Enterocyte Protection – a New Goal in ICU Nutrition
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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. -
4L Eosinophilic Granuloma of Gastro-Intestinal Tract Caused by Herring Parasite Eustoma Rotundatum
BsrrmsH 2 May 1964 MEDICAL JOURNAL 1141 4L Eosinophilic Granuloma of Gastro-intestinal Tract Caused by Herring Parasite Eustoma rotundatum B. STERRY ASHBY,* M.B., F.R.C.S.; P. J. APPLETONt M.B., B.S. IAN DAWSON,4 M.D., M.R.C.P. Brit. med.JY., 1964, 1, 1141-1145 For over 25 years sporadic reports have been appearing in the came from many countries in many different parts of the world. literature of cases of eosinophilic granuloma arising in various The essential details of these cases are recorded in Table I parts of the gastro-intestinal tract. Kaiiser (1937) described and Fig. 1. the first cases. In a search of the literature, which although The one feature common to all these case reports is the extensive is not claimed to be exhaustive, 47 papers were microscopical appearance of the lesion. No matter which part found, describing a total of 89 cases. They occurred through- of the alimentary tract is involved, the histological description out the alimentary tract from pharynx to rectum, though the is the same-an oedematous connective-tissue stroma with an majority were in the stomach and small intestine, and they increase of capillaries and lymphatics, and showing a massive diffuse eosinophil-cell infiltration, usually confined to the sub- * Surgical Registrar, Westminster Hospital and Medical School London. the muscularis mucosae and t House-Surgeon, Westminster Hospital and Medical School, Iondon. mucosa but sometimes splitting t Reader in Pathology, Westminster Hospital and Medical School, spreading into the muscle layer. The mucosa is almost always London. intact. -
Gastrointestinal Motility Physiology
GASTROINTESTINAL MOTILITY PHYSIOLOGY JAYA PUNATI, MD DIRECTOR, PEDIATRIC GASTROINTESTINAL, NEUROMUSCULAR AND MOTILITY DISORDERS PROGRAM DIVISION OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, CHILDREN’S HOSPITAL LOS ANGELES VRINDA BHARDWAJ, MD DIVISION OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION CHILDREN’S HOSPITAL LOS ANGELES EDITED BY: CHRISTINE WAASDORP HURTADO, MD REVIEWED BY: JOSEPH CROFFIE, MD, MPH NASPGHAN PHYSIOLOGY EDUCATION SERIES SERIES EDITORS: CHRISTINE WAASDORP HURTADO, MD, MSCS, FAAP [email protected] DANIEL KAMIN, MD [email protected] CASE STUDY 1 • 14 year old female • With no significant past medical history • Presents with persistent vomiting and 20 lbs weight loss x 3 months • Initially emesis was intermittent, occurred before bedtime or soon there after, 2-3 hrs after a meal • Now occurring immediately or up to 30 minutes after a meal • Emesis consists of undigested food and is nonbloody and nonbilious • Associated with heartburn and chest discomfort 3 CASE STUDY 1 • Initial screening blood work was unremarkable • A trial of acid blockade was started with improvement in heartburn only • Antiemetic therapy with ondansetron showed no improvement • Upper endoscopy on acid blockade was normal 4 CASE STUDY 1 Differential for functional/motility disorders: • Esophageal disorders: – Achalasia – Gastroesophageal Reflux – Other esophageal dysmotility disorders • Gastric disorders: – Gastroparesis – Rumination syndrome – Gastric outlet obstruction : pyloric stricture, pyloric stenosis • -
Studies of the Function of the Human Pylorus : and Its Role in The
+.1 Studúes OlTlæ Ftrnctíon OJTIrc Humanfolonts And,Iß R.ole InTlæ Riegulø;tíon OÍ Cústríß Drnptging David R. Fone Departments of Medicine and Gastroenterology, Royal Adelaide Hospital University of Adelaide August 1990 Table of Contents TABLE OF CONTENTS . SUMMARY vil DECLARATION...... X DED|CAT|ON.. .. ... xt ACKNOWLEDGMENTS xil CHAPTER 1 ANATOMY OF THE PYLORUS 1.1 INTRODUCTION.. 1 1.2 MUSCULAR ANATOMY 2 1.3 MUCOSAL ANATOMY 4 1.4 NEURALANATOMY 1.4.1 Extrinsic lnnervation of the Pylorus 5 1.4.2 lntrinsic lnnervation of the Pylorus 7 1.5 INTERSTITIAL CELLS OF CAJAL 8 1.6 CONCLUSTON 9 CHAPTER 2 MEASUREMENT OF PYLORIC MOTILITY 2.1 INTRODUCTION 10 2.2 METHODOLOG ICAL CHALLENGES 2.2.1 The Anatomical Mobility of the Pylorus . 10 2.2.2 The Narrowness of the Zone of Pyloric Contraction 12 2.3 METHODS USED TO MEASURE PYLORIC MOTILITY 2.3.1 lntraluminal Techniques 2.3.1.1 Balloon Measurements. 12 t 2.3 1.2 lntraluminal Side-hole Manometry . 13 2.3 1.9 The Sleeve Sensor 14 2.3 1.4 Endoscopy. 16 2.3 1.5 Measurements of Transpyloric Flow . 16 2.3 'I .6 lmpedance Electrodes 16 2.3.2 Extraluminal Techniques For Recording Pyl;'; l'¡"r¡iit¡l 2.3.2.'t Strain Gauges . 17 2.3.2.2 lnduction Coils . 17 2.3.2.3 Electromyography 17 2.3.3 Non-lnvasive Approaches For Recording 2.3.3.1 Radiology :ï:: Y:1":'1 18 2.3.9.2 Ultrasonography . 1B 2.3.3.3 Electrogastrography 19 2.3.4 ln Vitro Studies of Pyloric Muscle 19 2.4 CONCLUSTON. -
