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Caffeic acid does not protect human pancreatic β cells against stearic acid-induced ER stress and apoptosis

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11120%2F24%3A43926915" target="_blank" >RIV/00216208:11120/24:43926915 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://doi.org/10.1002/ejlt.202300206" target="_blank" >https://doi.org/10.1002/ejlt.202300206</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/ejlt.202300206" target="_blank" >10.1002/ejlt.202300206</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Caffeic acid does not protect human pancreatic β cells against stearic acid-induced ER stress and apoptosis

  • Popis výsledku v původním jazyce

    Long-term elevation of saturated fatty acids in blood has a deleterious effect on pancreatic beta-cell function and survival, leading to endoplasmic reticulum (ER) stress and apoptosis. This fundamentally contributes to type 2 diabetes development. Caffeic acid (CA) was found to protect various cell types against several proapoptotic stimuli, including fatty acids. However, its potential protective effect against fatty acid-induced apoptosis was not ascertained in pancreatic beta cells yet. Therefore, the objective of this study was to examine this in the human pancreatic beta-cell lines NES2Y and 1.1B4. In both cell lines, CA did not modify the effect of saturated stearic acid (SA) on beta-cell growth and viability. At higher concentrations, CA significantly even intensified the adverse effect of SA. Consistent with this, CA did not exhibit any inhibitory effect on SA-induced markers of ongoing apoptosis as well as ER stress. At higher concentrations, CA again slightly potentiated the effect of SA. CA applied alone was well tolerated up to 1 mM; however, at higher concentrations, it had detrimental effects in both cell lines. To conclude, we have shown that the treatment with caffeic acid has no inhibitory effect on SA-induced ER stress and apoptosis in the human pancreatic beta cells. Moreover, at higher concentrations, CA has proapoptotic potential.

  • Název v anglickém jazyce

    Caffeic acid does not protect human pancreatic β cells against stearic acid-induced ER stress and apoptosis

  • Popis výsledku anglicky

    Long-term elevation of saturated fatty acids in blood has a deleterious effect on pancreatic beta-cell function and survival, leading to endoplasmic reticulum (ER) stress and apoptosis. This fundamentally contributes to type 2 diabetes development. Caffeic acid (CA) was found to protect various cell types against several proapoptotic stimuli, including fatty acids. However, its potential protective effect against fatty acid-induced apoptosis was not ascertained in pancreatic beta cells yet. Therefore, the objective of this study was to examine this in the human pancreatic beta-cell lines NES2Y and 1.1B4. In both cell lines, CA did not modify the effect of saturated stearic acid (SA) on beta-cell growth and viability. At higher concentrations, CA significantly even intensified the adverse effect of SA. Consistent with this, CA did not exhibit any inhibitory effect on SA-induced markers of ongoing apoptosis as well as ER stress. At higher concentrations, CA again slightly potentiated the effect of SA. CA applied alone was well tolerated up to 1 mM; however, at higher concentrations, it had detrimental effects in both cell lines. To conclude, we have shown that the treatment with caffeic acid has no inhibitory effect on SA-induced ER stress and apoptosis in the human pancreatic beta cells. Moreover, at higher concentrations, CA has proapoptotic potential.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30202 - Endocrinology and metabolism (including diabetes, hormones)

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/LX22NPO5104" target="_blank" >LX22NPO5104: Národní institut pro výzkum metabolických a kardiovaskulárních onemocnění</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2024

  • Kód důvěrnosti údajů

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

Údaje specifické pro druh výsledku

  • Název periodika

    European Journal of Lipid Science and Technology

  • ISSN

    1438-7697

  • e-ISSN

    1438-9312

  • Svazek periodika

    126

  • Číslo periodika v rámci svazku

    6

  • Stát vydavatele periodika

    DE - Spolková republika Německo

  • Počet stran výsledku

    5

  • Strana od-do

    2300206

  • Kód UT WoS článku

    001197065700001

  • EID výsledku v databázi Scopus

    2-s2.0-85190394651