The trans10,cis12 (t10c12) isomer of conjugated linoleic acid (CLA) has bee
n shown to inhibit heparin-releasable lipoprotein lipase activity, reduce l
ipid stores in cultured 3T3-L1 adipocytes, and, when fed to mice, reduce bo
dy fat gain. We now report that t10c12 CLA significantly reduced leptin sec
retion from cultured 3T3-L1 adipocytes, and reduced leptin mRNA levels with
in the cells. Similar effects were produced by conjugated nonadecadienoic a
cid (a 19-carbon CLA cognate that is more effective than CLA in reducing bo
dy fat gain in mice), the lipoxygenase inhibitor nordihydroguaiaretic acid
(which is synergistic with CLA in reducing body fat gain in mice), and cigl
itazone (TZD, a PPAR gamma agonist). Feeding mice diet supplemented with 0.
5% t10c12 CLA for 4 weeks significantly reduced body fat gain, serum leptin
levels and adipocyte leptin mRNA expression, without affecting feed intake
or body weight. These data provide new insights into apparent mechanistic
similarities among t10c12 CLA, CNA NDGA, and TZD. (C) 2001 Academic Press.