Recent studies have demonstrated a reduction in body fat in growing animals
fed conjugated linoleic acid (CLA). Two experiments were conducted to exte
nd these observations to obese rats so that the mechanism of the actions of
CLA might be more easily elucidated. In experiment 1, male lean and obese
Zucker rats were fed diets containing either 0 or 0.5% CLA for 5 wk. There
was no effect of diet on growth rate or food intake. Dietary CLA reduced re
troperitoneal and inguinal fat pad weights in the lean rats but increased f
at pad weights in the obese genotype (diet x genotype interaction; P < 0.05
). Determination of fat pad cellularity indicated that these changes in fat
pad weight were due to a reduction or increase in average fat cell size fo
r the lean and obese Zucker rats, respectively. In experiment 2, we sought
to reproduce these effects on fat pad size, as well as to determine the eff
ect of dietary CLA on the catabolic response to bacterial endotoxin injecti
on in obese Zucker rats. Growing female lean and obese Zucker rats were fed
diets containing 0 or 0.5% CLA for 8 wk. On d 28, each rat was injected in
traperitoneally with lipopolysaccharide from Escherichia coli serotype 055:
B5 (1 mg/kg body weight) and body weight was determined over the next 96 h.
There was a diet x genotype interaction (P ( 0.05) for the body weight res
ponse to lipopolysaccharide 24 h postinjection. Lean rats fed CLA lost less
weight than did lean controls, but obese rats fed CLA lost more weight tha
n did obese controls. As in the first experiment, there was a diet x genoty
pe (P < 0.05) for the effect of treatment on retroperitoneal fat pad weight
s determined at the end of the experiment. Lean rats fed CLA had smaller RP
fat pads than did lean controls, but obese rats fed CLA once again had hea
vier RP fat pads than did obese controls. These results indicate that CLA r
educes body fat and catabolic response to endotoxin injection in lean Zucke
r rats but not in the obese genotype. The observed interaction between diet
and genotype warrants additional investigation into the specific mechanism
(s) of the biological activities of CLA.