New Developments in Goblet Cell Mucus Secretion and Function
REVIEW nature publishing group New developments in goblet cell mucus secretion and function GMH Birchenough1, MEV Johansson1, JK Gustafsson1, JH Bergstro¨m1 and GC Hansson1 Goblet cells and their main secretory product, mucus, have long been poorly appreciated; however, recent discoveries have changed this and placed these cells at the center stage of our understanding of mucosal biology and the immunology of the intestinal tract. The mucus system differs substantially between the small and large intestine, although it is built around MUC2 mucin polymers in both cases. Furthermore, that goblet cells and the regulation of their secretion also differ between these two parts of the intestine is of fundamental importance for a better understanding of mucosal immunology. There are several types of goblet cell that can be delineated based on their location and function. The surface colonic goblet cells secrete continuously to maintain the inner mucus layer, whereas goblet cells of the colonic and small intestinal crypts secrete upon stimulation, for example, after endocytosis or in response to acetyl choline. However, despite much progress in recent years, our understanding of goblet cell function and regulation is still in its infancy. THE INTESTINE system of mucus covering the epithelium. There is a The gastrointestinal tract is a remarkable organ. Not only can it two-layered mucus system in the stomach and colon and a digest most of our food into small components, but it is also single-layered mucus in the small intestine.5 The mucus layers filled with kilograms of microbes that live in stable equilibrium in these three regions perform their protective function using with us and our immune system. -
The Transcriptional Repressor Blimp1/Prdm1 Regulates Postnatal Reprogramming of Intestinal Enterocytes
The transcriptional repressor Blimp1/Prdm1 regulates postnatal reprogramming of intestinal enterocytes James Harpera, Arne Moulda, Robert M. Andrewsb, Elizabeth K. Bikoffa, and Elizabeth J. Robertsona,1 aSir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom; and bWellcome Trust Sanger Institute, Genome Campus, Hinxton-Cambridge CB10 1SA, United Kingdom Edited by Brigid L. M. Hogan, Duke University Medical Center, Durham, NC, and approved May 19, 2011 (received for review April 13, 2011) Female mammals produce milk to feed their newborn offspring rise to the developing crypts. The crypt derived adult enterocytes before teeth develop and permit the consumption of solid food. that emerge at postnatal day (P) 12 and repopulate the entire Intestinal enterocytes dramatically alter their biochemical signature epithelium lack Blimp1 expression. Conditional inactivation of during the suckling-to-weaning transition. The transcriptional re- Blimp1 results in globally misregulated gene expression patterns, pressor Blimp1 is strongly expressed in immature enterocytes in and compromises small intestine (SI) tissue architecture, nutrient utero, but these are gradually replaced by Blimp1− crypt-derived uptake, and survival of the neonate. In combination with tran- adult enterocytes. Here we used a conditional inactivation strategy scriptional profiling, the present experiments demonstrate that to eliminate Blimp1 function in the developing intestinal epithe- Blimp1/Prdm1 orchestrates orderly and extensive reprogramming lium. There was no noticeable effect on gross morphology or of the postnatal intestinal epithelium. formation of mature cell types before birth. However, survival of mutant neonates was severely compromised. Transcriptional Results profiling experiments reveal global changes in gene expression Down-Regulated Blimp1 Expression in Crypt Progenitors Beginning at patterns. -
GI Motility-I (Deglutition and Motor Functions of Stomach)
Lecture series Gastrointestinal tract Professor Shraddha Singh, Department of Physiology, KGMU, Lucknow GASTROINTESTINAL MOTILITY-1 (Deglutation and motor function of stomach) Mastication (Chewing) - the anterior teeth (incisors) providing a strong cutting action and the posterior teeth (molars), a grinding action – canine tearing - All the jaw muscles working together can close the teeth with a force as great as 25 Kg on the incisors and 90 Kg on the molars. - Most of the muscles of chewing are innervated by the motor branch of the 5th cranial nerve, and the chewing process is controlled by nuclei in the brain stem. - Stimulation of areas in the hypothalamus, amygdala, and even the cerebral cortex near the sensory areas for taste and smell can often cause chewing Chewing Reflex - The presence of a bolus of food in the mouth at first initiates reflex inhibition of the muscles of mastication, which allows the lower jaw to drop. ↓ - The drop in turn initiates a stretch reflex of the jaw muscles that leads to rebound contraction ↓ - raises the jaw to cause closure of the teeth ↓ - compresses the bolus again against the linings of the mouth, which inhibits the jaw muscles once again Chewing Reflex - most fruits and raw vegetables because these have indigestible cellulose membranes around their nutrient portions that must be broken before the food can be digested - Digestive enzymes act only on the surfaces of food particles - grinding the food to a very fine particulate consistency prevents excoriation of the GIT (Stomach) Swallowing (Deglutition) -
Human Body- Digestive System
Previous reading: Human Body Digestive System (Organs, Location and Function) Science, Class-7th, Rishi Valley School Next reading: Cardiovascular system Content Slide #s 1) Overview of human digestive system................................... 3-4 2) Organs of human digestive system....................................... 5-7 3) Mouth, Pharynx and Esophagus.......................................... 10-14 4) Movement of food ................................................................ 15-17 5) The Stomach.......................................................................... 19-21 6) The Small Intestine ............................................................... 22-23 7) The Large Intestine ............................................................... 24-25 8) The Gut Flora ........................................................................ 27 9) Summary of Digestive System............................................... 28 10) Common Digestive Disorders ............................................... 31-34 How to go about this module 1) Have your note book with you. You will be required to guess or answer many questions. Explain your guess with reasoning. You are required to show the work when you return to RV. 2) Move sequentially from 1st slide to last slide. Do it at your pace. 3) Many slides would ask you to sketch the figures. – Draw them neatly in a fresh, unruled page. – Put the title of the page as the slide title. – Read the entire slide and try to understand. – Copy the green shade portions in the note book. 4) -
The Arrest of Intestinal Epithelial ' Turnover' by the Use of X-Irradiation
Gut, 1962, 3, 26 Gut: first published as 10.1136/gut.3.1.26 on 1 March 1962. Downloaded from The arrest of intestinal epithelial ' turnover' by the use of x-irradiation G. WIERNIK, R. G. SHORTER, AND B. CREAMER From St. Thomas's Hospital and Medical School, London sYNoPsIs Mitotic activity and hence cell turnover has been abolished by x-irradiation with 1,000 r. in segments of the rat's gut. The whole stomach, the ascending colon, and 5 cm. of jejunum and ileum were irradiated and the changes observed histologically up to three days. Cessation of cell turnover in the small intestine is followed by cell death and desquamation within 24 hours, leading to denudation of the epithelium and collapse of villous structure. The pylorus and colon showed similar but less marked changes. In contrast the fundus and body of the stomach were unaffected by the absence of mitosis over a period of three days. It is concluded that cell turnover is, in part, necessary to maintain the mucosal structure, particularly the villous pattern in the small intestine. The gastro-intestinal epithelium is a dynamic METHODS structure. Although it appears an intact and lush Wistar rats of either sex weighing 200 g. were used. The membrane to histological examination, it is being animals were anaesthetized with intraperitoneal pento- continuously replaced and desquamated extremely barbitone sodium B.P. The segment of gut to be irradiated quickly. This replacement ofcells results from intense was delivered through an abdominal incision and its http://gut.bmj.com/ division in the crypts, the cells so formed migrating extent marked by fine silk loops. -
The Gallbladder
