Postprandial concentrations and distribution of apo C-III in type 2 diabetic patients. Effect of bezafibrate treatment

Citation
N. Attia et al., Postprandial concentrations and distribution of apo C-III in type 2 diabetic patients. Effect of bezafibrate treatment, ATHEROSCLER, 149(2), 2000, pp. 427-433
Citations number
33
Categorie Soggetti
Cardiovascular & Respiratory Systems","Cardiovascular & Hematology Research
Journal title
ATHEROSCLEROSIS
ISSN journal
00219150 → ACNP
Volume
149
Issue
2
Year of publication
2000
Pages
427 - 433
Database
ISI
SICI code
0021-9150(200004)149:2<427:PCADOA>2.0.ZU;2-D
Abstract
Apo C-III plays a key role in the metabolism of triglyceride-rich lipoprote ins. It has recently been implicated as a potential determinant of the trig lyceride (TG) lowering effect of fibrates, which down-regulate its expressi on. This hypothesis has been explored in ten moderately hypertriglyceridemi c (TG 4.50 +/- 2.40 mmol/l) male type 2 diabetic patients tested with a lip id load before and after 4 weeks of treatment with 400 mg bezafibrate daily . Treatment lowered apo C-III concentrations by 20%, mainly in VLDL. Postpr andially, apo C-III was transferred to chylomicrons in proportion to their TG content exclusively from HDL. VLDL retained their apo C-III and the apo C-III:TG ratio decreased as TG contents increased. At the end of the absorp tive period (8 h) HDL did not recover the totality of their apo C-III (net loss 19 and 28% respectively before and after treatment, P < 0.0001 for tim e effect). Bezafibrate lowered apo E by 33% (P < 0.03). The apo C-III:apo E ratio did not vary significantly under treatment but underwent a postprand ial decrease: 13% before and 18% (P = 0.01) after treatment. These results indicate that repression of apo C-III expression and lowering of the apo C- III:E ratio are not likely mechanisms for the lipid-lowering effects of fib rates in type 2 diabetic patients. The potent effects on postprandial lipem ia are suggestive of an apo C-III-independent stimulation of lipolysis. (C) 2000 Elsevier Science Ireland Ltd. All rights reserved.