Deficiency of heme oxygenase-1 impairs renal hemodynamics and exaggerates systemic inflammatory responses to renal ischemia.

Abstract

Heme oxygenase-1 may exert cytoprotective effects. In this study we examined the sensitivity of heme oxygenase-1 knockout (HO-1(-/-)) mice to renal ischemia by assessing glomerular filtration rate (GFR) and cytokine expression in the kidney, and inflammatory responses in the systemic circulation and in vital extrarenal organs. Four hours after renal ischemia, the GFR of HO-1(-/-) mice was much lower than that of wild-type mice in the absence of changes in renal blood flow or cardiac output. Eight hours after renal ischemia, there was a marked induction of interleukin-6 (IL-6) mRNA and its downstream signaling effector, phosphorylated signal transducer and activator of transcription 3 (pSTAT3), in the kidney, lung, and heart in HO-1(-/-) mice. Systemic levels of IL-6 were markedly and uniquely increased in HO-1(-/-) mice after ischemia as compared to wild-type mice. The administration of an antibody to IL-6 protected against the renal dysfunction and mortality observed in HO-1(-/-) mice following ischemia. We suggest that the exaggerated production of IL-6, occurring regionally and systemically following localized renal ischemia, in an HO-1-deficient state may underlie the heightened sensitivity observed in this setting.

• Authors: M J Tracz, J P Juncos, A J Croatt, A W Ackerman, J P Grande, K L Knutson, G C Kane, A Terzic, M D Griffin, K A Nath
• Journal: Kidney international (Kidney Int) Vol. 72 Issue 9 Pg. 1073-80 (Nov 2007) ISSN: 0085-2538 [Print] United States
• PMID: 17728706 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Cytokines
• Interleukin-6
• RNA, Messenger
• STAT3 Transcription Factor
• Stat3 protein, mouse
• Heme Oxygenase-1

Topics

• Animals
• Cardiac Output (physiology)
• Cytokines (blood)
• Female
• Glomerular Filtration Rate (physiology)
• Heme Oxygenase-1 (genetics, metabolism)
• Interleukin-6 (metabolism)
• Ischemia (metabolism, physiopathology)
• Kidney (blood supply, metabolism, physiopathology)
• Lung (metabolism)
• Male
• Mice
• Mice, Knockout
• Myocardium (metabolism)
• RNA, Messenger (genetics, metabolism)
• Regional Blood Flow (physiology)
• Reperfusion Injury (metabolism, physiopathology)
• STAT3 Transcription Factor (metabolism)
• Time Factors