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Insulin does not stimulate β-alanine transport into human skeletal muscle
Author(s) -
Lívia de Souza Gonçalves,
Caroline Kratz,
Lívia Santos,
Victor Henrique Carvalho,
Lucas Peixoto Sales,
Kleiner Nemezio,
Igor Longobardi,
Luiz Riani,
Marcelo Miranda de Oliveira Lima,
Tiemi Saito,
Alan Lins Fernandes,
J. Antunes Rodrigues,
Ruth M. James,
Craig Sale,
Bruno Gualano,
Bruno Geloneze,
Marisa Helena Gennari de Medeiros,
Guilherme Giannini Artioli
Publication year - 2020
Publication title -
ajp cell physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.432
H-Index - 181
eISSN - 1522-1563
pISSN - 0363-6143
DOI - 10.1152/ajpcell.00550.2019
Subject(s) - skeletal muscle , insulin , alanine , medicine , endocrinology , chemistry , biochemistry , amino acid
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 experiment 1, 12 men received supraphysiological amounts of β-alanine intravenously (0.11 g·kg −1 ·min −1 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 experiment 2, 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 experiment 1, no differences between conditions were shown for plasma β-alanine, muscle β-alanine, muscle carnosine and urinary β-alanine concentrations (all P > 0.05). In experiment 2, no differences between conditions were shown for plasma β-alanine or muscle β-alanine concentrations (all P > 0.05). Hyperinsulinemia did not increase β-alanine uptake by skeletal muscle cells, neither when substrate concentrations exceed the V max 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.

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