizo de Normalización Lingüística Universidade de Santiago de Compostela COLECCIÓN VOCABULARIOS TEMÁTICOS N.º 4 SERVIZO DE NORMALIZACIÓN LINGÜÍSTICA Vocabulario de Morfoloxía, anatomía e citoloxía veterinaria (galego-español-inglés) 2008 UNIVERSIDADE DE SANTIAGO DE COMPOSTELA VOCABULARIO de morfoloxía, anatomía e citoloxía veterinaria : (galego-español- inglés) / coordinador Xusto A. Rodríguez Río, Servizo de Normalización Lingüística ; autores Matilde Lombardero Fernández ... [et al.]. – Santiago de Compostela : Universidade de Santiago de Compostela, Servizo de Publicacións e Intercambio Científico, 2008. – 369 p. ; 21 cm. – (Vocabularios temáticos ; 4). - D.L. C 2458-2008. – ISBN 978-84-9887-018-3 1.Medicina �������������������������������������������������������������������������veterinaria-Diccionarios�������������������������������������������������. 2.Galego (Lingua)-Glosarios, vocabularios, etc. políglotas. I.Lombardero Fernández, Matilde. II.Rodríguez Rio, Xusto A. coord. III. Universidade de Santiago de Compostela. Servizo de Normalización Lingüística, coord. IV.Universidade de Santiago de Compostela. Servizo de Publicacións e Intercambio Científico, ed. V.Serie. 591.4(038)=699=60=20 Coordinador Xusto A. Rodríguez Río (Área de Terminoloxía. Servizo de Normalización Lingüística. Universidade de Santiago de Compostela) Autoras/res Matilde Lombardero Fernández (doutora en Veterinaria e profesora do Departamento de Anatomía e Produción Animal. -
Primary Processes in Sensory Cells: Current Advances
J Comp Physiol A (2009) 195:1–19 DOI 10.1007/s00359-008-0389-0 REVIEW Primary processes in sensory cells: current advances Stephan Frings Received: 14 September 2008 / Revised: 25 October 2008 / Accepted: 25 October 2008 / Published online: 15 November 2008 © The Author(s) 2008. This article is published with open access at Springerlink.com Abstract In the course of evolution, the strong and unre- INAD Inactivation no after-potential D mitting selective pressure on sensory performance has MEC Mechanosensitive channel-related protein driven the acuity of sensory organs to its physical limits. As OHC Outer hair cell a consequence, the study of primary sensory processes ORN Olfactory receptor neuron illustrates impressively how far a physiological function PDE Phosphodiesterase can be improved if the survival of a species depends on it. PDZ Domain postsynaptic density/discs-large/zonula Sensory cells that detect single-photons, single molecules, occludens domain mechanical motions on a nanometer scale, or incredibly TRP Channel transient receptor potential channel small Xuctuations of electromagnetic Welds have fascinated VNO Vomeronasal organ physiologists for a long time. It is a great challenge to understand the primary sensory processes on a molecular level. This review points out some important recent develop- Introduction ments in the search for primary processes in sensory cells that mediate touch perception, hearing, vision, taste, olfac- Sensory cells provide the central nervous system with vital tion, as well as the analysis of light polarization and the ori- information about the body and its environment. Each sen- entation in the Earth’s magnetic Weld. The data are screened sory cell detects speciWc stimuli using highly specialized for common transduction strategies and common transduc- structures which operate as sensors for adequate stimuli. -
Spinal Nerves, Ganglia, and Nerve Plexus Spinal Nerves
Chapter 13 Spinal Nerves, Ganglia, and Nerve Plexus Spinal Nerves Posterior Spinous process of vertebra Posterior root Deep muscles of back Posterior ramus Spinal cord Transverse process of vertebra Posterior root ganglion Spinal nerve Anterior ramus Meningeal branch Communicating rami Anterior root Vertebral body Sympathetic ganglion Anterior General Anatomy of Nerves and Ganglia • Spinal cord communicates with the rest of the body by way of spinal nerves • nerve = a cordlike organ composed of numerous nerve fibers (axons) bound together by connective tissue – mixed nerves contain both afferent (sensory) and efferent (motor) fibers – composed of thousands of fibers carrying currents in opposite directions Anatomy of a Nerve Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Epineurium Perineurium Copyright © The McGraw-Hill Companies, Inc. Permission required for reproduction or display. Endoneurium Nerve Rootlets fiber Posterior root Fascicle Posterior root ganglion Anterior Blood root vessels Spinal nerve (b) Copyright by R.G. Kessel and R.H. Kardon, Tissues and Organs: A Text-Atlas of Scanning Electron Microscopy, 1979, W.H. Freeman, All rights reserved Blood vessels Fascicle Epineurium Perineurium Unmyelinated nerve fibers Myelinated nerve fibers (a) Endoneurium Myelin General Anatomy of Nerves and Ganglia • nerves of peripheral nervous system are ensheathed in Schwann cells – forms neurilemma and often a myelin sheath around the axon – external to neurilemma, each fiber is surrounded by -
Spinal Cord Organization
