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J Surg Res. 2008 Oct;149(2):287-95. doi: 10.1016/j.jss.2007.12.756. Epub 2008 Jan 17.

Ozone oxidative preconditioning protects the rat kidney from reperfusion injury: the role of nitric oxide.

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1
Department of Urology, Renmin Hospital of Wuhan University, Wuhan University, Wuhan, China.

Abstract

BACKGROUND:

Ischemia/reperfusion (I/R) injury, which is commonly seen in the field of renal surgery or transplantation, is a major cause of acute renal failure. Previous studies have shown that ozone oxidative preconditioning (OzoneOP) attenuated renal I/R injury. The objective of this study was to examine the hypothesis that protective effects of OzoneOP in renal I/R injury were associated with endogenous NO.

MATERIALS AND METHODS:

In a right-nephrectomized rat mode, anesthetized rats underwent 45 min of renal ischemia. OzoneOP (1 mg/kg) was administered before I/R injury. Rats were killed at 24, 48, and 72 h after I/R injury and blood samples and renal tissues were obtained.

RESULTS:

OzoneOP prevented the renal dysfunction induced by I/R and increased nitric oxide (NO) release and renal NO synthase (endothelial, eNOS, and inducible, iNOS) expression. In contrast, enhancement of endothelin-1 in the kidney after the reperfusion was markedly suppressed by OzoneOP.

CONCLUSIONS:

Our findings indicated that the protective effect of OzoneOP was closely related to the NO production following the increase in eNOS and iNOS expression. Ozone treatment may have important clinical implications, particularly in view of the minimizing renal damage before transplantation.

PMID:
18262565
DOI:
10.1016/j.jss.2007.12.756
[Indexed for MEDLINE]

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