The Gallbladder Anatomy of the gallbladder Location: Right cranial abdominal quadrant. In the gallbladder fossa of the liver. o Between the quadrate and right medial liver lobes. Macroscopic: Pear-shaped organ Fundus, body and neck. o Neck attaches, via a short cystic duct, to the common bile duct. Opens into the duodenum via sphincter of Oddi at the major duodenal papilla. Found on the mesenteric margin of orad duodenum. o 3-6 cm aboral to pylorus. 1-2cm of distal common bile duct runs intramural. Species differences: Dogs: o Common bile duct enters at major duodenal papilla. Adjacent to pancreatic duct (no confluence prior to entrance). o Accessory pancreatic duct enters at minor duodenal papilla. ± 2 cm aboral to major duodenal papilla. MAJOR conduit for pancreatic secretions. Cats: o Common bile duct and pancreatic duct converge before opening at major duodenal papilla. Thus, any surgical procedure that affects the major duodenal papilla can affect the exocrine pancreatic secretions in cats. o Accessory pancreatic duct only seen in 20% of cats. 1 Gallbladder wall: 5 histologically distinct layers. From innermost these include: o Epithelium, o Submucosa (consisting of the lamina propria and tunica submucosa), o Tunica muscularis externa, o Tunica serosa (outermost layer covers gallbladder facing away from the liver), o Tunica adventitia (outermost layer covers gallbladder facing towards the liver). Blood supply: Solely by the cystic artery (derived from the left branch of the hepatic artery). o Susceptible to ischaemic necrosis should its vascular supply become compromised. Function: Storage reservoir for bile o Concentrated (up to 10-fold), acidified (through epithelial acid secretions) and modified (by the addition of mucin and immunoglobulins) before being released into the gastrointestinal tract at the major duodenal. -
Enterocyte Proliferation and Intracellular Bacteria in Animals
Gut 1994; 35: 1483-1486 1483 PROGRESS REPORT Gut: first published as 10.1136/gut.35.10.1483 on 1 October 1994. Downloaded from Enterocyte proliferation and intracellular bacteria in animals S McOrist, C J Gebhart, G H K Lawson Considerable proliferation of enterocytes, candidates for the bacteria involved.2 Recent forming adenomatous growths within the work shows that the intracellular bacteria are a intestinal mucosa, is a consistent feature of a new genus of obligate intracellular bacteria, number of enteric conditions in animals, now living within enterocytes. This report describes referred to under the general heading of pro- recent advances in the taxonomic status of the liferative enteropathy. These were originally bacteria and its association with disease patho- described in pigs as adenomas ofthe ileum and genesis in animals, focusing on how this can colon1 and this condition was found to have a aid an understanding of enterocyte prolifera- worldwide occurrence.2 Similar conditions tion. were subsequently described in a number of other animal species, again under the general heading of proliferative enteropathy or Intracellular bacteria enteritis. The degree, however, of mucosal The intracellular bacteria in proliferative proliferation, corresponding to a description of enteropathy in animals have been closely hyperplasia, through adenoma to a more studied in the pig and hamster species, in carcinomatous form, varies between species. which the disease is common and widespread. Occasional reports of the condition in the fox,3 Clinical diagnosis of infection and disease is, horse,4 and guinea pig5 describe a hyperplastic however, difficult2 and the disease might be condition of the mucosa whereas hamsters6 7 recognised more widely if diagnostic tools develop adenomatous lesions similar to the became available. -
Kaplan USMLE Step 1 Prep: Which Substance Will Confirm Diagnosis?
Kaplan USMLE Step 1 prep: Which substance will confirm diagnosis? JUL 6, 2020 Staff News Writer If you’re preparing for the United States Medical Licensing Examination® (USMLE®) Step 1 exam, you might want to know which questions are most often missed by test-prep takers. Check out this example from Kaplan Medical, and read an expert explanation of the answer. Also check out all posts in this series. The AMA selected Kaplan as a preferred provider to support you in reaching your goal of passing the USMLE® or COMLEX-USA®. AMA members can save 30% on access to additional study resources, such as Kaplan’s Qbank and High-yield courses. Learn more. This month’s stumper A 55-year-old man is admitted to the hospital because of hematemesis. Measurement fasting serum gastrin levels show them to be 8-fold higher compared with a normal individual and an upper gastrointestinal endoscopy shows multiple ulcers in the duodenum. A multiple endocrine neoplasia type 1 is suspected. Administration of which of the following substances will most likely confirm the diagnosis? A. Cholecystokinin. B. Gastric inhibitory peptide. C. Motilin. D. Pentagastrin. E. Secretin. URL: https://www.ama-assn.org/residents-students/usmle/kaplan-usmle-step-1-prep-which-substance-will-confirm- diagnosis Copyright 1995 - 2021 American Medical Association. All rights reserved. The correct answer is E. Kaplan Medical explains why The patient has Zollinger-Ellison syndrome (ZES); a positive secretin stimulation test is diagnostic. Zollinger-Ellison syndrome: Caused by a gastrin-secreting tumor (gastrinoma) typically located in the pancreas or duodenal wall.