Leucine and protein metabolism in rats with chronic renal insufficiency
Jazyk angličtina Země Německo Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
11370737
DOI
10.1078/0940-2993-00171
PII: S0940-2993(04)70011-1
Knihovny.cz E-zdroje
- MeSH
- acidóza etiologie metabolismus MeSH
- cholesterol krev MeSH
- chronické selhání ledvin metabolismus patologie MeSH
- isoleucin metabolismus MeSH
- kosterní svaly metabolismus MeSH
- kreatinin krev MeSH
- krysa rodu Rattus MeSH
- leucin metabolismus MeSH
- močovina krev MeSH
- modely nemocí na zvířatech MeSH
- nefrektomie MeSH
- potkani Wistar MeSH
- přijímání potravy fyziologie MeSH
- proteiny metabolismus MeSH
- tělesná hmotnost fyziologie MeSH
- uremie etiologie metabolismus MeSH
- valin metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- cholesterol MeSH
- isoleucin MeSH
- kreatinin MeSH
- leucin MeSH
- močovina MeSH
- proteiny MeSH
- valin MeSH
The aim of this study was to evaluate the effect of chronic uremia induced by 5/6 nephrectomy (5/6NX) on changes in protein and branched-chain amino acid (BCAA; valine, leucine and isoleucine) metabolism. The control group consisted of sham operated rats. Twenty eight weeks after surgery the parameters of protein and amino acid metabolism were evaluated using a primed constant intravenous infusion of L-[1-(14)C]leucine. A drop in BCAA levels and a significant increase in urea, creatinine and cholesterol were observed in plasma of all 5/6NX rats. However, severe uremia with acidosis developed only in one third of rats with 5/6NX. In 5/6NX rats with acidosis significant increases in proteolysis, leucine oxidation, leucine oxidized fraction, and leucine clearance were observed in comparison with the control group and rats with 5/6NX without acidosis. In addition, in 5/6NX rats with acidosis a significant decrease in valine concentration in gastrocnemius muscle was found. We conclude that marked activation of proteolysis occurs in severe chronic renal failure and is probably caused by metabolic changes related to acidosis development.
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