2016
Effect of glucose variability on pathways associated with glucotoxicity in diabetes: Evaluation of a novel in vitro experimental approach
KURICOVÁ, Katarína; Lukáš PÁCAL; Jan ŠOUPAL; Martin PRÁZNÝ; Kateřina KAŇKOVÁ et al.Základní údaje
Originální název
Effect of glucose variability on pathways associated with glucotoxicity in diabetes: Evaluation of a novel in vitro experimental approach
Autoři
Vydání
Diabetes Research and Clinical Practice, Clare, Elsevier Ireland Ltd. 2016, 0168-8227
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30202 Endocrinology and metabolism
Stát vydavatele
Irsko
Utajení
není předmětem státního či obchodního tajemství
Impakt faktor
Impact factor: 3.639
Označené pro přenos do RIV
Ano
Kód RIV
RIV/00216224:14110/16:00088852
Organizační jednotka
Lékařská fakulta
UT WoS
EID Scopus
Klíčová slova anglicky
Glycaemic variability; Continuous glucose monitoring; Diabetes complications; Hyperglycaemia; Hypoglycaemia; Pentose phosphate pathway
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 26. 4. 2017 10:33, Soňa Böhmová
Anotace
V originále
Aims: Glycaemic variability (GV) has been hypothesized to increase the risk of diabetes complications; however, results of clinical studies are contradictory. The effect of GV on cell phenotypes has been investigated in vitro showing that GV may have more deleterious effect on cells that high glucose itself. However, methodology used to study GV in vitro differs significantly between studies and does not reflect in vivo situation. Therefore we aimed to establish clinically relevant an in vitro experimental approach for the study of GV that reflects intra-day glucose fluctuations of subjects with type 1 diabetes mellitus (T1DM) and of healthy subjects and to test how low and high GV affect expression of genes that protects cells from hyperglycaemia-induced damage. Methods: Human umbilical vein endothelial cells (HUVEC) were cultured 24 h in medium with different glucose profiles: high GV, low GV and GV of healthy subjects—profiles created according to CGM of T1DM patients and healthy subjects. These profiles were compared to commonly used 5.5 and 25 mmol/l glucose concentrations. Gene expression was determined using quantitative PCR. Results: Our results showed general down-regulation of enzymes that are involved in the protection against hyperglycaemia-induced intracellular changes in both low and high GV compared to normal glycaemia similarly to the decrease induced by continuous hyperglycaemia. Gene expressions did not differ between high and low GV. Conclusion: Our data indicate that GV may have similar or even greater effect than continuous hyperglycaemia on the expression of several genes relevant to pathogenesis of diabetes microvascular complications.
Návaznosti
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