Effects of short-term administration of conjugated linoleic acid on lipid metabolism in white and brown adipose tissues of starved/refed Otsuka Long-Evans Tokushima Fatty rats

Citation
Sm. Rahman et al., Effects of short-term administration of conjugated linoleic acid on lipid metabolism in white and brown adipose tissues of starved/refed Otsuka Long-Evans Tokushima Fatty rats, FOOD RES IN, 34(6), 2001, pp. 515-520
Citations number
44
Categorie Soggetti
Food Science/Nutrition
Journal title
FOOD RESEARCH INTERNATIONAL
ISSN journal
09639969 → ACNP
Volume
34
Issue
6
Year of publication
2001
Pages
515 - 520
Database
ISI
SICI code
0963-9969(2001)34:6<515:EOSAOC>2.0.ZU;2-F
Abstract
The present study explored the short-term effects of dietary conjugated lin oleic acid (CLA) on body fat accumulation and lipid metabolism in starved/r efed Otsuka Long-Evans Tokushima Fatty (OLETF) rats. Male OLETF rats of 12- weeks-old were starved for 24 h and then re-fed for 48 h either with CLA di et [7.5% CLA and 7.5% safflower oil (SAF)] or SAF control diet (15% SAF oil ). The results demonstrated a 27% reduction of white adipose tissue wet wei ght (total of epididymal and perirenal adipose tissue weight) in the CLA gr oup compared to the control group. The activity of mitochondrial carnitine palmitoyltransferase (CPT), the rate-limiting enzyme for fatty acid oxidati on, was significantly elevated by 1.7- and 1.6-fold in perirenal white adip ose tissue and interscapular brown adipose tissues, respectively, in the CL A group compared to the control. In contrast, phosphatidate phosphohydrolas e (PAP), the rate-limiting enzyme for triglyceride (TG) synthesis, was foun d to be 23 and 15% lower, in perirenal white- and brown-adipose tissue of C LA-fed rats, respectively. In addition, CLA feeding led to a significant re duced concentration of serum total- and HDL-cholesterol and phospholipid. T hus, dietary CLA evidently lowers abdominal white adipose tissue wet weight through an enhanced fatty acid oxidation and a reduced TG synthesis. (C) 2 001 Elsevier Science Ltd. All rights reserved.