高脂饮食诱导肥胖抵抗大鼠MASLD和脂肪组织改变。

IF 2.5 Q3 CELL BIOLOGY
Amanda Rangel Madureira, Vinicius Valois Pereira Martins, Janete Corrêa Cardoso, Suellem Torezani-Sales, Kiany de Oliveira Miranda, Breno Souza Salgado, Lidianne Narducci Monteiro, Breno Valentim Nogueira, André Soares Leopoldo, Ana Paula Lima-Leopoldo
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引用次数: 0

摘要

背景/目的:肥胖抵抗(Obesity Resistance, OR)的特征是尽管有致肥性饮食,但体重增加有限,脂肪积累减少。然而,代谢风险,特别是代谢功能障碍相关的脂肪变性肝病(MASLD),仍不清楚。本研究旨在探讨高脂饮食(HFD)喂养的肥胖抵抗(OR) R大鼠中MASLD的存在,以及脂肪组织的代谢参数和形态学方面的变化。方法:雄性Wistar大鼠71只,随机分为标准饲粮组(SD, n=35)和高脂饲粮组(HFD, n=36)。该方案进行了14周,包括4周的诱导和10周的肥胖暴露。随后,应用分类学标准,将实验动物重新分为3组:a)对照组(C, n=12),饲喂标准日粮;b)易肥胖(OP, n=12);c) OR (n=12)。评估体重演变、肥胖、营养行为、代谢标志物和肝脏形态,以及MASLD的分期。结果:与OP相比,OR大鼠表现出较低的体重、总脂肪量和瘦素,但高于c。50%的OR动物观察到MASLD, 37.5%的OR动物进展为代谢功能障碍相关脂肪性肝炎(MASH)。OP大鼠的MASH发生率较高(87.5%)。结论:慢性HFD暴露导致OR大鼠的代谢变化和MASLD的发展,包括MASH,表明OR对HFD诱导的肝脏改变没有保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High-Fat Diet Induces MASLD and Adipose Tissue Changes in Obesity-Resistant Rats.

Background/aims: Obesity Resistance (OR) is characterized by limited weight gain and reduced fat accumulation despite an obesogenic diet. However, the metabolic risk, particularly regarding Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD), remains unclear. The current study aims to investigate the presence of MASLD, as well as metabolic parameters and morphological aspects of adipose tissues in obesity-resistant (OR) R rats fed a high-fat diet (HFD).

Methods: ale Wistar rats (n=71) were initially randomized into two groups: a) standard diet (SD, n=35) and b) high-fat diet (HFD, n=36). The protocol was performed for 14 weeks, including 4 weeks of induction and 10 weeks of exposure to obesity. Subsequently, after applying the tertile classification criterion, the animals were redistributed into three groups: a) control (C, n=12), fed a standard diet; b) obesity-prone (OP, n=12); and c) OR (n=12). Body weight evolution, adiposity, nutritional behavior, metabolic markers, and liver morphology were assessed, along with the staging of MASLD.

Results: OR rats exhibited lower body weight, total fat pads, and leptin compared to OP but higher values than C. MASLD was observed in 50% of OR animals, while 37.5% progressed to metabolic dysfunction-associated steatohepatitis (MASH). OP rats had a higher incidence of MASH (87.5%).

Conclusion: Chronic HFD exposure in OR rats lead to metabolic changes and MASLD development, including MASH, demonstrating that OR does not protect against HFD-induced hepatic alterations.

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来源期刊
CiteScore
5.80
自引率
0.00%
发文量
86
审稿时长
1 months
期刊介绍: Cellular Physiology and Biochemistry is a multidisciplinary scientific forum dedicated to advancing the frontiers of basic cellular research. It addresses scientists from both the physiological and biochemical disciplines as well as related fields such as genetics, molecular biology, pathophysiology, pathobiochemistry and cellular toxicology & pharmacology. Original papers and reviews on the mechanisms of intracellular transmission, cellular metabolism, cell growth, differentiation and death, ion channels and carriers, and the maintenance, regulation and disturbances of cell volume are presented. Appearing monthly under peer review, Cellular Physiology and Biochemistry takes an active role in the concerted international effort to unravel the mechanisms of cellular function.
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