Literature DB >> 35373128

Evaluation of Renal Biomarkers, Including Symmetric Dimethylarginine, following Gentamicin-Induced Proximal Tubular Injury in the Rat.

Diane M Hamlin1, A Eric Schultze1, Michael J Coyne2, Donald J McCrann2, Rebekah Mack2, Corie Drake2, Rachel E Murphy2, Julie Cross2, Marilyn Strong-Townsend2, Maha Yerramilli2, Mary K Leissinger2.   

Abstract

Symmetric dimethylarginine (SDMA) is an excretory renal function biomarker shown to correlate well with glomerular filtration rate in dogs, cats, humans, and rats. The objectives of this study were to determine utility of serum SDMA as a renal biomarker in a rat model of gentamicin-induced renal injury and to provide validation of a commercially available SDMA immunoassay for rat serum. Rats were randomly assigned to one of three dose levels of gentamicin (20, 50, or 100 mg/kg) or a vehicle control group and dosed once daily by subcutaneous injection for either four or ten days. Serum and urine renal biomarker evaluation, including serum SDMA, hematologic and serum biochemical analysis, urinalysis, and histologic examination of kidney, were performed. Before biologic validation, analytic validation of the SDMA immunoassay for rat serum was performed, including assessment of assay accuracy, precision, analytical sensitivity, linearity, analyte stability, and interference testing. Among markers of excretory renal function, SDMA and serum creatinine increased earliest and at the lowest gentamicin concentrations and were significantly increased in both the 50- and 100- mg/kg dose levels in the four- and ten-dose treatment groups compared with controls. Time- and dose-dependent increases were noted for all urinary biomarkers investigated in this study, with microalbumin being most responsive and osteopontin least responsive for detection of gentamicin-induced injury across dose levels and schedules investigated. The SDMA immunoassay met all set quality requirements assessed in analytical validation. This study is the first to investigate performance of serum SDMA compared with other excretory renal function markers in a rat gentamicin acute toxicity model. In this study, serum SDMA was an earlier biomarker for detection of gentamicin-induced toxicity than serum cystatin C, BUN, and creatinine clearance. The SDMA immunoassay provides a reliable commercially available assay for future renal investigations in rat models.
Copyright © 2022 by the American Society of Nephrology.

Entities:  

Keywords:  LC-MS/MS; Sprague Dawley rat; glomerular and tubulointerstitial diseases; glomerular filtration rate; renal biomarker

Mesh:

Substances:

Year:  2021        PMID: 35373128      PMCID: PMC8967625          DOI: 10.34067/KID.0006542020

Source DB:  PubMed          Journal:  Kidney360        ISSN: 2641-7650


  36 in total

1.  Asymmetrical dimethylarginine plasma clearance persists after acute total nephrectomy in rats.

Authors:  Katari A Carello; Steven E Whitesall; Mary C Lloyd; Scott S Billecke; Louis G D'Alecy
Journal:  Am J Physiol Heart Circ Physiol       Date:  2005-08-19       Impact factor: 4.733

Review 2.  The role of asymmetric and symmetric dimethylarginines in renal disease.

Authors:  Edzard Schwedhelm; Rainer H Böger
Journal:  Nat Rev Nephrol       Date:  2011-03-29       Impact factor: 28.314

3.  Multiscale Mathematical Model of Drug-Induced Proximal Tubule Injury: Linking Urinary Biomarkers to Epithelial Cell Injury and Renal Dysfunction.

Authors:  Yeshitila Gebremichael; James Lu; Harish Shankaran; Gabriel Helmlinger; Jerome Mettetal; K Melissa Hallow
Journal:  Toxicol Sci       Date:  2018-03-01       Impact factor: 4.849

4.  A simple and fast liquid chromatography-tandem mass spectrometry method for measurement of underivatized L-arginine, symmetric dimethylarginine, and asymmetric dimethylarginine and establishment of the reference ranges.

Authors:  Joe M El-Khoury; Dustin R Bunch; Edmunds Reineks; Raymond Jackson; Roxanne Steinle; Sihe Wang
Journal:  Anal Bioanal Chem       Date:  2011-11-29       Impact factor: 4.142

5.  Simultaneous determination of L-arginine, asymmetric dimethylarginine, and symmetric dimethylarginine in the plasma of rodents with LC-MS/MS.

Authors:  Jung-Woo Chae; In-Hwan Baek; Wonku Kang; Kwang-Il Kwon
Journal:  Arzneimittelforschung       Date:  2011

6.  Kidney injury molecule-1 outperforms traditional biomarkers of kidney injury in preclinical biomarker qualification studies.

Authors:  Vishal S Vaidya; Josef S Ozer; Frank Dieterle; Fitz B Collings; Victoria Ramirez; Sean Troth; Nagaraja Muniappa; Douglas Thudium; David Gerhold; Daniel J Holder; Norma A Bobadilla; Estelle Marrer; Elias Perentes; André Cordier; Jacky Vonderscher; Gérard Maurer; Peter L Goering; Frank D Sistare; Joseph V Bonventre
Journal:  Nat Biotechnol       Date:  2010-05       Impact factor: 54.908

7.  Comparison of symmetric dimethylarginine with creatinine, cystatin C and their eGFR equations as markers of kidney function.

Authors:  Joe M El-Khoury; Dustin R Bunch; Bo Hu; Drew Payto; Edmunds Z Reineks; Sihe Wang
Journal:  Clin Biochem       Date:  2016-07-21       Impact factor: 3.281

8.  Progression of glomerular filtration rate reduction determined in conscious Dahl salt-sensitive hypertensive rats.

Authors:  Allen W Cowley; Robert P Ryan; Terry Kurth; Meredith M Skelton; Daniel Schock-Kusch; Norbert Gretz
Journal:  Hypertension       Date:  2013-04-29       Impact factor: 10.190

Review 9.  Nephrotoxicity and Renal Pathophysiology: A Contemporary Perspective.

Authors:  Lillie M A Barnett; Brian S Cummings
Journal:  Toxicol Sci       Date:  2018-08-01       Impact factor: 4.849

10.  The clinical utility window for acute kidney injury biomarkers in the critically ill.

Authors:  Azrina Md Ralib; John W Pickering; Geoffrey M Shaw; Martin P Than; Peter M George; Zoltán H Endre
Journal:  Crit Care       Date:  2014-11-04       Impact factor: 9.097

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  1 in total

1.  Evaluation of renal injury and function biomarkers, including symmetric dimethylarginine (SDMA), in the rat passive Heymann nephritis (PHN) model.

Authors:  Michael J Coyne; A Eric Schultze; Donald J McCrann; Rachel E Murphy; Julie Cross; Marilyn Strong-Townsend; Corie Drake; Rebekah Mack
Journal:  PLoS One       Date:  2022-05-27       Impact factor: 3.752

  1 in total

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