Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1938873 | Biochemical and Biophysical Research Communications | 2007 | 6 Pages |
Leptin, an adipokine, a major regulator of food intake, was recently suggested to play a role in immune response. We previously showed that weight reduction following IFNα therapy is due, at least in part, to direct induction of adipose tissue apoptosis. We now studied the effect of leptin on IFNα treated adipocytes in vitro and in vivo. Diet induced obese C57/B6 mice were treated continually with recombinant (r) IFNαA/D + leptin (100 U/g body weight + 10 μg/day, respectably) or leptin (10 μg/day) alone for 8 days. Co-administration of IFNαA/D + leptin significantly reduced plasma cholesterol (P < 0.001), glucose (P < 0.007) and pro-apoptotic protein levels (P < 0.05). Additionally, co-administration prevented loss of body weight due to adipocyte apoptosis. Thus, leptin co-administration with IFNαA/D decreases some of the side effects of IFNα administration such as weight loss, cholesterol and glucose levels.