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Adverse Effects of Methylglyoxal on Transcriptome and Metabolic Changes in Visceral Adipose Tissue in a Prediabetic Rat Model

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11110%2F20%3A10417015" target="_blank" >RIV/00216208:11110/20:10417015 - isvavai.cz</a>

  • Alternative codes found

    RIV/00023001:_____/20:00080303 RIV/00064165:_____/20:10417015

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=S_qh5Idaa4" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=S_qh5Idaa4</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/antiox9090803" target="_blank" >10.3390/antiox9090803</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Adverse Effects of Methylglyoxal on Transcriptome and Metabolic Changes in Visceral Adipose Tissue in a Prediabetic Rat Model

  • Original language description

    Excessive methylglyoxal (MG) production contributes to metabolic and vascular changes by increasing inflammatory processes, disturbing regulatory mechanisms and exacerbating tissue dysfunction. MG accumulation in adipocytes leads to structural and functional changes. We used transcriptome analysis to investigate the effect of MG on metabolic changes in the visceral adipose tissue of hereditary hypetriglyceridaemic rats, a non-obese model of metabolic syndrome. Compared to controls, 4-week intragastric MG administration impaired glucose tolerance (p&lt; 0.05) and increased glycaemia (p&lt; 0.01) and serum levels of MCP-1 and TNF alpha (p&lt; 0.05), but had no effect on serum adiponectin or leptin. Adipose tissue insulin sensitivity and lipolysis were impaired (p&lt; 0.05) in MG-treated rats. In addition, MG reduced the expression of transcription factorNrf2(p&lt; 0.01), which controls antioxidant and lipogenic genes. Increased expression ofMcp-1andTNF alpha(p&lt; 0.05) together with activation of the SAPK/JNK signaling pathway can promote chronic inflammation in adipose tissue. Transcriptome network analysis revealed the over-representation of genes involved in insulin signaling (Irs1, Igf2, Ide), lipid metabolism (Nr1d1, Lpin1, Lrpap1) and angiogenesis (Dusp10, Tp53inp1).

  • 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

    10600 - Biological sciences

Result continuities

  • Project

  • Continuities

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Antioxidants [online]

  • ISSN

    2076-3921

  • e-ISSN

  • Volume of the periodical

    9

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    15

  • Pages from-to

    803

  • UT code for WoS article

    000580825900001

  • EID of the result in the Scopus database

    2-s2.0-85093876698