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Branched-chain amino acids in health and disease: metabolism, alterations in blood plasma, and as supplements

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11150%2F18%3A10374897" target="_blank" >RIV/00216208:11150/18:10374897 - isvavai.cz</a>

  • Result on the web

    <a href="https://nutritionandmetabolism.biomedcentral.com/articles/10.1186/s12986-018-0271-1" target="_blank" >https://nutritionandmetabolism.biomedcentral.com/articles/10.1186/s12986-018-0271-1</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1186/s12986-018-0271-1" target="_blank" >10.1186/s12986-018-0271-1</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Branched-chain amino acids in health and disease: metabolism, alterations in blood plasma, and as supplements

  • Original language description

    Branched-chain amino acids (BCAAs; valine, leucine, and isoleucine) are essential amino acids with protein anabolic properties, which have been studied in a number of muscle wasting disorders for more than 50 years. However, until today, there is no consensus regarding their therapeutic effectiveness. The aims of the article are: (i) to review the main metabolic pathways and supposed effects of the BCAA, (ii) explain the causes of altered metabolism and BCAA levels in various healthy and pathological conditions, and (iii) provide current views on their use as supplements for the possible main indications. The crucial role in BCAA metabolism play: (i) skeletal muscle as the initial site of BCAA catabolism accompanied with the release of alanine and glutamine to the blood; (ii) activity of branched-chain keto acid dehydrogenase (BCKD); and (iii) amination of branched-chain keto acids (BCKAs) to BCAAs. Enhanced consumption of BCAA for ammonia detoxification to glutamine in muscles is the cause of decreased BCAA levels in liver cirrhosis and urea cycle disorders. Increased BCKD activity is responsible for enhanced oxidation of BCAA in chronic renal failure, trauma, burn, sepsis, cancer, phenylbutyrate-treated subjects, and during exercise. Decreased BCKD activity is the main cause of increased BCAA levels and BCKAs in maple syrup urine disease, and plays a role in increased BCAA levels in diabetes type 2 and obesity. Increased BCAA concentrations during brief starvation and type 1 diabetes are explained by amination of BCKAs in visceral tissues and decreased uptake of BCAA by muscles. The studies indicate beneficial effects of BCAAs and BCKAs in therapy of chronic renal failure and a need of therapeutic strategies to avoid adverse effects of the BCAA administration on ammonia production in cirrhosis. Further studies are needed to elucidate the effects of BCAA supplementation in burn, trauma, sepsis, cancer and exercise. Whether increased BCAA levels are beneficial or harmful and whether contribute to insulin resistance should be known before the decision regarding their suitability in obese subjects and patients with type 2 diabetes. It is concluded that alterations in BCAA metabolism have been found common in a number of disease states, and careful studies are needed to elucidate their therapeutic effectiveness in most indications.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30202 - Endocrinology and metabolism (including diabetes, hormones)

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Nutrition &amp; Metabolism

  • ISSN

    1743-7075

  • e-ISSN

  • Volume of the periodical

    15

  • Issue of the periodical within the volume

    33

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    12

  • Pages from-to

    1-12

  • UT code for WoS article

    000431530300001

  • EID of the result in the Scopus database

    2-s2.0-85046552521