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橄榄苦苷对氯胺酮致大鼠心肌毒性的保护作用。

Protective effect of oleuropein on ketamine-induced cardiotoxicity in rats.

机构信息

Department of Anesthesiology and Reanimation, Faculty of Medicine, Hatay Mustafa Kemal University, 31300, Hatay, Turkey.

Department of Physiology, Faculty of Veterinary Medicine, Hatay Mustafa Kemal University, Hatay, Turkey.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 2020 Sep;393(9):1691-1699. doi: 10.1007/s00210-020-01870-w. Epub 2020 May 7.

Abstract

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.

摘要

橄榄苦苷具有抗氧化和心脏保护作用,已在几项研究中得到报道;然而,其对氯胺酮心脏毒性的影响尚不清楚。本研究旨在探讨橄榄苦苷对大鼠氯胺酮诱导的心脏毒性模型的影响。共有 28 只雄性 Wistar 白化大鼠纳入本研究,随机分为四组,每组 7 只。第 1 组(对照组):大鼠通过口服灌胃法给予 1 mL DMSO,连续 7 天。第 2 组(氯胺酮组):研究第 7 天,给予 60 mg/kg 氯胺酮腹膜内注射。然后,每 10 分钟给予 60 mg/kg 氯胺酮腹膜内注射,共 3 小时。第 3 组(橄榄苦苷组):大鼠通过口服灌胃法给予 200 mg/kg/天橄榄苦苷,连续 7 天。第 4 组(橄榄苦苷+氯胺酮组):大鼠通过口服灌胃法给予 1×200 mg/kg 橄榄苦苷,连续 7 天。此外,在实验第 7 天给予 60 mg/kg 氯胺酮腹膜内注射。然后,每 10 分钟给予 60 mg/kg 氯胺酮腹膜内注射,共 3 小时。测定血清心脏标志物(TnI、CK-MB 和 CK)水平。对心脏组织的一部分进行组织病理学分析。测定心脏组织氧化应激和抗氧化标志物(MDA、GSH、GSH.Px 和 CAT)、TNF-α、IL-6、NF-κB、COX-2 和 Nrf-2 基因表达以及相关基因的蛋白转化水平。结果表明,氯胺酮给药增加了 MDA(p<0.001)、TNF-α(p<0.01)、IL-6(p<0.01)、COX-2(p<0.001)和 NF-κB(p<0.001)水平,以及血清 TnI(p<0.001)、CK-MB(p<0.001)和 CK(p<0.01)水平,同时降低了 GSH(p<0.05)和 Nrf-2(p<0.05)水平,以及 GSH-Px(p<0.001)和 CAT(p<0.05)酶活性。橄榄苦苷给药可使 MDA、TNF-α、IL-6、COX-2、NF-κB、TnI、CK-MB 和 CK 水平接近对照组,并使 GSH 水平和 GSH-Px 和 CAT 酶活性接近对照组,从而降低氧化应激和炎症。本研究表明,橄榄苦苷给药可逆转氯胺酮使用引起的氧化应激和炎症增加,并对心脏具有保护作用。

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