İstanbul, Turkey
İstanbul, Turkey

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Saglam I.Y.,Goztepe Park Medical Hospital | Ozdamar E.N.,Maltepe University | Demiralay E.,Baskent University | Sehirli A.O.,Marmara University | And 2 more authors.
Turkish Neurosurgery | Year: 2013

Aim: The purpose of this study was to determine the possible protective effects of captopril treatment against apoptosis in the brain induced by burn injury. Ma terIal and Methods: Under ether anaesthesia, Wistar albino rats (200-250 g) were exposed to a 900C (burn) or 250C (sham) water bath for 10 s. The ACE group was treated with i.p. 10 mg/kg captopril immediately after burn injury and this treatment was repeated twice daily. At the end of the 24 hours, brain samples were taken. Apoptotic brain cells marked by terminal deoxynucleotidyl transferase-mediated d-UTPnick end labeling (TUNEL) were evaluated in the cerebellum and midbrain of rats. Results: Apoptotic cells in the cerebellum were significantly decreased after captopril treatment and found to be lower when compared to the burn group (p<0.001). In the midbrain of rats, the numbers of TUNEL-positive cells and apoptotic bodies were significantly increased in the burn group when compared to the control group (p<0.001). The burn-induced changes were reduced in the captopril-treated burn group (p<0.01). ConclusIon: Captopril has beneficial effects in burn injury and should be assessed as a therapeutic agent in the management of this condition.


PubMed | Goztepe Park Medical Hospital
Type: Journal Article | Journal: Turkish neurosurgery | Year: 2013

The purpose of this study was to determine the possible protective effects of captopril treatment against apoptosis in the brain induced by burn injury.Under ether anaesthesia, Wistar albino rats (200-250 g) were exposed to a 900C (burn) or 250C (sham) water bath for 10 s. The ACE group was treated with i.p. 10 mg/kg captopril immediately after burn injury and this treatment was repeated twice daily. At the end of the 24 hours, brain samples were taken. Apoptotic brain cells marked by terminal deoxynucleotidyl transferase-mediated d-UTPnick end labeling (TUNEL) were evaluated in the cerebellum and midbrain of rats.Apoptotic cells in the cerebellum were significantly decreased after captopril treatment and found to be lower when compared to the burn group (p < 0.001). In the midbrain of rats, the numbers of TUNEL-positive cells and apoptotic bodies were significantly increased in the burn group when compared to the control group (p < 0.001). The burn-induced changes were reduced in the captopril-treated burn group (p < 0.01).Captopril has beneficial effects in burn injury and should be assessed as a therapeutic agent in the management of this condition.

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