2008Chinese Remedies & ClinicsRequires access

Ulinastatin provides protection against endotoxin-induced acute kidney injury in rats

B Wang

Open publisher page 0 citations

Abstract

Objective To explore the role of Ulinastatin (UTI) in lipopolysaccharide (LPS)-induced acute kidney injury (AKI) in rats. Methods Thirty male Wistar rats were randomized to receive caudal injection of 1 ml normal saline (control group), or 5 mg/kg LPS (LPS group) or 5 mg/kg LPS plus 105 U/kg UTI (LPS+UTI group). Six hours later, the blood and urine levels of IL-18 were determined with enzyme-linked immunosorbent assay (ELISA), serum creatinine (SCr) with Jaffe′s reaction and the morphology of kidneys observed under an electron microscope. Results The level of Scr was significantly elevated in the LPS group compared with normal controls and the LPS+UTI group, as were levels of blood and urine IL-18. Microscopically, the renal tubular epithelium in normal rats showed large and round-shaped nuclei, intact brush border and mitochondria, whereas pyknosis, rupture of mitochondrial cristae, vacuolization and disrupted microvilla were found for the LPS group in contrast to the nearly normal morphology in the LPS+UIT group except for sparsely identifiable resolution of mitochondrial cristae. Conclusion UTI may reduce the expression of pro-inflammatory IL-18, hence its protection against LPS-induced AKI in rats.

About this research paper

What this paper is about

Objective To explore the role of Ulinastatin (UTI) in lipopolysaccharide (LPS)-induced acute kidney injury (AKI) in rats. Methods Thirty male Wistar rats were randomized to receive caudal injection of 1 ml normal saline (control group), or 5 mg/kg LPS (LPS group) or 5 mg/kg LPS plus 105 U/kg UTI (LPS+UTI group). Six hours later, the blood and urine levels of IL-18 were determined with enzyme-linked immunosorbent assay (ELISA), serum creatinine (SCr) with Jaffe′s reaction and the morphology of kidneys observed under an electron microscope. Results The level of Scr was significantly elevated in the LPS group compared with normal controls and the LPS+UTI group, as were levels of blood and urine IL-18. Microscopically, the renal tubular epithelium in normal rats showed large and round-shaped nuclei, intact brush border and mitochondria, whereas pyknosis, rupture of mitochondrial cristae, vacuolization and disrupted microvilla were found for the LPS group in contrast to the nearly normal morphology in the LPS+UIT group except for sparsely identifiable resolution of mitochondrial cristae. Conclusion UTI may reduce the expression of pro-inflammatory IL-18, hence its protection against LPS-induced AKI in rats.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objective To explore the role of Ulinastatin (UTI) in lipopolysaccharide (LPS)-induced acute kidney injury (AKI) in rats. Methods Thirty male Wistar rats were randomized to receive caudal injection of 1 ml normal saline (control group), or 5 mg/kg LPS (LPS group) or 5 mg/kg LPS plus 105 U/kg UTI (LPS+UTI group). Six hours later, the blood and urine levels of IL-18 were determined with enzyme-linked immunosorbent assay (ELISA), serum creatinine (SCr) with Jaffe′s reaction and the morphology of kidneys observed under an electron microscope. Results The level of Scr was significantly elevated in the LPS group compared with normal controls and the LPS+UTI group, as were levels of blood and urine IL-18. Microscopically, the renal tubular epithelium in normal rats showed large and round-shaped nuclei, intact brush border and mitochondria, whereas pyknosis, rupture of mitochondrial cristae, vacuolization and disrupted microvilla were found for the LPS group in contrast to the nearly normal morphology in the LPS+UIT group except for sparsely identifiable resolution of mitochondrial cristae. Conclusion UTI may reduce the expression of pro-inflammatory IL-18, hence its protection against LPS-induced AKI in rats.

Key concepts: Ulinastatin, Vacuolization, Lipopolysaccharide, Brush border, Saline, Acute kidney injury, Internal medicine, Creatinine

Related papers

Back to paper searchBrowse research topicsOriginal source
Ulinastatin provides protection against endotoxin-induced acute kidney injury in rats — Research Paper | ScholarLens