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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, Renal Tubule – Dilation
Kidney, Renal Tubule – Dilation Figure Legend: Figure 1 Kidney, Renal tubule - Dilation in a male B6C3F1 mouse from a chronic study. Dilated tubules are noted as tracts running through the cortex and outer medulla. Figure 2 Kidney, Renal tubule - Dilation in a male F344/N rat from a chronic study. Tubule dilation is present throughout the outer stripe of the outer medulla, extending into the cortex. Figure 3 Kidney, Renal tubule - Dilation in a male B6C3F1 mouse from a chronic study. Slight tubule dilation is associated with degeneration and necrosis. Figure 4 Kidney, Renal tubule - Dilation in a male F344/N rat from a chronic study. Tubule dilation is associated with chronic progressive nephropathy. Comment: Renal tubule dilation may occur anywhere along the nephron or collecting duct system. It may occur in focal areas or as tracts running along the entire length of kidney sections (Figure 1). 1 Kidney, Renal Tubule – Dilation Renal tubule dilation may occur from xenobiotic administration, secondary mechanisms, or an unknown pathogenesis (see Kidney – Nephropathy, Obstructive (Figure 2). Dilation may result from direct toxic injury to the tubule epithelium interfering with absorption and secretion (Figure 3). It may also occur secondary to renal ischemia or from prolonged diuresis related to drug administration. Secondary mechanisms of tubule dilation may result from lower urinary tract obstruction, the deposition of tubule crystals, interstitial inflammation and/or fibrosis, and chronic progressive nephropathy (Figure 4). A few dilated tubules may be regarded as normal histologic variation. Recommendation: Renal tubule dilation should be diagnosed and given a severity grade. The location of tubule dilation should be included in the diagnosis as a site modifier. -
Female Urethra
OBJECTIVES: • By the end of this lecture, student should understand the anatomical structure of urinary system. General Information Waste products of metabolism are toxic (CO2, ammonia, etc.) Removal from tissues by blood and lymph Removal from blood by Respiratory system And Urinary system Functions of the Urinary System Elimination of waste products Nitrogenous wastes Toxins Drugs Functions of the Urinary System Regulate homeostasis Water balance Acid-base balance in the blood Electrolytes Blood pressure Organs of the Urinary system Kidneys Ureters Urinary bladder Urethra Kidneys Primary organs of the urinary system Located between the 12th thoracic and 3rd lumbar vertebrae. Right is usually lower due to liver. Held in place by connective tissue [renal fascia] and surrounded by thick layer of adipose [perirenal fat] Each kidney is approx. 3 cm thick, 6 cm wide and 12 cm long Regions of the Kidney Renal cortex: outer region Renal medulla: pyramids and columns Renal pelvis: collecting system Kidneys protected by three connective tissue layers Renal fascia -Attaches to abdominal wall Renal capsule: -Surrounds each kidney -Fibrous sac -Protects from trauma and infection Adipose capsule -Fat cushioning kidney Nephrons Each kidney contains over a million nephrons [functional structure] • Blood enters the nephron from a network that begins with the renal artery. • This artery branches into smaller and smaller vessels and enters each nephron as an afferent arteriole. • The afferent arteriole ends in a specialized capillary called the Glomerulus. • Each kidney has a glomerulus contained in Bowman’s Capsule. • Any cells that are too large to pass into the nephron are returned to the venous blood supply via the efferent arteriole. -
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. -
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. -
Kidney Function • Filtration • Reabsorption • Secretion • Excretion • Micturition
About This Chapter • Functions of the kidneys • Anatomy of the urinary system • Overview of kidney function • Filtration • Reabsorption • Secretion • Excretion • Micturition © 2016 Pearson Education, Inc. Functions of the Kidneys • Regulation of extracellular fluid volume and blood pressure • Regulation of osmolarity • Maintenance of ion balance • Homeostatic regulation of pH • Excretion of wastes • Production of hormones © 2016 Pearson Education, Inc. Anatomy of the Urinary System • Kidneys, ureters, bladder, and urethra • Kidneys – Bean-shaped organ – Cortex and medulla © 2016 Pearson Education, Inc. Anatomy of the Urinary System • Functional unit is the nephron – Glomerulus in the Bowman’s capsule – Proximal tubule – The loop of Henle • Descending limb and ascending limb twisted between arterioles forming the juxtaglomerular apparatus – Distal tubule – Collecting ducts © 2016 Pearson Education, Inc. Figure 19.1b Anatomy summary The kidneys are located retroperitoneally at the level of the lower ribs. Inferior Diaphragm vena cava Aorta Left adrenal