TY - JOUR
T1 - Ovarian hormones inhibit fat intake under binge-type conditions in ovariectomized rats
AU - Yu, Zhiping
AU - Geary, Nori
AU - Corwin, Rebecca L.
N1 - Funding Information:
The authors thank Allison Brown for her excellent technical assistance with the carcass composition analysis. We also would like to thank Kim Feeney, Lauren Chuday, Jessica Hedden, and Maggie Sikora for their assistance with data collection. This work was supported by NIH 1-R01-MH6794301, as well as the Women in Science and Engineering Research Program (WISER) funded by the Pennsylvania Space Grant Consortium.
PY - 2008/10/20
Y1 - 2008/10/20
N2 - Binge eating is more common in females than in males. This study investigated the effects of ovarian hormones on binge-eating behavior in a diet-related rat model. Six groups of ovariectomized Sprague-Dawley rats were used (n = 13/group). All rats had continuous access to chow and water throughout the study. One half of the rats were injected every fourth day with estradiol benzoate (2 μg/100 μl sesame oil) and progesterone (500 μg/100 μl sesame oil); the other half received only the sesame oil vehicle. Three feeding protocols were tested in each hormone injection condition: (1) chow only: no additional dietary fat access; (2) low-restriction: 1-h fat access every day; (3) high-restriction: 1-h fat access on Monday, Wednesday, and Friday. As previously reported in intact male and female rats, the high-restriction groups exhibited binge-like increases in 1-h energy intake during fat access. The major new finding of this study is that 1-h energy intake was tonically, but not cyclically, reduced in the hormone-treated high-restriction (binge) rats. Specifically, both low- and high-restriction hormone-treated rats consumed significantly less energy than did the oil-treated rats during the 1-h fat period (p < 0.0001) and overall (p < 0.0001), indicating a tonic inhibition of eating. However, food intake during the 1-h fat access period was also cyclically reduced in the hormone-treated low-restriction rats, but not in the hormone-treated high-restriction rats. These results indicate that the normal cyclic inhibitory influence of ovarian hormones on eating, but not their normal tonic inhibitory influence, is disrupted by conditions leading to binge-type eating.
AB - Binge eating is more common in females than in males. This study investigated the effects of ovarian hormones on binge-eating behavior in a diet-related rat model. Six groups of ovariectomized Sprague-Dawley rats were used (n = 13/group). All rats had continuous access to chow and water throughout the study. One half of the rats were injected every fourth day with estradiol benzoate (2 μg/100 μl sesame oil) and progesterone (500 μg/100 μl sesame oil); the other half received only the sesame oil vehicle. Three feeding protocols were tested in each hormone injection condition: (1) chow only: no additional dietary fat access; (2) low-restriction: 1-h fat access every day; (3) high-restriction: 1-h fat access on Monday, Wednesday, and Friday. As previously reported in intact male and female rats, the high-restriction groups exhibited binge-like increases in 1-h energy intake during fat access. The major new finding of this study is that 1-h energy intake was tonically, but not cyclically, reduced in the hormone-treated high-restriction (binge) rats. Specifically, both low- and high-restriction hormone-treated rats consumed significantly less energy than did the oil-treated rats during the 1-h fat period (p < 0.0001) and overall (p < 0.0001), indicating a tonic inhibition of eating. However, food intake during the 1-h fat access period was also cyclically reduced in the hormone-treated low-restriction rats, but not in the hormone-treated high-restriction rats. These results indicate that the normal cyclic inhibitory influence of ovarian hormones on eating, but not their normal tonic inhibitory influence, is disrupted by conditions leading to binge-type eating.
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U2 - 10.1016/j.physbeh.2008.07.021
DO - 10.1016/j.physbeh.2008.07.021
M3 - Article
C2 - 18706435
AN - SCOPUS:52949101346
SN - 0031-9384
VL - 95
SP - 501
EP - 507
JO - Physiology and Behavior
JF - Physiology and Behavior
IS - 3
ER -