Lecture 4 Spinal Cord Organization The spinal cord . Afferent tract • connects with spinal nerves, through afferent BRAIN neuron & efferent axons in spinal roots; reflex receptor interneuron • communicates with the brain, by means of cell ascending and descending pathways that body form tracts in spinal white matter; and white matter muscle • gives rise to spinal reflexes, pre-determined gray matter Efferent neuron by interneuronal circuits. Spinal Cord Section Gross anatomy of the spinal cord: The spinal cord is a cylinder of CNS. The spinal cord exhibits subtle cervical and lumbar (lumbosacral) enlargements produced by extra neurons in segments that innervate limbs. The region of spinal cord caudal to the lumbar enlargement is conus medullaris. Caudal to this, a terminal filament of (nonfunctional) glial tissue extends into the tail. terminal filament lumbar enlargement conus medullaris cervical enlargement A spinal cord segment = a portion of spinal cord that spinal ganglion gives rise to a pair (right & left) of spinal nerves. Each spinal dorsal nerve is attached to the spinal cord by means of dorsal and spinal ventral roots composed of rootlets. Spinal segments, spinal root (rootlets) nerve roots, and spinal nerves are all identified numerically by th region, e.g., 6 cervical (C6) spinal segment. ventral Sacral and caudal spinal roots (surrounding the conus root medullaris and terminal filament and streaming caudally to (rootlets) reach corresponding intervertebral foramina) collectively constitute the cauda equina. Both the spinal cord (CNS) and spinal roots (PNS) are enveloped by meninges within the vertebral canal. Spinal nerves (which are formed in intervertebral foramina) are covered by connective tissue (epineurium, perineurium, & endoneurium) rather than meninges. -
The Peripheral Nervous System
The Peripheral Nervous System Dr. Ali Ebneshahidi Peripheral Nervous System (PNS) – Consists of 12 pairs of cranial nerves and 31 pairs of spinal nerves. – Serves as a critical link between the body and the central nervous system. – peripheral nerves contain an outermost layer of fibrous connective tissue called epineurium which surrounds a thinner layer of fibrous connective tissue called perineurium (surrounds the bundles of nerve or fascicles). Individual nerve fibers within the nerve are surrounded by loose connective tissue called endoneurium. Cranial Nerves Cranial nerves are direct extensions of the brain. Only Nerve I (olfactory) originates from the cerebrum, the remaining 11 pairs originate from the brain stem. Nerve I (Olfactory)- for the sense of smell (sensory). Nerve II (Optic)- for the sense of vision (sensory). Nerve III (Oculomotor)- for controlling muscles and accessory structures of the eyes ( primarily motor). Nerve IV (Trochlear)- for controlling muscles of the eyes (primarily motor). Nerve V (Trigeminal)- for controlling muscles of the eyes, upper and lower jaws and tear glands (mixed). Nerve VI (Abducens)- for controlling muscles that move the eye (primarily motor). Nerve VII (Facial) – for the sense of taste and controlling facial muscles, tear glands and salivary glands (mixed). Nerve VIII (Vestibulocochlear)- for the senses of hearing and equilibrium (sensory). Nerve IX (Glossopharyngeal)- for controlling muscles in the pharynx and to control salivary glands (mixed). Nerve X (Vagus)- for controlling muscles used in speech, swallowing, and the digestive tract, and controls cardiac and smooth muscles (mixed). Nerve XI (Accessory)- for controlling muscles of soft palate, pharynx and larynx (primarily motor). Nerve XII (Hypoglossal) for controlling muscles that move the tongue ( primarily motor). -
PN1 (Midha) Microanatomy of Peripheral Nerves-Part1.Pdf
Peripheral Nerve Basics • Consist of processes of cell bodies found in the DRG, anterior horn, and autonomic ganglia • Organized by several distinct connective tissue layers – the epineurium, perineurium, and endoneurium • Vascular supply provided by the vasa nervorum Peripheral Nerve Basics • Neuronal processes bound into fascicles by perineurium • Fascicles bound into nerves by epineurium • Endoneurium is a division of the perineurium which form thin layers of connective tissue surrounding neuronal fibers in a fascicle Sural nerve in cross-section Epineurium • Loose areolar tissue with sparse, longitudinally-oriented collagen fibers • Some elastic fibers where epineurium abuts perineurium • Able to accommodate a significant amount of nerve stretching and movement • Increases in thickness where nerves cross joints • Constitutes an increasing proportion of nerves as they increase in size • Epineurial fat helps cushion nerves from compressive injury • Decreased epineurial fat found in patients with diabetes Perineurium • Cellular component composed of laminated fibroblasts of up to 15 layers in thickness which are bounded by a basal lamina • Semi-permeable: inner lamellae have tight junctions, providing a barrier to intercellular transport of macromolecules – Tight junctions can be loosened with topical anaesthetics and with osmotic change Perineurium • Exhibits a slightly positive internal pressure – Fascicular contents herniate upon perineurial injury • Under tension longitudinally – Nerve segment shortens upon transection – may complicate surgical repair as nerve can be stretched only approximately 10% before being inhibited by collagen Endoneurium • Intrafascicular connective tissue consisting of a collagenous matrix in the interstitial space • Develops into partitions of dense connective tissue between diverging fascicles and eventually becomes perineurium when the fascicles separate • Collagen fibers are longitudinally-oriented and run along nerve fibers and capillaries.