Urinary System
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Te2, Part Iii
TERMINOLOGIA EMBRYOLOGICA Second Edition International Embryological Terminology FIPAT The Federative International Programme for Anatomical Terminology A programme of the International Federation of Associations of Anatomists (IFAA) TE2, PART III Contents Caput V: Organogenesis Chapter 5: Organogenesis (continued) Systema respiratorium Respiratory system Systema urinarium Urinary system Systemata genitalia Genital systems Coeloma Coelom Glandulae endocrinae Endocrine glands Systema cardiovasculare Cardiovascular system Systema lymphoideum Lymphoid system Bibliographic Reference Citation: FIPAT. Terminologia Embryologica. 2nd ed. FIPAT.library.dal.ca. Federative International Programme for Anatomical Terminology, February 2017 Published pending approval by the General Assembly at the next Congress of IFAA (2019) Creative Commons License: The publication of Terminologia Embryologica is under a Creative Commons Attribution-NoDerivatives 4.0 International (CC BY-ND 4.0) license The individual terms in this terminology are within the public domain. Statements about terms being part of this international standard terminology should use the above bibliographic reference to cite this terminology. The unaltered PDF files of this terminology may be freely copied and distributed by users. IFAA member societies are authorized to publish translations of this terminology. Authors of other works that might be considered derivative should write to the Chair of FIPAT for permission to publish a derivative work. Caput V: ORGANOGENESIS Chapter 5: ORGANOGENESIS -
Kidney, Ureter, Urinary Bladder & Urethra
Kidney, Ureter, Urinary bladder & Urethra Red: important. Black: in male|female slides. Gray: notes|extra. Editing file ➢ OBJECTIVES • The microscopic structure of the renal cortex and medulla. • The histology of renal corpuscle, proximal and distal tubules, loop of Henle, and collecting tubules & ducts. • The histological structure of juxtaglomerular apparatus. • The functional structures of the different parts of the kidney. • The microscopic structure of the Renal pelvis and ureter. • The microscopic structure of the urinary bladder and male and female urethra Histology team 437 | Renal block | All lectures ➢ KIDNEY o Cortex: Dark brown and granular. Content of cortex (renal corpuscle, PCT, loop of Henle, DCT, part of collecting tubule) o Medulla: 6-12 pyramid-shape regions (renal pyramids) content of medulla ( collecting duct, loop of Henle, collecting tubule) o The base of pyramid is toward the cortex (cortico-medullary border) o The apex (renal papilla) toward the hilum, it is perforated by 12 openings of the ducts of Bellini (Papillary “collecting” ducts) in region called area cribrosa. o The apex is surrounded by a minor calyx. o 3 or 4 minor calyces join to form 3 or 4 major calyces that form renal pelvis. o Pyramids are separated by cortical columns of Bertin (renal column) ➢ URINIFEROUS TUBULE o It is the functional unit of the kidney. o Is formed of: 1- Nephron. 2-Collecting tubule. o The tubules are densely packed. o The tubules are separated by thin stroma and basal lamina. Histology team 437 | Renal block | All lectures ➢ NEPHRON o There are 2 types of nephrons: a- Cortical nephrons. b- Juxtamedullary nephrons. -
NROSCI/BIOSC 1070 and MSNBIO 2070 September 27, 2017
NROSCI/BIOSC 1070 and MSNBIO 2070 September 27, 2017 Cardiovascular 6 Special Circulations Coronary Muscle The coronary arteries branch directly from the aorta, and provide the perfusion of the heart. Although blood actually is pumped through the heart, only ~ 100 µm of the inner endocardial surface can obtain significant amounts of nutrition directly from the blood supply in the cardiac chambers. Blood flow through the coronary capillaries during systole and diastole is different than in most other tissues of the body. The blood flow to the ventricles falls during systole, and increases during diastole. During ventricular contrac- tion, blood flow through