大麻二酚油和强的松龙对镉中毒雄性Wistar大鼠肝酶、氧化应激标志物和肝脏组织学的影响

S. K. Mobisson, P. C. Onyebuagu, I. Wopara, D. Izunwanne, Emmanuel C. Madu, Augustine C. Emeruem, J. B. Monye, A. O. Obembe
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引用次数: 0

摘要

背景:本研究旨在探讨大麻二酚(CBD)油和强的松龙对镉中毒雄性Wistar大鼠血清肝酶标志物和肝脏氧化应激标志物的影响。选取体重150 ~ 200g的雄性Wistar大鼠40只,分为8组(A-H),每组5只。1组作为对照组,2 ~ 8组给予强的松龙1mg/kg体重;镉1.5mg/kg bw;强的松龙1mg/kg bw + cbd油0.2mg/kg bw;cbd油0.2mg/kg bw +镉2mg/kg bw;强的松龙3mg/kg bw +镉2mg/kg;分别为0.1mg/kg bw和0.2mg/kg bw。经胃管灌胃给药14天。结果显示,与对照组相比,所有治疗组的天冬氨酸转氨酶(AST)浓度均显著降低。血清谷丙转氨酶(ALT)显著高于对照组(p0.05)。治疗组肝脏谷胱甘肽过氧化物酶显著低于对照组。肝还原性谷胱甘肽在治疗组显著低于对照组。强的松龙、强的松龙+镉和CBD油(0.2mg/kg)组肝脏组织学显示肝细胞变性和血管充血。我们得出结论,不同剂量的CBD油、强的松龙和镉可以降低血清肝酶和氧化应激标志物的浓度,但会引起肝脏局部炎症。如果这项研究适用于人类,cbd油和强的松龙应谨慎服用,因为它们可能会产生不良反应,特别是对肝病患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Cannabidiol oil and prednisolone on liver enzymes, oxidative stress markers and liver histology in cadmium induced toxicity in male Wistar rats
Background: This study aimed to ascertain the effect of cannabidiol (CBD) oil and prednisolone on serum liver enzyme markers and hepatic oxidative stress markers on cadmium-induced toxicity in male Wistar rats. Forty (40) male Wistar rats weighing between 150g to 200g were assigned into 8 groups (A-H) of five animals each. Group 1 served as control, Groups 2-8 received 1mg/kg body weight of prednisolone; 1.5mg/kg bw of cadmium; 1mg/kg bw of prednisolone + 0.2mg/kg bw of CBD-oil; 0.2mg/kg bw of CBD-oil + 2mg/kg bw of cadmium; 3mg/kg bw of prednisolone + 2mg/kg of cadmium; 0.1mg/kg bw of CBD-oil and 0.2mg/kg bw of CBD-oil respectively. The administration was done using an orogastric tube (gavage) for 14 days. Results revealed a significant decrease in the concentration of aspartate aminotransferase (AST) in all treated groups compared to control. Furthermore, serum alanine aminotransferase (ALT) showed a significant (p<0.05) decrease in all treated groups compared to control. There was a significant decrease in the concentration of alkaline phosphatase (ALP) in treated groups compared to the control. Liver catalase significantly increased in rats fed with pred +cadmium compared to control and other treated groups. Liver superoxide dismutase (SOD) significantly decreased in (p<0.05) the group treated with cadmium compared to the control and prednisolone groups. Liver malondialdehyde concentration did not reveal any significant change (p>0.05). Liver glutathione peroxidase significantly decreased in treated groups than in control. Liver-reduced glutathione significantly decreased across treated groups than the control. Histology of the liver revealed degeneration of hepatocytes and vascular congestion in groups treated with prednisolone, prednisolone+ cadmium, and CBD oil (0.2mg/kg). We conclude that CBD oil, prednisolone, and Cadmium administration at different doses decreased the concentration of serum liver enzyme and oxidative stress markers but caused local inflammation of the liver. If this study is applicable to humans, CBD-oil and prednisolone should be cautiously taken as they may likely present adverse effects, especially in people with liver disease.
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