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兔肝中的胆固醇动态:高脂肪饮食、橄榄油和协同的饮食效应。

Cholesterol dynamics in rabbit liver: High-fat diet, olive oil, and synergistic dietary effects.

机构信息

Laboratorio de Biología Molecular del Metabolismo & Nutrición (MeNu). IHEM, Universidad Nacional de Cuyo, CONICET, Mendoza, Argentina; Laboratorio de Investigaciones Andrológicas de Mendoza (LIAM). IHEM, Universidad Nacional de Cuyo, CONICET, Mendoza, Argentina; Laboratorio de Enfermedades Metabólicas (LEM), Universidad Juan Agustín Maza, Mendoza, Argentina.

Laboratorio de Enfermedades Metabólicas (LEM), Universidad Juan Agustín Maza, Mendoza, Argentina.

出版信息

Biochem Biophys Res Commun. 2024 Nov 12;733:150675. doi: 10.1016/j.bbrc.2024.150675. Epub 2024 Sep 12.

Abstract

BACKGROUND & AIMS: Lipid metabolism disorders contribute to a range of human diseases, including liver-related pathologies. Rabbits, highly sensitive to dietary cholesterol, provide a model for understanding the development of liver disorders. Sterol regulatory element-binding protein isoform 2 (SREBP2) crucially regulates intracellular cholesterol pathways. Extra-virgin olive oil (EVOO) has shown reducing cholesterol levels and restoring liver parameters affected by HFD. The aim was to investigate the molecular impact of an HFD and supplemented with EVOO on rabbit liver cholesterol metabolism.

APPROACH & RESULTS: Male rabbits were assigned to dietary cohorts, including control, acute/chronic HFD, sequential HFD with EVOO, and EVOO. Parameters such as serum lipid profiles, hepatic enzymes, body weight, and molecular analyses. After 6 months of HFD, plasma and hepatic cholesterol increased with decreased SREBP2 and 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase (HMGCR) expression. Prolonged HFD increased cholesterol levels, upregulating SREBP2 mRNA and HMGCR protein. Combining this with EVOO lowered cholesterol, increased SREBP2 mRNA, and upregulated low-density lipoprotein receptor (LDLR) expression. HFD-induced metabolic dysfunction-associated fatty liver disease was mitigated by EVOO. In conclusion, the SREBP2 system responds to dietary changes.

CONCLUSIONS

In rabbits, the SREBP2 system responds to dietary changes. Acute HFD hinders cholesterol synthesis, while prolonged HFD disrupts regulation, causing SREBP2 upregulation. EVOO intake prompts LDLR upregulation, potentially enhancing cholesterol clearance and restoring hepatic alterations.

摘要

背景与目的

脂质代谢紊乱与多种人类疾病有关,包括肝脏相关疾病。兔子对饮食胆固醇高度敏感,为理解肝脏疾病的发展提供了模型。固醇调节元件结合蛋白 2 异构体(SREBP2)对细胞内胆固醇途径的调节至关重要。特级初榨橄榄油(EVOO)已被证明可降低胆固醇水平并恢复 HFD 影响的肝脏参数。本研究旨在研究 HFD 及其补充 EVOO 对兔肝脏胆固醇代谢的分子影响。

方法和结果

雄性兔子被分配到不同的饮食组,包括对照组、急性/慢性 HFD 组、HFD 序贯补充 EVOO 组和 EVOO 组。评估了血清脂质谱、肝酶、体重和分子分析等参数。在 HFD 喂养 6 个月后,血浆和肝脏胆固醇增加,SREBP2 和 3-羟基-3-甲基戊二酰基辅酶 A 还原酶(HMGCR)表达降低。长期 HFD 增加胆固醇水平,上调 SREBP2 mRNA 和 HMGCR 蛋白。与此相结合,补充 EVOO 可降低胆固醇,增加 SREBP2 mRNA,并上调低密度脂蛋白受体(LDLR)表达。EVOO 减轻了 HFD 诱导的代谢功能障碍相关脂肪性肝病。结论:SREBP2 系统对饮食变化做出反应。急性 HFD 阻碍胆固醇合成,而长期 HFD 破坏调节,导致 SREBP2 上调。EVOO 摄入促使 LDLR 上调,可能增强胆固醇清除并恢复肝脏改变。

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