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采用两阶段胰岛素输注研究评估超重/肥胖、非糖尿病女性中脂肪分解的胰岛素抑制作用与胰岛素介导的葡萄糖摄取之间的关系。

Use of a two-stage insulin infusion study to assess the relationship between insulin suppression of lipolysis and insulin-mediated glucose uptake in overweight/obese, nondiabetic women.

机构信息

Stanford University School of Medicine, Division of Endocrinology, Stanford, CA 94305-5103, USA.

出版信息

Metabolism. 2011 Dec;60(12):1741-7. doi: 10.1016/j.metabol.2011.05.008. Epub 2011 Aug 4.

Abstract

Differences in insulin regulation of free fatty acids (FFAs) are not readily apparent at the same insulin concentrations used to differentiate relative insulin-mediated glucose disposal. Resistance to insulin-mediated glucose disposal and higher daylong FFA concentrations occur more commonly in obese individuals. However, the relationship between the ability of insulin to suppress FFA release from adipose tissue and stimulate glucose disposal in muscle has not been clearly defined in this population. The current study was initiated to test the hypothesis that these 2 facets of insulin action are related, with greater defects in insulin-mediated glucose disposal associated with less effective insulin inhibition of FFA release from adipose tissue. Subjects included 56 healthy nondiabetic overweight/moderately obese women classified as insulin resistant or insulin sensitive based on whole-body glucose disposal. All underwent a modified 240-minute 2-stage insulin infusion with basal (∼15 µU/mL) and physiologically elevated (∼80 µU/mL) steady-state insulin concentrations. Plasma glucose, insulin, FFA, and glycerol were measured throughout. Whereas plasma glucose differed most during physiological hyperinsulinemia in insulin-resistant vs insulin-sensitive subjects, plasma FFA/glycerol differed most during basal insulin concentrations. The FFA concentrations during the basal insulin steady state correlated highly (r = 0.85, P < .001) with glucose concentrations during the hyperinsulinemic steady state. Overweight/moderately obese women exhibit dramatic differences in the ability of insulin to suppress plasma FFA, which correlate highly with differences in insulin-mediated glucose disposal. Variability in insulin regulation of FFA is most apparent at basal insulin concentrations, whereas differences in glucose disposal are most apparent during physiologic hyperinsulinemia. Both can be quantified using a simple 2-stage insulin infusion study, with first-stage FFA concentrations and second-stage glucose concentrations being most informative.

摘要

胰岛素对游离脂肪酸(FFA)的调节作用在用于区分相对胰岛素介导的葡萄糖处置的相同胰岛素浓度下并不明显。在肥胖个体中,胰岛素介导的葡萄糖处置抵抗和全天较高的 FFA 浓度更为常见。然而,在该人群中,胰岛素抑制脂肪组织释放 FFA 和刺激肌肉葡萄糖摄取的能力之间的关系尚未明确界定。本研究旨在检验以下假设:即这两个胰岛素作用的方面是相关的,胰岛素介导的葡萄糖处置缺陷越大,胰岛素抑制脂肪组织释放 FFA 的作用越不有效。研究对象包括 56 名健康的非糖尿病超重/中度肥胖女性,根据全身葡萄糖处置情况分为胰岛素抵抗或胰岛素敏感。所有受试者均接受改良的 240 分钟 2 期胰岛素输注,基础(约 15 µU/mL)和生理升高(约 80 µU/mL)稳态胰岛素浓度。整个过程中测量血浆葡萄糖、胰岛素、FFA 和甘油。尽管在胰岛素抵抗与胰岛素敏感的受试者中,生理高胰岛素血症期间的血浆葡萄糖差异最大,但基础胰岛素浓度期间的血浆 FFA/甘油差异最大。基础胰岛素稳态期间的 FFA 浓度与高胰岛素血症稳态期间的葡萄糖浓度高度相关(r = 0.85,P <.001)。超重/中度肥胖女性在胰岛素抑制血浆 FFA 的能力方面存在明显差异,这与胰岛素介导的葡萄糖处置差异高度相关。FFA 与葡萄糖的胰岛素调节差异在基础胰岛素浓度下最为明显,而葡萄糖处置的差异在生理高胰岛素血症期间最为明显。这两种情况都可以使用简单的 2 期胰岛素输注研究来量化,其中第一阶段的 FFA 浓度和第二阶段的葡萄糖浓度最具信息量。

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