The Kidneys – a Basic Guide
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Detection of Continuous Erythropoietin Receptor Activator in Blood And
Letters to the Editor 5 A Pugliese-Ciaccio, Catanzaro; Dipartimento di Oncologia, 1.0 Biologia e Genetica Università degli Studi di Genova, Italy. Funding: supported from Associazione Italiana Ricerca sul Cancro 0.8 (AIRC) (to FM and MF) and Fondazione ‘Amelia Scorza’ β2-mneg Onlus, Cosenza, Italy. 0.6 Acknowledgments: we would like to acknowledge Dr. Vincenzo not treated Callea, Prof Luca Baldini, Dr Ugo Consoli and Dr Serena Matis 0.4 for their contribution and useful suggestions.We thank Laura Veroni and Brigida Gulino for precious secretarial assistance. Proportion 0.2 p=0.002 pos β β2-m Key words: 2-microglobulin, CD38, IgVH mutational status, CLL, prognosis. 0.0 Correspondence: Fortunato Morabito, Unità Operativa Complessa di Ematologia, Dipartimento di Medicina Interna, 0 3 6 9 12 15 Azienda Ospedaliera di Cosenza, Viale della Repubblica, years 87100 Cosenza, Italy. Phone: international +39.0984.681329. B Fax: international +39.0984.791751. Univariate analysis E-mail: [email protected] Risk categories HR (95% C.I., p value) Citation: Gentile M, Cutrona G, Neri A, Molica S, Ferrarini M, No factor 1 and Morabito F. Predictive value of B2-microglobulin (B2-m) levels One factor 1,5 (0.7-3.4, p=ns) in chronic lymphocytic leukemia since Binet A stages. Two factor 5.0 (2.5-10.2, p<0.0001) Haematologica 2009; 94:887-888. Three factors 15.4 (7.3-32.5, p<0.0001) doi:10.3324/haematol.2009.005561 C 1.0 References 0.8 1. Rossi D, Zucchetto A, Rossi FM, Capello D, Cerri M, no factor Deambrogi C, et al. -
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. -
Extracellular Volume in the Brain- the Relevance of the Chloride Space
Pediat. Res. 12: 635-645 (1978) A Review: Extracellular Volume in the Brain- The Relevance of the Chloride Space DONALD B. CHEEK(lZ2'AND A. BARRY HOLT Royal Children's Hospital Research Foundation, Parkville, Victoria, Australia By simultaneous infusion of anions into the blood and into the concerning brain water and the chloride space (C1 space) as a ventriculocisternal area it is possible to define two compart- measure of extracellular volume (ECV) . ments, one of blood plus brain and one of cerebrospinal fluid The rhesus monkey (Macaca mulatta) is a useful experimental (CSF) plus brain, with a zone of slow equilibration within the model. Comparisons of the macaque brain with the human brain brain where the two components meet. It would appear that during can prove rewarding. Our work on the growth of halogens (Br- and I-) have a much more remarkable and rapid the macaque brain and the distribution of C1- and H,O extends entrance into brain tissue from blood and, with increasing blood from midgestation (80 days) to term (165 days) and well into concentration, penetrate the second compartment significantly. the postnatal period (120 days after birth). The results of this Chloride is more strongly transported across the choroid plexus work have been documented in a recent publication (21). from blood to CSF (in comparison with I- or Br-). Chloride should resemble Br- and I- in diffusing rapidly through the intercellular canals back into the blood. However, knowledge I. CSF CIRCULATION AND ITS BARRIERS concerning C1- distribution dynamics is meager. The dynamics of chloride distribution, diffusion, and transport Homeostasis and the constancy of Claude Bernard's "Milieu using, for example, 36Cl-, 38Cl-, and stable C1-, have not been Interne" is essential for normal function of the central nervous studied sufficiently (in the two compartments), but circumstan- system (CNS). -
Pathophysiology of Acid Base Balance: the Theory Practice Relationship