the capillaries is obstructed by compression of the vessels. Thus, blood flow increases during diastole when the muscle around the vessels relaxes. Autoregulatory mechanisms are paramount in adjusting the blood flow through the heart. Another major influence on dilation of the coronary arteries is epinephrine released from the adrenal gland. Cerebral Circulation The cerebral circulation is almost completely insensitive to neural and hormonal influences that produce vasoconstriction elsewhere in the body. By far the predominant factor that controls blood flow through the cerebral circulation is paracrine release. In particular, carbon dioxide has a strong vasodilation effect on the cerebral vessels. Skeletal Muscle Circulation Control of blood flow to skeletal muscle is in many respects similar to that in the heart. Paracrine fac- tors have strong influences, and vasodilation is induced by the release of epinephrine from the adrenal gland. A major difference between the two circulations is that skeletal muscle arterioles are richly in- nervated by sympathetic vasoconstrictor fibers, and are major resistance vessels to contribute to total peripheral resistance. -
Calcium Phosphate Microcrystals in the Renal Tubular Fluid Accelerate Chronic Kidney Disease Progression
The Journal of Clinical Investigation RESEARCH ARTICLE Calcium phosphate microcrystals in the renal tubular fluid accelerate chronic kidney disease progression Kazuhiro Shiizaki,1,2 Asako Tsubouchi,3 Yutaka Miura,1 Kinya Seo,4 Takahiro Kuchimaru,5 Hirosaka Hayashi,1 Yoshitaka Iwazu,1,6,7 Marina Miura,1,6 Batpurev Battulga,8 Nobuhiko Ohno,8,9 Toru Hara,10 Rina Kunishige,3 Mamiko Masutani,11 Keita Negishi,12 Kazuomi Kario,12 Kazuhiko Kotani,7 Toshiyuki Yamada,7 Daisuke Nagata,6 Issei Komuro,13 Hiroshi Itoh,14 Hiroshi Kurosu,1 Masayuki Murata,3 and Makoto Kuro-o1 1Division of Anti-aging Medicine, Center for Molecular Medicine, Jichi Medical University, Shimotsuke, Japan. 2Yurina Medical Park, Shimotsuga, Japan. 3Graduate School of Arts and Sciences, University of Tokyo, Tokyo, Japan. 4Division of Cell and Molecular Medicine, 5Division of Cardiology and Metabolism, Center for Molecular Medicine, 6Division of Nephrology, Department of Internal Medicine, 7Department of Clinical Laboratory Medicine, and 8Division of Histology and Cell Biology, Department of Anatomy, Jichi Medical University, Shimotsuke, Japan. 9Division of Ultrastructural Research, National Institute for Physiological Sciences, Okazaki, Japan. 10Electron Microscopy Analysis Station, Research Network and Facility Service Division, National Institute for Materials Science, Tsukuba, Japan. 11Healthcare Business Unit, Nikon Corporation, Yokohama, Japan. 12Division of Cardiovascular Medicine, Department of Internal Medicine, Jichi Medical University, Shimotsuke, Japan. 13Department of Cardiovascular Medicine, Graduate School of Medicine, University of Tokyo, Tokyo, Japan. 14Division of Endocrinology, Metabolism and Nephrology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan. The Western pattern diet is rich not only in fat and calories but also in phosphate. -
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. -
Excretory Products and Their Elimination
290 BIOLOGY CHAPTER 19 EXCRETORY PRODUCTS AND THEIR ELIMINATION 19.1 Human Animals accumulate ammonia, urea, uric acid, carbon dioxide, water Excretory and ions like Na+, K+, Cl–, phosphate, sulphate, etc., either by metabolic System activities or by other means like excess ingestion. These substances have to be removed totally or partially. In this chapter, you will learn the 19.2 Urine Formation mechanisms of elimination of these substances with special emphasis on 19.3 Function of the common nitrogenous wastes. Ammonia, urea and uric acid are the major Tubules forms of nitrogenous wastes excreted by the animals. Ammonia is the most toxic form and requires large amount of water for its elimination, 19.4 Mechanism of whereas uric acid, being the least toxic, can be removed with a minimum Concentration of loss of water. the