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胰岛素不会刺激β-丙氨酸进入人体骨骼肌的转运。

Insulin does not stimulate β-alanine transport into human skeletal muscle.

机构信息

Applied Physiology and Nutrition Research Group; School of Physical Education and Sport, Rheumatology Division, Faculdade de Medicina FMUSP, Universidade de São Paulo, São Paulo, Brazil.

Musculoskeletal Physiology Research Group, Sport, Health, and Performance Enhancement Research Centre, Nottingham Trent University, Nottingham, United Kingdom.

出版信息

Am J Physiol Cell Physiol. 2020 Apr 1;318(4):C777-C786. doi: 10.1152/ajpcell.00550.2019. Epub 2020 Feb 26.

DOI:10.1152/ajpcell.00550.2019
PMID:32101455
Abstract

To test whether high circulating insulin concentrations influence the transport of β-alanine into skeletal muscle at either saturating or subsaturating β-alanine concentrations, we conducted two experiments whereby β-alanine and insulin concentrations were controlled. In , 12 men received supraphysiological amounts of β-alanine intravenously (0.11 g·kg·min for 150 min), with or without insulin infusion. β-Alanine and carnosine were measured in muscle before and 30 min after infusion. Blood samples were taken throughout the infusion protocol for plasma insulin and β-alanine analyses. β-Alanine content in 24-h urine was assessed. In , six men ingested typical doses of β-alanine (10 mg/kg) before insulin infusion or no infusion. β-Alanine was assessed in muscle before and 120 min following ingestion. In , no differences between conditions were shown for plasma β-alanine, muscle β-alanine, muscle carnosine and urinary β-alanine concentrations (all > 0.05). In , no differences between conditions were shown for plasma β-alanine or muscle β-alanine concentrations (all > 0.05). Hyperinsulinemia did not increase β-alanine uptake by skeletal muscle cells, neither when substrate concentrations exceed the of β-alanine transporter TauT nor when it was below saturation. These results suggest that increasing insulin concentration is not necessary to maximize β-alanine transport into muscle following β-alanine intake.

摘要

为了测试高循环胰岛素浓度是否会影响β-丙氨酸在饱和或亚饱和β-丙氨酸浓度下向骨骼肌的转运,我们进行了两项实验,分别控制β-丙氨酸和胰岛素浓度。在实验 1 中,12 名男性接受了静脉内超生理剂量的β-丙氨酸(0.11 g·kg·min 持续 150 分钟),同时或不接受胰岛素输注。输注前和输注后 30 分钟测量肌肉中的β-丙氨酸和肉碱。在整个输注方案中采集血液样本,用于检测血浆胰岛素和β-丙氨酸分析。评估 24 小时尿液中的β-丙氨酸含量。在实验 2 中,6 名男性在胰岛素输注或无输注前摄入了典型剂量的β-丙氨酸(10 mg/kg)。在摄入前和 120 分钟后测量肌肉中的β-丙氨酸。在实验 3 中,两种条件下的血浆β-丙氨酸、肌肉β-丙氨酸、肌肉肉碱和尿β-丙氨酸浓度均无差异(均>0.05)。在实验 4 中,两种条件下的血浆β-丙氨酸或肌肉β-丙氨酸浓度均无差异(均>0.05)。高胰岛素血症并未增加骨骼肌细胞对β-丙氨酸的摄取,无论是在底物浓度超过β-丙氨酸转运体 TauT 的 时,还是在低于饱和时。这些结果表明,在摄入β-丙氨酸后,增加胰岛素浓度对于将β-丙氨酸最大程度地转运到肌肉中并不是必需的。

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