首页> 外文期刊>Molecular genetics and metabolism >Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation.
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Influence of dietary fatty acid chain-length on metabolic tolerance in mouse models of inherited defects in mitochondrial fatty acid beta-oxidation.

机译:在线粒体脂肪酸β-氧化遗传缺陷的小鼠模型中,饮食脂肪酸链长对代谢耐受性的影响。

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Fasting-induced metabolic disease of all inherited deficiencies of the acyl-CoA dehydrogenases is characterized by hypoglycemia, hypoketonemia, and organic aciduria. Mice with these enzyme deficiencies are cold intolerant. To evaluate the potential role that dietary fatty acid chain-length has on a patient's ability to compensate during a metabolic challenge, we fed long-chain acyl CoA dehydrogenase (LCAD) deficient and short-chain acyl CoA dehydrogenase (SCAD) deficient mice a diet rich in medium-chain triglycerides (MCT) or long-chain triglycerides (LCT). To elucidate the importance of maintaining adequate serum glucose concentrations on compensation mechanisms during metabolic challenge, we treated LCAD-/- mice with a solution of 12.5% glucose or saline prior to fasting and a cold-challenge. We found that feeding SCAD deficient mice the LCT diet from weaning increased survival from 40 to 94% during metabolic challenge of cold tolerance. In contrast, there was no benefit to feeding the MCT diet at weaning to LCAD-/- mice; however, there was significant benefit when LCAD-/- mice were fed the MCT diet from the beginning of gestation. Survival during cold-challenge increased from 50 to 93%. In the LCAD-/- mice treated with glucose, despite maintaining serum glucose concentrations at normal or higher concentrations, the LCAD-/- mice were still unable to compensate during metabolic challenge. These results indicate the important influences dietary fatty acids may have by providing enhanced metabolic tolerance in patients with inborn errors of fatty acid oxidation. Furthermore, these studies demonstrate that there may be crucial variables involved in the treatment of these patients, including the patient's specific enzyme deficiency, the quantity and chain-length of dietary fat, which may provide positive effects, as well as the time in development when it was administered.
机译:空腹诱发的酰基辅酶A脱氢酶所有遗传缺陷的代谢性疾病的特点是低血糖,低血钾和有机酸尿。具有这些酶缺陷的小鼠不耐寒冷。为了评估膳食脂肪酸链长对患者在代谢挑战中的补偿能力的潜在作用,我们以长链酰基辅酶A脱氢酶(LCAD)不足和短链酰基辅酶A脱氢酶(SCAD)不足的小鼠为食富含中链甘油三酸酯(MCT)或长链甘油三酸酯(LCT)。为了阐明在代谢激发过程中在补偿机制中维持足够的血清葡萄糖浓度的重要性,我们在禁食和冷攻击之前用12.5%的葡萄糖或盐水溶液处理了LCAD-/-小鼠。我们发现,喂养SCAD缺陷的小鼠断奶的LCT饮食在耐寒性的代谢挑战期间将生存率从40%提高到94%。相反,断奶时给LCAD-/-小鼠饲喂MCT饮食没有任何好处。但是,从怀孕开始就给LCAD-/-小鼠饲喂MCT饮食具有明显的好处。寒冷挑战中的生存时间从50%增加至93%。在用葡萄糖治疗的LCAD-/-小鼠中,尽管将血清葡萄糖浓度维持在正常或更高的水平,但LCAD-/-小鼠在代谢激发过程中仍然无法补偿。这些结果表明,通过增加先天脂肪酸氧化错误的患者的代谢耐受性,饮食中的脂肪酸可能具有重要影响。此外,这些研究表明,对这些患者的治疗可能涉及一些关键变量,包括患者特定的酶缺乏症,饮食脂肪的数量和链长,这可能会产生积极影响,以及发育的时间。它被管理。

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