KURICOVÁ, Katarína, Lukáš PÁCAL and Kateřina KAŇKOVÁ. Hypoglycemia increases expression of several genes upregulated by hyperglycemia. In ADA, American diabetes association. 2014. ISSN 0012-1797.
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Basic information
Original name Hypoglycemia increases expression of several genes upregulated by hyperglycemia
Name in Czech Hypoglykémie zvyšuje expresi nekterých genů ovlivnených hyperglykémii
Authors KURICOVÁ, Katarína, Lukáš PÁCAL and Kateřina KAŇKOVÁ.
Edition ADA, American diabetes association, 2014.
Other information
Original language English
Type of outcome Conference abstract
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 8.095
Organization unit Faculty of Medicine
ISSN 0012-1797
Keywords (in Czech) diabetes, hypoglykémie, oxidační stres
Keywords in English diabetes, hypoglycemia, oxidative stress
Changed by Changed by: Mgr. Katarína Chalásová, Ph.D., učo 184643. Changed: 20/6/2014 10:50.
Abstract
Hyperglycemia-induced overproduction of mitochondrial reactive oxygen species (ROS) is the key event in the development and progression of diabetic microvascular complications. ROS activates several harmful pathways including increased production of advanced glycation end products (AGEs), increased expression of receptor for AGEs or polyol pathway flux. The effect of hypoglycemia on pathways activated by hyperglycemia is much less explored. Therefore we aimed to test the effect of low glucose on the expression of proteins/enzymes with established role in the hyperglycemia-driven cell damage in vitro. Specifically, we evaluated mRNA expression of superoxide dismutase (SOD1), heme oxygenase (HMOX), p65 subunit of nuclear factor kappa B, glyoxalase 1 (GLO1), receptor for advanced glycation end products and DJ-1 (an enzyme with established glyoxalase activity). Primary human umbilical vein endothelial cells were grown in EBM2 medium for 48 hours and then cultured for 24 hours in medium with different content of glucose: (i) normoglycemic (5.5 mmol/l), (ii) hyperglycemic (25.5 mmol/l) and (iii) hypoglycemic (2.75 mmol/l). Total RNA was extracted and reverse transcribed using commercial kits (Roche). Gene expression was determined using predesigned TaqMan probes (Life Technologies). Results were normalized to 18-S RNA. mRNA expression of all studied genes was increased in response to hyperglycemia compared to normoglycemia as expected although statistical significance was reached only in case of SOD1 and p65 (P < 0.05). Similar trends were observed in low glucose conditions compared to normoglycemia with exception of HMOX expression which was slightly but not significantly lower (P > 0.05). Our results suggest that hypoglycemia may have similar effect on primary endothelial cells with respect to established damaging pathways.
Links
NT13198, research and development projectName: Pentózový cyklus jako potenciální nový terapeutický cíl v prevenci diabetických komplikací
Investor: Ministry of Health of the CR
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