Filtrate The process of excreting ammonia is Ammonotelism. Many bony fishes, 19.5 Regulation of aquatic amphibians and aquatic insects are ammonotelic in nature. Kidney Function Ammonia, as it is readily soluble, is generally excreted by diffusion across 19.6 Micturition body surfaces or through gill surfaces (in fish) as ammonium ions. Kidneys do not play any significant role in its removal. Terrestrial adaptation 19.7 Role of other necessitated the production of lesser toxic nitrogenous wastes like urea Organs in and uric acid for conservation of water. Mammals, many terrestrial Excretion amphibians and marine fishes mainly excrete urea and are called ureotelic 19.8 Disorders of the animals. Ammonia produced by metabolism is converted into urea in the Excretory liver of these animals and released into the blood which is filtered and System excreted out by the kidneys. -
« Glomerulogenesis and Renal Tubular Differentiation : Role of Hnf1β »
THESE DE DOCTORAT DE L’UNIVERSITE PARIS DESCARTES Ecole doctorale « Bio Sorbonne Paris Cité », ED 562 Département Développement, Génétique, Reproduction, Neurobiologie et Vieillissement (DGRNV) Spécialité : Développement Présentée pour obtenir le titre de DOCTEUR de l’Université Paris Descartes « Glomerulogenesis and renal tubular differentiation : Role of HNF1 β » Par Mlle Arianna FIORENTINO Soutenance le 13 décembre 2016 Composition du jury : Mme. Evelyne Fischer Directrice de thèse M. Marco Pontoglio Examinateur M. Jean-Jacques Boffa Rapporteur M. Yves Allory Rapporteur M Rémi Salomon Examinateur M Jean-Claude Dussaule Examinateur Equipe "Expression Génique, Développement et Maladies" (EGDM) INSERM U1016/ CNRS UMR 8104 / Université Paris-Descartes Institut Cochin, Dpt. Développement, Reproduction et Cancer 24, Rue du Faubourg Saint Jacques, 75014 Paris, France A. Fiorentino HNF1beta in kidney development “Connaître ce n'est pas démontrer, ni expliquer. C'est accéder à la vision.” (Le Petit Prince- Antoine de Saint-Exupéry) 2 A. Fiorentino HNF1beta in kidney development Aknowledgments - Remerciements – Ringraziamenti During this long adventure of the PhD, I was surrounded by many people that I will try to thank to in these pages. In first place, I would like to thank the members of the jury that have kindly accepted to evaluate my work: Jean-Jacques Boffa, Yves Allory, Jean-Claude Dussaule and Rémi Salomon. For the supervision and the precious advices, I would like to thank Evelyne Fischer and Marco Pontoglio that overviewed all my work. I thank Evelyne, my thesis director, for the scientific exchanges of ideas, for the guidance to complete my project and for her help in difficult moments. I thank Marco for the discussions, even for the heated ones, because the pressure in the environment not only helped me to work harder on science but more importantly on my character, to face the problems and solve them. -
24. the Endothelial Glycocalyx (C Alphonsus)
Part I Anaesthesia Refresher Course – 2018 24 University of Cape Town The Endothelial Glycocalyx Dr Christella Alphonsus Dept of Anaesthesia & Perioperative Medicine University of Cape Town Overview The glycocalyx is a complex gel layer that coats all healthy vascular endothelium. This layer exists in dynamic interaction between flowing blood and the endothelial cell wall. It plays a pivotal role in vascular protection, modulation and haemostasis. Components The endothelial glycocalyx is essentially made up of glycoproteins or proteoglycans but there is great diversity in structure and function within these two groups. Proteoglycans have a protein core to which are attached negatively charged glycosaminoglycan (GAG) side chains. There are different types of proteoglycans and they vary according to: the core protein size, the number of GAG side chains and whether they are bound or not bound to the cell membrane. Syndecans and glypicans are first bound to the cell membrane and the GAG side chains are attached later. Other proteoglycans (perlecans, versicans, decorins, biglycans, mimecans) are first bound to