| Journal: |
Zagazig University Medical Journal,
Zagazig University Medical Journal
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Volume: |
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| Abstract: |
Background: Renal ischemia/reperfusion is an imperative cause of acute
kidney damage which in turn releases detrimental mediators into the
circulation leading to subsequent remote organ injury.
:
Aim of the study: to assess the possible protective effects of diacerein
(DIA),
interleukin-1
receptor
antagonistail address,
renal
ischemia/reperfusion (I/R) induced kidney and lung injuries in male
albino
against
rats.
Material, Methods: Rats were randomly assigned into: sham, I/R, and
DIA-pretreated I/R groups. DIA was orally administered in doses of 25,
50 and 100 mg/kg/day for 20 days, then, both right and left renal pedicles
were clamped for 45 min followed by reperfusion for 24 h. One-way
ANOVA followed by Post-Hoc test were used to compare the results. P
Value of <0.05 was considered as statistically significant.
Results : DIA significantly reduced serum creatinine and blood urea
nitrogen (BUN), improved both kidney and lung histoarchitecture,
reduced pulmonary interleukin-1 beta (IL-1β), tumor necrosis factor
alpha
(TNF-α),
osteopontin
(OPN),
elevated
superoxide
dismutase(SOD), glutathione (GSH), nuclear factor erythroid 2–related
factor 2 (Nrf-2), Heme oxygenase 1 (HO-1), and reduced
malondialdehyde (MDA) lung levels.
Conclusion: Our results show that DIA has a
promising protective impact against kidney and lung
injuries prompted by renal I/R. This effect is proposed
to be mediated, partially, by downregulation of
osteopontin and upregulation of Nrf-2/HO-1.
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