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禁食状态下胰高血糖素的动力学:血清3,5,3'-三碘甲状腺原氨酸的生理性升高会增加胰高血糖素的代谢清除率。

Glucagon kinetics in fasting: physiological elevations in serum 3,5,3'-triiodothyronine increase the metabolic clearance rate of glucagon.

作者信息

Burman K D, Smallridge R C, Jones L, Ramos E A, O'Brien J T, Wright F D, Wartofsky L

出版信息

J Clin Endocrinol Metab. 1980 Nov;51(5):1158-65. doi: 10.1210/jcem-51-5-1158.

Abstract

We have attempted to determine if the elevated plasma glucagon concentration and delayed MCR of glucagon (MCRg) observed during caloric restriction are related to the decreased serum T3 that also occurs during fasting. Twelve obese subjects received a 3-h iv glucagon infusion during a 4-day fed period (1000 kCal/day) and again on approximately the third fasting day. Five patients fasted without receiving exogenous T3 (control group), whereas seven subjects fasted but also received 5 micrograms T3 orally every 4 h (T3 group) to maintain approximately the same serum T3 levels in the fed and fasting periods. Glucagon production rates (GPR) were derived by multiplying the MCRg by the respective basal plasma glucogon concentrations. In the control group, the MCRg was 442 +/- 55 ml/m2 . min in the postabsorptive state and decreased to 312 +/- 49 ml/m2 . min (P < 0.025) during fasting, whereas in the T3-treated group, the postabsorptive MCRg was 304 +/- 22 ml/m2 . min and increased during fasting to 417 +/- 47 ml/m2 . min (P < 0.025). The GPRs in the control group were statistically unaltered between the fed (27.7 +/- 3.0 ng/m2 . min) and fasted (22.9 +/- 1.8 ng/m2 . min) intervals, but GPR increased from 37.9 +/- 6.1 ng/m2 . min during fasting to 49.2 +/- 9.1 ng/m2 . min when T3 was administered (5 micrograms every 4 h). The net plasma glucose increment in response to glucagon decreased from 18 mg/dl (fed) to 5 mg/dl (fast) in the control patients and from 10 mg/dl (fed) to 7 mg/dl (fast) in the T3-treated subjects. In the T3-treated patients, serum T3 averaged 124 ng/dl during both feeding and fasting, and rT3 was 55 +/- 6 ng/dl during feeding and 49 +/- 5 ng/dl during fasting. In summary, the results from this study indicate that during fasting 1) slight physiological alterations in serum T3 influence the MCRg, and 2) T3 increases the GPR and blocks the customary fasting-induced rise in rT3. Conceivably, decreased T3 is an early event in the fasting state which serves to decrease the MCRg, a process which subsequently regulates glucose homeostasis.

摘要

我们试图确定在热量限制期间观察到的血浆胰高血糖素浓度升高和胰高血糖素代谢清除率(MCRg)延迟是否与禁食期间也会出现的血清T3降低有关。12名肥胖受试者在为期4天的进食期(1000千卡/天)接受了3小时的静脉注射胰高血糖素,大约在禁食的第三天再次接受注射。5名患者禁食但未接受外源性T3(对照组),而7名受试者禁食但也每4小时口服5微克T3(T3组),以在进食期和禁食期维持大致相同的血清T3水平。胰高血糖素产生率(GPR)通过将MCRg乘以各自的基础血浆胰高血糖素浓度得出。在对照组中,吸收后状态下的MCRg为442±55毫升/平方米·分钟,禁食期间降至312±49毫升/平方米·分钟(P<0.025),而在T3治疗组中,吸收后MCRg为304±22毫升/平方米·分钟,禁食期间增加至417±47毫升/平方米·分钟(P<0.025)。对照组的GPR在进食期(27.7±3.0纳克/平方米·分钟)和禁食期(22.9±1.8纳克/平方米·分钟)之间无统计学改变,但当给予T3(每4小时5微克)时,GPR从禁食期间的37.9±6.1纳克/平方米·分钟增加至49.2±9.1纳克/平方米·分钟。对照组患者对胰高血糖素的血浆葡萄糖净增量从进食时的18毫克/分升降至禁食时的5毫克/分升,T3治疗的受试者从进食时的10毫克/分升降至禁食时的7毫克/分升。在T3治疗的患者中,进食和禁食期间血清T3平均为124纳克/分升,反T3(rT3)在进食时为55±6纳克/分升,禁食时为49±5纳克/分升。总之,本研究结果表明,在禁食期间:1)血清T3的轻微生理改变会影响MCRg;2)T3会增加GPR并阻止禁食引起的rT3通常升高。可以想象,T3降低是禁食状态下的一个早期事件,其作用是降低MCRg,这一过程随后调节葡萄糖稳态。

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