Acute effects of phenylbutyrate on glutamine, branched-chain amino acid and protein metabolism in skeletal muscles of rats
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
28621016
PubMed Central
PMC5573773
DOI
10.1111/iep.12231
Knihovny.cz E-zdroje
- Klíčová slova
- Phenylbutyrate, branched-chain amino acids, glutamine, leucine, maple syrup urine disease, muscle protein,
- MeSH
- fenylbutyráty farmakologie MeSH
- glutamin metabolismus MeSH
- kosterní svaly účinky léků metabolismus MeSH
- leucin metabolismus MeSH
- oxidace-redukce účinky léků MeSH
- potkani Wistar MeSH
- proteosyntéza účinky léků MeSH
- svalové proteiny metabolismus MeSH
- techniky tkáňových kultur MeSH
- větvené aminokyseliny metabolismus MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- fenylbutyráty MeSH
- glutamin MeSH
- leucin MeSH
- svalové proteiny MeSH
- větvené aminokyseliny MeSH
Phenylbutyrate (PB) acts as chemical chaperone and histone deacetylase inhibitor, which is used to decrease ammonia in urea cycle disorders and has been investigated for use in the treatment of a number of lethal illnesses. We performed in vivo and in vitro experiments to examine the effects of PB on glutamine (GLN), branched-chain amino acid (BCAA; valine, leucine and isoleucine) and protein metabolism in rats. In the first study, animals were sacrificed one hour after three injections of PB (300mg/kg b.w.) or saline. In the second study, soleus (SOL, slow twitch) and extensor digitorum longus (EDL, fast twitch) muscles were incubated in a medium with or without PB (5 mM). L-[1-14 C] leucine was used to estimate protein synthesis and leucine oxidation, and 3-methylhistidine release was used to evaluate myofibrillar protein breakdown. PB treatment decreased GLN, BCAA and branched-chain keto acids (BCKAs) in blood plasma, decreased BCAA and increased GLN concentrations in muscles, and increased GLN synthetase activities in muscles. Addition of PB to incubation medium increased leucine oxidation (55% in EDL, 29% in SOL), decreased BCKA and increased GLN in medium of both muscles, increased GLN in muscles, decreased protein synthesis in SOL and increased proteolysis in EDL. It is concluded that PB decreases BCAA, BCKA and GLN in blood plasma, activates BCAA catabolism and GLN synthesis in muscle and exerts adverse effects on protein metabolism. The results indicate that BCAA and GLN supplementation is needed when PB is used therapeutically and that PB may be a useful prospective agent which could be effective in management of maple syrup urine disease.
Department of Biochemistry Faculty of Medicine Charles University Hradec Kralove Czech Republic
Department of Physiology Faculty of Medicine Charles University Hradec Kralove Czech Republic
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