The Intestinal Neuro-Immune Axis: Crosstalk Between Neurons, Immune Cells, and Microbes
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The Baseline Structure of the Enteric Nervous System and Its Role in Parkinson’S Disease
life Review The Baseline Structure of the Enteric Nervous System and Its Role in Parkinson’s Disease Gianfranco Natale 1,2,* , Larisa Ryskalin 1 , Gabriele Morucci 1 , Gloria Lazzeri 1, Alessandro Frati 3,4 and Francesco Fornai 1,4 1 Department of Translational Research and New Technologies in Medicine and Surgery, University of Pisa, 56126 Pisa, Italy; [email protected] (L.R.); [email protected] (G.M.); [email protected] (G.L.); [email protected] (F.F.) 2 Museum of Human Anatomy “Filippo Civinini”, University of Pisa, 56126 Pisa, Italy 3 Neurosurgery Division, Human Neurosciences Department, Sapienza University of Rome, 00135 Rome, Italy; [email protected] 4 Istituto di Ricovero e Cura a Carattere Scientifico (I.R.C.C.S.) Neuromed, 86077 Pozzilli, Italy * Correspondence: [email protected] Abstract: The gastrointestinal (GI) tract is provided with a peculiar nervous network, known as the enteric nervous system (ENS), which is dedicated to the fine control of digestive functions. This forms a complex network, which includes several types of neurons, as well as glial cells. Despite extensive studies, a comprehensive classification of these neurons is still lacking. The complexity of ENS is magnified by a multiple control of the central nervous system, and bidirectional communication between various central nervous areas and the gut occurs. This lends substance to the complexity of the microbiota–gut–brain axis, which represents the network governing homeostasis through nervous, endocrine, immune, and metabolic pathways. The present manuscript is dedicated to Citation: Natale, G.; Ryskalin, L.; identifying various neuronal cytotypes belonging to ENS in baseline conditions. -
Journal of Neuroimmunology
JOURNAL OF NEUROIMMUNOLOGY AUTHOR INFORMATION PACK TABLE OF CONTENTS XXX . • Description p.1 • Audience p.1 • Impact Factor p.1 • Abstracting and Indexing p.1 • Editorial Board p.2 • Guide for Authors p.3 ISSN: 0165-5728 DESCRIPTION . The Journal of Neuroimmunology affords a forum for the publication of works applying immunologic methodology to the furtherance of the neurological sciences. Studies on all branches of the neurosciences, particularly fundamental and applied neurobiology, neurology, neuropathology, neurochemistry, neurovirology, neuroendocrinology, neuromuscular research, neuropharmacology and psychology, which involve either immunologic methodology (e.g. immunocytochemistry) or fundamental immunology (e.g. antibody and lymphocyte assays), are considered for publication. Works pertaining to multiple sclerosis, AIDS, amyotrophic lateral sclerosis, Guillain Barré Syndrome, myasthenia gravis, and brain tumors form a major focus. The scope of the Journal is broad, covering both research and clinical problems of neuroscientific interest. A major aim of the Journal is to encourage the development of immunologic approaches to analyse in further depth the interactions and specific properties of nervous tissue elements during development and disease. AUDIENCE . Researchers in neurology, immunology, neuroscience, neuropathology, and experimental neurology IMPACT FACTOR . 2020: 3.478 © Clarivate Analytics Journal Citation Reports 2021 ABSTRACTING AND INDEXING . BIOSIS Citation Index Chemical Abstracts Current Contents - Life Sciences Embase PubMed/Medline Pascal Francis Reference Update Scopus AUTHOR INFORMATION PACK 23 Sep 2021 www.elsevier.com/locate/jneuroim 1 EDITORIAL BOARD . Editors-in-Chief Robyn Klein, Washington University in St Louis School of Medicine, Campus Box 8301660 S. Euclid Ave., MO 63110-1093, Saint Louis, Missouri, United States of America Laura Piccio, The University of Sydney Brain and Mind Centre, Camperdown, Australia Gregory Wu, Washington University in St Louis School of Medicine, Campus Box 8301660 S. -
2021 Psychiatry CC-MOC Content Specifications
