2021
DOI: 10.1007/s00726-021-03090-9
|View full text |Cite
|
Sign up to set email alerts
|

Insulin stimulates β-alanine uptake in skeletal muscle cells in vitro

Abstract: We evaluated whether insulin could stimulate β-alanine uptake by skeletal muscle cells in vitro. Mouse myoblasts (C2C12) (n = 3 wells per condition) were cultured with β-alanine (350 or 700 µmol·L−1), with insulin (100 µU·mL−1) either added to the media or not. Insulin stimulated the β-alanine uptake at the lower (350 µmol·L−1) but not higher (700 µmol·L−1) β-alanine concentration in culture medium, indicating that transporter saturation might blunt the stimulatory effects of insulin.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
3

Relationship

1
2

Authors

Journals

citations
Cited by 3 publications
(1 citation statement)
references
References 19 publications
(23 reference statements)
0
1
0
Order By: Relevance
“…The degree of their involvement in the cellular transportation of amino acids and peptides into the myocardium is unknown. β-alanine and taurine regulate the expression of the transporter TauT within skeletal muscle and decreased β-alanine uptake was shown in an immortalized mouse skeletal muscle cell line (C2C12) exposed to hypotaurine (a TauT inhibitor), suggesting that TauT may be the primary transporter of β-alanine in skeletal muscle ( 44 ). Due to the abundance of taurine in myocardial tissue ( 45 ), it can be postulated that β-alanine would also enter myocardial tissue via this transporter.…”
Section: Myocardial Carnosine Metabolismmentioning
confidence: 99%
“…The degree of their involvement in the cellular transportation of amino acids and peptides into the myocardium is unknown. β-alanine and taurine regulate the expression of the transporter TauT within skeletal muscle and decreased β-alanine uptake was shown in an immortalized mouse skeletal muscle cell line (C2C12) exposed to hypotaurine (a TauT inhibitor), suggesting that TauT may be the primary transporter of β-alanine in skeletal muscle ( 44 ). Due to the abundance of taurine in myocardial tissue ( 45 ), it can be postulated that β-alanine would also enter myocardial tissue via this transporter.…”
Section: Myocardial Carnosine Metabolismmentioning
confidence: 99%