Kidney factors that enhance risk for drug-induced nephrotoxicity.

Slides:



Advertisements
Similar presentations
Vertebrate kidney structure and function ap biology chapter 44.
Advertisements

Introduction to Renal Histology Part 2 of 2 Anjali Satoskar MD PhD Department of Pathology
Biotransformation and metabolism
Renal tubular reabsorption/Secretion. Urine Formation Preview.
16.2 Anatomy of the Kidney and Excretion There are three regions to a kidney ___________ Nephrons are the functional units of the kidney  Each kidney.
Bio 449Lecture 26 – Renal Physiology IINov. 10, 2010 Nephrons (cont’d) Urine formation Glomerular filtration Proximal tubule Loop of Henle & initial distal.
Topic 11.3 The Kidney & Osmoregulation
Proximal and distal tubules and the loop of Henle. A
Copyright © 2017 American Academy of Pediatrics.
The Kidney.
Urinary System.
Renal autacoids Domina Petric, MD.
Renal tubule transport mechanisms
Figure 7 Overview of crystal deposition in the
Topic 11.3 The Kidney & Osmoregulation
Tubulointerstitial Injury Associated With Chemotherapeutic Agents
Peter A. McCullough, MD, MPH, Timothy Larsen, DO, Jeremiah R
Driving change: kidney proximal tubule CSF-1 polarizes macrophages
Volume 55, Issue 4, Pages (April 1999)
Toxic Nephropathies: Core Curriculum 2010
A trail of research on potassium
Apical membrane handling of substances, in this example aminoglycosides, by proximal tubular cells. Apical membrane handling of substances, in this example.
Renal and extrarenal regulation of potassium
Kidney specific factors that enhance nephrotoxic risk are noted.
Pharmacology behind Common Drug Nephrotoxicities Perazella, Mark A
A ‘complexity’ of urate transporters
Vasopressin in chronic kidney disease: an elephant in the room?
Figure 3 Pathophysiological events and preventive
Volume 60, Issue 6, Pages (December 2001)
R. Willi Grunewald, Claudius H. Reisse, Gerhard A. Müller 
Volume 83, Issue 4, Pages (April 2013)
Transcellular movement of organic cations (OCs) and organic anions (OAs) in kidney proximal tubule epithelial cells. Transcellular movement of organic.
Volume 83, Issue 4, Pages (April 2013)
Mechanism of action of drugs commonly used to treat hyponatremia.
Driving change: kidney proximal tubule CSF-1 polarizes macrophages
Schematic illustration of the reabsorption of calcium, phosphorus, and magnesium by different segments of the nephron. Schematic illustration of the reabsorption.
Distribution of postsynaptic density proteins in rat kidney: Relationship to neuronal nitric oxide synthase  Akihiro Tojo, David S. Bredt, Christopher.
Characteristics of isolated perfused juxtaglomerular apparatus
Volume 80, Issue 4, Pages (August 2011)
Insulin resistance and hypertension: new insights
New drug toxicities in the onco-nephrology world
Renal potassium channels: Function, regulation, and structure
Luminal signal in tubuloglomerular feedback: What about potassium?
Volume 62, Issue 4, Pages (October 2002)
Study of isolated perfused tubular segments allowed study of each of the different nephron segments independently. Study of isolated perfused tubular segments.
Volume 77, Issue 10, Pages (May 2010)
Volume 55, Issue 3, Pages (March 1999)
Volume 72, Issue 4, Pages (August 2007)
Model of proximal ammonia transport.
Pharmacology American Journal of Kidney Diseases
Drug factors associated with increased risk for nephrotoxicity.
Basolateral transport of drugs.
Apical transport of drugs in the proximal tubule.
Patient factors that increase risk for drug-induced nephrotoxicity.
Bisphosphonate nephrotoxicity
Structure of the nephron.
Cetuximab (C) is an EGF receptor (EGFR) antibody that causes renal magnesium wasting by competing with EGF for its receptor. Cetuximab (C) is an EGF receptor.
The proximal kidney tubule is the target for tenofovir-associated nephrotoxicities. The proximal kidney tubule is the target for tenofovir-associated nephrotoxicities.
Potential roles of biomarkers
Measured urea permeabilities in the different nephron sections of a rat kidney. Measured urea permeabilities in the different nephron sections of a rat.
Algorithm for management of drug-induced acute interstitial nephritis
Urea transporters along the nephron.
Cisplatin (Cis) nephrotoxicity is, in part, related to its uptake by proximal tubular cells. Cisplatin (Cis) nephrotoxicity is, in part, related to its.
Integrated overview of renal ammonia metabolism.
Pathophysiologic pathways of hematuria-induced kidney damage.
Tubulointerstitial changes and arteriolar hyalinosis in diabetic kidney disease. Tubulointerstitial changes and arteriolar hyalinosis in diabetic kidney.
The medullary interstitium has a concentration >4 times that of its surrounding fluid, and must be both generated and maintained. The medullary interstitium.
Pemetrexed (Pmx) nephrotoxicity may result from proximal tubular cell uptake of drug through apical (folate receptor-α [FR-α]) and basolateral (reduced.
Speculative mechanism by which gadolinium (Gd3+) might trigger nephrogenic systemic fibrosis. Speculative mechanism by which gadolinium (Gd3+) might trigger.
A urine sediment score of 0–4 is used to quantitatively evaluate AKI
Presentation transcript:

Kidney factors that enhance risk for drug-induced nephrotoxicity. Kidney factors that enhance risk for drug-induced nephrotoxicity. High RBF increases drug delivery and exposure to the kidney. High metabolic rates of TALH tubular cells increase risk for drug nephrotoxicity. Kidney metabolism of drugs to toxic metabolites and ROS overwhelms local antioxidants and promotes tubular injury. Increased concentrations of potentially nephrotoxic drugs in the medulla and interstitium increase kidney injury. Apical uptake of certain drugs (aminoglycosides, hydroxyethyl starch) and basolateral transport of drugs through the organic anion transporter (tenofovir) and organic cation transporter (cisplatin) increase kidney toxicity. PCT, proximal convoluted tubule; RBF, renal blood flow; ROS, reactive oxygen species; TALH, thick ascending loop of Henle. Mark A. Perazella CJASN 2018;13:1897-1908 ©2018 by American Society of Nephrology