Department of Anatomy & Embryology, Maastricht University, Maastricht, The Netherlands; School for Nutrition, Toxicology and Metabolism (NUTRIM), Maastricht University, Maastricht, The Netherlands.
Department of Anatomy & Embryology, Maastricht University, Maastricht, The Netherlands; School for Nutrition, Toxicology and Metabolism (NUTRIM), Maastricht University, Maastricht, The Netherlands.
Clin Nutr. 2017 Feb;36(1):229-237. doi: 10.1016/j.clnu.2015.11.005. Epub 2015 Dec 8.
BACKGROUND & AIMS: Non-alcoholic fatty-liver disease (NAFLD) is the hepatic manifestation of the metabolic syndrome. Previously, we showed that a high-protein diet minimized diet-induced development of fatty liver and even reversed pre-existing steatosis. A high-protein diet leads to amino-acid catabolism, which in turn causes anaplerosis of the tricarboxylic-acid (TCA) cycle. Therefore, we hypothesized that anaplerosis of the TCA cycle could be responsible for the high-protein diet-induced improvement of NAFLD by channeling amino acids into the TCA cycle. Next we considered that an efficient anaplerotic agent, the odd-carbon medium-chain triglyceride triheptanoin (TH), might have similar beneficial effects.
C57BL/6J mice were fed low-fat (8en%) or high-fat (42en%) oleate-containing diets with or without 15en% TH for 3 weeks.
TH treatment enhanced the hepatic capacity for fatty-acid oxidation by a selective increase in hepatic Ppara, Acox, and Cd36 expression, and a decline in plasma acetyl-carnitines. It also induced pyruvate cycling through an increased hepatic PCK1 protein concentration and it increased thermogenesis reflected by an increased Ucp2 mRNA content. TH, however, did not reduce hepatic lipid content.
The comparison of the present effects of dietary triheptanoin with a previous study by our group on protein supplementation shows that the beneficial effects of the high-protein diet are not mimicked by TH. This argues against anaplerosis as the sole explanatory mechanism for the anti-steatotic effect of a high-protein diet.
非酒精性脂肪性肝病(NAFLD)是代谢综合征的肝脏表现。此前,我们发现高蛋白饮食可最大程度地减少饮食诱导的脂肪肝发生,甚至逆转已存在的脂肪变性。高蛋白饮食会导致氨基酸分解代谢,进而导致三羧酸(TCA)循环的氨酰化。因此,我们假设 TCA 循环的氨酰化可以通过将氨基酸导入 TCA 循环来解释高蛋白饮食改善 NAFLD 的原因。接下来,我们考虑到一种有效的氨酰化剂,奇数碳中链甘油三酯三庚酸酯(TH)可能具有类似的有益效果。
用含或不含 15%TH 的低脂肪(8en%)或高脂肪(42en%)油酸盐饮食喂养 C57BL/6J 小鼠 3 周。
TH 治疗通过选择性增加肝 Ppara、Acox 和 Cd36 的表达以及降低血浆乙酰肉碱水平,增强了脂肪酸氧化的肝脏能力。它还通过增加肝 PCK1 蛋白浓度诱导丙酮酸循环,并通过增加 Ucp2 mRNA 含量增加产热。然而,TH 并未减少肝内脂质含量。
与我们之前关于蛋白质补充的研究相比,目前饮食中 TH 的影响表明,高蛋白饮食的有益效果不能被 TH 模拟。这表明氨酰化不是高蛋白饮食抗脂肪变性作用的唯一解释机制。