Liraglutide improves lipid and carbohydrate metabolism of ovariectomized rats

被引:14
作者
Argenta Model, Jorge Felipe [1 ]
Lima, Matheus Vieira [1 ]
Ohlweiler, Renata [1 ]
Vogt, Everton Lopes [1 ]
Rocha, Debora Santos [1 ]
de Souza, Samir Khal [1 ]
Turck, Patrick [1 ]
da Rosa Araujo, Alex Sander [1 ]
Vinagre, Anapaula Sommer [1 ]
机构
[1] Univ Fed Rio Grande do Sul UFRGS, Dept Physiol, Porto Alegre, RS, Brazil
关键词
Lipid metabolism; Carbohydrate metabolism; Brown adipose tissue; White adipose tissue; Heart; Redox homeostasis; Oxidative stress; BROWN ADIPOSE-TISSUE; GLUCAGON-LIKE PEPTIDE-1; GLP-1 RECEPTOR AGONIST; BEIGE FAT DEVELOPMENT; OXIDATIVE STRESS; GENE-EXPRESSION; EPICARDIAL FAT; GLYCOGEN FORMATION; INDUCED OBESITY; ESTROGEN;
D O I
10.1016/j.mce.2021.111158
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Considering that post-menopausal women and ovariectomized rodents develop obesity associated with increased visceral fat, this study was developed to investigate if liraglutide, a glucagon-like peptide 1 (GLP1) analogue, could improve the metabolism of estrogen (E2) deficient females. Wistar rats were ovariectomized (OVX), and subdivided in four groups: sham saline, sham liraglutide, OVX saline, and OVX liraglutide. After sixty days, metabolic parameters of blood, heart, liver, brown (BAT) and white adipose tissue (WAT) visceral depots, and, heart oxidative homeostasis, were evaluated. Castration increased the animals' body weight, the relative weight of the WAT depots, hepatic triglycerides and cardiac glycogen content. Liraglutide treatment reversed these effects, decreased WAT depots weight and increased glucose oxidation and lipogenesis in BAT and WAT. In addition, liraglutide enhanced adrenalin (A) lipolytic effect. These results indicate that liraglutide may be a promising treatment to restore lipid homeostasis and prevent weight gain associated with E2 deficiency.
引用
收藏
页数:11
相关论文
共 107 条
[1]  
AEBI H, 1984, METHOD ENZYMOL, V105, P121
[2]   ROLE OF OVARIAN HORMONES IN THE LONG-TERM CONTROL OF GLUCOSE-HOMEOSTASIS GLYCOGEN FORMATION AND GLUCONEOGENESIS [J].
AHMEDSOROUR, H ;
BAILEY, CJ .
ANNALS OF NUTRITION AND METABOLISM, 1981, 25 (04) :208-212
[3]   Changes in thiol content and expression of glutathione redox system genes in the hippocampus and cerebellum in Alzheimer's disease [J].
Aksenov, MY ;
Markesbery, WR .
NEUROSCIENCE LETTERS, 2001, 302 (2-3) :141-145
[4]   'Browning' the cardiac and peri-vascular adipose tissues to modulate cardiovascular risk [J].
Aldiss, Peter ;
Davies, Graeme ;
Woods, Rachel ;
Budge, Helen ;
Sacks, Harold S. ;
Symonds, Michael E. .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2017, 228 :265-274
[5]   The glucagon-like peptide-1 analogue exendin-4 reverses impaired intracellular Ca2+ signalling in steatotic hepatocytes [J].
Ali, Eunues S. ;
Hua, Jin ;
Wilson, Claire H. ;
Tallis, George A. ;
Zhou, Fiona H. ;
Rychkov, Grigori Y. ;
Barritt, Greg J. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2016, 1863 (09) :2135-2146
[6]  
[Anonymous], 1985, HDB METHODS OXYG RAD
[7]   Liver glyconeogenesis:: a pathway to cope with postprandial amino acid excess in high-protein fed rats? [J].
Azzout-Marniche, Dalila ;
Gaudichon, Claire ;
Blouet, Clemence ;
Bos, Cecile ;
Mathe, Veronique ;
Huneau, JeanFrancois ;
Tome, Daniel .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2007, 292 (04) :R1400-R1407
[8]   Biology of incretins: GLP-1 and GIP [J].
Baggio, Laurie L. ;
Drucker, Daniel J. .
GASTROENTEROLOGY, 2007, 132 (06) :2131-2157
[9]   Myocardial antioxidant and oxidative stress changes due to sex hormones [J].
Barp, J ;
Araújo, ASR ;
Fernandes, TRG ;
Rigatto, KV ;
Llesuy, S ;
Belló-Klein, A ;
Singal, P .
BRAZILIAN JOURNAL OF MEDICAL AND BIOLOGICAL RESEARCH, 2002, 35 (09) :1075-1081
[10]   Metformin ameliorates body mass gain and early metabolic changes in ovariectomized rats [J].
Barthem, Clarissa Souza ;
Rossetti, Camila Ludke ;
Carvalho, Denise P. ;
da-Silva, Wagner Seixas .
ENDOCRINE CONNECTIONS, 2019, 8 (12) :1568-1578