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胰岛素对人体肝脏酮体生成的非脂肪酸依赖性抑制作用。

Fatty acid-independent inhibition of hepatic ketone body production by insulin in humans.

作者信息

Keller U, Gerber P P, Stauffacher W

机构信息

Department of Medicine, University Hospital, Basel, Switzerland.

出版信息

Am J Physiol. 1988 Jun;254(6 Pt 1):E694-9. doi: 10.1152/ajpendo.1988.254.6.E694.

Abstract

To investigate whether elevated plasma insulin or glucagon concentrations are capable of modifying hepatic ketogenesis independently of plasma free fatty acid (FFA) concentrations, ketone body production was determined by [3-14C]acetoacetate infusions in overnight-fasted normal subjects during exogenous supply of FFA (Intralipid and heparin infusion). When plasma FFA concentrations were elevated from 0.73 +/- 0.07 to 1.53 +/- 0.16 mmol/l during low insulin concentrations (approximately equal to 13 microU/ml) in group A (n = 7), total ketone body production increased from 3.6 +/- 0.6 to 8.2 +/- 1.0 mumol.kg-1.min-1 (P less than 0.001). When plasma FFA were similarly elevated during raised plasma insulin concentrations (approximately equal to 110 microU/ml) in group B (n = 5), total ketone body production was only 3.8 +/- 0.8 mumol.kg-1.min-1 (P less than 0.01 vs. group A). Low plasma FFA and low insulin concentrations resulted in total ketone body production of 0.70 +/- 0.18 mumol.kg-1.min-1 in group C (n = 7; P less than 0.01 vs. groups A and B). Elevation of plasma glucagon during Intralipid infusion in group D (n = 7) failed to affect ketogenesis, but the beta-hydroxybutyrate-to-acetoacetate concentration ratio decreased significantly (P less than 0.01). The data indicate that elevation of plasma insulin to high physiological concentrations restrains FFA-induced ketogenesis.

摘要

为了研究血浆胰岛素或胰高血糖素浓度升高是否能够独立于血浆游离脂肪酸(FFA)浓度而改变肝脏生酮作用,通过在空腹过夜的正常受试者外源性供应FFA(输注英脱利匹特和肝素)期间输注[3-14C]乙酰乙酸来测定酮体生成。在A组(n = 7)低胰岛素浓度(约等于13微单位/毫升)期间,当血浆FFA浓度从0.73±0.07毫摩尔/升升高至1.53±0.16毫摩尔/升时,总酮体生成从3.6±0.6增加至8.2±1.0微摩尔·千克-1·分钟-1(P<0.001)。在B组(n = 5)血浆胰岛素浓度升高(约等于110微单位/毫升)期间,当血浆FFA同样升高时,总酮体生成仅为3.8±0.8微摩尔·千克-1·分钟-1(与A组相比,P<0.01)。低血浆FFA和低胰岛素浓度导致C组(n = 7)的总酮体生成量为0.70±0.18微摩尔·千克-1·分钟-1(与A组和B组相比,P<0.01)。在D组(n = 7)输注英脱利匹特期间血浆胰高血糖素升高并未影响生酮作用,但β-羟基丁酸与乙酰乙酸的浓度比显著降低(P<0.01)。数据表明,血浆胰岛素升高至较高的生理浓度会抑制FFA诱导的生酮作用。

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