Increased Incretin But Not Insulin Response after Oral versus Intravenous Branched Chain Amino Acids
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
PubMed
28595189
DOI
10.1159/000475604
PII: 000475604
Knihovny.cz E-zdroje
- Klíčová slova
- Branched chain amino acids, Glucagon-like peptide 1, Glucose-dependent insulinotropic peptide, Incretin effect, Insulin response,
- MeSH
- aplikace orální MeSH
- C-peptid krev MeSH
- dospělí MeSH
- glukagon krev MeSH
- glukagonu podobný peptid 1 krev MeSH
- inkretiny krev MeSH
- intravenózní podání MeSH
- inzulin krev MeSH
- isoleucin krev MeSH
- krevní glukóza metabolismus MeSH
- leucin krev MeSH
- lidé MeSH
- mladý dospělý MeSH
- valin krev MeSH
- větvené aminokyseliny aplikace a dávkování krev MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- žaludeční inhibiční polypeptid krev MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- srovnávací studie MeSH
- Názvy látek
- C-peptid MeSH
- glukagon MeSH
- glukagonu podobný peptid 1 MeSH
- inkretiny MeSH
- inzulin MeSH
- isoleucin MeSH
- krevní glukóza MeSH
- leucin MeSH
- valin MeSH
- větvené aminokyseliny MeSH
- žaludeční inhibiční polypeptid MeSH
BACKGROUND/AIMS: Branched chain amino acids (BCAAs) are known to exert an insulinotropic effect. Whether this effect is mediated by incretins (glucagon like peptide 1 [GLP-1] or glucose-dependent insulinotropic peptide [GIP]) is not known. The aim of this study was to show whether an equivalent dose of BCAA elicits a greater insulin and incretin response when administered orally than intravenously (IV). METHODS: Eighteen healthy, male subjects participated in 3 tests: IV application of BCAA solution, oral ingestion of BCAA and placebo in an equivalent dose (30.7 ± 1.1 g). Glucose, insulin, C-peptide, glucagon, GLP-1, GIP, valine, leucine and isoleucine concentrations were measured. RESULTS: Rise in serum BCAA was achieved in both BCAA tests, with incremental areas under the curve (iAUC) being 2.1 times greater for IV BCAA compared with those of the oral BCAA test (p < 0.0001). Oral and IV BCAA induced comparable insulin response greater than placebo (240 min insulin iAUC: oral 3,411 ± 577 vs. IV 2,361 ± 384 vs. placebo 961.2 ± 175 pmol/L, p = 0.0006). Oral BCAA induced higher GLP-1 (p < 0.0001) and GIP response (p < 0.0001) compared with the IV or placebo. Glucose levels declined significantly (p < 0.001) in the same pattern during both BCAA tests with no change in the placebo group. CONCLUSIONS: An equivalent dose of BCAA elicited a comparable insulin and greater incretin response when administered orally and not when administered through IV. We conclude that insulinotropic effects of BCAA are partially incretin dependent.
Citace poskytuje Crossref.org
ClinicalTrials.gov
NCT02697305