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. 2010 Oct 6;299(6):R1634–R1642. doi: 10.1152/ajpregu.00219.2010

Table 1.

Morphometric and plasma characteristics

Group
P Value
Lean
Obese
Variable Cycling OVX Cycling OVX Obesity effect OVX effect
Weight gain, g/day 0.51 ± 0.49 2.91 ± 0.35 0.44 ± 0.30 3.01 ± 0.41 0.976 <0.001
Body wt,* g 308.8 ± 7.4 318.1 ± 6.1 380.3 ± 14.0 390.4 ± 9.3 <0.001 0.342
FFM,* g 237.6 ± 5.1 246.7 ± 3.9 268.9 ± 9.2 275.7 ± 6.1 <0.001 0.240
FM*
    g 71.2 ± 5.0 71.5 ± 4.9 111.4 ± 6.0 114.8 ± 6.2 <0.001 0.753
    % 22.9 ± 1.3 22.3 ± 1.2 29.2 ± 0.9 29.2 ± 1.2 <0.001 0.796
Glucose, mM 9.84 ± 0.5 12.95 ± 0.8 11.05 ± 0.7 14.02 ± 0.7 0.207 <0.001
Cholesterol, mM 2.06 ± 0.3 2.11 ± 0.4 1.88 ± 0.3 2.34 ± 0.3 0.953 0.459
TGs,* mM 0.93 ± 0.1 1.08 ± 0.2 1.53 ± 0.3 2.43 ± 0.6 0.008 0.140
NEFAs, μM 714.0 ± 79.6 433.4 ± 58.0 650.8 ± 55.3 602.8 ± 66.8 0.546 0.048
Estradiol, pM 167.2 ± 18.3 52.7 ± 8.6 187.6 ± 19.3 49.5 ± 5.3 0.886 <0.001

Values are means ± SE. For rate of weight gain, all animals (n = 20–25 per group) were included in the analysis; for plasma and some morphometric measurements, a representative subset of animals (n = 10–14 per group) was used. FFM, fat-free mass; FM, fat mass; TGs, triglycerides; NEFAs, nonesterified fatty acids. Body composition was determined through a combination of dual-energy X-ray absorptiometry and quantitative magnetic resonance imaging. Plasma was collected on diestrus 2 (cycling animals) or at the time of death [ovariectomized (OVX) animals], and cholesterol, TGs, NEFAs, glucose, and estradiol were measured using standard assays. Data were examined by ANOVA, with significance set at P < 0.05:

*

obesity effect;

OVX effect.