Liquorice root extract and isoliquiritigenin attenuate high-fat diet-induced hepatic steatosis and damage in rats by regulating AMPK.

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Mohammed Abdo Yahya, Ghedeir M Alshammari, Magdi A Osman, Laila Naif Al-Harbi, Abu ElGasim A Yagoub, Sahar Abdulaziz AlSedairy
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引用次数: 0

Abstract

Objective: This study compared the ability of Liquorice roots aqueous extract (LRE) and its ingredient, isoliquiritigenin (ISL), in alleviating high-fat diet (HFD)-induced hepatic steatosis and examined if this effect involves activation of AMPK.Materials and methods: Control or HFD-fed rats were treated with the vehicle, LRE (200 mg/kg), or ISL (30 mg/kg) for 8 weeks orally.Results: ISL and LRE reduced HFD-induced hyperglycaemia, improved liver structure, lowered serum and hepatic lipids, and attenuated hepatic oxidative stress and inflammation. In the control and HFD-fed rats, ISL and LRE significantly stimulated the muscular and hepatic mRNA and protein levels of AMPK, improved oral glucose tolerance, reduced hepatic mRNA levels of SREBP1/2, and upregulated hepatic levels of PPARα and Bcl2. These effects were comparable for ISL and LRE and were prevented by co-administration of compound C, an AMPK inhibitor.Discussion and conclusion: ISL and LRE provide an effective theory to alleviate hepatic steatosis through activating AMPK.

甘草根提取物和甘草次甙元通过调节 AMPK 减轻高脂饮食引起的大鼠肝脏脂肪变性和损伤
研究目的本研究比较了甘草根水提取物(LRE)及其成分ISL(isiquiritigenin)在缓解高脂饮食(HFD)诱导的肝脏脂肪变性方面的能力,并考察了这种作用是否涉及AMPK的激活:对照组或高脂饮食喂养的大鼠口服载体、LRE(200 毫克/千克)或 ISL(30 毫克/千克)治疗 8 周:结果:ISL和LRE降低了HFD诱导的高血糖,改善了肝脏结构,降低了血清和肝脏脂质,减轻了肝脏氧化应激和炎症反应。在对照组和高氟日粮喂养的大鼠中,ISL 和 LRE 能显著刺激肌肉和肝脏中 AMPK 的 mRNA 和蛋白质水平,改善口服葡萄糖耐量,降低肝脏中 SREBP1/2 的 mRNA 水平,上调肝脏中 PPARα 和 Bcl2 的水平。这些效应在 ISL 和 LRE 中具有可比性,同时服用 AMPK 抑制剂化合物 C 可防止这些效应:ISL和LRE为通过激活AMPK缓解肝脏脂肪变性提供了一种有效的理论。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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