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饥饿对小鼠胰岛胰岛素分泌和葡萄糖代谢的影响。

The effect of starvation on insulin secretion and glucose metabolism in mouse pancreatic islets.

作者信息

Hedeskov C J, Capito K

出版信息

Biochem J. 1974 Jun;140(3):423-33. doi: 10.1042/bj1400423.

Abstract
  1. Rates of insulin secretion, glucose utilization, lactate output, incorporation of glucose into glycogen, contents of glucose 6-phosphate, fructose 1,6-diphosphate and ATP, and maximally extractable enzyme activities of hexokinase, high-K(m) glucose-phosphorylating activity (;glucokinase'), glucose 6-phosphatase and unspecific acid phosphatase were measured in isolated pancreatic islets from fed and 48-h-starved mice. 2. In the fed state insulin secretion from isolated islets was increased five- to six-fold when the extracellular glucose concentration was raised from 2.5mm to 16.7mm; 5mm-caffeine potentiated this effect. The secretory response to glucose of islets from mice starved for 48h was diminished at all glucose concentrations from 2.5mm up to approx. 40mm. Very high glucose concentrations (60mm and above) restored the secretory response to that found in the fed state, suggesting that the K(m) value for the overall secretory process had been increased (approx. fourfold) by starvation. Addition of 5mm-caffeine to islets from starved mice also restored the insulin secretory response to 2.5-16.7mm-glucose to normal values. 3. Extractable hexokinase, ;glucokinase', glucose 6-phosphatase and unspecific phosphatase activities were not changed by starvation. 4. Glucose utilization and glycolysis (measured as the rate of formation of (3)H(2)O from [5-(3)H]glucose over a 2h period) was decreased in islets from starved mice at all glucose concentrations up to approx. 55mm. At still higher glucose concentrations up to approx. 100mm, there was no difference between the fed and starved state, suggesting that the K(m) value for the rate-limiting glucose phosphorylation had been increased (approx. twofold) by starvation. Preparation of islets omitting substrates (glucose, pyruvate, fumarate and glutamate) from the medium during collagenase treatment lowered the glucose utilization measured subsequently at 16.7mm-glucose by 38 and 30% in islets from fed and starved mice respectively. Also the 2h lactate output by the islets at 16.7mm extracellular glucose was diminished by starvation. Incorporation of glucose into glycogen was extremely low, but the rate of incorporation was more than doubled by starvation. 5. After incubation for 30min at 16.7mm-glucose the content of glucose 6-phosphate was unchanged by starvation, that of ATP was increased and the concentration of (fructose 1,6-diphosphate plus triose phosphates) was decreased. 6. Possible mechanisms behind the correlated impairment in insulin secretion and islet glucose metabolism during starvation are discussed.
摘要
  1. 测定了喂食小鼠和饥饿48小时小鼠分离胰岛中的胰岛素分泌速率、葡萄糖利用率、乳酸输出量、葡萄糖合成糖原的掺入量、6-磷酸葡萄糖、1,6-二磷酸果糖和ATP的含量,以及己糖激酶、高K(m)葡萄糖磷酸化活性(“葡萄糖激酶”)、6-磷酸葡萄糖酶和非特异性酸性磷酸酶的最大可提取酶活性。2. 在喂食状态下,当细胞外葡萄糖浓度从2.5mmol/L升高到16.7mmol/L时,分离胰岛的胰岛素分泌增加了五到六倍;5mmol/L咖啡因增强了这种作用。在2.5mmol/L至约40mmol/L的所有葡萄糖浓度下,饥饿48小时小鼠胰岛对葡萄糖的分泌反应均减弱。非常高的葡萄糖浓度(60mmol/L及以上)使分泌反应恢复到喂食状态下的水平,表明饥饿使整个分泌过程的K(m)值增加(约四倍)。向饥饿小鼠的胰岛中添加5mmol/L咖啡因也使对2.5 - 16.7mmol/L葡萄糖的胰岛素分泌反应恢复到正常水平。3. 可提取的己糖激酶、“葡萄糖激酶”、6-磷酸葡萄糖酶和非特异性磷酸酶活性不受饥饿影响。4. 在高达约55mmol/L的所有葡萄糖浓度下,饥饿小鼠胰岛中的葡萄糖利用率和糖酵解(以2小时内[5-(3)H]葡萄糖生成(3)H(2)O的速率衡量)均降低。在高达约100mmol/L的更高葡萄糖浓度下,喂食和饥饿状态之间没有差异,表明饥饿使限速葡萄糖磷酸化的K(m)值增加(约两倍)。在胶原酶处理期间从培养基中省略底物(葡萄糖、丙酮酸、富马酸和谷氨酸)来制备胰岛,随后在16.7mmol/L葡萄糖下测定的喂食和饥饿小鼠胰岛的葡萄糖利用率分别降低了38%和30%。同样,在细胞外葡萄糖浓度为16.7mmol/L时,胰岛2小时的乳酸输出量因饥饿而减少。葡萄糖合成糖原的掺入量极低,但饥饿使掺入速率增加了一倍多。5. 在16.7mmol/L葡萄糖下孵育30分钟后,饥饿对6-磷酸葡萄糖的含量没有影响,ATP含量增加,(1,6-二磷酸果糖加磷酸丙糖)的浓度降低。6. 讨论了饥饿期间胰岛素分泌和胰岛葡萄糖代谢相关损伤背后的可能机制。

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