A Compendium of Research
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ANS: 600 Ml/Min This Is the Renal Plasma Flow, Which Is Given As the Clearance of PAH
Bio390 Clearance and Reabsorption thanks to Dr. J.F. Anderson, Dept Zoology Univ. of Florida, Gainesville Use the following data to answer these questions. 100 ml renal inulin clearance: min 0.5 mg [inulin]arterial plasma: ml hematocrit: 0.40 600 ml renal PAH clearance: min 0.8 mg [glucose]arterial plasma: ml 0.0 mg [glucose]urine: ml 0.5 ml rate of urine formation: min ESTIMATE: a. plasma flow rate in the afferent arterioles: ANS: 600 mL/min This is the renal plasma flow, which is given as the Clearance of PAH. b. plasma flow rate in the efferent arterioles: ANS: This will be the renal plasma flow rate (RPF) minus the amount that the plasma volume is reduced by filtration. The amount of plasma lost by filtration must equal the GFR which is the clearance of inulin (100 ml/min here). Thus, the blood flow 1 in the efferent arteriole is 600 - 100 ml/min = 500 ml/min in this problem c. plasma flow rate in the renal veins: ANS: by the time that blood enters the veins, nearly all of the water lost during filtration has made its way back to the blood (especially if the subject is dehydrated!). If urine is being formed at a rate of 0.5 mL/min, then that represents (essentially) the volume of water lost per min. So, the renal venous plasma flow rate = RPF- urine loss = 600 - 0.5 = 599.5 ml/min d. renal blood flow rate in renal artery in ml/min ANS: 833 mL/min the hct = 40% (0.4). -
Impaired Tubular Secretion of Organic Solutes in Acute Kidney Injury
Original Investigation Impaired Tubular Secretion of Organic Solutes in Acute Kidney Injury Frank J. O’Brien,1 Robert D. Mair,2,3 Natalie S. Plummer,2,3 Timothy W. Meyer,2,3 Scott M. Sutherland,4 and Tammy L. Sirich2,3 Abstract Background Impairment of kidney function is routinely assessed by measuring the accumulation of creatinine, an organic solute cleared largely by glomerular filtration. We tested whether the clearance of solutes that undergo tubular secretion is reduced in proportion to the clearance of creatinine in humans with AKI. Methods Four endogenously produced organic solutes (phenylacetylglutamine [PAG], hippurate [HIPP], indoxyl sulfate [IS], and p-cresol sulfate [PCS]) were measured in spot urine and plasma samples from ten patients with AKI and 17 controls. Fractional clearance relative to creatinine was calculated to assess tubular secretion. Fractional clearance values were calculated in terms of the free, unbound levels of HIPP, IS, and PCS that bind to plasma proteins. Results Fractional clearance values for PAG, HIPP, IS, and PCS were .1.0 in patients with AKI as well as controls, indicating that these solutes were still secreted by the tubules of the injured kidneys. Fractional clearance values were, however, significantly lower in patients with AKI than controls, indicating that kidney injury reduced tubular secretion more than glomerular filtration (AKI versus control: PAG, 2.160.7 versus 4.661.4, P,0.001; HIPP, 1065 versus 1567, P50.02; IS, 1066 versus 2867, P,0.001; PCS, 3.361.8 versus 1063, P,0.001). Free plasma levels rose out of proportion to total plasma levels for each of the bound solutes in AKI, so that calculating their fractional clearance in terms of their total plasma levels failed to reveal their impaired secretion. -
Evaluation of Chronic Autonomic Symptoms in Gulf War Veterans with Unexplained Fatigue
Evaluation of Chronic Autonomic Symptoms in Gulf War Veterans with Unexplained Fatigue • Principal Investigator: Dr. Mian Li, WRIISC-DC and Neurology Service at VAMC-DC; Associate Clinical Professor of Neurology • Co-Investigators: Drs Han Kang, Pamela Karasik, Clara Mahan, Friedhelm Sandbrink, Ping Zhai • Post-doctoral fellow: Changqing Xu • Study Coordinator (Volunteer Status): Wenguo Yao • Funded by VA Merit Review Clinical Science R & D • Research approved by local IRB/R & D and conducted in VAMC- DC with compliance of stipulated human research regulations and VA policies regarding report or dissemination of research and non- research information. 