McNamara J P
Department of Animal Sciences and Nutrition Program, Washington State University, Pullman 99164-6320.
J Nutr. 1994 Aug;124(8 Suppl):1383S-1391S. doi: 10.1093/jn/124.suppl_8.1383S.
The flux of energy-yielding compounds through the pathways of lipogenesis, esterification into triglycerides and lipolysis in adipose tissue plays a pivotal role in supplying the demands of lactation and maternal health. The critical importance of these pathways is demonstrated by the number of highly coordinated and redundant metabolic control elements that regulate the enzyme activity in these pathways, including protein and several steroid hormones, catecholamines, and blood concentrations of several nutrients. Control on these pathways is exerted by all of these elements during lactation. Insights have been gained recently into the adaptations of these pathway reactions due to genetic propensity for milk production, stage of lactation, and intake of energy-yielding components such as starch, cellulose and triglycerides. The rates of these pathways vary exponentially with the intakes of key substrates and demands for milk precursors. The parameters of equations describing these pathways are not constant, but vary with genotype and with prolonged changes in nutritional and environmental conditions. Two major regulatory systems are critical to alterations of carbon flux during the entire lactational period. One is the interaction of growth hormone and insulin to control lipogenesis; the other is the counter-regulation by norepinephrine and insulin on cyclic AMP-initiated enzyme phosphorylation to regulate lipolysis. Examples of specific control points having a critical impact on lactational success and that are associated with genetic selection for milk production are the activities of acetyl-CoA carboxylase and hormone sensitive lipase. Further insights into the mechanisms of these adaptations will help us to improve the efficiency of metabolic flux during lactation.(ABSTRACT TRUNCATED AT 250 WORDS)
产能化合物通过脂肪生成、酯化形成甘油三酯以及脂肪组织中的脂肪分解途径所产生的通量,在满足泌乳需求和母体健康方面起着关键作用。这些途径的至关重要性体现在众多高度协调且冗余的代谢控制元件上,这些元件调节着这些途径中的酶活性,包括蛋白质、几种类固醇激素、儿茶酚胺以及几种营养素的血浓度。在泌乳期间,所有这些元件都会对这些途径施加控制。最近,人们对这些途径反应因产奶的遗传倾向、泌乳阶段以及淀粉、纤维素和甘油三酯等产能成分的摄入而产生的适应性有了深入了解。这些途径的速率会随着关键底物的摄入量和对乳汁前体的需求呈指数变化。描述这些途径的方程参数并非恒定不变,而是会随基因型以及营养和环境条件的长期变化而变化。在整个泌乳期,有两个主要调节系统对碳通量的改变至关重要。一个是生长激素和胰岛素相互作用以控制脂肪生成;另一个是去甲肾上腺素和胰岛素对环磷酸腺苷引发的酶磷酸化进行反调节以控制脂肪分解。对泌乳成功具有关键影响且与产奶遗传选择相关的特定控制点的例子包括乙酰辅酶A羧化酶和激素敏感性脂肪酶的活性。对这些适应性机制的进一步深入了解将有助于我们提高泌乳期间代谢通量的效率。(摘要截断于250字)