Protective effect of oleuropein on ketamine-induced cardiotoxicity in rats

被引:0
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作者
Mehmet Selim Çömez
Mustafa Cellat
Hüseyin Özkan
Yakup Borazan
Tuba Aydın
İshak Gökçek
Erdinç Türk
Mehmet Güvenç
Ahmet Çakır
Şule Yurdagül Özsoy
机构
[1] Hatay Mustafa Kemal University,Department of Anesthesiology and Reanimation, Faculty of Medicine
[2] Hatay Mustafa Kemal University,Department of Physiology, Faculty of Veterinary Medicine
[3] Hatay Mustafa Kemal University,Department of Genetics, Faculty of Veterinary Medicine
[4] Adıyaman University,Department of Pharmacognosy, Faculty of Pharmacy
[5] Education And Research Hospital,Department of Pharmacology and Toxicology, Faculty of Veterinary Medicine
[6] Ağrı İbrahim Çeçen University,Department of Chemistry, Faculty of Science and Letters
[7] Hatay Mustafa Kemal University,Department of Pathology, Faculty of Veterinary Medicine
[8] Kilis 7 Aralık University,undefined
[9] Adnan Menderes University,undefined
来源
Naunyn-Schmiedeberg's Archives of Pharmacology | 2020年 / 393卷
关键词
Ketamine; Oleuropein; Cardiotoxicity;
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摘要
The antioxidant and cardioprotective effects of oleuropein have been reported in several studies; however, its effect on ketamine cardiotoxicity has not been known yet. The aim of this study was to investigate the effects of oleuropein in ketamine-induced cardiotoxicity model in rats. A total of 28 male Wistar Albino rats were included in the study and they were randomly divided into four groups, each having seven rats. Group 1 (control): rats were given 1 mL of DMSO by oral gavage method for 7 days. Group 2 (ketamine): on the seventh day of the study, 60 mg/kg ketamine was administered intraperitoneally. Then, 60 mg/kg ketamine was administered intraperitoneally every 10 min for 3 h. Group 3 (oleuropein): rats were given 200 mg/kg/day oleuropein by oral gavage method for 7 days. Group 4 (oleuropein + ketamine): rats were given 1 × 200 mg/kg oleuropein by oral gavage method for 7 days. Furthermore, 60 mg/kg ketamine was administered intraperitoneally on the seventh day of the experiment. Then, 60 mg/kg ketamine was administered intraperitoneally every 10 min for 3 h. Serum cardiac marker (TnI, CK-MB and CK) levels were measured. Histopathological analysis was performed on a portion of the cardiac tissue. Cardiac tissue oxidative stress and antioxidant markers (MDA, GSH, GSH.Px and CAT), TNF-α, IL-6, NF-κB, COX-2 and Nrf-2 gene expressions, and protein conversion levels of related genes were determined. Data obtained showed that ketamine administration increased MDA (p < 0.001), TNF-α (p < 0.01), IL-6 (p < 0.01), COX-2 (p < 0.001) and NF-κB (p < 0.001) levels, as well as serum TnI (p < 0.001), CK-MB (p < 0.001) and CK (p < 0.01) levels whereas decreased GSH (p < 0.05) and Nrf-2 (p < 0.05) levels, as well as GSH-Px (p < 0.001) and CAT (p < 0.05) enzyme activities. Oleuropein administration was observed to decrease MDA, TNF-α, IL-6, COX-2, NF-κB, TnI, CK-MB and CK levels close to the control group and to increase GSH levels and GSH-Px and CAT enzyme activities close to the control group. This study showed that oleuropein administration reversed the increased oxidative stress and inflammation as a result of the use of ketamine and had protective effects on the heart.
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页码:1691 / 1699
页数:8
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