Intensive and Critical Care Nursing (2008) 24, 28—40 ORIGINAL ARTICLE Pathophysiology of acid base balance: The theory practice relationship Sharon L. Edwards ∗ Buckinghamshire Chilterns University College, Chalfont Campus, Newland Park, Gorelands Lane, Chalfont St. Giles, Buckinghamshire HP8 4AD, United Kingdom Accepted 13 May 2007 KEYWORDS Summary There are many disorders/diseases that lead to changes in acid base Acid base balance; balance. These conditions are not rare or uncommon in clinical practice, but every- Arterial blood gases; day occurrences on the ward or in critical care. Conditions such as asthma, chronic Acidosis; obstructive pulmonary disease (bronchitis or emphasaemia), diabetic ketoacidosis, Alkalosis renal disease or failure, any type of shock (sepsis, anaphylaxsis, neurogenic, cardio- genic, hypovolaemia), stress or anxiety which can lead to hyperventilation, and some drugs (sedatives, opoids) leading to reduced ventilation. In addition, some symptoms of disease can cause vomiting and diarrhoea, which effects acid base balance. It is imperative that critical care nurses are aware of changes that occur in relation to altered physiology, leading to an understanding of the changes in patients’ condition that are observed, and why the administration of some immediate therapies such as oxygen is imperative. © 2007 Elsevier Ltd. All rights reserved. Introduction the essential concepts of acid base physiology is necessary so that quick and correct diagnosis can The implications for practice with regards to be determined and appropriate treatment imple- acid base physiology are separated into respi- mented. ratory acidosis and alkalosis, metabolic acidosis The homeostatic imbalances of acid base are and alkalosis, observed in patients with differing examined as the body attempts to maintain pH bal- aetiologies. -
The Urinary Tract and How It Works
The Urinary Tract and How It Works National Kidney and Urologic Diseases Information Clearinghouse What is the urinary tract and how does it work? The urinary tract is the body’s drainage system for removing urine, which is composed of wastes and extra fluid. In order for normal urination to occur, all body parts in the urinary tract need to work together in the correct order. Kidneys Kidneys. The kidneys are two bean-shaped organs, each about the size of a fist. They are located just below the rib cage, one on each side of the spine. Every day, the kidneys filter about 120 to 150 quarts of blood to produce about 1 to 2 quarts of urine. The kidneys work around the clock; a person does not control what they do. Ureters Ureters. Ureters are the thin tubes of muscle—one on each side of the bladder— Bladder that carry urine from each of the kidneys to Urethra the bladder. Bladder. The bladder, located in the pelvis The urinary tract between the pelvic bones, is a hollow, muscular, balloon-shaped organ that expands as it fills with urine. Although a urination. The bladder stores urine until person does not control kidney function, the person finds an appropriate time and a person does control when the bladder place to urinate. A normal bladder acts empties. Bladder emptying is known as like a reservoir and can hold 1.5 to 2 cups of urine. How often a person needs to urinate depends on how quickly the kidneys Why is the urinary tract produce the urine that fills the bladder. -
GFR (Glomerular Filtration Rate) a Key to Understanding How Well Your Kidneys Are Working
GFR (Glomerular Filtration Rate) A Key to Understanding How Well Your Kidneys Are Working www.kidney.org About the Information in this Booklet Did you know that the National Kidney Foundation (NKF) offers guidelines and commentaries that help your healthcare provider make decisions about your medical treatment? The information in this booklet is based on those recommended guidelines. Stages of Kidney Disease There are five stages of kidney disease. They are shown in the table below. Your healthcare provider determines your stage of kidney disease, based on the presence of kidney damage and your glomerular filtration rate (GFR), which is a measure of your kidney function. Your treatment is based on your stage of kidney disease. Speak to your healthcare provider if you have any questions about your stage of kidney disease or your treatment. STAGES OF KIDNEY DISEASE Glomerular Stage Description Filtration Rate (GFR)* Kidney damage (e.g., protein 1 90 or above in the urine) with normal GFR Kidney damage with mild 2 60 to 89 decrease in GFR 3 Moderate decrease in GFR 30 to 59 4 Severe reduction in GFR 15 to 29 5 Kidney failure Less than 15 *Your GFR number tells your healthcare provider how much kidney function you have. As chronic kidney disease progresses, your GFR number decreases. 2 NATIONAL KIDNEY FOUNDATION Why is GFR Important? Most people are aware that their blood pressure and cholesterol numbers are important in knowing their risk for heart and blood vessel disease. Yet few know about glomerular filtration rate (GFR), one of the numbers that tells them about the health of their 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. -
