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胰岛素和血浆氨基酸浓度对肝硬化患者亮氨酸代谢的影响。

Effect of insulin and plasma amino acid concentration on leucine metabolism in cirrhosis.

作者信息

Petrides A S, Luzi L, Reuben A, Riely C, DeFronzo R A

机构信息

Department of Medicine, University of Texas Health Science Center, San Antonio 78284.

出版信息

Hepatology. 1991 Sep;14(3):432-41.

PMID:1874488
Abstract

Clinically stable patients with cirrhosis demonstrate insulin resistance with regard to glucose metabolism. However, much less is known about the two major factors, insulin and plasma amino acid concentration, that regulate protein metabolism in cirrhotic patients. To examine this question, we performed paired euglycemic insulin clamp studies in combination with 14C-leucine and indirect calorimetry. In the first study insulin alone was infused, and the plasma amino acid concentration was allowed to decline. During the second study a balanced amino acid solution was infused with insulin to increase the total plasma amino acid concentration approximately twofold. Insulin-mediated glucose disposal (4.68 vs. 6.45 mg/kg-min, p less than 0.01) was significantly impaired by 30% in cirrhotic patients during both insulin clamp studies. In the postabsorptive state, cirrhotic patients manifested low plasma leucine (76 vs. 102 mumol/L) and alpha-ketoisocaproate (19 vs. 30 mumol/L) concentrations, but all parameters of leucine turnover were normal. When insulin alone was infused, the endogenous leucine flux (an index of protein degradation) declined similarly in cirrhotic patients (30.8 mumol/m2-min) and control (26.9) subjects, and this was accompanied by a similar decrease in plasma leucine concentration (31% vs. 33%). The decline in circulating leucine concentration was accompanied by a parallel decline in leucine oxidation (5.1 vs. 4.6 mumol/m2-min) and nonoxidative (28.9 vs. 26.0 mumol/m2-min) leucine disposal, which were of similar magnitude in cirrhotic patients and control subjects, respectively. In both cirrhotic patients and control subjects, combined hyperinsulinemia/hyperaminoacidemia elicited a similar stimulation of nonoxidative leucine disposal (an index of protein synthesis) and leucine oxidation while causing a greater suppression of endogenous leucine flux than observed with insulin alone. Thus the suppressive effect of insulin on protein degradation and the stimulatory effect of insulin/amino acid infusion on protein synthesis are not impaired in cirrhotic patients, demonstrating a clear-cut dissociation between the effects of insulin on protein and glucose metabolism.

摘要

临床稳定的肝硬化患者在葡萄糖代谢方面表现出胰岛素抵抗。然而,对于调节肝硬化患者蛋白质代谢的两个主要因素——胰岛素和血浆氨基酸浓度,我们所知甚少。为了研究这个问题,我们进行了配对的正常血糖胰岛素钳夹研究,并结合14C-亮氨酸和间接测热法。在第一项研究中,仅输注胰岛素,使血浆氨基酸浓度下降。在第二项研究中,将平衡氨基酸溶液与胰岛素一起输注,以使总血浆氨基酸浓度增加约两倍。在两项胰岛素钳夹研究中,肝硬化患者的胰岛素介导的葡萄糖处置(分别为4.68对6.45mg/kg-分钟,p小于0.01)均显著受损30%。在吸收后状态下,肝硬化患者的血浆亮氨酸(分别为76对102μmol/L)和α-酮异己酸(分别为19对30μmol/L)浓度较低,但亮氨酸周转的所有参数均正常。当仅输注胰岛素时,肝硬化患者(30.8μmol/m2-分钟)和对照(26.9)受试者的内源性亮氨酸通量(蛋白质降解指标)下降相似,同时血浆亮氨酸浓度也有相似程度的下降(分别为31%对33%)。循环亮氨酸浓度的下降伴随着亮氨酸氧化(分别为5.1对4.6μmol/m2-分钟)和非氧化(分别为28.9对26.0μmol/m2-分钟)亮氨酸处置的平行下降,这在肝硬化患者和对照受试者中幅度相似。在肝硬化患者和对照受试者中,联合高胰岛素血症/高氨基酸血症均引起了对非氧化亮氨酸处置(蛋白质合成指标)和亮氨酸氧化的相似刺激,同时与单独使用胰岛素相比,对内源性亮氨酸通量的抑制作用更大。因此,胰岛素对蛋白质降解的抑制作用以及胰岛素/氨基酸输注对蛋白质合成的刺激作用在肝硬化患者中并未受损,这表明胰岛素对蛋白质和葡萄糖代谢的作用之间存在明显的分离。

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