CONTINUING CERTIFICATION/MOC EXAMINATION IN PSYCHIATRY The American Board of Psychiatry and Neurology, Inc. (ABPN) has issued new, two- dimensional content specifications for the psychiatry, neurology and child neurology continuing certification/MOC examinations. Questions for the 2021 psychiatry, neurology and child neurology continuing certification examinations will conform to these new content specifications. Within the two-dimensional format, one dimension is comprised of disorders and topics while the other is comprised of competencies and mechanisms that cut across the various disorders of the first dimension. By design, the two dimensions are interrelated and not independent of each other. All of the questions on the examination will fall into one of the disorders/topics and will be aligned with a competency/mechanism. For example, an item on substance use could focus on treatment, or it could focus on systems-based practice. The psychiatry, neurology and child neurology continuing certification content specifications can be accessed from the Specialty MOC Exams section of our website. Candidates should use the new detailed content specifications as a guide to prepare for a continuing certification examination. Scores for these examinations will be reported in a standardized format rather than the previous percent correct format. In addition to these three continuing certification examinations, ABPN examinations will gradually conform to the new two-dimensional content specification starting in 2018. The American Board of Psychiatry and Neurology, Inc. is a not-for-profit corporation dedicated to serving the public interest and the professions of psychiatry and neurology by promoting excellence in practice through certification and continuing certification processes. For more information, please contact us at [email protected] or visit our website at www.abpn.com . -
The Vagus Nerve Can Predict and Possibly Modulate Non- Communicable Chronic Diseases: Introducing a Neuroimmunological Paradigm to Public Health
12/17/19, 08:13 Page 1 of 15 J Clin Med. 2018 Oct; 7(10): 371. PMCID: PMC6210465 Published online 2018 Oct 19. doi: 10.3390/jcm7100371 PMID: 30347734 The Vagus Nerve Can Predict and Possibly Modulate Non- Communicable Chronic Diseases: Introducing a Neuroimmunological Paradigm to Public Health Yori Gidron,1,* Reginald Deschepper,2 Marijke De Couck,2,3 Julian F. Thayer,4 and Brigitte Velkeniers5 1SCALAB UMR CNRS 9193, Université Lille, BP 60149, Villeneuve d’Ascq CEDEX 59653, France 2Mental Health and Wellbeing Research Group, Vrije Universiteit Brussel (VUB), Laerbeeklaan 103, 1090 Jette, Brussels, Belgium; [email protected] (R.D.); [email protected] (M.D.C.) 3Faculty of Health Care, University College Odisee, 9302 Aalst, Belgium 4Department of Neuroscience and Psychology, College of Medicine, Ohio State University, 33 Psychology Building, 1835 Neil Ave. Columbus, OH 43210, USA; [email protected] 5Faculty of Medicine and Pharmacy, Vrije Universiteit Brussel (VUB), Laerbeeklaan 103, 1090 Jette, Brussels, Belgium; [email protected] *Correspondence: [email protected]; Tel.: +32-498-56-82-77 Received 2018 Sep 19; Accepted 2018 Oct 15. Copyright © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). Abstract Global burden of diseases (GBD) includes non-communicable conditions such as cardiovascular diseases, cancer and chronic obstructive pulmonary disease. These share important behavioral risk factors (e.g., smoking, diet) and pathophysiological contributing factors (oxidative stress, inflammation and excessive sympathetic activity). -
Enteric Nervous System (ENS): 1) Myenteric (Auerbach) Plexus & 2
Enteric Nervous System (ENS): 1) Myenteric (Auerbach) plexus & 2) Submucosal (Meissner’s) plexus à both triggered by sensory neurons with chemo- and mechanoreceptors in the mucosal epithelium; effector motors neurons of the myenteric plexus control contraction/motility of the GI tract, and effector motor neurons of the submucosal plexus control secretion of GI mucosa & organs. Although ENS neurons can function independently, they are subject to regulation by ANS. Autonomic Nervous System (ANS): 1) parasympathetic (rest & digest) – can innervate the GI tract and form connections with ENS neurons that promote motility and secretion, enhancing/speeding up the process of digestion 2) sympathetic (fight or flight) – can innervate the GI tract and inhibit motility & secretion by inhibiting neurons of the ENS Sections and dimensions of the GI tract (alimentary canal): Esophagus à ~ 10 inches Stomach à ~ 12 inches and holds ~ 1-2 L (full) up to ~ 3-4 L (distended) Duodenum à first 10 inches of the small intestine Jejunum à next 3 feet of small intestine (when smooth muscle tone is lost upon death, extends to 8 feet) Ileum à final 6 feet of small intestine (when smooth muscle tone is lost upon death, extends to 12 feet) Large intestine à 5 feet General Histology of the GI Tract: 4 layers – Mucosa, Submucosa, Muscularis Externa, and Serosa Mucosa à epithelium, lamina propria (areolar connective tissue), & muscularis mucosae Submucosa à areolar connective tissue Muscularis externa à skeletal muscle (in select parts of the tract); smooth muscle (at least 2 layers – inner layer of circular muscle and outer layer of longitudinal muscle; stomach has a third layer of oblique muscle under the circular layer) Serosa à superficial layer made of areolar connective tissue and simple squamous epithelium (a.k.a. -
1 the Anatomy and Physiology of the Oesophagus
111 2 3 1 4 5 6 The Anatomy and Physiology of 7 8 the Oesophagus 9 1011 Peter J. Lamb and S. Michael Griffin 1 2 3 4 5 6 7 8 911 2011 location deep within the thorax and abdomen, 1 Aims a close anatomical relationship to major struc- 2 tures throughout its course and a marginal 3 ● To develop an understanding of the blood supply, the surgical exposure, resection 4 surgical anatomy of the oesophagus. and reconstruction of the oesophagus are 5 ● To establish the normal physiology and complex. Despite advances in perioperative 6 control of swallowing. care, oesophagectomy is still associated with the 7 highest mortality of any routinely performed ● To determine the structure and function 8 elective surgical procedure [1]. of the antireflux barrier. 9 In order to understand the pathophysiol- 3011 ● To evaluate the effect of surgery on the ogy of oesophageal disease and the rationale 1 function of the oesophagus. for its medical and surgical management a 2 basic knowledge of oesophageal anatomy and 3 physiology is essential. The embryological 4 Introduction development of the oesophagus, its anatomical 5 structure and relationships, the physiology of 6 The oesophagus is a muscular tube connecting its major functions and the effect that surgery 7 the pharynx to the stomach and measuring has on them will all be considered in this 8 25–30 cm in the adult. Its primary function is as chapter. 9 a conduit for the passage of swallowed food and 4011 fluid, which it propels by antegrade peristaltic 1 contraction. It also serves to prevent the reflux Embryology 2 of gastric contents whilst allowing regurgita- 3 tion, vomiting and belching to take place. -
Reliability of Quantitative Sudomotor Axon Reflex Testing and Quantitative Sensory Testing in Neuropathy of Impaired Glucose Regulation
ABSTRACT: Reproducible neurophysiologic testing paradigms are critical for multicenter studies of neuropathy associated with impaired glucose regulation (IGR), yet the best methodologies and endpoints remain to be established. This study evaluates the reproducibility of neurophysiologic tests within a multicenter research setting. Twenty-three participants with neuropathy and IGR were recruited from two study sites. The reproducibility of quantitative sudomotor axon reflex test (QSART) and quantitative sensory test (QST) (using the CASE IV system) was determined in a subset of patients at two sessions, and it was calculated from intraclass correlation coefficients (ICCs). QST (cold detection threshold: ICC ϭ 0.80; vibration detection threshold: ICC ϭ 0.75) was more reproducible than QSART (ICC foot ϭ 0.52). The performance of multiple tests in one setting did not improve reproducibility of QST. QST reproducibility in our IGR patients was similar to reports of other studies. QSART reproducibility was significantly lower than QST. In this group of patients, the reproducibility of QSART was unaccept- able for use as a secondary endpoint measure in clinical research trials. Muscle Nerve 39: 529–535, 2009 RELIABILITY OF QUANTITATIVE SUDOMOTOR AXON REFLEX TESTING AND QUANTITATIVE SENSORY TESTING IN NEUROPATHY OF IMPAIRED GLUCOSE REGULATION AMANDA PELTIER, MD,1 A. GORDON SMITH, MD,2,3 JAMES W. RUSSELL, MD, MS,4 KIRAN SHEIKH, MD,5 BILLIE BIXBY, BS,2 JAMES HOWARD, BS,2 JONATHAN GOLDSTEIN, MD,6 YANNA SONG, MS,7 LILY WANG, PhD,7 EVA L. FELDMAN, MD, -
Neuroscience: the Science of the Brain
