Age sensitizes the kidney to heme protein-induced acute kidney injury

Karl A. Nath, Joseph P. Grande, Gianrico Farrugia, Anthony J. Croatt, John D Belcher, Robert P Hebbel, Gregory M Vercellotti, Zvonimir S. Katusic

Research output: Contribution to journalArticle

17 Citations (Scopus)

Abstract

Age increases the risk for ischemic acute kidney injury (AKI). We questioned whether a similar age-dependent injury occurs following exposure to hemoglobin, a known nephrotoxin. Old mice (~16 mo old), but not young mice (~6 mo old), when administered hemoglobin, exhibited marked elevation in blood urea nitrogen (BUN) and serum creatinine, and acute tubular necrosis with prominent tubular cast formation. The aged kidney exhibited induction of heme oxygenase-1 (HO-1) and other genes/proteins that may protect against heme-mediated renal injury, including ferritin, ferroportin, haptoglobin, and hemopexin. Old mice did not evince induction of HO-2 mRNA by hemoglobin, whereas a modest induction of HO-2 mRNA was observed in young mice. To determine the functional significance of HO-2 in heme protein-induced AKI, we administered hemoglobin to relatively young HO-2+/+ and HO-2-/- mice: HO-2-/- mice, compared with HO-2+/+ mice, exhibited greater renal dysfunction and histologic injury when administered hemoglobin. In addition to failing to elicit a protective system such as HO-2 in response to hemoglobin, old mice exhibited an exaggerated maladaptive response typified by markedly greater induction of the nephrotoxic cytokine IL-6 (130-fold increase vs. 10-fold increase in mRNA in young mice). We conclude that aged mice, unlike relatively younger mice, are exquisitely sensitive to the nephrotoxicity of hemoglobin, an effect attended by a failure to induce HO-2 mRNA and a fulminant upregulation of IL-6. Age thus markedly augments the sensitivity of the kidney to heme proteins, and HO-2 confers resistance to such insults.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Renal Physiology
Volume304
Issue number3
DOIs
StatePublished - Feb 8 2013

Fingerprint

Hemeproteins
Acute Kidney Injury
Kidney
Hemoglobins
Messenger RNA
Interleukin-6
Wounds and Injuries
Hemopexin
Heme Oxygenase-1
Haptoglobins
Blood Urea Nitrogen
Ferritins
Heme
Creatinine
Necrosis
Up-Regulation

Keywords

  • Acute kidney injury
  • Age
  • Heme oxygenase-2
  • Heme proteins
  • Interleu-kin-6

Cite this

Age sensitizes the kidney to heme protein-induced acute kidney injury. / Nath, Karl A.; Grande, Joseph P.; Farrugia, Gianrico; Croatt, Anthony J.; Belcher, John D; Hebbel, Robert P; Vercellotti, Gregory M; Katusic, Zvonimir S.

In: American Journal of Physiology - Renal Physiology, Vol. 304, No. 3, 08.02.2013.

Research output: Contribution to journalArticle

Nath, Karl A. ; Grande, Joseph P. ; Farrugia, Gianrico ; Croatt, Anthony J. ; Belcher, John D ; Hebbel, Robert P ; Vercellotti, Gregory M ; Katusic, Zvonimir S. / Age sensitizes the kidney to heme protein-induced acute kidney injury. In: American Journal of Physiology - Renal Physiology. 2013 ; Vol. 304, No. 3.
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