1 Rationale • GW veterans (7.7%) reported dizziness/imbalance. blurred vision, excessive fatigue, or tremor (Kang HK, et al. Illnesses among United States veterans of the Gulf War: a population- based survey of 30,000 veterans. J Occup Environ Med 2000; 42(5): 491-501 • Reported neurological symptoms are similar or identical to those from patients with diseases of autonomic nervous system • Ill group (deployed) with post-exertion fatigue • Control (deployed) without fatigue • Objective of this study • Autonomic parameters useful in treatment 2 Peripheral Autonomic Nervous System • Afferent Pathways • Efferent Components parasympathetic and sympathetic • Neurotoxin may preferentially affect small nerve fiber • Small fiber neuropathy vs Autonomic neuropathy • Long delay in diagnosing autonomic system disorder: a) unclear nature course of acquired autonomic disorders b) lack of appropriate -
Production of Hypertonic Urine in the Absence of Pituitary Antidiuretic Hormone
Production of Hypertonic Urine in the Absence of Pituitary Antidiuretic Hormone Robert W. Berliner, Douglas G. Davidson J Clin Invest. 1957;36(10):1416-1427. https://doi.org/10.1172/JCI103541. Research Article Find the latest version: https://jci.me/103541/pdf PRODUCTION OF HYPERTONIC URINE IN THE ABSENCE OF PITUITARY ANTIDIURETIC HORMONE 1 BY ROBERT W. BERLINER AND DOUGLAS G. DAVIDSON 2 (From the Laboratory of Kidney and Electrolyte Metabolism, National Heart Institute, National Institutes of Health, Public Health Sertice, Department of Health, Education, and Welfare, Bethesda, Md.) (Submitted for publication May 1, 1957; accepted May 23, 1957) The mechanism by which pituitary antidiuretic permeability of the tubule membrane to water. hormone (ADH) produces its renal effect has The change to hypertonicity cannot be so readily not been clearly established. Under ordinary con- attributed to an effect on water permeability with- ditions, in the absence of ADH, urine of a con- out some assumptions as to the mechanism by centration considerably below that of plasma is which the hypertonicity is produced. However, produced in large volume. With increasing it is a reasonable hypothesis that the mechanism amounts of ADH, administered or secreted, the for the production of hypertonicity is not depen- osmotic pressure of the urine rises to and above dent upon ADH but that its effects are unmasked, that of plasma. With respect to total water bal- in the presence of ADH, by 1) changes in the vol- ance, the quantitatively more important contri- ume and concentration of urine delivered to it and, bution to water economy is the change between possibly, 2) changes in the permeability of the maximally dilute and isotonic urine, since this, in membranes separating the concentrating mecha- normal man, may involve a change in water ex- nism from the urine in the tubule lumen. -
Aging of the Autonomic Nervous System
Autonomic Nervous System in Old Age Interdisciplinary Topics in Gerontology Vol. 33 Series Editors Patrick R. Hof, New York, N.Y. Charles V. Mobbs, New York, N.Y. Editorial Board Constantin Bouras, Geneva Christine K. Cassel, New York, N.Y. Anthony Cerami, Manhasset, N.Y. H. Walter Ettinger, Winston-Salem, N.C. Caleb E. Finch, Los Angeles, Calif. Kevin Flurkey, Bar Harbor, Me. Laura Fratiglioni, Stockholm Terry Fulmer, New York, N.Y. Jack Guralnik, Bethesda, Md. Jeffrey H. Kordower, Chicago, Ill. Bruce S. McEwen, New York, N.Y. Diane Meier, New York, N.Y. Jean-Pierre Michel, Geneva John H. Morrison, New York, N.Y. Mark Moss, Boston, Mass. Nancy Nichols, Melbourne S. Jay Olshansky, Chicago, Ill. James L. Roberts, San Antonio, Tex. Jesse Roth, Baltimore, Md. Albert Siu, New York, N.Y. John Q. Trojanowski, Philadelphia, Pa. Bengt Winblad, Huddinge Autonomic Nervous System in Old Age Volume Editors George A. Kuchel, Farmington, Conn. Patrick R. Hof, New York, N.Y. 11 figures and 9 tables, 2004 Basel · Freiburg · Paris · London · New York · Bangalore · Bangkok · Singapore · Tokyo · Sydney George A. Kuchel, MD FRCP UConn Center on Aging University of Connecticut Health Center Farmington, Conn., USA Patrick R. Hof, MD Associate Professor, Kastor Neurobiology of Aging Laboratories Dr. Arthur Fishberg Research Centre for Neurobiology Mount Sinai School of Medicine New York, N.Y., USA Library of Congress Cataloging-in-Publication Data Autonomic nervous system in old age / volume editors, George A. Kuchel, Patrick R. Hof. p. ; cm. – (Interdisciplinary topics in gerontology, ISSN 0074–1132 ; v. 33) Includes bibliographical references and index. -
