Title of article :
CAFFEIC ACID PHENETHYL ESTER DECREASES THE LEVEL OF S-100B PROTEIN AFTER MIDDLE CEREBRAL AFTER OCCLUSION IN RABBITS
Author/Authors :
SERARSLAN, YURDAL Mustafa Kemal University - Tayfur Ata Sökmen Medical Faculty - Department of Neurosurgery, Turkey , BAL, RAMAZAN Fırat University - Faculty of Medicine - Department of Biophysics, Turkey , ALTUĞ, MUHAMMED ENES Mustafa Kemal University - Veterinary Faculty - Department of Surgery, Turkey , KONTAŞ, TÜNAY Mustafa Kemal University - Veterinary Faculty - Department of Biochemistry, Turkey , MELEK, İSMET MURAT Mustafa Kemal University - Tayfur Ata Sökmen Medical Faculty - Department of Neurology, Turkey
From page :
313
To page :
316
Abstract :
Effects of caffeic acid phenethyl ester (CAPE) on the serum S-100B levels were studied as an index for brain damage after permanent middle cerebral artery (MCA) occlusion in rabbits. Twenty rabbits were divided into four groups (n=5): control, sham, non-treatment and CAPE. The right MCA was occluded using a microsurgical procedure with bipolar coagulation and was then transected in non-treatment and CAPE groups. The rabbits in the sham group underwent a surgical procedure but the MCA was not occluded. No surgery was performed in the control group. CAPE was administered after MCA occlusion at the dose of 10μg/kg, once a day intraperitoneally for 7 days in the CAPE group. Serum S-100B levels were determined on days 1, 2, 4 and 7. Serum S-100B level was significantly increased following permanent MCA occlusion. Posttreatment of CAPE significantly reduced the serum S-100B level. This study demonstrated that CAPE is capable of attenuating increased serum S-100B level induced by MCA occlusion in rabbits. CAPE may be useful as a neuroprotective agent.
Keywords :
Brain , caffeic acid phenethyl ester , CAPE , experimental stroke , middle cerebral artery occlusion , MCA , S100B
Journal title :
Pakistan Journal Of Pharmaceutical Sciences
Journal title :
Pakistan Journal Of Pharmaceutical Sciences
Record number :
2647224
Link To Document :
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