Abstract
Leptin has been believed to exert its weight-reducing action not only by inducing hypophagia but also by increasing energy expenditure/thermogenesis. Leptin-deficient ob/ob mice have correspondingly been thought to be thermogenically limited and to show hypothermia, mainly due to atrophied brown adipose tissue (BAT). In contrast to these established views, we found that BAT is fully functional and that leptin treatment did not increase thermogenesis in wild-type or in ob/ob mice. Rather, ob/ob mice showed a decreased but defended body temperature (i.e., were anapyrexic, not hypothermic) that was normalized to wild-type levels after leptin treatment. This was not accompanied by increased energy expenditure or BAT recruitment but, instead, was mediated by decreased tail heat loss. The weight-reducing hypophagic effects of leptin are, therefore, not augmented through a thermogenic effect of leptin; leptin is, however, pyrexic, i.e., it alters centrally regulated thresholds of thermoregulatory mechanisms, in parallel to effects of other cytokines.
| Original language | English |
|---|---|
| Journal | Cell Reports |
| Volume | 14 |
| Issue number | 7 |
| Pages (from-to) | 1621-1631 |
| Number of pages | 11 |
| DOIs | |
| Publication status | Published - 23.02.2016 |
Funding
The authors thank Jörg Heeren, Markus Heine, and Christian Schlein for discussions and Robert Csikasz and Sarina Paesler for technical assistance. The study was supported by grants from the Swedish Research Council, The Knut and Alice Wallenberg Foundation, the Studienstiftung des Deutschen Volkes, and the German Research Council DFG.
Research Areas and Centers
- Academic Focus: Center for Brain, Behavior and Metabolism (CBBM)