Metabolic and Other Causes of Dysautonomia, Orthostatic
AUTONOMIC DISORDERS AND AUTONOMIC TESTING Kamal R. Chémali, MD Associate Professor of Clinical Neurology Eastern Virginia Medical School Director, Sentara Neuromuscular and Autonomic Center Director, Sentara Music and Medicine Center Kevin McNeeley Sentara Autonomic Laboratory Coordinator The Upright Posture • Significant stress on the body to maintain adequate cerebral flow • Pooling of 500ml to 1000ml of blood • Decreased venous return to the heart • Reduced cardiac output and blood pressure • Compensatory baroreflex activation (CNS, afferent and efferent PNS pathways) • When this system fails, OH, cerebral hypoperfusion, syncope occur The 3 Orthostatic Syndromes Orthostatic Postural Reflex Hypotension Tachycardia Syncope Definition Gradual, Sustained ↑HR>30 1st 10’ Sudden ↓sBP>20 or ↓dBP>10 up; no ↓ BP ↓BP & HR BP Pattern Physiology Arterial denervation – Venous return Brainstem main impact diastole impact systole threshold CV reflexes Usually abnormal Usually normal Usually nl Associated Disease-based Syndromic Syndromic Dysauton. Poor prognosis Good Prognosis SFN Type Severe, Diffuse Mild, Focal None Somatic Small Fiber System Small fiber anterolateral system Large fiber dorsal column – medial lemniscal system CCF 2001 Purves: Neuroscience. 2004 Case 1 (Somatic Small Fiber Neuropathy) • A 48 year-old man presents to your clinic because of a burning sensation in his toes that started 3 months ago and has progressed to involve the entire foot up to the ankle bilaterally. He denies any past medical history but has gained 25 lbs in the past year, due to overeating and inactivity. • On examination, he has a mild sensory gradient to pinprick and temperature in stockings distribution up to the ankles. Vibration is mildly reduced at the toes and joint position sense is intact. -
Autonomic Symptom Burden Is an Independent Contributor to Multiple Sclerosis Related Fatigue
Clinical Autonomic Research (2019) 29:321–328 https://doi.org/10.1007/s10286-018-0563-6 RESEARCH ARTICLE Autonomic symptom burden is an independent contributor to multiple sclerosis related fatigue Magdalena Krbot Skorić1,2 · Luka Crnošija1 · Ivan Adamec1 · Barbara Barun1,3 · Tereza Gabelić1,3 · Tomislav Smoljo3 · Ivan Stanić3 · Tin Pavičić3 · Ivan Pavlović3 · Jelena Drulović4 · Tatjana Pekmezović5 · Mario Habek1,3 Received: 13 June 2018 / Accepted: 30 August 2018 / Published online: 12 September 2018 © Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Objectives To investigate a possible association between autonomic dysfunction and fatigue in people with multiple sclerosis. Methods In 70 people with multiple sclerosis early in the disease course (51 females, mean age 33.8 ± 9.1), quantitative sudomotor axon refex tests, cardiovascular refex tests (heart rate and blood pressure responses to the Valsalva maneuver and heart rate response to deep breathing), and the tilt table test were performed. Participants completed the Composite Autonomic Symptom Score 31, the Modifed Fatigue Impact Scale, and the Epworth Sleepiness Scale, as well as the Beck Depression Inventory. Cutof scores of ≥ 38 or ≥ 45 on the Modifed Fatigue Impact Scale were used to stratify patients into a fatigued subgroup (N = 17 or N = 9, respectively). Results We found clear associations between fatigue and scores in subjective tests of the autonomic nervous system: fatigued patients scored signifcantly worse on Composite Autonomic Symptom Score 31, and there was a strong correlation between the Modifed Fatigue Impact Scale and the Composite Autonomic Symptom Score 31 (rs = 0.607, p < 0.001). On the other hand, we found only modest associations between fatigue and scores in objective tests of the autonomic nervous system: there was a clear trend for lower sweating outputs at all measured sites, which reached statistical signifcance for the distal leg and foot. -
The Tilt Table Test in Autonomic Medicine