gland Left kidney Right kidney Renal artery Renal vein Ureter Peritoneum Urinary Rectum (cut) bladder (cut) © 2016 Pearson Education, Inc. Figure 19.1c Anatomy summary © 2016 Pearson Education, Inc. Figure 19.1d Anatomy summary © 2016 Pearson Education, Inc. Figure 19.1f-h Anatomy summary Some nephrons dip deep into the medulla. One nephron has two arterioles and two sets of capillaries that form a portal system. Efferent arteriole Arterioles Peritubular Juxtaglomerular capillaries The cortex apparatus contains all Bowman’s Nephrons Afferent capsules, arteriole Glomerulus proximal Juxtamedullary nephron and distal (capillaries) with vasa recta tubules. Peritubular capillaries Glomerulus The medulla contains loops of Henle and Vasa recta collecting ducts. Collecting duct Loop of Henle © 2016 Pearson Education, Inc. -
The Renal Vascular System of the Monkey: a Gross Anatomical Description MARK J
J. Anat. (1987), 153, pp. 123-137 123 With 8 figures Printed in Great Britain The renal vascular system of the monkey: a gross anatomical description MARK J. HORACEK, ALVIN M. EARLE AND JOSEPH P. GILMORE Departments ofAnatomy and Physiology and Biophysics, University of Nebraska College of Medicine, Omaha, Nebraska 68105, U.S.A. (Accepted 12 September 1986) INTRODUCTION Monkeys are frequently used as a model for physiological experiments involving the kidney. It is known that physiological disparity between mammalian species can often be elucidated by a study of the structural differences between these species. Despite this fact, the monkey's renal vasculature has not been described in sufficient detail. Such a description would be useful since monkey experimentation plays an important role in understanding human physiology. Also, the branching pattern and segmen- tation of the monkey's renal vasculature is interesting from both comparative and experimental viewpoints. Fourman & Moffat (1971) indicated that although all mammalian kidneys are somewhat similar, there are several species-specific differences in terms oforganisation, microstructure and function. They conducted several extensive vascular studies on mammals, including several rodents and carnivores, but did not include any specific information concerning the monkey. Graves (1971) and Fine & Keen (1966) have described the branching patterns and segmentation of human kidneys. However, comparable information pertaining to the monkey kidney is not available. The purpose of the present study is to provide a detailed morphological description of the gross renal vasculature in the kidneys of two species of monkeys, Macacafascicularis and Macaca mulatta. MATERIALS AND METHODS Twelve monkeys (Macacafascicularis and Macaca mulatta) were used in this study after they had been utilised for electrophysiological experimentation. -
Anatomy and Physiology of the Bowel and Urinary Systems
PMS1 1/26/05 10:52 AM Page 1 Anatomy and Physiology of the Bowel and 1 Urinary Systems Anthony McGrath INTRODUCTION The aim of this chapter is to increase the reader’s under- standing of the small and large bowel and urinary system as this will enhance their knowledge base and allow them to apply this knowledge when caring for patients who are to undergo stoma formation. LEARNING OBJECTIVES By the end of this chapter the reader will have: ❏ an understanding of the anatomy and physiology of the small and large bowel; ❏ an understanding of the anatomy and physiology of the urinary system. GASTROINTESTINAL TRACT The gastrointestinal (GI) tract (Fig. 1.1) consists of the mouth, pharynx, oesophagus, stomach, duodenum, jejunum, small and large intestines, rectum and anal canal. It is a muscular tube, approximately 9m in length, and it is controlled by the autonomic nervous system. However, while giving a brief outline of the whole system and its makeup, this chapter will focus on the anatomy and physiology of the small and large bowel and the urinary system. The GI tract is responsible for the breakdown, digestion and absorption of food, and the removal of solid waste in the form of faeces from the body. As food is eaten, it passes through each section of the GI tract and is subjected to the action of various 1 PMS1 1/26/05 10:52 AM Page 2 1 Anatomy and Physiology of the Bowel and Urinary Systems Fig. 1.1 The digestive system. Reproduced with kind permission of Coloplast Ltd from An Introduction to Stoma Care 2000 2 PMS1 1/26/05 10:52 AM Page 3 Gastrointestinal Tract 1 digestive fluids and enzymes (Lehne 1998). -
Urinary Tract Eod Stage & Treatment
