Cholesteryl Ester Transfer Protein (CETP) expression does not affect glucose homeostasis and insulin secretion: studies in human CETP transgenic mice

Autor: Emerielle C. Vanzela, Helena Fonseca Raposo, Helena C. F. Oliveira, J.A. Berti
Rok vydání: 2016
Předmět:
0301 basic medicine
medicine.medical_specialty
Glucose uptake
Endocrinology
Diabetes and Metabolism

medicine.medical_treatment
Clinical Biochemistry
Cholesteryl ester transfer protein (CETP)
Mice
Obese

Mice
Transgenic

030204 cardiovascular system & hematology
Carbohydrate metabolism
Glucose homeostasis
03 medical and health sciences
chemistry.chemical_compound
0302 clinical medicine
Endocrinology
Internal medicine
Insulin Secretion
Cholesterylester transfer protein
medicine
Animals
Homeostasis
Insulin
RNA
Messenger

Biochemistry
medical

Glucose tolerance test
Glucose Transporter Type 4
biology
medicine.diagnostic_test
Research
Biochemistry (medical)
Torcetrapib
Glucose Tolerance Test
Insulin sensitivity
Cholesterol Ester Transfer Proteins
carbohydrates (lipids)
Glucose
030104 developmental biology
Adipose Tissue
Gene Expression Regulation
chemistry
biology.protein
Female
lipids (amino acids
peptides
and proteins)
Zdroj: Lipids in Health and Disease
ISSN: 1476-511X
DOI: 10.1186/s12944-016-0179-6
Popis: Background Cholesteryl ester transfer protein (CETP) is a plasma protein that mediates the exchange of triglycerides for esterified cholesterol between HDL and apoB-lipoproteins. Previous studies suggest that CETP may modify glucose metabolism in patients or cultured cells. In this study, we tested if stable CETP expression would impair glucose metabolism. Methods We used human CETP transgenic mice and non-transgenic littermate controls (NTg), fed with control or high fat diet, as well as in dyslipidemic background and aging conditions. Assays included glucose and insulin tolerance tests, isolated islets insulin secretion, tissue glucose uptake and adipose tissue GLUT mRNA expression. Results CETP expression did not modify glucose or insulin tolerance in all tested conditions such as chow and high fat diet, adult and aged mice, normo and dyslipidemic backgrounds. Fasting and fed state plasma levels of insulin were not differ in CETP and NTg mice. Direct measurements of isolated pancreatic islet insulin secretion rates induced by glucose (11, 16.7 or 22 mM), KCl (40 mM), and leucine (10 mM) were similar in NTg and CETP mice, indicating that CETP expression did not affect β-cell function in vivo and ex vivo. Glucose uptake by insulin target tissues, measured in vivo using 3H-2-deoxyglucose, showed that CETP expression had no effect on the glucose uptake in liver, muscle, perigonadal, perirenal, subcutaneous and brown adipose tissues. Accordingly, GLUT1 and GLUT4 mRNA in adipose tissue were not affected by CETP. Conclusions In summary, by comparing the in vivo all-or-nothing CETP expressing mouse models, we demonstrated that CETP per se has no impact on the glucose tolerance and tissue uptake, global insulin sensitivity and beta cell insulin secretion rates.
Databáze: OpenAIRE