Gender differences between hypocretin/orexin knockout and wild type mice: age, body weight, body composition, metabolic markers, leptin and insulin resistance.
|Title||Gender differences between hypocretin/orexin knockout and wild type mice: age, body weight, body composition, metabolic markers, leptin and insulin resistance.|
|Publication Type||Journal Article|
|Year of Publication||2014|
|Authors||Ramanathan L, Siegel JM|
|Date Published||2014 Dec|
|Keywords||Aging, Animals, Body Composition, Body Weight, Female, Insulin Resistance, Intracellular Signaling Peptides and Proteins, Leptin, Male, Mice, Mice, Inbred C57BL, Mice, Knockout, Neuropeptides, Orexins, Sex Characteristics|
Female hypocretin knockout (Hcrt KO) mice have increased body weight despite decreased food intake compared to wild type (WT) mice. In order to understand the nature of the increased body weight, we carried out a detailed study of Hcrt KO and WT, male, and female mice. Female KO mice showed consistently higher body weight than WT mice, from 4 to 20 months (20-60%). Fat, muscle, and free fluid levels were all significantly higher in adult (7-9 months) as well as old (18-20 months) female KO mice compared to age-matched WT mice. Old male KO mice showed significantly higher fat content (150%) compared to age-matched WT mice, but no significant change in body weight. Respiratory quotient (-19%) and metabolic rates (-14%) were significantly lower in KO mice compared to WT mice, regardless of gender or age. Female KO mice had significantly higher serum leptin levels (191%) than WT mice at 18-20 months, but no difference between male mice were observed. Conversely, insulin resistance was significantly higher in both male (73%) and female (93%) KO mice compared to age- and sex-matched WT mice. We conclude that absence of the Hcrt peptide has gender-specific effects. In contrast, Hcrt-ataxin mice and human narcoleptics, with loss of the whole Hcrt cell, show weight gain in both sexes.
|Alternate Journal||J. Neurochem.|
|Grant List||MH64109 / MH / NIMH NIH HHS / United States |
NS14610 / NS / NINDS NIH HHS / United States