Clinical Autonomic Research (2019) 29:215–230 https://doi.org/10.1007/s10286-019-00598-9 REVIEW ARTICLE Autonomic uprising: the tilt table test in autonomic medicine William P. Cheshire Jr.1 · David S. Goldstein2 Received: 25 January 2019 / Accepted: 21 February 2019 / Published online: 5 March 2019 © Springer-Verlag GmbH Germany, part of Springer Nature 2019 Abstract This perspective piece on head-up tilt table testing is part of a series on autonomic function testing. The tilt table can be a useful diagnostic test, but methodologies vary, and the results are sometimes misinterpreted. The intent here is not to review comprehensively the utility of various tilt table testing protocols but to convey a number of general points that may give perspective and have practical clinical value, based on an understanding of autonomic physiology and our long clini- cal and research experience in the evaluation of autonomic disorders. The goals of tilt table testing are to assess orthostatic hypotension (OH), chronic orthostatic intolerance (COI), and unexplained syncope. The testing is useful for distinguishing neurogenic from non-neurogenic OH, identifying failure of the sympathetic noradrenergic system in autonomic neuropathies and ganglionopathies, and assessing barorefex-sympathoneural function in α-synucleinopathies. For COI, the testing can provide objective data related to the patient’s symptoms, diagnose postural tachycardia syndrome (POTS), and distinguish POTS from other causes of tachycardia. Provocative tilt table testing can help understand bases for recurrent transient loss of consciousness in patients with syncope, distinguish neurally mediated syncope from psychogenic pseudosyncope, and separate syncope-related convulsion from epileptic seizures. For each of these purposes, the goals, formats, endpoints, and clinical utility are diferent. -
Syncope and Atypical Seizures
Syncope and Atypical Seizures Ravi Mandapati, M.D., FACC.; FHRS Director, Specialized Program for Arrhythmias in Congenital Heart Disease UCLA Cardiac Arrhythmia Center David Geffen School of Medicine at UCLA Director, Pediatric Cardiac Electrophysiology Loma Linda University Medical Center Syncope • Sy ncope is a transient loss of consciousness d ue to transient global cerebral hypo perfusion characterized by rapid onset, short duration, and spontaneous complete recovery. • Without qualifying transient global hypo perfusion, the definition of syncope becomes wide enough to include disorders such as epileptic seizures and concussion. •January 14-15, 2011 SCA Conference •1 Seizures are frequently and inappropriately classified as syncope Seizures •Sheldon et al. Diagnosis of Syncope and Seizures, JACC 2002 •January 14-15, 2011 SCA Conference •2 Seizures •Sheldon et al. Diagnosis of Syncope and Seizures, JACC 2002 Breath holding spells • Infantile reflex syncopal attacks or pallid breath holding spells elicited by noxious stimuli are caused by vagally mediated cardiac inhibition. • Cyanotic breath holding spells that occur with expiratory cessation of respiration during crying •January 14-15, 2011 SCA Conference •3 Neurally Mediated Reflex Syncope/Triggers • Emotion/pain • Prolonged standing • Micturition • Post exercise • Hyperventilation and straining • Stretching • Coughing • Standing up suddenly • Deglution Syncope : Mechanical /Structural • Aortic Stenosis • Hypertrophic cardiomyopathy • Anomalous coronary artery • Severe pulmonary -
Renal Function in Mice: Effects of Volume Expansion and Angiotensin II
J Am Soc Nephrol 10: 2631–2636, 1999 Renal Function in Mice: Effects of Volume Expansion and Angiotensin II LUDEK CERVENKA,* KENNETH D. MITCHELL,† and L. GABRIEL NAVAR† *Department of Experimental Medicine, Institute for Clinical and Experimental Medicine, Prague, Czech Republic; and †Department of Physiology, Tulane University School of Medicine, New Orleans, Louisiana. Abstract. The present study was performed to validate a simple (83 6 2 mmHg), but led to significantly greater values in both means for assessing renal function in anesthetized mice and to GFR and RPF (1.35 6 0.14 versus 1.01 6 0.1 ml/min z g and characterize the renal hemodynamic responses to acute volume 11.26 6 1.39 versus 6.29 6 0.5 ml/min z g, respectively). expansion and how these responses are altered by concurrent Infusion of AngII during volume expansion led to significant angiotensin II (AngII) infusions. Inulin and para-aminohippu- elevations of MAP (100 6 3 mmHg, P , 0.05) and prevented rate clearances were used to assess GFR and renal plasma flow the increases in GFR and RPF elicited by volume expansion (RPF) in three groups of male C57Bl/6 mice anesthetized with (0.77 6 0.08 and 5.35 6 0.48 ml/min z g, respectively). inactin (100 mg/kg, intraperitoneally) and ketamine (10 mg/ Volume expansion also elicited marked increases in absolute kg). To avoid the hypotension associated with repeated blood and fractional sodium excretion (6.1 6 1.0 versus 0.62 6 0.2 sampling, a single blood sample was taken after three timed mEq/min z g and 3.1 6 0.7 versus 0.4 6 0.1%, respectively). -