GAGs and then secreted by the endothelial cells. There are five types of GAG side chains: heparan sulphate makes up 50–90%, with the remainder composed of hyaluronic acid and chondroiton, dermatan and keratin sulphates. Hyaluronic acid is the only GAG not usually bound to a core protein and forms viscous solutions with water. Glycoproteins act as adhesion molecules and contribute to the coagulation, fibrinolytic and haemostatic systems. These include E and P selectin which are expressed after stimulation by histamine, thrombin, interleukin-1 and tumour necrosis factora (TNF-α). Ligands for leucocyte and platelet adhesion ICAM-1, ICAM-2, VCAM-1, PECAM-1 are also expressed within the glycocalyx. -
Urinary System
URINARY SYSTEM Ján Líška DVM, PhD Institut of Histology and Embryology, Faculty of Medicine, Comenius University Urinary system • The kidneys are the organ with multiple functions: • filtration of the blood • excretion of metabolic waste products and related removal of toxins • maintenance blood volume • regulation of acid-base balance • regulation of fluid and electrolyte balance • production of the hormones The other components of urinary system are accessory. Their function is essentially in order to eliminate urine. Urinary system - anatomy • Kidney are located in the retroperitoneal space • The surface of the kidney is covered by a fibrous capsule of dense connective tissue. • This capsule is coated with adipose capsule. • Each kidney is attached to a ureter, which carries urine to the bladder and urine is discharged out through the urethra. ANATOMIC STRUCTURE OF THE KIDNEY RENAL LOBES CORTEX outer shell columns Excretory portion medullary rays MEDULLA medullary pyramids HILUM Collecting system blood vessels lymph vessels major calyces nerves RENAL PELVIS minor calyces ureter Cortex is the outer layer surrounding the internal medulla. The cortex contains renal corpuscles, convoluted parts of prox. and dist. tubules. Renal column: the renal tissue projection between two medullary pyramids which supports the cortex. Renal pyramids: the conical segments within the medulla. They contain the ductal apparatus and stright parts of the tubules. They posses papilla - having openings through which urine passes into the calyces. Each pyramid together with the associated overlying cortex forms a renal lobe. renal pyramid papilla minor calix minor calyx Medullary rays: are in the middle of cortical part of the renal lobe, consisting of a group of the straight portiones of nephrons and the collec- medullary rays ting tubules (only straight tubules). -
Claudins in the Renal Collecting Duct
International Journal of Molecular Sciences Review Claudins in the Renal Collecting Duct Janna Leiz 1,2 and Kai M. Schmidt-Ott 1,2,3,* 1 Department of Nephrology and Intensive Care Medicine, Charité-Universitätsmedizin Berlin, 12203 Berlin, Germany; [email protected] 2 Molecular and Translational Kidney Research, Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association (MDC), 13125 Berlin, Germany 3 Berlin Institute of Health (BIH), 10178 Berlin, Germany * Correspondence: [email protected]; Tel.: +49-(0)30-450614671 Received: 22 October 2019; Accepted: 20 December 2019; Published: 28 December 2019 Abstract: The renal collecting duct fine-tunes urinary composition, and thereby, coordinates key physiological processes, such as volume/blood pressure regulation, electrolyte-free water reabsorption, and acid-base homeostasis. The collecting duct epithelium is comprised of a tight epithelial barrier resulting in a strict separation of intraluminal urine and the interstitium. Tight junctions are key players in enforcing this barrier and in regulating paracellular transport of solutes across the epithelium. The features of tight junctions across different epithelia are strongly determined by their molecular composition. Claudins are particularly important structural components of tight junctions because they confer barrier and transport properties. In the collecting duct, a specific set of claudins (Cldn-3, Cldn-4, Cldn-7, Cldn-8) is expressed, and each of these claudins has been implicated in mediating aspects of the specific properties of its tight junction. The functional disruption of individual claudins or of the overall barrier function results in defects of blood pressure and water homeostasis. In this concise review, we provide an overview of the current knowledge on the role of the collecting duct epithelial barrier and of claudins in collecting duct function and pathophysiology. -
