Effect of Dexmedetomidine on Lung Tissue Lower Extremity Ischemia Reperfusion Injury in Streptozotocin Induced Diabetic Rats
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Original Investigation
P: 358-362
July 2020

Effect of Dexmedetomidine on Lung Tissue Lower Extremity Ischemia Reperfusion Injury in Streptozotocin Induced Diabetic Rats

GMJ 2020;31(3):358-362
1. Kırıkkale University School of Medicine, Department of Histology and Embryology, Kırıkkale, Turkey
2. Yıldırım Beyazıt University School of Medicine, Department of Thoracic Surgery, Ankara, Turkey
3. Gazi University School of Medicine, Department of Anesthesia and Reanimation, Ankara, Turkey
4. Gazi University School of Medicine, Department of Biochemistry, Ankara, Turkey
No information available.
No information available
Received Date: 12.04.2018
Accepted Date: 17.05.2018
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ABSTRACT

Objective:

The aim of our study was to investigate the effects of dexmedetomidine on lung tissue in rat’s lower extremity after undergoing an ischemia reperfusion (I/R) injury.

Material and methods:

After obtaining ethical committee approval, 24 Wistar albino rats (200-270 gr) were randomly divided into four groups: (Control (Group C), diabetes-control (Group DC), diabetes I/R (Group DIR), and diabetes-I/R-dexmedetomidine (Group DIRD). In diabetes groups, single-dose (55 mg/kg) streptozotocin was administered intraperitoneally. Rats with a blood glucose level above 250 mg/dl at the 72nd hour were accepted as diabetic. At the end of four weeks, laparotomy was performed in all rats. Nothing else was done in Group C and DC. In Group DIR, ischemia reperfusion was produced via two-hour periods of clamping and subsequent declamping of infra-renal abdominal aorta. In Group DIRD, 100 μg/kg of dexmedetomidine were administered intraperitoneally.

Results:

When the groups’ lung tissue neutrophil infiltration/aggregation light microscopic findings were compared to each other, a significant difference was observed among the groups (p=0.003). When the groups’ lung tissue injury score light microscopic findings were compared, a significant difference was observed among the groups (p=0.001). When groups were compared to each other in terms of lung tissue MDA levels and SOD activities, a significant difference was observed (p=0.002, p=0.018, respectively).

Conclusion:

Our results confirm that dexmedetomidine has protective effects against the lung damage resulting from IR in diabetic rats. However, future studies should be conducted to evaluate these effects.

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