Role of ChREBP and SREBP-1c in gestational diabetes: two key players in glucose and lipid metabolism

被引:3
作者
Eroglu, Nurgul [1 ]
Yerlikaya, Fatma Humeyra [2 ]
Onmaz, Duygu Eryavuz [2 ]
Colakoglu, Mehmet Cengiz [3 ]
机构
[1] Necmettin Erbakan Univ, Meram Fac Med, Dept Biochem, Konya, Turkey
[2] Selcuk Univ, Fac Med, Dept Biochem, Alaaddin Keykubat Campus, TR-42075 Selcuklu, Konya, Turkey
[3] Necmettin Erbakan Univ, Meram Fac Med, Dept Obstet & Gynecol, Konya, Turkey
关键词
Gestational diabetes; Insulin resistance; SREBP-1c; ChREBP; Lipid metabolism; INSULIN-RESISTANCE; TRANSCRIPTION FACTOR; ADIPOSE-TISSUE; HEPATIC STEATOSIS; EXPRESSION; OBESITY; MELLITUS; ISOFORM; LIVERS; MICE;
D O I
10.1007/s13410-022-01050-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Gestational diabetes mellitus (GDM) is any degree of glucose intolerance diagnosed during pregnancy. Metabolic abnormalities in GDM are associated with pancreatic beta-cell destruction and decreased insulin sensitivity. Carbohydrate-responsive element-binding protein (ChREBP) and sterol regulatory element-binding protein-1c (SREBP-1c) are two transcription factors that play a key role in carbohydrate and lipid metabolism homeostasis. Our aim in this study was to elucidate the role of these proteins in GDM. Methods The study included 50 pregnant women diagnosed with GDM and 52 pregnant women with normal glucose tolerance. Maternal blood samples were collected from pregnant women between the 24th and 28th weeks of pregnancy. Serum SREBP-1c and ChREBP levels were measured with commercial ELISA kits according to the manufacturer's instructions. Results Serum ChREBP (p=0.044) and SREBP1c (p=0.042) levels of pregnant women with normal glucose tolerance were found to be statistically significantly higher than women with GDM.
引用
收藏
页码:587 / 591
页数:5
相关论文
共 27 条
[1]   Gestational diabetes mellitus [J].
Alfadhli, Eman M. .
SAUDI MEDICAL JOURNAL, 2015, 36 (04) :399-406
[2]   The lipogenic transcription factor ChREBP dissociates hepatic steatosis from insulin resistance in mice and humans [J].
Benhamed, Fadila ;
Denechaud, Pierre-Damien ;
Lemoine, Maud ;
Robichon, Celine ;
Moldes, Marthe ;
Bertrand-Michel, Justine ;
Ratziu, Vlad ;
Serfaty, Lawrence ;
Housset, Chantal ;
Capeau, Jacqueline ;
Girard, Jean ;
Guillou, Herve ;
Postic, Catherine .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (06) :2176-2194
[3]  
Chelakkadan M., 2016, J CURR PHARM RES, V9, P1, DOI [10.22159/ijcpr.2017v9i1.16615, DOI 10.22159/IJCPR.2017V9I1.16615]
[4]   Carbohydrate response element binding protein (ChREBP) modulates the inflammatory response of mesangial cells in response to glucose [J].
Chen, Yan ;
Wang, Yan-Jun ;
Zhao, Ying ;
Wang, Jin-Cheng .
BIOSCIENCE REPORTS, 2018, 38
[5]   Liver-specific inhibition of ChREBP improves hepatic steatosis and insulin resistance in ob/ob mice [J].
Dentin, Renaud ;
Benhamed, Fadila ;
Hainault, Isabelle ;
Fauveau, Veronique ;
Foufelle, Fabienne ;
Dyck, Jason R. B. ;
Girard, Jean ;
Postic, Catherine .
DIABETES, 2006, 55 (08) :2159-2170
[6]   Gestational diabetes from A to Z [J].
Dirar, AbdelHameed Mirghani ;
Doupis, John .
WORLD JOURNAL OF DIABETES, 2017, 8 (12) :489-511
[7]   Recent Insights Into SREBP as a Direct Mediator of Kidney Fibrosis via Lipid-Independent Pathways [J].
Dorotea, Debra ;
Koya, Daisuke ;
Ha, Hunjoo .
FRONTIERS IN PHARMACOLOGY, 2020, 11
[8]   Colostrum and mature breast milk analysis of serum irisin and sterol regulatory element-binding proteins-1c in gestational diabetes mellitus [J].
Fatima, Syeda Sadia ;
Khalid, Erum ;
Ladak, Asma Akbar ;
Ali, Syed Adnan .
JOURNAL OF MATERNAL-FETAL & NEONATAL MEDICINE, 2019, 32 (18) :2993-2999
[9]   SREBP-1c transcription factor and lipid homeostasis:: Clinical perspective [J].
Ferre, P. ;
Foufelle, F. .
HORMONE RESEARCH, 2007, 68 (02) :72-82
[10]   A critical role for ChREBP-mediated FGF21 secretion in hepatic fructose metabolism [J].
Fisher, Ffolliott M. ;
Kim, MiSung ;
Doridot, Ludivine ;
Cunniff, Jeremy C. ;
Parker, Thomas S. ;
Levine, Daniel M. ;
Hellerstein, Marc K. ;
Hudgins, Lisa C. ;
Maratos-Flier, Eleftheria ;
Herman, Mark A. .
MOLECULAR METABOLISM, 2017, 6 (01) :14-21