HSP72 is an early biomarker to detect cisplatin and acetaminophen nephrotoxicity

Biomarkers. 2017 Sep;22(6):548-556. doi: 10.1080/1354750X.2017.1315616. Epub 2017 Apr 19.

Abstract

Objective: To evaluate whether the urinary HSP72 levels (uHSP72) are a useful biomarker for early diagnosis of acute kidney injury (AKI) induced by two widely used drugs: cisplatin and acetaminophen.

Materials and methods: To analyze the time-course of nephrotoxic injury and uHSP72 levels, male Wistar rats were administered a single high dose of cisplatin (7 mg/kg) or acetaminophen (750 mg/kg) and were assessed at 6, 12, 24, 48, 72, 96 and 120 h.

Results: AKI induced by cisplatin was characterized by tubular injury that started at 6 h and was enhanced after 48 h. Plasma creatinine was increased only after 72 h. In contrast, uHSP72 levels were augmented after 6 h and were enhanced after 48 h of cisplatin administration, which was consistent with the tubular injury. In acetaminophen-induced AKI, the tubular lesions were less severe and predominantly characterized by tubular cell detachment. Interestingly, uHSP72 levels were increased after 6 h of acetaminophen injection and remained elevated at the following time points, reflecting the tubular injury, even in the absence of major functional changes.

Conclusions: In two models of renal injury induced by nephrotoxic drugs, we showed that uHSP72 could be used as an early biomarker to detect subtle to severe tubular injury.

Keywords: Drug-induced AKI; tubular injury; urine biomarkers.

MeSH terms

  • Acetaminophen / adverse effects*
  • Acetaminophen / toxicity
  • Acute Kidney Injury / chemically induced*
  • Acute Kidney Injury / diagnosis*
  • Animals
  • Biomarkers / urine
  • Cisplatin / adverse effects*
  • Cisplatin / toxicity
  • Early Diagnosis
  • HSP72 Heat-Shock Proteins / urine*
  • Kidney Tubules / injuries
  • Male
  • Rats
  • Rats, Wistar
  • Time Factors

Substances

  • Biomarkers
  • HSP72 Heat-Shock Proteins
  • Acetaminophen
  • Cisplatin