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胰岛素和收缩对正常及链脲佐菌素处理大鼠灌注膈肌葡萄糖代谢的影响。

The influence of insulin and of contraction on glucose metabolism in the perfused diaphragm muscle from normal and streptozotocin-treated rats.

作者信息

Beloff-Chain A, Chain E B, Rookledge K A

出版信息

Biochem J. 1971 Nov;125(1):97-103. doi: 10.1042/bj1250097.

Abstract
  1. The metabolism of [U-(14)C]glucose in perfused resting and contracting diaphragm muscle from normal rats and rats made diabetic with streptozotocin was studied in the presence and absence of insulin. 2. The incorporation of [U-(14)C]-glucose into glycogen and oligosaccharides was stimulated by insulin under all experimental conditions studied. 3. In the normal perfused resting diaphragm muscle the incorporation of radioactivity from [(14)C]glucose into lactate and CO(2) was not affected by insulin. 4. Periodic contractions, induced by electrical stimulation of the perfused diaphragm muscle in the absence of insulin, caused an increased incorporation of (14)C into glycogen and hexose phosphate esters, whereas incorporation of (14)C into lactate was greatly decreased. Production of (14)CO(2) in the contracting muscle was not significantly different from that in resting muscle. Addition of insulin to the perfusion liquid caused a further increase in formation of [(14)C]-glycogen in contracting muscle to values reached in the resting muscle in the presence of insulin. Formation of [(14)C]lactate was also stimulated by insulin, to values close to those found in the resting muscle in the presence of insulin. 5. In the diabetic resting muscle the rate of glucose metabolism was very low in the absence of insulin. Insulin increased formation of [(14)C]glycogen to the value found in normal muscle in the absence of insulin. Production of (14)CO(2) and formation of [(14)C]hexose phosphate remained unchanged. 6. In the diabetic contracting muscle production of (14)CO(2) was increased to values approaching those found in normal contracting muscle. Formation of [(14)C]lactate and [(14)C]glycogen was also increased by contraction, to normal values. Only traces of [(14)C]hexose phosphate were detectable. Addition of insulin to the perfusion medium stimulated formation of [(14)C]glycogen, to values found in normal contracting muscle. Production of [(14)C]hexose phosphate was stimulated by insulin, to approximately the values found in the normal contracting muscle. Production of (14)CO(2) and [(14)C]lactate, however, was not significantly affected by insulin. 7. These results indicate that the defects of glucose metabolism observed in perfused resting diabetic diaphragm muscle can be partially corrected by contraction, and in the presence of insulin the contracting diabetic muscle has a completely normal pattern of glycogen synthesis and lactate production, but CO(2) production remains impaired.
摘要
  1. 在有胰岛素和无胰岛素的情况下,研究了正常大鼠以及用链脲佐菌素诱导糖尿病大鼠的灌注静止和收缩膈肌中[U-(14)C]葡萄糖的代谢情况。2. 在所有研究的实验条件下,胰岛素均刺激[U-(14)C]葡萄糖掺入糖原和寡糖。3. 在正常灌注的静止膈肌中,[(14)C]葡萄糖的放射性掺入乳酸和CO(2)不受胰岛素影响。4. 在无胰岛素的情况下,通过电刺激灌注的膈肌诱导周期性收缩,导致(14)C掺入糖原和己糖磷酸酯增加,而(14)C掺入乳酸则大大减少。收缩肌中(14)CO(2)的产生与静止肌中无显著差异。向灌注液中添加胰岛素导致收缩肌中[(14)C]糖原的形成进一步增加,达到有胰岛素时静止肌中的水平。[(14)C]乳酸的形成也受到胰岛素刺激,接近有胰岛素时静止肌中的水平。5. 在糖尿病静止肌中,无胰岛素时葡萄糖代谢率非常低。胰岛素将[(14)C]糖原的形成增加到无胰岛素时正常肌中的水平。(14)CO(2)的产生和[(14)C]己糖磷酸的形成保持不变。6. 在糖尿病收缩肌中,(14)CO(2)的产生增加到接近正常收缩肌中的水平。收缩也使[(14)C]乳酸和[(14)C]糖原的形成增加到正常水平。仅可检测到微量的[(14)C]己糖磷酸。向灌注介质中添加胰岛素刺激[(14)C]糖原的形成,达到正常收缩肌中的水平。[(14)C]己糖磷酸的产生受到胰岛素刺激,达到正常收缩肌中大致的水平。然而,(14)CO(2)和[(14)C]乳酸的产生不受胰岛素显著影响。7. 这些结果表明,灌注的糖尿病静止膈肌中观察到的葡萄糖代谢缺陷可通过收缩部分纠正,并且在有胰岛素存在时,收缩的糖尿病肌具有完全正常的糖原合成和乳酸产生模式,但CO(2)产生仍受损。

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