首页> 外文期刊>American Journal of Physiology >Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profile
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Parenteral and enteral metabolism of anaplerotic triheptanoin in normal rats. II. Effects on lipolysis, glucose production, and liver acyl-CoA profile

机译:正常大鼠Anplerotic三肽肠道肠外和肠内代谢。 II。 对脂解,葡萄糖生产和肝酰基 - COA型谱的影响

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摘要

The anaplerotic odd-medium-chain triglyceride triheptanoin is used in clinical trials for the chronic dietary treatment of patients with long-chain fatty acid oxidation disorders. We previously showed (Kinman RP, Kasumov T, Jobbins KA, Thomas KR, Adams JE, Brunengraber LN, Kutz G, Brewer WU, Roe CR, Brunengraber H. Am J Physiol Endocrinol Metab 291: E860-E866, 2006) that the intravenous infusion of triheptanoin increases lipolysis traced by the turnover of glycerol. In this study, we tested whether lipolysis induced by triheptanoin infusion is accompanied by the potentially harmful release of long-chain fatty acids. Rats were infused with heptanoate ± glycerol or triheptanoin. Intravenous infusion of triheptanoin at 40% of caloric requirement markedly increased glycerol endogenous Ra but not oleate endogenous Ra. Thus, the activation of lipolysis was balanced by fatty acid reesterification in the same cells. The liver acyl-CoA profile showed the accumulation of intermediates of heptanoate (3-oxidation and Cs-ketogenesis and a decrease in free CoA but no evidence of metabolic perturbation of liver metabolism such as propionyl overload. Our data suggest that triheptanoin, administered either intravenously or intraduodenally, could be used for intensive care and nutritional support of metabolically decompensated long-chain fatty acid oxidation disorders.
机译:Anplerotic奇介质链甘油三酯三肽用于临床试验,用于长链脂肪酸氧化疾病患者的慢性膳食治疗。我们以前展示(Kinman RP,Kasumov T,Jobbins Ka,Thomas Kr,Adams Je,Brunengraber Ln,Kutz G,Brewer Wu,Roe Cr,Brunengraber H.AM J Physocrinol Metab 291:E860-E866,291)即静脉注射intiheptanoin的输注增加了甘油的成交量追踪的脂解。在这项研究中,我们测试了三肽输注诱导的脂肪解是否伴有长链脂肪酸的潜在有害的释放。将大鼠注入庚酸盐±甘油或三肽。静脉内输注三肽在40%的热量要求中显着增加甘油内源性Ra,但不是含油内源性Ra。因此,通过在同一细胞中通过脂肪酸酸盐渗透来平衡脂肪分解的活化。肝脏酰基-CoA分布显示庚酸盐中间体(3-氧化和Cs-keetogenesis的中间体的积累,并没有减少免费的COA,但没有肝脏代谢的代谢扰动,例如丙酰基过载。我们的数据表明Triheptanoin,静脉内给药或颅内细胞,可用于代谢失代偿的长链脂肪酸氧化障碍的重症监护和营养支持。

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