甘草酸和磷脂酰胆碱复方制剂作为实验性小鼠非酒精性脂肪性肝炎的预防疗法

Livers Pub Date : 2024-01-29 DOI:10.3390/livers4010006
V. Prikhodko, T. M. Matuzok, Vadim E. Karev, A. V. Karavaeva, O. M. Spasenkova, Nadezhda V. Kirillova, D. Ivkin, S. V. Okovityi
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摘要

非酒精性代谢相关性脂肪性肝炎(MASH)是一种发病率和患病率越来越高的疾病,同时也是一种尚未得到有效药物治疗的重要医疗需求。在这项工作中,我们旨在探索联合使用甘草酸(GA)和磷脂酰胆碱(PC)协同预防实验性 MASH 的治疗可能性。成年 C57Bl/6 小鼠被用来建立饮食/毒性 MASH 模型,并接受 GA(34.3 毫克/千克/天)或 GA + PC 组合(34.3 + 158.1 毫克/千克/天)口服治疗 3 个月。对动物的运动、行为、短期记忆、体能、神经肌肉关节功能、血液生化和氧化应激标记物水平进行评估,然后对肝脏、骨骼肌和坐骨神经进行组织学检查,并测定组织氨和脂质含量。采用实时聚合酶链反应测量了几种致病转录标记物的相对表达。GA 和 PC 在抗炎、抗氧化、低血氨、降血糖和促进认知等方面显示出适度的相加协同作用。在焦虑和抑郁样行为以及基因表达方面,这些药物的作用存在差异。我们的研究结果表明了 GA 和 PC 之间的部分药理协同作用,并验证了对其潜在临床应用的进一步研究。
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Glycyrrhizinic Acid and Phosphatidylcholine Combination as a Preventive Therapy for Experimental Murine Non-Alcoholic Steatohepatitis
Non-alcoholic metabolic-associated steatohepatitis (MASH) is a condition characterized by increasingly high prevalence and incidence, and also represents an important unmet medical need when it comes to effective pharmacotherapy. In this work, we aimed to explore the therapeutic possibilities of the synergistic combined use of glycyrrhizinic acid (GA) and phosphatidylcholine (PC) to prevent experimental MASH. Adult C57Bl/6 mice were used to model dietary/toxic MASH and treated orally by either GA (34.3 mg/kg/d) or a GA + PC combination (34.3 + 158.1 mg/kg/d) for 3 months. Animal locomotion, behaviour, short-term memory, physical performance, neuromuscular joint function, blood biochemistry, and oxidative stress marker levels were evaluated, followed by histological examination of the liver, skeletal muscle and sciatic nerve with tissue ammonia and lipid content determination. Real-time polymerase chain reaction was used to measure the relative expression of several pathogenetic transcript markers. GA and PC showed moderate additive synergism in their anti-inflammatory, antioxidant, hypoammonaemic, hypoglycaemic, and pro-cognitive activities. Differential effects of the agents were seen in regard to anxiety- and depression-like behaviour as well as gene expression. Our results indicate partial pharmacological synergism between GA and PC and validate further research of its potential clinical applications.
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