L7-Renal Regulation of Body Fluid [PDF]
Iden8fy and describe the role of the Sensors and Objectives Effectors in the Abbreviations renal regulaon of body fluid volume ADH An8diurec hormone & osmolality ECF Extracellular fluid ECV Effec8ve Circulang Iden8fy the site and Volume describe the Describe the role of ANF Atrial natriure8c factor influence of the kidney in aldosterone on regulaon of body ANP ATRIAL NATRIURETIC PEPTIDE reabsorp8on of Na+ fluid volume & in the late distal osmolality tubules. PCT Proximal convoluted tubules AVP arginine vasopressin Understand the role of ADH in the reabsorp8on of water and urea Mind map Blood volume remains exactly constant despite extreme changes in daily fluid intake and the reason for that is : 1- slight change in blood volume ! Renal regulaNon of marked change in Extra Cellular cardiac output Volume Is a reflex 2- a slight change mechanism in RegulaNon of ECF Thus, regulaon of in cardiac output which variables volume = Na+ also dependent !large change in reflecng total RegulaNon of body upon blood pressure body sodium and Na+= RegulaNon BP baroreceptors. 3-slight change in ECV are monitor by blood pressure ! appropriate sensor large change in (receptors) URINE OUTPUT . Con. Blood Volume regulation : Sensors Effectors Affecng 1- Rennin angiotensin, aldosterone. 1- Caro8d sinus Urinary Na excre8on. 2- ADH ( the result will cause a change in NA+ and water excre8on either 3- Renal sympathe8c nerve by increasing it or 2- Volume receptors decreasing it ) . (large vein, atria, intrarenalartery) 4- ANP Con. Blood Volume regulation : Cardiac atria Low pressure receptors Pulmonary vasculature Central vascular sensors Carod sinus Sensors in the CNS High pressure receptors AorNc arch Juxtaglomerular apparatus (renal afferent arteriole) Sensors in the liver ECF volume Receptors Con. -
Renal Effects of Atrial Natriuretic Peptide Infusion in Young and Adult ~Ats'
003 1-3998/88/2403-0333$02.00/0 PEDIATRIC RESEARCH Vol. 24, No. 3, 1988 Copyright O 1988 International Pediatric Research Foundation, Inc. Printed in U.S.A. Renal Effects of Atrial Natriuretic Peptide Infusion in Young and Adult ~ats' ROBERT L. CHEVALIER, R. ARIEL GOMEZ, ROBERT M. CAREY, MICHAEL J. PEACH, AND JOEL M. LINDEN WITH THE TECHNICAL ASSISTANCE OF CATHERINE E. JONES, NANCY V. RAGSDALE, AND BARBARA THORNHILL Departments of Pediatrics [R.L.C., A.R.G., C.E.J., B. T.], Internal Medicine [R.M.C., J.M. L., N. V.R.], Pharmacology [M.J.P.], and Physiology [J.M.L.], University of Virginia, School of Medicine, Charlottesville, Virginia 22908 ABSTRAm. The immature kidney appears to be less GFR, glomerular filtration rate responsive to atrial natriuretic peptide (ANP) than the MAP, mean arterial pressure mature kidney. It has been proposed that this difference UeC~pV,urinary cGMP excretion accounts for the limited ability of the young animal to UN,V, urinary sodium excretion excrete a sodium load. To delineate the effects of age on the renal response to exogenous ANP, Sprague-Dawley rats were anesthetized for study at 31-32 days of age, 35- 41 days of age, and adulthod. Synthetic rat A* was infused intravenously for 20 min at increasing doses rang- By comparison to the adult kidney, the immature kidney ing from 0.1 to 0.8 pg/kg/min, and mean arterial pressure, responds to volume expansion with a more limited diuresis and glomerular filtration rate, plasma ANP concentration, natriuresis (I). A number of factors have been implicated to urine flow rate, and urine sodium excretion were measured explain this phenomenon in the neonatal kidney, including a at each dose. -
1. Urine Diversion
