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Effect of alloxan-diabetes and treatment with anti-insulin serum on pathways of glucose metabolism in lactating rat mammary gland

机译:四氧嘧啶糖尿病和抗胰岛素血清对泌乳大鼠乳腺葡萄糖代谢途径的影响

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摘要

1. The overall metabolic changes in lactating mammary gland in alloxan-diabetic and anti-insulin-serum-treated rats were assessed by measurement of the incorporation of 14C from specifically labelled glucose, pyruvate and acetate into carbon dioxide and lipid, together with measurements of enzymes concerned with the pentose phosphate pathway and with citrate metabolism. 2. Alloxan-diabetes depressed the rate of formation of 14CO2 from [1-14C]glucose and [2-14C]glucose to approx. 10% of the control rate; this was partially reversed by addition of insulin in vitro. The quotient Oxidation of [1-14C]glucose/Oxidation of [6-14C]glucose fell from a value of 17·6 in the control group to 3·9 in the diabetic group and was restored to 14·3 in the presence of insulin in vitro. In keeping with these results it was shown that glucose 6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities were significantly decreased in alloxan-diabetic rats. 3. Alloxan-diabetes depressed the decarboxylation and the oxidation of labelled pyruvate, but not the oxidation of labelled acetate. 4. The synthesis of lipid from specifically labelled glucose was greatly decreased, that from [2-14C]pyruvate was almost unchanged and that from [1-14C]acetate alone was increased in alloxandiabetic rats. However, the stimulation of lipid synthesis from acetate by glucose was small in the alloxan-diabetic rats compared with the controls. Insulin in vitro partially reversed all these effects. Both citrate-cleavage enzyme and acetate thiokinase activities were decreased in alloxan-diabetic rats. 5. Treatment of rats with anti-insulin serum depressed the formation of 14CO2 from [1-14C]glucose and [2-14C]glucose, but increased that from [6-14C]glucose. This was completely restored by the presence of insulin in vitro. The quotient Oxidation of [1-14C]glucose/Oxidation of [6-14C]glucose fell from a value of 17·6 in the control group to 3·8 in the anti-insulin-serum-treated group. There were no changes in the activity of glucose 6-phosphate dehydrogenase or 6-phosphogluconate dehydrogenase, but the hexokinase distribution changed and the content of the soluble fraction increased significantly. 6. The synthesis of lipid from specifically labelled glucose was depressed in anti-insulin-serum-treated rats; this effect was completely reversed by addition of insulin in vitro to the tissue slices.
机译:1.通过测量专门标记的葡萄糖,丙酮酸和乙酸盐中碳含量 14 的掺入,评估了四氧嘧啶糖尿病和抗胰岛素血清治疗的大鼠泌乳乳腺的总体代谢变化。二氧化碳和脂质,以及与戊糖磷酸途径和柠檬酸盐代谢有关的酶的测定。 2.四氧嘧啶糖尿病降低了由[1- 14 C]葡萄糖和[2- 14 C]葡萄糖形成 14 CO2的速率到大约控制率的10%;通过在体外添加胰岛素可以部分逆转这种情况。 [1- 14 C]葡萄糖的商氧化/ [6- 14 C]葡萄糖的商数从对照组的17·6降至3·糖尿病组为9,在胰岛素存在下可恢复至14·3。与这些结果一致,表明在四氧嘧啶糖尿病大鼠中葡萄糖6-磷酸脱氢酶和6-磷酸葡萄糖酸酯脱氢酶活性显着降低。 3.四氧嘧啶糖尿病抑制了标记的丙酮酸的脱羧和氧化,但没有抑制标记的乙酸盐的氧化。 4.特异性标记葡萄糖的脂质合成大大减少,[2- 14 C]丙酮酸盐几乎没有变化,[1- 14 C]乙酸盐几乎没有变化单独的四氧嘧啶糖尿病大鼠增加。然而,与对照相比,在四氧嘧啶糖尿病大鼠中,葡萄糖对乙酸盐的脂质合成的刺激很小。体外胰岛素可部分逆转所有这些作用。在四氧嘧啶糖尿病大鼠中,柠檬酸盐切割酶和乙酸盐硫激酶的活性均降低。 5.用抗胰岛素血清处理的大鼠抑制了[1- 14 C]葡萄糖和[2- 14 形成的 14 CO2 C]葡萄糖,但从[6- 14 C]葡萄糖增加。体外存在胰岛素可以完全恢复这种状态。 [1- 14 C]葡萄糖的商氧化/ [6- 14 C]葡萄糖的商数从对照组的17·6降至3·抗胰岛素血清治疗组为8。葡萄糖6-磷酸脱氢酶或6-磷酸葡萄糖酸酯脱氢酶的活性没有变化,但是己糖激酶分布发生了变化,可溶性部分的含量显着增加。 6.在抗胰岛素血清治疗的大鼠中,由特异性标记的葡萄糖合成脂质的过程受到抑制。通过在组织切片中体外添加胰岛素,这种作用被完全逆转。

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