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谷蛋白通过影响饮食诱导肥胖载脂蛋白 E 缺陷小鼠的脂肪生成和脂肪酸氧化而使非酒精性脂肪性肝病恶化。

Gluten worsens non-alcoholic fatty liver disease by affecting lipogenesis and fatty acid oxidation in diet-induced obese apolipoprotein E-deficient mice.

机构信息

Department of Biochemistry and Immunology, ICB - Federal University of Minas Gerais, Caixa Postal 486, Belo Horizonte, 30161-970, Brazil.

Precision Immunology Institute at the Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

Mol Cell Biochem. 2024 Jun;479(6):1335-1347. doi: 10.1007/s11010-023-04802-3. Epub 2023 Jul 4.

DOI:10.1007/s11010-023-04802-3
PMID:37402020
Abstract

Obesity is closely associated with non-alcoholic fatty liver disease (NAFLD), characterized by hepatic fat accumulation and hepatocyte injury. Preclinical studies have shown exacerbated weight gain associated with an obesogenic gluten-containing diet. However, whether gluten affects obesity-induced hepatic lipid accumulation still remains unclear. We hypothesized that gluten intake could affect fatty liver development in high-fat diet (HFD)-induced obese mice. Thus, we aimed to investigate the impact of gluten intake on NAFLD in HFD-induced obese mice. Male apolipoprotein E-deficient (Apoe-/-) mice were fed with a HFD containing (GD) or not (GFD) vital wheat gluten (4.5%) for 10 weeks. Blood and liver were collected for further analysis. We found that gluten exacerbated weight gain, hepatic fat deposition, and hyperglycemia without affecting the serum lipid profile. Livers of the GD group showed a larger area of fibrosis, associated with the expression of collagen and MMP9, and higher expression of apoptosis-related factors, p53, p21, and caspase-3. The expression of lipogenic factors, such as PPARγ and Acc1, was more elevated and factors related to beta-oxidation, such as PPARα and Cpt1, were lower in the GD group compared to the GFD. Further, gluten intake induced a more significant expression of Cd36, suggesting higher uptake of free fatty acids. Finally, we found lower protein expression of PGC1α followed by lower activation of AMPK. Our data show that gluten-containing high-fat diet exacerbated NAFLD by affecting lipogenesis and fatty acid oxidation in obese Apoe-/- mice through a mechanism involving lower activation of AMPK.

摘要

肥胖与非酒精性脂肪性肝病(NAFLD)密切相关,其特征为肝内脂肪堆积和肝细胞损伤。临床前研究表明,富含麸质的致肥胖饮食可导致体重明显增加。然而,麸质是否影响肥胖引起的肝脂质蓄积仍不清楚。我们假设麸质的摄入可能会影响高脂肪饮食(HFD)诱导肥胖小鼠的脂肪肝发展。因此,我们旨在研究麸质的摄入对 HFD 诱导肥胖小鼠非酒精性脂肪性肝病的影响。雄性载脂蛋白 E 基因缺陷(Apoe-/-)小鼠喂食含有(GD)或不含有(GFD)生命小麦麸质(4.5%)的 HFD 10 周。收集血液和肝脏进行进一步分析。我们发现,麸质加重了体重增加、肝脂肪沉积和高血糖,而对血清脂质谱没有影响。GD 组的肝脏显示出更大的纤维化面积,与胶原蛋白和 MMP9 的表达以及凋亡相关因子 p53、p21 和 caspase-3 的表达增加有关。与脂肪生成相关的因子,如 PPARγ 和 Acc1,在 GD 组中的表达更高,而与β氧化相关的因子,如 PPARα 和 Cpt1,在 GD 组中的表达更低。此外,麸质的摄入诱导 Cd36 的表达更显著,表明游离脂肪酸的摄取增加。最后,我们发现 PGC1α 的蛋白表达降低,随后 AMPK 的激活降低。我们的数据表明,富含麸质的高脂肪饮食通过降低 AMPK 的激活,影响肥胖 Apoe-/-小鼠的脂肪生成和脂肪酸氧化,从而加重非酒精性脂肪性肝病。

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Rev Cardiovasc Med. 2021 Sep 24;22(3):755-768. doi: 10.31083/j.rcm2203082.
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Gluten-degrading bacteria: availability and applications.降解麸质的细菌:可用性与应用
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