Selecthealth Medical Policies Physical Medicine Policies
SelectHealth Medical Policies Physical Medicine Policies Table of Contents Policy Title Policy Last Number Revised Acute Inpatient Rehabilitation 443 12/20/18 Chiropractic Care (Adult) 643 09/08/21 Computerized Microprocessor-Controlled Knee Prostheses (OttoBock C-Leg, 233 08/21/17 Endolite Adaptive Prosthesis, Ossur Prosthesis) Diagnostic and Therapeutic Interventions for Spinal Pain 626 07/21/21 Epidural Adhesiolysis (Percutaneous or Endoscopic) for the Treatment of 249 11/29/12 Chronic Back Pain Functional Anaesthetic Discography 422 08/13/09 Functional Electrical Stimulation (FES); Neuromuscular Electrical 413 01/12/09 Stimulation (NMES) Infusion Pumps (External or Implantable) 609 07/31/17 Lymphedemia Therapy 147 04/21/11 Manipulation Under Anesthesia (MUA) for Management of Back and Pelvic Pain 425 10/12/09 Negative Pressure Wound Therapy 185 05/27/21 Nonsurgical Spinal Compression for the Treatment of Chronic Low Back Pain 323 10/31/06 Percutaneous Electrical Nerve Stimulation (PENS) 162 12/19/09 Percutaneous Sacroplasty 433 12/26/09 Phonophoresis 306 05/20/06 Physical Therapy (PT); Occupational Therapy (OT) 518 10/11/18 Platelet Rich Plasma (PRP) Grafting for Bone and Soft Tissue Healing/ 315 12/17/09 Autologous Platelet-Derived Preparations Pressure Specified Sensory Device (PSSD) for Assessment of 217 02/18/10 Peripheral Neuropathy Pulsed Electrical Stimulation with an Integrated Unloading Brace 251 10/19/17 (e.g., BioniCare® Stimulator) Radiofrequency Ablation (RFA) of the Dorsal Root Ganglion (DRG) of the Spine 226 05/15/15 Radiofrequency Ablation (RFA) of the Genicular Nerve 557 11/04/20 Radiofrequency Ablation (RFA) of the Sacroiliac (SI) Joint 389 01/01/20 Sanexas Therapy 649 07/13/21 Table of Contents Continued on Page 2.. -
Assessment of Gastrointestinal Autonomic Dysfunction: Present and Future Perspectives
Journal of Clinical Medicine Review Assessment of Gastrointestinal Autonomic Dysfunction: Present and Future Perspectives Ditte S. Kornum 1,2,* , Astrid J. Terkelsen 3, Davide Bertoli 4, Mette W. Klinge 1, Katrine L. Høyer 1,2, Huda H. A. Kufaishi 5, Per Borghammer 6, Asbjørn M. Drewes 4,7, Christina Brock 4,7 and Klaus Krogh 1,2 1 Department of Hepatology and Gastroenterology, Aarhus University Hospital, DK8200 Aarhus, Denmark; [email protected] (M.W.K.); [email protected] (K.L.H.); [email protected] (K.K.) 2 Steno Diabetes Centre Aarhus, Aarhus University Hospital, DK8200 Aarhus, Denmark 3 Department of Neurology, Aarhus University Hospital, DK8200 Aarhus, Denmark; [email protected] 4 Mech-Sense, Department of Gastroenterology and Hepatology, Aalborg University Hospital, DK9100 Aalborg, Denmark; [email protected] (D.B.); [email protected] (A.M.D.); [email protected] (C.B.) 5 Steno Diabetes Centre Copenhagen, Gentofte Hospital, DK2820 Gentofte, Denmark; [email protected] 6 Department of Nuclear Medicine and PET-Centre, Aarhus University Hospital, DK8200 Aarhus, Denmark; [email protected] 7 Steno Diabetes Centre North Jutland, Aalborg University Hospital, DK9100 Aalborg, Denmark * Correspondence: [email protected] Abstract: The autonomic nervous system delicately regulates the function of several target organs, including the gastrointestinal tract. Thus, nerve lesions or other nerve pathologies may cause autonomic dysfunction (AD). Some of the most common causes of AD are diabetes mellitus and α-synucleinopathies such as Parkinson’s disease. Widespread dysmotility throughout the gastroin- Citation: Kornum, D.S.; Terkelsen, testinal tract is a common finding in AD, but no commercially available method exists for direct A.J.; Bertoli, D.; Klinge, M.W.; Høyer, K.L.; Kufaishi, H.H.A.; Borghammer, verification of enteric dysfunction.