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三例脂肪萎缩性糖尿病患者胰岛素抵抗的体内和体外特征分析

In vivo and in vitro characterization of insulin resistance in three cases of lipoatrophic diabetes.

作者信息

Robert J J, Magre J, Reynet C, Darmaun D, Picard J, Capeau J

机构信息

Unité d'Endocrinologie et Diabétologie de l'Enfant, INSERM U 30, Hôpital des Enfants Malades, Paris, France.

出版信息

Diabete Metab. 1990 May-Jun;16(3):240-7.

PMID:2210020
Abstract

Insulin resistance was explored in vivo and in vitro in 3 lipoatrophic diabetic girls (12, 15 and 19 years old = L1, L2 and L3). Patients L1 and L2 were explored with fasting hyperglycaemia (9 mmol/l); patient L3 was normoglycaemic. All had abnormal OGTT with marked hyperinsulinemia. Their basal glucose productions, measured by [6,6(-2)H] glucose constant infusion, were 3.3, 2.6 and 3.4 mg kg-1 min-1, respectively; they did not correlate with fasting plasma glucose. Glucose production in response to a 2 mg kg-1 min- unlabeled glucose infusion, was normally suppressed in L2, but was incompletely suppressed (by 1.5 mg kg-1 min-1) in L1 and L3. The dose-response curve during hyperinsulinemic euglycaemic clamp at 1, 2 and 10 mU kg-1 min-1 insulin infusion was shifted to the right in all three patients. However the maximal glucose disposal rates were close to normal (9 and 9 mg kg-1 min-1) in L1 and L3, while it remained very low (3.6 mg kg-1 min-1 at 10 mU kg-1 min-1 insulin infusion) in L2. The endogenous insulin secretion (plasma C-peptide) was also incompletely suppressed during insulin infusion. Thus, the in vivo insulin resistance of lipoatrophic diabetes concerns not only glucose disposal but also hepatic glucose output and insulin secretion; in addition, the alterations of glucose metabolism were not the same in all subjects. The in vitro studies showed no pre-receptor defect (anti-insulin antibodies, insulin receptor antibodies). Insulin binding to erythrocytes and cultured fibroblasts was normal.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对3名脂肪萎缩性糖尿病女孩(分别为12岁、15岁和19岁,即L1、L2和L3)进行了体内和体外胰岛素抵抗研究。L1和L2患者存在空腹高血糖(9 mmol/l);L3患者血糖正常。所有人的口服葡萄糖耐量试验均异常,伴有明显高胰岛素血症。通过[6,6(-2)H]葡萄糖持续输注测量的基础葡萄糖生成量分别为3.3、2.6和3.4 mg·kg-1·min-1;它们与空腹血糖不相关。在输注2 mg·kg-1·min-1未标记葡萄糖后,L2的葡萄糖生成正常被抑制,但L1和L3中抑制不完全(仅降低1.5 mg·kg-1·min-1)。在1、2和10 mU·kg-1·min-1胰岛素输注的高胰岛素正常血糖钳夹期间,三名患者的剂量反应曲线均右移。然而,L1和L3的最大葡萄糖处置率接近正常(9和9 mg·kg-1·min-1),而L2仍然很低(在10 mU·kg-1·min-1胰岛素输注时为3.6 mg·kg-1·min-1)。胰岛素输注期间内源性胰岛素分泌(血浆C肽)也未被完全抑制。因此,脂肪萎缩性糖尿病的体内胰岛素抵抗不仅涉及葡萄糖处置,还涉及肝脏葡萄糖输出和胰岛素分泌;此外,所有受试者的葡萄糖代谢改变并不相同。体外研究未显示受体前缺陷(抗胰岛素抗体、胰岛素受体抗体)。胰岛素与红细胞和培养的成纤维细胞的结合正常。(摘要截短于250字)

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