迷迭香和辅酶q10通过加速对乙酰氨基酚和卡马西平的代谢和消除,减轻了对乙酰氨基酚和卡马西平同时服用的有害影响

Marwa Magdy Hamido, N. Zaki, S. Nasr, W. El-Sayed
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引用次数: 0

摘要

背景:卡马西平(CBZ)与对乙酰氨基酚(APAP)相互作用可导致肝功能衰竭和死亡。本研究旨在分析迷迭香乙醇提取物(REE)或辅酶Q10 (CoQ10)缓解CBZ与APAP相互作用的潜力。方法:48只成年雄性大鼠按分组进行不同处理。测定肝脏氧化应激参数,包括丙二醛(MDA)、谷胱甘肽(GSH)、谷胱甘肽过氧化物酶(GPx)、超氧化物歧化酶(SOD)、过氧化氢酶、谷胱甘肽s -转移酶(GST),以及CYP3A4、CYP2E1、IL-6、TNF-α、IL-1B的表达水平。同时进行肝脏组织病理学检查,测定血浆CBZ和APAP清除率。结果:CBZ联合APAP可显著提高大鼠肝脏丙氨酸转氨酶(ALT)活性和MDA,降低肝脏GPx、GST、GSH活性。CBZ和CoQ10分别上调CYP3A4和CYP2E1的基因表达。单用CBZ或联用APAP治疗组IL-6表达降低。CBZ、APAP、REE、CoQ10或CBZ与APAP联合治疗组TNF-α表达显著下调。CBZ和APAP联合组肝脏表现为小叶中央变性和坏死。REE和CoQ10能够减轻大部分这些有害影响。联合应用CBZ和APAP可使APAP和CBZ的血浆清除时间分别从6小时延长至24小时和从9小时延长至24小时。结论:REE和CoQ10通过增强细胞抗氧化环境,诱导代谢酶,降低APAP和CBZ的血浆半衰期,防止它们的积累和潜在的相互作用,减轻了CBZ和APAP联合的有害影响。关键词:对乙酰氨基酚、抗氧化剂、卡马西平、辅酶q10、CYP3A4、CYP2E1、谷胱甘肽、脂质过氧化、迷迭香
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rosemary and CoQ10 Alleviated the Detrimental Effects of Concomitant Administration of Acetaminophen and Carbamazepine by Accelerating Their Metabolism and Elimination
BACKGROUND: The interaction of carbamazepine (CBZ) and acetaminophen (APAP) could result in hepatic failure and mortality. This study was conducted to analyzed the potential of rosemary ethanol extract (REE) or coenzyme Q10 (CoQ10) to alleviate the interactions between CBZ and APAP.METHODS: Fourty-eight adult male rats were treated differently based on the assigned groups. Oxidative stress parameters, including malondialdehyde (MDA), glutathione (GSH), glutathione peroxidase (GPx), superoxide dismutase (SOD), catalase, and glutathione S-transferase (GST), and the expression levels of CYP3A4, CYP2E1, IL-6, TNF-α, and IL-1B in the liver were estimated. In addition, the histopathology of liver was examined and the plasma clearance rate of CBZ and APAP was estimated.RESULTS: Combination of CBZ and APAP significantly elevated alanine aminotransferase (ALT) activity and hepatic MDA, and reduced the activities of GPx, GST, and GSH level in liver. The gene expression of CYP3A4 and CYP2E1 was upregulated by CBZ and CoQ10, respectively. The expression of IL-6 has decreased in the groups treated with CBZ alone or in combination with APAP. TNF-α expression was significantly downregulated in the groups treated with CBZ, APAP, REE, CoQ10, or combination CBZ and APAP. The liver from CBZ and APAP combination group showed centrolobular degeneration and necrosis. REE and CoQ10 were able to alleviate most of these detrimental effects. The combined administration of CBZ and APAP extended the plasma clearance time of APAP and CBZ from 6 to 24 and from 9 to 24 hours, respectively.CONCLUSION: REE and CoQ10 alleviated the detrimental effects of the combination of CBZ and APAP through enhancing the cellular antioxidant milieu, induction of metabolizing enzymes, reduction of the plasma half-life of APAP and CBZ preventing their accumulation and potential interaction.KEYWORDS: acetaminophen, antioxidants, carbamazepine, CoQ10, CYP3A4, CYP2E1, glutathione, lipid peroxidation, rosemary
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