NEUROSCIENCE SCIENCE OF THE BRAIN AN INTRODUCTION FOR YOUNG STUDENTS British Neuroscience Association European Dana Alliance for the Brain Neuroscience: the Science of the Brain 1 The Nervous System P2 2 Neurons and the Action Potential P4 3 Chemical Messengers P7 4 Drugs and the Brain P9 5 Touch and Pain P11 6 Vision P14 Inside our heads, weighing about 1.5 kg, is an astonishing living organ consisting of 7 Movement P19 billions of tiny cells. It enables us to sense the world around us, to think and to talk. The human brain is the most complex organ of the body, and arguably the most 8 The Developing P22 complex thing on earth. This booklet is an introduction for young students. Nervous System In this booklet, we describe what we know about how the brain works and how much 9 Dyslexia P25 there still is to learn. Its study involves scientists and medical doctors from many disciplines, ranging from molecular biology through to experimental psychology, as well as the disciplines of anatomy, physiology and pharmacology. Their shared 10 Plasticity P27 interest has led to a new discipline called neuroscience - the science of the brain. 11 Learning and Memory P30 The brain described in our booklet can do a lot but not everything. It has nerve cells - its building blocks - and these are connected together in networks. These 12 Stress P35 networks are in a constant state of electrical and chemical activity. The brain we describe can see and feel. It can sense pain and its chemical tricks help control the uncomfortable effects of pain. -
B-Afferents: a Fundamental Division of the Nervous System Mediating Hoxneostasis?
Zurich Open Repository and Archive University of Zurich Main Library Strickhofstrasse 39 CH-8057 Zurich www.zora.uzh.ch Year: 1990 Dichotomic classification of sensory neurons: Elegant but problematic Neuhuber, W L DOI: https://doi.org/10.1017/s0140525x00078882 Posted at the Zurich Open Repository and Archive, University of Zurich ZORA URL: https://doi.org/10.5167/uzh-154322 Journal Article Published Version Originally published at: Neuhuber, W L (1990). Dichotomic classification of sensory neurons: Elegant but problematic. Behav- ioral and Brain Sciences, 13(02):313-314. DOI: https://doi.org/10.1017/s0140525x00078882 BEHAVIORAL AND BRAIN SCIENCES (1990) 13, 289-331 Printed in the United States of America B-Afferents: A fundamental division of the nervous system mediating hoxneostasis? James C. Prechtl* Terry L* Powley Laboratory of Regulatory Psychobiology, Department of Psychological Sciences, Purdue University, West Lafayette, IN 47907 Electronic mail: [email protected]@brazil.psych.edu *Reprint requests should be addressed to: James C. Prechtl, Department of Neuroscience, A-001, University of California, San Diego, La Jolla, CA 92093 Abstract? The peripheral nervous system (PNS) has classically been separated into a somatic division composed of both afferent and efferent pathways and an autonomic division containing only efferents. J. N. Langley, who codified this asymmetrical plan at the beginning of the twentieth century, considered different afferents, including visceral ones, as candidates for inclusion in his concept of the "autonomic nervous system" (ANS), but he finally excluded all candidates for lack of any distinguishing histological markers. Langley's classification has been enormously influential in shaping modern ideas about both the structure and the function of the PNS. -
Neuroimmunology: the Brain As a Cognitive Antigen
Neuroimmunology: The brain as a cognitive antigen Prof Anat Achiron, MD, PhD Director, Multiple Sclerosis Center & Neurogenomic Laboratory Sheba Medical Center, Tel-Hashomer ISRAEL Itinerary • Self-recognition • Basic brain immunology • The brain as an antigen • BBB • PML • Myelin • Autoimmunity • Multiple sclerosis • Brain plasticity • The brain as a cognitive antigen Multiple Sclerosis Center Sheba Multiple Sclerosis Center Multiple Sclerosis Center, Sheba Medical Center, Tel-Hashomer, ISRAEL 1995 – 2016…. No of MS patients = 4071 http://research.sheba.co.il/e/13/ SheBa Comprehensive Multiple Sclerosis Center Nursing Physiotherapy Neurology Sport, Gait, Balance Hydrotherapy Neuro- Occupational Ophthalmology therapy Patient Speech Orthopedics therapy Expert MS Center Neuro-urology Social work Sexual counseling Creative art Psychiatry Psychology Family Group therapy counseling Sheba