| First Author | Torres DJ | Year | 2021 |
| Journal | Int J Mol Sci | Volume | 22 |
| Issue | 20 | PubMed ID | 34681674 |
| Mgi Jnum | J:313682 | Mgi Id | MGI:6786789 |
| Doi | 10.3390/ijms222011010 | Citation | Torres DJ, et al. (2021) Female Mice with Selenocysteine tRNA Deletion in Agrp Neurons Maintain Leptin Sensitivity and Resist Weight Gain While on a High-Fat Diet. Int J Mol Sci 22(20) |
| abstractText | The role of the essential trace element selenium in hypothalamic physiology has begun to come to light over recent years. Selenium is used to synthesize a family of proteins participating in redox reactions called selenoproteins, which contain a selenocysteine residue in place of a cysteine. Past studies have shown that disrupted selenoprotein expression in the hypothalamus can adversely impact energy homeostasis. There is also evidence that selenium supports leptin signaling in the hypothalamus by maintaining proper redox balance. In this study, we generated mice with conditional knockout of the selenocysteine tRNA([Ser]Sec) gene (Trsp) in an orexigenic cell population called agouti-related peptide (Agrp)-positive neurons. We found that female Trsp(Agrp)KO mice gain less weight while on a high-fat diet, which occurs due to changes in adipose tissue activity. Female Trsp(Agrp)KO mice also retained hypothalamic sensitivity to leptin administration. Male mice were unaffected, however, highlighting the sexually dimorphic influence of selenium on neurobiology and energy homeostasis. These findings provide novel insight into the role of selenoproteins within a small yet heavily influential population of hypothalamic neurons. |
