Nd libitum. They had not been used in priory another study and they had not been given a drug regularly, in addition they had not a disease, previously. The rats were deprived of food for 12 h before the experiment but had free access to water. Experiments were carried out under steril conditions and antibiotic prophylaxis with cefazolin sodium (30 mg/kg intramuscularly, single preoperative dose) was given. Isotonic NaCl solution was given intravenously at the rate of 3 ml/kg/h. During all MS023MedChemExpress MS023 experimental manipulations, to prevent the effects of hypothermia and to provide the stability of hemodynamic parameters, the body temperature was maintained at 37.2 with a rectal probe. For this, animals were placed on an operating table with thermoregulatory, and were used heat pad.Study groupsTwenty-seven rats were randomly allocated into 3 groups. Sham group underwent a surgical procedure similar to the other groups but the aorta was not occluded. This group of animals was used to elicit the effects of anesthesia and operation on the results and also to determine the biochemical parameters of normalThe rats were anesthetized with intramuscular injection of 15 mg/kg ketamine hydrochloride (Ketalar; Pfizer, Istanbul, Turkey) and 2 mg/kg xylazine hydrochloride (Rompun, Bayer, Turkey) before the surgical procedure. The rats were shaved from abdomen to leg. The surgical area was painted with batticon. Surgical area was cleaned and draped. Intraperitoneal cephalosporine (10 mg/kg) was administered before skin incision. After steril surgical preparation, a midline laparotomy was made and the intestines were taken out by deflecting them to the right and covering them with warm and wet compresses to decrease the loss of heat and fluid. After the retroperitoneal area was opened, the abdominal aorta and inferior vena cava were identified and isolated. The maintenance of anesthesia was established with intermittent delivery of ketamine, without endotracheal intubation and mechanical ventilation. 400 IU/kg of heparin was administered intraperitoneally to all animals immediately before the procedure. Spinal cord ischemia was created by clamping the aorta just below the renal vein with an atraumatic microvascular clamp (vascustatts II, midi straight 1001?532; Scanlan Int., PubMed ID:https://www.ncbi.nlm.nih.gov/pubmed/28549975 St. Paul, MN, USA) 3 min after heparin administration. Another clamp was placed above the aortic bifurcation to occlude the iliac collateral circulation. During procedure, temperature probe was inserted into the rectum. Body temperature was maintained close to 37 using a heated operation table. The systemic blood pressure was measured as 70?0 mmHg in the aorta. Electrocardiographic monitoring was performed on all animals throughout the experiment. The heart rate was maintained at 176?90 beats/min. After experimental procedure, all animals received protamine sulfate (1 mg/kg intravenously) to antagonize the effects of heparin. After bleeding was controlled, 10 ml of warm ringer lactate solution was given intraperitoneally. The muscles of the abdomen and skin were closed in a routine manner with 3? silk sutures. Prophylactic antibacterial therapy was carried out with the intramuscular administration of Cefazoline Na (15 mg/kg/day; Mustafa Nevzat AS, Istanbul, Turkey) preoperatively and postoperatively. ForErkut and Onk Journal of Cardiothoracic Surgery (2015) 10:Page 3 ofpostoperative analgesia, morphine HCl (400 mcg/kg/day, i.m., Galen AS, Istanbul, Turkey) was given to all subjects.Evaluat.