2/20/2020 SHRI VIDEO TRAINING SERIES 2018 DX forward Recorded 2/2020 URINARY TRACT EOD STAGE & TREATMENT PRESENTED BY LORI SOMERS, RN IOWA CANCER REGISTRY 1 BLADDER C670‐C679 EOD PRIMARY TUMOR EOD REGIONAL LYMPH NODES EOD METASTASIS 2 1 2/20/2020 EOD • General Coding instructions, 32 pg pdf • https://seer.cancer.gov/tools/staging/2018‐ EOD‐General‐Instructions.pdf • Timing rules • What to include re clinical or path findings • Rules re neoadjuvant therapy • Discrepancies between op/path 3 BLADDER EOD PRI TUMOR • Note 1: Two main types of bladder cancer – Flat (sessile) • Called in situ when tumor has not penetrated basement membrane – Papillary type • Called noninvasive when tumor has not penetrated basement membrane 4 2 2/20/2020 EOD PRI TUMOR • Note 2: Noninvasive papillary transitional carcinoma: Pathologists use many descriptive terms for noninvasive papillary TCC. Frequently the path report does not contain a definitive statement of non‐invasion. – Non‐invasion can be inferred from microscopic description – List of terms in SEER*RSA schema 5 Definite statements non‐invasion ‘for papillary TCC’ • Noninfiltrating • Noninvasive • No evidence of invasion • No extension into lamina propria • No stromal invasion • No extension into underlying supporting tissue • Neg lamina propria and superficial muscle • Neg muscle and (subepithelial) connective tissue • No infiltrative behavior/component 6 3 2/20/2020 Inferred descriptions of non‐invasion ‘for papillary TCC’ • No involvement of musc propria and no mention of subepthelium/submucosa • No statement of invasion (microscopic description present • (Underlying) tissue insufficient to judge depth of invasion • No involvement of muscularis propria • Benign deeper tissue • Microscopic description problematic (non‐invas vs superficial invas) • Frond surfaced by transitional cell • No mural infiltration • No evid of invasion (no sampled stroma) • Confined to mucosa 7 EOD PRI TUMOR Note 3: Noninvasive (in situ) flat transitional cell carcinoma: . -
The Kidneys (Nephros)
THE KIDNEYS (NEPHROS) Functions 1. Removal of excess water, salts and products of protein metabolism 2. Maintenance of PH 3. Production and release of erythopoietin, which controls blood cell production 4. Synthesis and release of renin to influence blood pressure 5. Production of 1, 25-hydroxycholecalciferol (activated form of vitamin D) for control of calcium metabolism. There are 2 kidneys in the body, one on either side of the median plane. The kidneys are bean-shaped about 10cm long, 5cm wide and weigh about 150g. The kidneys are intra-abdominal extending from T12-L3. The left kidney is about 1cm higher than the right one, owing to the large right lobe of the liver. The kidneys lay retroperitoneally on the posterior abdominal wall against Psoas major muscle. Each kidney is covered by a tough fibrous renal capsule. This is surrounded by fat known as perirenal /perinephric fat. The latter is enclosed in a renal fascia which attaches it firmly to the posterior abdominal wall. However, the renal fascia is flexible enough to allow kidneys shift slightly as the diaphragm moves during respiration. The kidney has • Anterior and posterior surfaces • Medial and lateral borders • Superior and inferior poles The lateral border is convex and lies against psoas major muscle. The medial border is concave. The hilus/hilum is a prominent medial indentation on this border. It’s a point of entry for the renal artery, renal nerves and exit for the renal vein and renal pelvis. From anterior to posterior are the; renal vein, renal artery and renal pelvis. The posterior surface of the superior pole is related to the diaphragm while the anteromedial surface to the suprarenal gland. -
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. -
L8-Urine Conc. [PDF]
The loop of Henle is referred to as countercurrent multiplier and vasa recta as countercurrent exchange systems in concentrating and diluting urine. Explain what happens to osmolarity of tubular fluid in the various segments of the loop of Henle when concentrated urine is being produced. Explain the factors that determine the ability of loop of Henle to make a concentrated medullary gradient. Differentiate between water diuresis and osmotic diuresis. Appreciate clinical correlates of diabetes mellitus and diabetes insipidus. Fluid intake The total body water Antidiuretic hormone is controled by : Renal excretion of water Hyperosmolar medullary Changes in the osmolarity of tubular fluid : interstitium 1 2 3 Low osmolarity The osmolarity High osmolarity because of active decrease as it goes up because of the transport of Na+ and because of the reabsorbation of water co-transport of K+ and reabsorption of NaCl Cl- 4 5 Low osmolarity because of High osmolarity because of reabsorption of NaCl , also reabsorption of water in reabsorption of water in present of ADH , present of ADH reabsorption of urea Mechanisms responsible for creation of hyperosmolar medulla: Active Co- Facilitated diffusion transport : transport : diffusion : of : Na+ ions out of the Only of small thick portion of the K+ , Cl- and other amounts of water ascending limb of ions out of the thick from the medullary the loop of henle portion of the Of urea from the tubules into the into the medullary ascending limb of inner medullary medullary interstitium the loop of henle collecting