Gan-Jiang-Ling-Zhu Decoction Prevents Paigen's Diet-induced Lean Metabolic Dysfunction-associated Steatotic Liver disease by Regulating Bile Acid Metabolism.

IF 1.7 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Zansong Ma, Milian Chen, Ying Cao, Deji Song, Li Zhang
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引用次数: 0

Abstract

Introduction: Metabolic dysfunction-associated steatotic liver disease (MASLD) is a global health concern, even among lean individuals. The Gan-Jiang-Ling-Zhu decoction (GZD), a traditional Chinese medicine formula, shows therapeutic potential against MASLD. This study investigated the efficacy of GZD in lean MASLD and explored its mechanisms of action.

Methods: A lean MASLD mouse model was established using C57BL/6 mice fed with a cholesterol- rich Paigen's diet (PD). Following successful modeling, mice were administered GZD (1.8, 3.6, or 7.2 g/kg) or vehicle control. Body weight, food intake, and liver weight were monitored. Hepatic steatosis and lipid accumulation were assessed via H&E and Oil Red O staining, while serum enzymes were quantified biochemically. Gut microbiota composition was analyzed by 16S rRNA gene sequencing, and bile acid (BA) profiles in feces and serum were measured using UPLC-TQMS.

Results: Twelve weeks of PD feeding induced a lean MASLD phenotype characterized by reduced body weight alongside hepatic steatosis and dyslipidemia. The GZD treatment dosedependently ameliorated liver steatosis and lipid accumulation, with the highest dose (7.2 g/kg) showing superior efficacy. GZD restored gut microbiota balance by reducing pathogenic bacteria and enriching taxa involved in BA metabolism, leading to increased fecal excretion of secondary BAs. Conversely, serum levels of secondary BAs were significantly reduced after GZD treatment.

Discussion: Our study highlights the promising role of GZD in lean MASLD, the involvement of gut microbiota and related BA metabolism that aligns with emerging evidence that gut dysbiosis and disrupted BA homeostasis are central to MASLD pathogenesis, even in lean individuals. However, the mechanistic links between specific microbial changes, BA pool composition, and hepatic outcomes remain to be elucidated.

Conclusion: GZD ameliorates hepatic steatosis in lean MASLD mice, an effect associated with modulation of gut microbiota composition and increased fecal excretion of secondary BAs. These findings suggest the potential of GZD as a therapeutic option for lean MASLD through gutliver axis regulation.

肝降灵助汤通过调节胆汁酸代谢预防白原饮食诱导的瘦代谢功能障碍相关脂肪变性肝病
代谢功能障碍相关的脂肪变性肝病(MASLD)是一个全球性的健康问题,即使在瘦人中也是如此。中药甘姜灵珠汤(GZD)显示出治疗MASLD的潜力。本研究考察了GZD对精益MASLD的疗效,并探讨了其作用机制。方法:采用高胆固醇Paigen日粮(PD)喂养C57BL/6小鼠,建立瘦型MASLD小鼠模型。成功建模后,小鼠给予GZD(1.8、3.6或7.2 g/kg)或对照。监测体重、食物摄入量和肝脏重量。通过H&E和油红O染色评估肝脏脂肪变性和脂质积累,同时生化定量血清酶。采用16S rRNA基因测序分析肠道菌群组成,采用UPLC-TQMS检测粪便和血清胆汁酸(BA)谱。结果:12周的PD喂养诱导了瘦弱的MASLD表型,其特征是体重减轻,同时伴有肝脏脂肪变性和血脂异常。GZD剂量依赖性地改善了肝脏脂肪变性和脂质积累,最高剂量(7.2 g/kg)显示出优越的疗效。GZD通过减少致病菌和丰富参与BA代谢的分类群来恢复肠道菌群平衡,导致继发性BA的粪便排泄增加。相反,GZD治疗后血清继发性BAs水平显著降低。讨论:我们的研究强调了GZD在瘦型MASLD中有希望的作用,肠道微生物群和相关BA代谢的参与与肠道生态失调和BA稳态破坏是MASLD发病机制的核心的新证据一致,即使在瘦型个体中也是如此。然而,特定微生物变化、BA池组成和肝脏预后之间的机制联系仍有待阐明。结论:GZD改善了瘦型MASLD小鼠的肝脏脂肪变性,其作用与调节肠道菌群组成和增加继发性BAs的粪便排泄有关。这些研究结果表明,GZD通过调节肝脏轴,有可能成为精益MASLD的治疗选择。
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来源期刊
CiteScore
3.10
自引率
5.60%
发文量
327
审稿时长
7.5 months
期刊介绍: Combinatorial Chemistry & High Throughput Screening (CCHTS) publishes full length original research articles and reviews/mini-reviews dealing with various topics related to chemical biology (High Throughput Screening, Combinatorial Chemistry, Chemoinformatics, Laboratory Automation and Compound management) in advancing drug discovery research. Original research articles and reviews in the following areas are of special interest to the readers of this journal: Target identification and validation Assay design, development, miniaturization and comparison High throughput/high content/in silico screening and associated technologies Label-free detection technologies and applications Stem cell technologies Biomarkers ADMET/PK/PD methodologies and screening Probe discovery and development, hit to lead optimization Combinatorial chemistry (e.g. small molecules, peptide, nucleic acid or phage display libraries) Chemical library design and chemical diversity Chemo/bio-informatics, data mining Compound management Pharmacognosy Natural Products Research (Chemistry, Biology and Pharmacology of Natural Products) Natural Product Analytical Studies Bipharmaceutical studies of Natural products Drug repurposing Data management and statistical analysis Laboratory automation, robotics, microfluidics, signal detection technologies Current & Future Institutional Research Profile Technology transfer, legal and licensing issues Patents.
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