Weight gain in response to high-fat feeding in CD-1 male mice

2010 ◽  
Vol 44 (3) ◽  
pp. 231-237 ◽  
Author(s):  
W L Breslin ◽  
K Strohacker ◽  
K C Carpenter ◽  
L Esposito ◽  
Brian K Mcfarlin
Keyword(s):  
High Fat ◽  
Endocrinology ◽  
2013 ◽  
Vol 154 (10) ◽  
pp. 3817-3825 ◽  
Author(s):  
Laura K. Fonken ◽  
Rebecca A. Lieberman ◽  
Zachary M. Weil ◽  
Randy J. Nelson

2015 ◽  
Author(s):  
Nicole M Templeman ◽  
Arya Mehran ◽  
James Johnson

Insulin is an essential hormone with key roles in energy homeostasis and body composition. Mice and rats, unlike other mammals, have two insulin genes: the rodent-specific Ins1 gene and the ancestral Ins2 gene. The relationships between insulin gene dosage and obesity has previously been explored in male and female Ins2-/- mice with full or reduced Ins1 dosage, as well as in female Ins1-/- mice with full or partial Ins2 dosage. We report herein unexpected hyper-variability in circulating insulin and physiological responses to high fat feeding in male Ins1-/-:Ins2+/- mice. Two large cohorts of Ins1-/-:Ins2+/- mice and their Ins1-/-:Ins2+/+ littermates were fed chow diet or high fat diet (HFD) from weaning and housed in specific pathogen-free (SPF) conditions. Cohort A and cohort B were studied one year apart. Contrary to female mice from the same litters, inactivating one Ins2 allele on the complete Ins1-null background did not cause a consistent reduction of circulating insulin in male mice. In cohort A, HFD-fed males showed an equivalent degree of insulin hypersecretion and weight gain, regardless of Ins2 dosage. In cohort B, Ins1-/-:Ins2+/- males showed decreased insulin levels and body mass, compared to Ins1-/-:Ins2+/+ littermates. While experimental conditions were held consistent between cohorts, we found that HFD-fed Ins1-/-:Ins2+/- mice with lower insulin levels had increased corticosterone. Collectively, these observations highlight the hyper-variability and range of phenotypic characteristics modulated by Ins2 gene dosage, specifically in male mice.


2011 ◽  
Vol 52 (9) ◽  
pp. 1723-1732 ◽  
Author(s):  
David W. Nelson ◽  
Yu Gao ◽  
Nicole M. Spencer ◽  
Taylor Banh ◽  
Chi-Liang Eric Yen

2007 ◽  
Vol 113 (4-5) ◽  
pp. 173-185 ◽  
Author(s):  
E. Korsheninnikova ◽  
P. J. Voshol ◽  
B. Baan ◽  
G. C. M. van der Zon ◽  
L. M. Havekes ◽  
...  

Metabolites ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 800
Author(s):  
Federica La Rosa ◽  
Letizia Guiducci ◽  
Maria Angela Guzzardi ◽  
Andrea Cacciato Insilla ◽  
Silvia Burchielli ◽  
...  

Maternal high-fat diet (HFD) affects metabolic and immune development. We aimed to characterize the effects of maternal HFD, and the subsequent diet-normalization of the mothers during a second pregnancy, on the liver and thymus metabolism in their offspring, in minipigs. Offspring born to high-fat (HFD) and normal diet (ND) fed mothers were studied at week 1 and months 1, 6, 12 of life. Liver and thymus glucose uptake (GU) was measured with positron emission tomography during hyperinsulinemic-isoglycemia. Histological analyses were performed to quantify liver steatosis, inflammation, and hepatic hematopoietic niches (HHN), and thymocyte size and density in a subset. The protocol was repeated after maternal-diet-normalization in the HFD group. At one week, HFDoff were characterized by hyperglycemia, hyperinsulinemia, severe insulin resistance (IR), and high liver and thymus GU, associating with thymocyte size and density, with elevated weight-gain, liver IR, and steatosis in the first 6 months of life. Maternal diet normalization reversed thymus and liver hypermetabolism, and increased HHN at one week. It also normalized systemic insulin-sensitivity and liver fat content at all ages. Instead, weight-gain excess, hyperglycemia, and hepatic IR were still observed at 1 month, i.e., end-lactation. We conclude that intra-uterine HFD exposure leads to time-changing metabolic and immune-correlated abnormalities. Maternal diet-normalization reversed most of the effects in the offspring.


2015 ◽  
Vol 29 (S1) ◽  
Author(s):  
Laelie Snook ◽  
Scott Frendo‐Cumbo ◽  
Rebecca MacPherson ◽  
Laura Castellani ◽  
Willem Peppler ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document