| Objective(s)
:
Sepsis can result in severe organ injury by provoking inflammatory cascades and
oxidative stress. Several studies are currently underway to find a drug with anti-inflammatory effects
to prevent mortality and morbidity during sepsis. The present study was undertaken to assess the
effects of metformin on oxidative stress and antioxidant status in sepsis induced by the Cecal Ligation
and Puncture (CLP) method.
Materials and Methods:
Male Wistar rats were divided into 4 groups (n=10): sham, CLP, and 50 and 100 mg/
kg metformin-treated CLP groups. After 12 hr, blood samples were collected and lung tissue was removed for
histopathological study to detect tissue damage and degree of inflammation based on neutrophil infiltration
and assay of the oxidative stress biomarkers superoxide dismutase (SOD), total antioxidant capacity (TAC),
malondialdehyde (MDA), myeloperoxidase (MPO), glutathione peroxidase (GPx), and plasminogen activator
inhibitor-1 (PAI-1).
Results:
The MPO activity and MDA level were decreased in the metformin-treated groups (
P<
0.05).
Moreover, the groups receiving metformin showed lower inflammation scores than the CLP group
(
P<
0.05). No significant differences in SOD, GPx, or PAI in the different groups were observed. The TAC
level was reduced in the CLP group compared to the sham group (
P<
0.05), and interestingly, this value
was reduced even further in the metformin-treated groups (
P<
0.05 compared with the CLP group).
Conclusion:
It was concluded that metformin protects lung tissue against sepsis-induced oxidative
damage, and this protective effect may be more related to its anti-inflammatory and reduced
neutrophil accumulation and less to its anti-oxidative properties. |