Back to Search Start Over

The impact of pretreatment with simvastatin on kidney tissue of rats with acute sepsis.

Authors :
Özkök E
Yorulmaz H
Ateş G
Aydın I
Ergüven M
Tamer Ş
Source :
Physiology international [Physiol Int] 2017 Jun 01; Vol. 104 (2), pp. 158-170.
Publication Year :
2017

Abstract

It has been reported that changes in cytokine levels affect mitochondrial functions, levels of hypoxia-inducible factor α (HIF-1α), and tissue damage during sepsis. We aimed to investigate the effects of simvastatin pretreatment on mitochondrial enzyme activities, and on levels of ghrelin, HIF-1α, and thiobarbituric acid reactive substances (TBARS) in kidney tissue during sepsis. Rats were separated into four groups, namely, control, lipopolysaccharides (LPS) (20 mg/kg), simvastatin (20 mg/kg), and simvastatin + LPS. We measured the levels of mitochondrial enzyme activities and TBARS in the kidney using spectrophotometry. The histological structure of the kidney sections was examined after staining with hematoxylin and eosin. Tumor necrosis factor α (TNF-α), IL-10, HIF-1α, and ghrelin immunoreactivity were examined using proper antibodies. In tissue, TNF-α (p < 0.01) and HIF-1α (p < 0.05) levels were increased in the simvastatin + LPS and LPS groups. TBARS levels were higher in the LPS group than in the other groups (p < 0.01), but they were similar in the simvastatin + LPS and control groups (p > 0.05). Ghrelin immunoreactivity was lower in the LPS group (p < 0.05) and higher in the simvastatin + LPS group than in the LPS group (p < 0.01). We observed tubular damage in the sections of the LPS group. There were no differences in mitochondrial enzyme activities between the groups (p > 0.05). We observed that pretreatment of simvastatin caused favorable changes on ghrelin and TBARS levels in rats with sepsis.

Details

Language :
English
ISSN :
2498-602X
Volume :
104
Issue :
2
Database :
MEDLINE
Journal :
Physiology international
Publication Type :
Academic Journal
Accession number :
28665194
Full Text :
https://doi.org/10.1556/2060.104.2017.2.8