Application of Negative Tissue Interstitial Pressure Improves Functional Capillary Density After Hemorrhagic Shock in the Absence of Volume Resuscitation
UC San Diego UC San Diego Previously Published Works Title Application of negative tissue interstitial pressure improves functional capillary density after hemorrhagic shock in the absence of volume resuscitation. Permalink https://escholarship.org/uc/item/3pc6m5m7 Journal Physiological reports, 9(5) ISSN 2051-817X Authors Jani, Vinay P Jani, Vivek P Munoz, Carlos J et al. Publication Date 2021-03-01 DOI 10.14814/phy2.14783 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Received: 21 January 2021 | Accepted: 5 February 2021 DOI: 10.14814/phy2.14783 ORIGINAL ARTICLE Application of negative tissue interstitial pressure improves functional capillary density after hemorrhagic shock in the absence of volume resuscitation Vinay P. Jani1 | Vivek P. Jani2 | Carlos J. Munoz1 | Krianthan Govender1 | Alexander T. Williams1 | Pedro Cabrales1 1Department of Bioengineering, University of California, San Diego, La Abstract Jolla, CA, USA Microvascular fluid exchange is primarily dependent on Starling forces and both the ac- 2 Division of Cardiology, Department of tive and passive myogenic response of arterioles and post-capillary venules. Arterioles Medicine, The Johns Hopkins University, The Johns Hopkins School of Medicine are classically considered resistance vessels, while venules are considered capacitance Baltimore, MD, USA vessels with high distensibility and low tonic sympathetic stimulation at rest. However, few studies have investigated the effects of modulating interstitial hydrostatic pressure, Correspondence Pedro Cabrales, University of particularly in the context of hemorrhagic shock. The objective of this study was to in- California, San Diego Department of vestigate the mechanics of arterioles and functional capillary density (FCD) during appli- Bioengineering, 0412 9500 Gilman cation of negative tissue interstitial pressure after 40% total blood volume hemorrhagic Dr. -
Urinary System
OUTLINE 27.1 General Structure and Functions of the Urinary System 818 27.2 Kidneys 820 27 27.2a Gross and Sectional Anatomy of the Kidney 820 27.2b Blood Supply to the Kidney 821 27.2c Nephrons 824 27.2d How Tubular Fluid Becomes Urine 828 27.2e Juxtaglomerular Apparatus 828 Urinary 27.2f Innervation of the Kidney 828 27.3 Urinary Tract 829 27.3a Ureters 829 27.3b Urinary Bladder 830 System 27.3c Urethra 833 27.4 Aging and the Urinary System 834 27.5 Development of the Urinary System 835 27.5a Kidney and Ureter Development 835 27.5b Urinary Bladder and Urethra Development 835 MODULE 13: URINARY SYSTEM mck78097_ch27_817-841.indd 817 2/25/11 2:24 PM 818 Chapter Twenty-Seven Urinary System n the course of carrying out their specific functions, the cells Besides removing waste products from the bloodstream, the uri- I of all body systems produce waste products, and these waste nary system performs many other functions, including the following: products end up in the bloodstream. In this case, the bloodstream is ■ Storage of urine. Urine is produced continuously, but analogous to a river that supplies drinking water to a nearby town. it would be quite inconvenient if we were constantly The river water may become polluted with sediment, animal waste, excreting urine. The urinary bladder is an expandable, and motorboat fuel—but the town has a water treatment plant that muscular sac that can store as much as 1 liter of urine. removes these waste products and makes the water safe to drink.