Abstract
Laboratory mouse models with genetically altered growth hormone (GH) signaling and subsequent endocrine disruptions, have longer lifespans than control littermates. As such, these mice are commonly examined to determine the role of the somatotropic axis as it relates to healthspan and longevity in mammals. The two most prominent mouse mutants in this context are the genetically dwarf Ames and Snell models which have been studied extensively for over two decades. However, it has only been proposed recently that both white and brown adipose tissue depots may contribute to their delayed aging. Here we review the current state of the field and supplement it with recent data from our labs.
| Original language | English (US) |
|---|---|
| Article number | 176 |
| Journal | Metabolites |
| Volume | 10 |
| Issue number | 5 |
| DOIs | |
| State | Published - May 2020 |
| Externally published | Yes |
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
- Brown adipose tissue
- IGF-1
- Lipids
- Pituitary specific factor 1 (Pit-I)
- Prophet of Pituitary 1 (PropI)
- White adipose tissue
ASJC Scopus subject areas
- Endocrinology, Diabetes and Metabolism
- Biochemistry
- Molecular Biology
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