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血浆非酯化脂肪酸水平生理性升高对胰岛素分泌无影响。

Lack of effect of a physiological elevation of plasma non-esterified fatty acid levels on insulin secretion.

作者信息

Frias J P, Basabe L, Macaraeg G, Kruszynska Y T

机构信息

Department Medicine, Division of Endocrinology & Metabolism, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.

出版信息

Diabetes Metab. 2000 Apr;26(2):133-9.

Abstract

Elevated plasma non-esterified fatty acid (NEFA) levels in obese subjects may contribute to their higher insulin secretory rates by direct effects on the islet B-cells. This may involve short-term metabolic effects, or long-term effects on islet B-cell mass, which is characteristically increased in obesity. We examined the effects of elevating plasma NEFA levels for 5.5 to 7 h on insulin secretion after an overnight fast and during a 90 min 12 mmol/l hyperglycemic clamp in 9 normal women (40.1 +/- 9.5 years [mean +/- SD]; BMI: 25.2 +/- 3.72 kg/m(2) ). Subjects were studied twice. In one study plasma NEFA levels were increased approximately 2-fold by infusion of 20% Intralipid (60 ml/h) and heparin (900 U/h) for 5.5 h before and throughout the glucose clamp. Elevated NEFA levels were associated with a small increase in fasting plasma glucose (5.0 +/- 0.1 vs 4.7 +/- 0.1 mmol/l, P <0.05) and C-peptide levels (0.54 +/- 0.09 vs 0.41 +/- 0.06 nmol/l, P <0.05). The increase in fasting insulin levels did not, however, reach statistical significance (9.0 +/- 2.5 vs 5.3 +/- 1.4 mU/l, NS). During the glucose clamp, plasma NEFA levels were suppressed to very low levels in the saline control study. Although plasma NEFA levels also fell in the lipid/heparin study, they remained significantly higher than on the control day, and somewhat higher than might be expected postprandially in obese subjects. During the glucose clamps, plasma glucose, insulin, and C-peptide profiles were similar on the two study days. No difference in either first or second phase insulin secretion was observed between the two studies. In conclusion, our findings do not support the idea that the exaggerated insulin secretion in obesity is mediated by short-term effects of plasma NEFA levels on islet B-cell metabolism, independent of plasma glucose levels.

摘要

肥胖受试者血浆非酯化脂肪酸(NEFA)水平升高可能通过对胰岛B细胞的直接作用导致其胰岛素分泌率更高。这可能涉及短期代谢效应,或对胰岛B细胞量的长期影响,而胰岛B细胞量在肥胖中通常会增加。我们研究了在9名正常女性(40.1±9.5岁[平均值±标准差];体重指数:25.2±3.72kg/m²)中,禁食过夜后以及在90分钟12mmol/L高血糖钳夹期间,将血浆NEFA水平升高5.5至7小时对胰岛素分泌的影响。受试者进行了两次研究。在一项研究中,在葡萄糖钳夹前及整个过程中,通过输注20%英脱利匹特(60ml/h)和肝素(900U/h)5.5小时,使血浆NEFA水平升高约2倍。NEFA水平升高与空腹血糖小幅升高(5.0±0.1 vs 4.7±0.1mmol/L,P<0.05)和C肽水平升高(0.54±0.09 vs 0.41±0.06nmol/L,P<0.05)相关。然而,空腹胰岛素水平的升高未达到统计学显著性(9.0±2.5 vs 5.3±1.4mU/L,无显著性差异)。在葡萄糖钳夹期间,生理盐水对照研究中血浆NEFA水平被抑制至非常低的水平。尽管在脂质/肝素研究中血浆NEFA水平也下降,但仍显著高于对照日,且略高于肥胖受试者餐后预期水平。在葡萄糖钳夹期间,两项研究日的血浆葡萄糖、胰岛素和C肽曲线相似。两项研究之间在第一或第二阶段胰岛素分泌方面未观察到差异。总之,我们的研究结果不支持肥胖中过度的胰岛素分泌是由血浆NEFA水平对胰岛B细胞代谢的短期作用介导的这一观点,且该作用独立于血浆葡萄糖水平。

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