1. Urine diversion – hygienic risks and microbial guidelines for reuse © Caroline Schönning Department of Parasitology, Mycology and Environmental Microbiology Swedish Institute for Infectious Disease Control (SMI) SE-171 82 Solna Sweden [email protected] This chapter is based on the doctoral thesis published by the author in February 2001: Höglund, C. (2001). Evaluation of microbial health risks associated with the reuse of source separated human urine. PhD thesis, Department of Biotechnology, Royal Institute of Technology, Stockholm, Sweden. ISBN 91-7283-039-5. The full thesis (87 pages, without published papers) can be downloaded from: http://www.lib.kth.se/Sammanfattningar/hoglund010223.pdf Dr Håkan Jönsson, Swedish University for Agricultural Sciences is acknowledged for compiling Section 3, and Dr Jan-Olof Drangert, Linköping University is acknowledged for compiling Section 9. TABLE OF CONTENTS TABLE OF CONTENTS 1 1. INTRODUCTION 2 1.1 History 2 1.2 Nutrient content and volume of domestic wastewater 3 2. URINE DIVERSION 3 2.1 Urine diversion in Sweden 4 2.2 Source-separation of urine in other parts of the world 6 2.3 Ecological Sanitation 6 3. URINE AS A FERTILISER IN AGRICULTURE 7 3.1 Characteristics of diverted human urine 7 3.2 Collection and storage of the urine – developing countries 7 3.3 Urine as a fertiliser 8 3.4 Crops to fertilise 9 3.5 Dosage 9 3.6 Fertilising experiments 10 3.7 Acceptance 11 4. PATHOGENIC MICROORGANISMS IN URINE 11 5. FAECAL CONTAMINATION 13 5.1 Analysis of indicator bacteria to determine faecal contamination 14 5.2 Analysis of faecal sterols to determine faecal contamination 15 5.3 Discussion 16 6. -
Intravenous Fluid Therapy: a Review
INTRAVENOUS FLUID THERAPY: A REVIEW Joanne Gaffney, RN, CANP, MS If this common intervention isn’t managed vigilantly, it actually can exacerbate the risks it’s designed to alleviate. umerous conditions— In this article, I’ll review the ba- The body loses fluid through metabolic, infective, sics of fluid balance and the etiology such normal physiologic func- traumatic, and iatro- of fluid loss. I’ll discuss how to as- tions as breathing and urination. N genic—can cause fluid sess fluid depletion, outline the prin- But when certain diseases or en- depletion. In such cases, initiat- ciples of fluid replacement therapy, vironmental conditions substan- ing intravenous (IV) fluid replace- and explain the context in which tially increase fluid loss, the body ment is commonplace. In fact, IV various types of solutions are ad- may be unable to maintain ho- fluid replacement therapy is one ministered. I will not, however, meostasis, and fluid replacement of the most common invasive cover the treatment of diabetes mel- may be necessary. procedures hospitalized patients litus and diabetes insipidus, which undergo, and it’s performed in cer- follow different principles that are NORMAL FLUID LOSS tain outpatient and home care set- beyond the scope of this article. Normal fluid loss includes both in- tings as well. sensible and sensible losses. Each Fluid loss can put patients at FLUID MECHANICS day the skin loses approximately substantial risk for fluid and elec- Body water represents approxi- 300 mL and the lungs lose approxi- trolyte imbalances, which can lead mately 60% of a person’s total mately 700 mL of water from evap- to shock and multiple organ failure. -
Urinalysis and Kidney Disease: What You Need to Know
URINALYSIS AND KIDNEY DISEASE What You Need To Know www.kidney.org About the Information in this Booklet Did you know that the National Kidney Foundation (NKF) offers guidelines and commentaries that help your healthcare provider make decisions about your medical treatment? The information in this booklet is based on those recommended guidelines. Stages of Kidney Disease There are five stages of kidney disease. They are shown in the table below. Your healthcare provider determines your stage of kidney disease based on the presence of kidney damage and your glomerular filtration rate (GFR), which is a measure of your kidney function. Your treatment is based on your stage of kidney disease. Speak to your healthcare provider if you have any questions about your stage of kidney disease or your treatment. STAGES OF KIDNEY DISEASE Glomerular Stage Description Filtration Rate (GFR)* Kidney damage (e.g., protein 1 90 or above in the urine) with normal GFR Kidney damage with mild 2 60 to 89 decrease in GFR 3 Moderate decrease in GFR 30 to 59 4 Severe reduction in GFR 15 to 29 5 Kidney failure Less than 15 *Your GFR number tells your healthcare provider how much kidney function you have. As chronic kidney disease progresses, your GFR number decreases. What is a urinalysis (also called a “urine test”)? A urinalysis is a simple test that looks at a small sample of your urine. It can help find conditions that may need treatment, including infections or kidney problems. It can also help find serious diseases in the early stages, like chronic kidney disease, diabetes, or liver disease.