Comprehensive Multiple Sclerosis Center Epidemiology Image Analysis Cognition Multiple Sclerosis Neuroimmunology Center Gene expression Education Rehabilitation Clinical trials Immune system– Basic definitions n Innate immune system aimed at acute rapid immune response. n Detects pathogens or PAMPs (pathogen-associated molecular patterns) which are characteristic structures present in microorganisms by receptors belonging to two diverse receptor families: the Toll-like receptor family and the Nod protein (or NBD-LRR protein) family. n In vertebrates, the innate immune system activates the more evolved adaptive immune system, which is composed of T and B lymphocytes. Immune system – detection & response Innate immune response: 1) Antigen-presenting cells (APCs) are activated through recognition of pathogens (or PAMPs) by receptors such as TLRs or NBD-LRR proteins. 2) This activation leads to the production of inflammatory cytokines and the expression of co-stimulatory molecules on the cell surface. Adaptive immune response: 3) Antigens will be presented by MHC molecules on APCs to T lymphocytes (Signal 1). -
Manuscript Postprint
This is the peer reviewed version of the following article: J Child Psychol Psychiatry. 2018 Sep 3, which has been published in final form at http://dx.doi.org/10.1111/jcpp.12958 This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self- Archiving. Bidirectional relationship between eating disorders and autoimmune diseases Hedman A, Breithaupt L, Hübel C, Thornton LM, Tillander A, Norring C, Birgegård A, Larsson H, Ludvigsson JF, Sävendahl L, Almqvist C, Bulik CM. Access to the published version may require subscription. Published with permission from: Wiley Bidirectional relationship between eating disorders and autoimmune diseases Anna Hedman, Ph.D.1, Lauren Breithaupt, M.A.1,2, Christopher Hübel, M.D., M.Sc.,1,3 Laura M. Thornton, Ph.D.4, Annika Tillander, Ph.D.1,5, Claes Norring, Ph.D.6, Andreas Birgegård, Ph.D.6, Henrik Larsson, Ph.D.1,7, Jonas Ludvigsson, M.D., Ph.D.1,8, Lars Sävendahl, M.D., Ph.D.9, Catarina Almqvist, M.D., Ph.D.1,10, Cynthia M. Bulik, Ph.D.1,4,11 1Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm, Sweden 2Department of Psychology, George Mason University, Fairfax, VA, USA 3Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King’s College London, UK 4Department of Psychiatry, University of North Carolina at Chapel Hill, Chapel Hill, NC 5Department of Computer and Information Science, Linköping University, Linköping, Sweden 6Centre for Psychiatry Research, Department of Clinical -
NROSCI/BIOSC 1070 and MSNBIO 2070 November 15, 2017 Gastrointestinal 1 Functions of the Digestive Tract
NROSCI/BIOSC 1070 and MSNBIO 2070 November 15, 2017 Gastrointestinal 1 Functions of the Digestive Tract. The digestive system has two primary roles: digestion, or the chemical and mechanical breakdown of foods into small molecules that can absorbed, or moved across the intestinal mucosa into the bloodstream. In order to accomplish these functions, the secretion of enzymes, hormones, mucus, and paracrines by the gastrointestinal organs is needed. Furthermore, motility, or controlled movement of materials through the digestive tract is required. In addition to these primary functions, the gastrointestinal tract faces a number of challenges. Almost 7 liters of fluid must be released into the lumen of the digestive tract per day to allow for digestion and absorption to occur. Clearly, most of this fluid must be reabsorbed or dehydration will occur. Furthermore, the inner surface of the digestive tract is technically in contact with the external environment; for this reason, protective mechanisms are needed. In part, these mechanisms must protect against the secretions of the GI tract, including acid and enzymes. Anatomy of the Gastrointestinal System November 15, 2017 Page 1 GI 1 The anatomy of the GI system is illustrated in the previous 2 figures. The organs involved in digestion and absorption include the salivary glands, esophagus, stomach, small intestine, liver, pancreas, and large intestine. In addition, 7 sphincters control the movement of material and secretions between the organs. The total length of the GI tract is about 15 feet, of which 13 feet are comprised of intestine. The processed material within the GI tract is referred to as chyme.