Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 626-631 |
| Number of pages | 6 |
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 355 |
| Issue number | 3 |
| DOIs | |
| State | Published - 13 Apr 2007 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adipocytes
- Body weight
- Diet-induce obesity
- IFNα
- Leptin
ASJC Scopus subject areas
- Biophysics
- Biochemistry
- Molecular Biology
- Cell Biology
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