Sex differences in the metabolic effects of diet-induced obesity vary by age of onset

2018 ◽  
Vol 42 (5) ◽  
pp. 1088-1091 ◽  
Author(s):  
Abigail E. Salinero ◽  
Brian M. Anderson ◽  
Kristen L. Zuloaga
Sleep Health ◽  
2021 ◽  
Author(s):  
Nina C. Polyné ◽  
Katherine E. Miller ◽  
Janeese Brownlow ◽  
Philip R. Gehrman

2011 ◽  
Vol 7 (3) ◽  
pp. 399-400
Author(s):  
Tatiana Zupekan ◽  
Sandhya Bondada ◽  
Catherine E. Lewis ◽  
Daniel A. DeUgarte

1990 ◽  
Vol 156 (6) ◽  
pp. 842-845 ◽  
Author(s):  
Charles D. T. Sibisi

Data from a UK national sample showed differences between the sexes in age-specific inception rates for mania. Women had a higher inception rate than men during the middle years. The cumulative admission rates were nearly equal between the sexes.


Author(s):  
Luciano F. Drager ◽  
Jiango Li ◽  
Christian Reinke ◽  
S Bevans-Fonti ◽  
J Jun ◽  
...  

2019 ◽  
Vol 29 ◽  
pp. S215-S216
Author(s):  
Chuan Jiao ◽  
Richard Kopp ◽  
Elizabeth Kuney ◽  
Chao Chen ◽  
Chunyu Liu

Endocrinology ◽  
2006 ◽  
Vol 147 (12) ◽  
pp. 5855-5864 ◽  
Author(s):  
Jonathan D. Roth ◽  
Heather Hughes ◽  
Eric Kendall ◽  
Alain D. Baron ◽  
Christen M. Anderson

Effects of amylin and pair feeding (PF) on body weight and metabolic parameters were characterized in diet-induced obesity-prone rats. Peripherally administered rat amylin (300 μg/kg·d, 22d) reduced food intake and slowed weight gain: approximately 10% (P < 0.05), similar to PF. Fat loss was 3-fold greater in amylin-treated rats vs. PF (P < 0.05). Whereas PF decreased lean tissue (P < 0.05 vs. vehicle controls; VEH), amylin did not. During wk 1, amylin and PF reduced 24-h respiratory quotient (mean ± se, 0.82 ± 0.0, 0.81 ± 0.0, respectively; P < 0.05) similar to VEH (0.84 ± 0.01). Energy expenditure (EE mean ± se) tended to be reduced by PF (5.67 ± 0.1 kcal/h·kg) and maintained by amylin (5.86 ± 0.1 kcal/h·kg) relative to VEH (5.77 ± 0.0 kcal/h·kg). By wk 3, respiratory quotient no longer differed; however, EE increased with amylin treatment (5.74 ± 0.09 kcal/·kg; P < 0.05) relative to VEH (5.49 ± 0.06) and PF (5.38 ± 0.07 kcal/h·kg). Differences in EE, attributed to differences in lean mass, argued against specific amylin-induced thermogenesis. Weight loss in amylin and pair-fed rats was accompanied by similar increases arcuate neuropeptide Y mRNA (P < 0.05). Amylin treatment, but not PF, increased proopiomelanocortin mRNA levels (P < 0.05 vs. VEH). In a rodent model of obesity, amylin reduced body weight and body fat, with relative preservation of lean tissue, through anorexigenic and specific metabolic effects.


1993 ◽  
Vol 34 (3) ◽  
pp. 187-191 ◽  
Author(s):  
Richard C. Evenson ◽  
Scott T. Meier ◽  
Brian J. Hagan

2018 ◽  
Vol 239 (2) ◽  
pp. 229-240 ◽  
Author(s):  
A Feraco ◽  
A Armani ◽  
R Urbanet ◽  
A Nguyen Dinh Cat ◽  
V Marzolla ◽  
...  

Obesity is a major risk factor that contributes to the development of cardiovascular disease and type 2 diabetes. Mineralocorticoid receptor (MR) expression is increased in the adipose tissue of obese patients and several studies provide evidence that MR pharmacological antagonism improves glucose metabolism in genetic and diet-induced mouse models of obesity. In order to investigate whether the lack of adipocyte MR is sufficient to explain these beneficial metabolic effects, we generated a mouse model with inducible adipocyte-specific deletion of Nr3c2 gene encoding MR (adipo-MRKO). We observed a significant, yet not complete, reduction of Nr3c2 transcript and MR protein expression in subcutaneous and visceral adipose depots of adipo-MRKO mice. Notably, only mature adipocyte fraction lacks MR, whereas the stromal vascular fraction maintains normal MR expression in our mouse model. Adipo-MRKO mice fed a 45% high-fat diet for 14 weeks did not show any significant difference in body weight and fat mass compared to control littermates. Glucose and insulin tolerance tests revealed that mature adipocyte MR deficiency did not improve insulin sensitivity in response to a metabolic homeostatic challenge. Accordingly, no significant changes were observed in gene expression profile of adipogenic and inflammatory markers in adipose tissue of adipo-MRKO mice. Moreover, pharmacological MR antagonism in mature primary murine adipocytes, which differentiated ex vivo from WT mice, did not display any effect on adipokine expression. Taken together, these data demonstrate that the depletion of MR in mature adipocytes displays a minor role in diet-induced obesity and metabolic dysfunctions.


2017 ◽  
Vol 216 (1) ◽  
pp. S15-S16 ◽  
Author(s):  
Andrea G. Edlow ◽  
Larissa H. Mattei ◽  
Ingy O. Khattaby ◽  
Charlotte A. Williamson ◽  
Sanaya Daruvala ◽  
...  

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