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首页> 外文期刊>The biochemical journal >Regulation of lactating-rat mammary-gland lipogenesis by insulin and glucagon in vivo. The role and site of action of insulin in the transition to the starved state
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Regulation of lactating-rat mammary-gland lipogenesis by insulin and glucagon in vivo. The role and site of action of insulin in the transition to the starved state

机译:在体内通过胰岛素和胰高血糖素对泌乳大鼠乳腺脂肪生成的调节。胰岛素在饥饿状态下的作用和作用部位

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pStarvation for 6h and 24h caused an 80% and 95% decrease in the rate of mammary-gland lipogenesis respectively in conscious lactating rats. 2. Plasma insulin concentrations decreased and circulating ketone-body concentrations increased with the length of starvation. 3. The inhibition of lipogenesis after 24h starvation was accompanied by increased concentrations of glucose, glucose 6-phosphate and citrate in the mammary gland. Qualitatively similar changes were observed after 6h starvation. 4. Infusion of insulin at physiological concentrations caused a 100% increase in the rate of lipogenesis in fed animals and partially reversed the inhibition of lipogenesis caused by starvation. 5. Infusion of insulin tended to reverse the changes seen in intracellular metabolite concentrations. 4. Infusion of glucagon into fed rats caused no change in the rates of lipogenesis in mammary gland, liver or white adipose tissue. 7. It is concluded that (a) insulin acts physiologically to regulate lipogenesis in the mammary gland, (b) hexokinase and phosphofructokinase are important regulatory enzymes in the short-term control of lipogenesis in the mammary gland, which are under the influence of insulin, and (c) the unresponsiveness of mammary-gland lipogenesis iin vivo/i to infusions of glucagon is consistent with an adaptive mechanism which diverts substrate towards the lactating mammary gland and away from other tissues./p
机译:饥饿6h和24h导致清醒的泌乳大鼠乳腺脂肪生成率分别降低80%和95%。 2.随着饥饿时间的延长,血浆胰岛素浓度降低,循环酮体浓度升高。 3.饥饿24小时后脂肪形成的抑制伴随着乳腺中葡萄糖,6-磷酸葡萄糖和柠檬酸盐浓度的增加。饥饿6小时后观察到定性相似的变化。 4.以生理浓度输注胰岛素可使饲喂动物的脂肪生成速率增加100%,并且部分逆转了饥饿引起的脂肪生成的抑制作用。 5.输注胰岛素倾向于逆转细胞内代谢物浓度的变化。 4.将胰高血糖素注入喂养的大鼠中不会引起乳腺,肝脏或白色脂肪组织中脂肪生成速率的变化。 7.结论是:(a)胰岛素在乳腺中以生理方式调节脂肪生成,(b)己糖激酶和磷酸果糖激酶是短期控制乳腺中脂肪生成的重要调节酶,它们受胰岛素的影响。 ,以及(c)体内乳腺脂肪生成对胰高血糖素输注的无反应性与一种适应性机制相一致,该机制可将底物转移到泌乳的乳腺并远离其他组织。

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