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中链甘油三酯可改善阿尔茨海默病小鼠模型的认知和全身代谢。

Medium-chain triglycerides improve cognition and systemic metabolism in mouse models of Alzheimer's disease.

作者信息

M'Bra Paule E H, Hamilton Laura K, Moquin-Beaudry Gaël, Mangahas Chenicka L, Pratesi Federico, Castonguay Anne, Mailloux Sophia, Galoppin Manon, Avila Lopez Jessica, Bernier Megan, Turri Marta, Mayhue Marian, Aumont Anne, Tétreault Martine, Cunnane Stephen C, Fernandes Karl J L

机构信息

Research Center on Aging, CIUSSS de l'Estrie-CHUS, J1H 2J7, Sherbrooke, Canada.

Department of Medicine, Faculty of Medicine and Health Sciences, Université de Sherbrooke, J1H 5H3, Sherbrooke, Canada.

出版信息

Brain. 2025 Aug 6. doi: 10.1093/brain/awaf267.

Abstract

Lifestyle-based interventions, including dietary modifications, can reduce dementia risk. In this regard, dietary supplementation with medium-chain triglycerides (MCT) has shown potential therapeutic benefits in individuals with Alzheimer's disease (AD). These effects are widely presumed to be mediated by hepatic conversion of MCT into circulating ketones. However, the physiological and cellular mechanisms underlying the benefits of MCT remain understudied, particularly in the context of AD. Here, we investigated the cellular and molecular changes occurring in the brain and systemically in response to dietary supplementation with MCT versus a ketogenic diet (KD). The experimental design consisted of comparing a 70% carbohydrate control diet to either a control diet supplemented with 10% MCT or a carbohydrate-free high fat KD. Diets were tested in two AD mouse models, slow-progressing 3xTg-AD mice that model pre-symptomatic/early stages and rapidly-progressing 5xFAD mice that model late stages of the disease. We found that MCT supplementation and KD both improved hippocampal-dependent spatial learning and memory, increased dendritic spine density of hippocampal neurons, and modulated hippocampal expression of genes associated with mitochondrial functions, synaptic structure, and insulin signaling in AD mouse models. However, unlike KD, MCT supplementation did not elevate circulating ketones, suggesting different mechanisms. Indeed, MCT enhanced the peripheral insulin response of AD mice, while KD conversely unveiled their latent metabolic vulnerability, increasing their hyperglycaemia, body weight gain, and adiposity. The systemic metabolic disturbances of AD mice correlated with transcriptomic alterations in hepatic lipid metabolism and ketogenesis genes and increased lipid droplet accumulation. These liver metabolic abnormalities were partially reversed by both MCT supplementation and KD, but in distinct ways. Notably, KD selectively triggered hepatic neutral lipid depletion and prominent proinflammatory gene expression while MCT down-regulated expression of cholesterol-related genes. Collectively, these findings reveal that MCT supplementation in the context of AD improves cognition and systemic metabolism without elevating circulating ketone levels.

摘要

包括饮食调整在内的基于生活方式的干预措施可以降低痴呆症风险。在这方面,补充中链甘油三酯(MCT)已在阿尔茨海默病(AD)患者中显示出潜在的治疗益处。人们普遍认为这些作用是由肝脏将MCT转化为循环酮介导的。然而,MCT益处背后的生理和细胞机制仍未得到充分研究,尤其是在AD的背景下。在这里,我们研究了在大脑中以及全身因补充MCT与生酮饮食(KD)而发生的细胞和分子变化。实验设计包括将70%碳水化合物的对照饮食与补充10%MCT的对照饮食或无碳水化合物的高脂肪KD进行比较。在两种AD小鼠模型中测试了这些饮食,即模拟症状前/早期阶段的进展缓慢的3xTg-AD小鼠和模拟疾病晚期阶段的进展迅速的5xFAD小鼠。我们发现,在AD小鼠模型中,补充MCT和KD均改善了海马体依赖的空间学习和记忆,增加了海马神经元的树突棘密度,并调节了与线粒体功能、突触结构和胰岛素信号相关的海马基因表达。然而,与KD不同的是,补充MCT并未提高循环酮水平,这表明存在不同的机制。事实上,MCT增强了AD小鼠的外周胰岛素反应,而KD则相反地揭示了它们潜在的代谢脆弱性,增加了它们的高血糖、体重增加和肥胖。AD小鼠的全身代谢紊乱与肝脏脂质代谢和生酮基因的转录组改变以及脂滴积累增加相关。补充MCT和KD均部分逆转了这些肝脏代谢异常,但方式不同。值得注意的是,KD选择性地引发肝脏中性脂质消耗和显著的促炎基因表达,而MCT下调了胆固醇相关基因的表达。总的来说,这些发现表明,在AD背景下补充MCT可改善认知和全身代谢,而不会提高循环酮水平。

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