Cholesteryl ester transfer protein expression is down-regulated in hyperinsulinemic transgenic mice

Autor: P.R. Patricio, Everardo M. Carneiro, E.J.B. Bighetti, J.A. Berti, A.C. Casquero, Helena C. F. Oliveira, Antonio C. Boschero
Rok vydání: 2003
Předmět:
medicine.medical_specialty
medicine.medical_treatment
Lipoproteins
experimental diabetes
cholesteryl ester transfer protein gene expression
lipoprotein lipase
Down-Regulation
Mice
Transgenic

QD415-436
Carbohydrate metabolism
Biochemistry
chemistry.chemical_compound
Mice
Endocrinology
Downregulation and upregulation
Internal medicine
Hyperinsulinism
Cholesterylester transfer protein
medicine
Hyperinsulinemia
Animals
Humans
Insulin
RNA
Messenger

triglycerides
Glycoproteins
biology
Triglyceride
Cell Biology
medicine.disease
Streptozotocin
Cholesterol Ester Transfer Proteins
carbohydrates (lipids)
Glucose
chemistry
Gene Expression Regulation
Liver
Cholesteryl ester
biology.protein
Body Composition
lipids (amino acids
peptides
and proteins)

hyperglycemia
Cholesterol Esters
Carrier Proteins
medicine.drug
Zdroj: Journal of Lipid Research, Vol 44, Iss 10, Pp 1870-1876 (2003)
ISSN: 0022-2275
Popis: Cholesteryl ester transfer protein (CETP) mediates cholesteryl ester (CE) and triglyceride redistribution among plasma lipoproteins. In this work, we investigated whether varying levels of insulin regulate the CETP expression in vivo. Insulin deficiency [streptozotocin (STZ) injection], and hyperinsulinemia (insulin injections, 14 days) were induced in transgenic mice expressing a human CETP minigene flanked by its natural regulatory sequences. Glucose supplementation was provided to the hyperinsulinemic group (INS+GLUC) and to an extra group of mice (GLUC). In the STZ group, endogenous CE transfer rate, plasma CETP, and hepatic CETP mRNA levels were enhanced 3.0-, 1.5-, and 2.5-fold, respectively, as compared with controls. Insulin replacement in STZ mice normalized their glycemia and liver mRNA levels. Higher plasma CETP levels were observed in GLUC mice, which were decreased in INS+GLUC mice. Hepatic CETP mRNA was not altered in GLUC mice and was reduced by one-third in INS+GLUC mice. These results show that: 1) STZ treatment increases CETP plasma levels and liver mRNA expression; 2) diet glucose supplementation increases plasma CETP levels but does not change liver mRNA abundance; and 3) daily insulin injections blunt the glucose-stimulated CETP expression by reducing its liver mRNA levels. These data suggest that insulin down-regulates CETP gene expression.
Databáze: OpenAIRE