Published May 1, 2013 | Version v1
Journal article

Assessment of cisplatin-induced kidney injury using an integrated rodent platform

  • 1. Global Safety Assessment, AstraZeneca R and D Waltham, MA 02451 (United States)
  • 2. Patient Safety, AstraZeneca R and D Wilmington, DE 19850 (United States)
  • 3. Discovery Statistics, AstraZeneca R and D Waltham, MA 02451 (United States)
  • 4. DMPK, AstraZeneca R and D Waltham, MA 02451 (United States)
  • 5. Global Safety Assessment, AstraZeneca R and D Alderley Park, Macclesfield, SK10 4TG (United Kingdom)

Description

Current diagnosis of drug-induced kidney injury (DIKI) primarily relies on detection of elevated plasma creatinine (Cr) or blood urea nitrogen (BUN) levels; however, both are indices of overall kidney function and changes are delayed with respect to onset of nephron injury. Our aim was to investigate whether early changes in new urinary DIKI biomarkers predict plasma Cr, BUN, renal hemodynamic and kidney morphological changes associated with kidney injury following a single dose of cisplatin (CDDP) using an integrated platform in rodent. Conscious surgically prepared male Han Wistar rats were given a single intraperitoneal dose of CDDP (15 mg/kg). Glomerular filtration rate (GFR), effective renal plasma flow (ERPF), urinalysis, DIKI biomarkers, CDDP pharmacokinetics, blood pressures, heart rate, body temperature and electroencephalogram (EEG) were measured in the same vehicle- or CDDP-treated animals over 72 h. Plasma chemistry (including Cr and BUN) and renal tissues were examined at study termination. Cisplatin caused progressive reductions of GFR, ERPF, heart rate and body temperature from day 1 (0–24 h). DIKI biomarkers including alpha-glutathione S-transferase (α-GST) significantly increased as early as 6 h post-dose, which preceded significant declines of GFR and ERPF (24 h), increased plasma Cr and BUN (72 h), and associated with renal acute tubular necrosis at 72 h post-dose. The present study adds to the current understanding of CDDP action by demonstrating that early increases in urinary excretion of α-GST predict DIKI risk following acute exposure to CDDP in rats, before changes in traditional DIKI markers are evident. - Highlights: ► CDDP causes direct damage to kidneys without affecting EEG or CVS function. ► α-GST and albumin detect DIKI earlier when compared with traditional indices. ► Integrated "cardiovascular-EEG-renal" model to better understand DIKI mechanisms ► Promotes 3R's principles in drug discovery and development

Availability note (English)

Available from http://dx.doi.org/10.1016/j.taap.2013.01.032

Additional details

Identifiers

DOI
10.1016/j.taap.2013.01.032;
PII
S0041-008X(13)00063-X;

Publishing Information

Journal Title
Toxicology and Applied Pharmacology
Journal Volume
268
Journal Issue
3
Journal Page Range
p. 352-361
ISSN
0041-008X
CODEN
TXAPA9

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.