| Literature DB >> 32101455 |
Lívia de Souza Gonçalves1, Caroline Kratz1, Lívia Santos2, Victor Henrique Carvalho3, Lucas Peixoto Sales1, Kleiner Nemezio1, Igor Longobardi1, Luiz Augusto Riani1, Marcelo Miranda de Oliveira Lima4, Tiemi Saito1, Alan Lins Fernandes1, Joice Rodrigues3, Ruth Margaret James2, Craig Sale2, Bruno Gualano1, Bruno Geloneze4, Marisa Helena Gennari de Medeiros3, Guilherme Giannini Artioli1.
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 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 Vmax 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.Entities:
Keywords: carnosine; human skeletal muscle; hyperinsulinemia; taurine transporter; β-alanine
Year: 2020 PMID: 32101455 DOI: 10.1152/ajpcell.00550.2019
Source DB: PubMed Journal: Am J Physiol Cell Physiol ISSN: 0363-6143 Impact factor: 4.249