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超常肝糖原含量对高胰高血糖素血症诱导的肝糖原分解的影响。

Effects of supranormal liver glycogen content on hyperglucagonemia-induced liver glycogen breakdown.

作者信息

Bélanger P, Couturier K, Latour M G, Lavoie J M

机构信息

Département de Kinésiologie, Université de Montréal, Québec, Canada.

出版信息

Eur J Appl Physiol. 2000 Nov;83(4 -5):328-35. doi: 10.1007/s004210000286.

Abstract

The purpose of the present study was to test the hypothesis that a higher hepatic glycogen level is associated with higher glucagon-induced hepatic glycogen depletion. Four groups of anesthetized rats received three injections (at times 0, 30, and 60 min) of glucagon (intravenously, 20 [microg/kg). Among these groups, hepatic glycogen levels had previously been manipulated either by an overloading diet (Fast-refed), a reduction in food intake (1/2-fast), or exercise (75 min of running, 26 m/ min, 0% grade). A fourth group had normal hepatic glycogen levels. A fifth group of rats was injected only with saline (0.9% NaCl). Liver glycogen concentrations were measured every 30 min during the course of the 90-min experiment, using liver samples obtained from the open liver biopsy technique. Plasma glucagon concentrations were significantly higher (P < 0.05) in the glucagon-injected groups than in the saline-injected group. As expected, liver glycogen levels were significantly higher (P < 0.01; 1.6-fold) in the Fast-refed group than in all other groups. Glucagon-induced decreases in liver glycogen concentrations were similar in Fast-refed than in normally fed and exercised rats when the overall 90-min period was considered. However, during the course of the last 30-min period, liver glycogen was significantly (P < 0.01) decreased only in the Fast-refed group. The Fast-refed, normally fed, and exercised groups had a similar glucagon-induced hyperglycemia that was significantly more elevated (P < 0.01) than glucose levels measured in the saline-injected group. Glucagon-induced reactive hyperinsulinemia was observed only in the Fast-refed and normally fed rats, and not in the exercised and 1/2-fast rats. It is concluded that supranormal levels of liver glycogen may be associated with a larger hyperglucagonemia-induced liver glycogen breakdown.

摘要

本研究的目的是检验以下假设

较高的肝糖原水平与较高的胰高血糖素诱导的肝糖原消耗有关。四组麻醉大鼠接受三次胰高血糖素注射(分别在0、30和60分钟时静脉注射,剂量为20μg/kg)。在这些组中,肝糖原水平先前已通过超载饮食(快速再喂养)、减少食物摄入量(半禁食)或运动(以26米/分钟的速度跑步75分钟,坡度为0%)进行了调控。第四组肝糖原水平正常。第五组大鼠仅注射生理盐水(0.9%氯化钠)。在90分钟的实验过程中,每隔30分钟使用通过开放式肝活检技术获取的肝脏样本测量肝糖原浓度。注射胰高血糖素的组血浆胰高血糖素浓度显著高于注射生理盐水的组(P<0.05)。如预期的那样,快速再喂养组的肝糖原水平显著高于所有其他组(P<0.01;高1.6倍)。当考虑整个90分钟时间段时,快速再喂养组中胰高血糖素诱导的肝糖原浓度降低与正常喂养和运动的大鼠相似。然而,在最后30分钟期间,仅快速再喂养组的肝糖原显著降低(P<0.01)。快速再喂养组、正常喂养组和运动组具有相似的胰高血糖素诱导的高血糖症,其血糖水平显著高于注射生理盐水组测量的血糖水平(P<0.01)。仅在快速再喂养组和正常喂养的大鼠中观察到胰高血糖素诱导的反应性高胰岛素血症,而在运动组和半禁食组大鼠中未观察到。结论是肝糖原的超常水平可能与更大的高胰高血糖素血症诱导的肝糖原分解有关。

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