| First Author | Bohlen TM | Year | 2016 |
| Journal | Mol Cell Endocrinol | Volume | 423 |
| Pages | 11-21 | PubMed ID | 26762764 |
| Mgi Jnum | J:237320 | Mgi Id | MGI:5811978 |
| Doi | 10.1016/j.mce.2015.12.022 | Citation | Bohlen TM, et al. (2016) Fatness rather than leptin sensitivity determines the timing of puberty in female mice. Mol Cell Endocrinol 423:11-21 |
| abstractText | Leptin is a permissive factor for the onset of puberty. However, changes in adiposity frequently influence leptin sensitivity. Thus, the objective of the present study was to investigate how changes in body weight, fatness, leptin levels and leptin sensitivity interact to control the timing of puberty in female mice. Pre-pubertal obesity, induced by raising C57BL/6 mice in small litters, led to an early puberty onset. Inactivation of Socs3 gene in the brain or exclusively in leptin receptor-expressing cells reduced the body weight and leptin levels at pubertal onset, and increased leptin sensitivity. Notably, these female mice exhibited significant delays in vaginal opening, first estrus and onset of estrus cyclicity. In conclusion, our findings suggest that increased leptin sensitivity did not play an important role in favoring pubertal onset in female mice. Rather, changes in pubertal body weight, fatness and/or leptin levels were more important in influencing the timing of puberty. |
