Effects of stereoisomers of estradiol on food intake, body weight and hoarding behavior in female rats

The effects of 17-alpha and 17-beta estradiol on food intake, body weight and hoarding behavior in ovariectomised rats were investigated. For five days, ten animals received subcutaneous injections of both isomers (10 micrograms/kg/day) in a counterbalanced design. Hoarding tests were conducted on the last three days of each 5-day injection period. 17-Alpha estradiol significantly reduced food intake but was without effect on body weight. 17-Beta estradiol reduced food intake significantly more than the alpha form and also significantly reduced body weight. These differential effects suggest that stereoisomers of estradiol may be acting on separate regulatory systems. The treatments did not change hoarding activity compared to pre-treatment levels.     

Effects of voluntary exercise on sexual behavior in female rats

In two experiments, ovariectomized rats given access to activity wheels showed significantly higher lordosis ratings following estradiol treatment than animals maintained in individual hanging cages. Estrogen-induced decreases in body weight also were greater in wheel-housed animals. We suggest that access to running wheels may alter responsiveness to estradiol.     

Effects of ovariectomy and estradiol on body weight and food intake in gold thioglucose-treated mice

Two experiments investigated the effects of ovariectomy and estradiol replacement on the body weight and food intake of mice that had previously been treated with either gold thioglucose or saline. Ovariectomy and estradiol benzoate injections altered food intake in gold thioglucose-treated mice as much as in saline controls. Ovariectomy increased body weight in saline controls but it was without effect on the body weight of gold thioglucose-treated mice.     

Effect of treadmill exercise on food intake and body weight in lean and obese rats

Body weight and food intake of lean and obese, male and female Osborne-Mendel rats following treadmill exercise were compared. Rats were assigned, separately by sex, to one of three diet groups; Group 1 was fed a low fat (10%) diet throughout the study, Group 2 was fed a high fat (55%) diet for 16 weeks and then switched to the low fat diet 1 week prior to exercise, and Group 3 was fed the high fat diet throughout the study. To control for differences in work output between the leanest and heaviest animals, exercise intensity was adjusted across groups such that all exercised rats had equivalent energy expenditure. After a 3 day training period, the exercise was successively increased over 8 days until a work output of 374.9J was reached. Relative to their respective controls, obese exercised males showed a reduction in body weight but no change in food intake. In contrast, exercised females showed no change in body weight or food intake, regardless of dietary condition.     

Behavioral effects of ethynyl estrogens in the female rat

The synthetic analogues of estradiol, ethynyl estradiol and mestranol, are used in oral contraceptives. Their effects on food intake and sexual behavior were evaluated in female rats, and compared with those of estradiol. It was found (Experiment 1) that both ethynyl estradiol and mestranol reduced food intake reliably, and more than estradiol. Water intake and body weight followed similar trends. Ethynyl estradiol, but not mestranol, plus progesterone stimulated proceptive and receptive behavior in ovariectomized female rats. Daily administration of ethynyl estrogens without progesterone showed similar trends (Experiment 3). It is hoped that these studies provide guidelines for further work on the effects of synthetic estrogens on sub-primate and primate behavior.     

Modulation of food intake by amygdaloid estradiol benzoate implants in female rats

Bilateral implants of estradiol benzoate into the corticomedial nuclei of the amygdala significantly reduced food intake in ovariectomised rats over a 72-hour stimulation period. The effect was similar in magnitude to those following diencephalic estrogen implants. A decrease in food intake was also observed following amygdaloid estradiol benzoate implants in ovariectomised rats which had previously sustained electrolytic lesions of the ventromedial-arcuate region of the hypothalamus. It is concluded that estradiol benzoate may act directly on both the hypothalamus and amygdala (as well as peripherally) to modulate food intake.     

Effects of wheel running on food intake and weight gain of male and female rats

Adult male and female rats were housed in a sedentary condition or given free access to a running wheel for 50 days. Running wheel activity of female rats was higher than that of males throughout the experiment. Food intake, of both male and female rats that could take exercise increased, and the rate of increase of females was greater than that of males. In both males and females there was a positive correlation between food intake and running wheel activity. These findings suggest that the sex difference in the rate of increase in food intake elicited by wheel running is at least partly explained by the sex difference in running wheel activity. Although food intake increased as a function of running wheel activity, the weight gains of both sexes were slower than those of sedentary rats. In both sexes this slower weight gain was mainly due to less accumulation of fat.     

Food deprivation effects on some estrogen-sensitive responses in female rats

Thirty-six female rats were placed on food deprivation schedules to reduce them to 4 groups having 100, 90, 80, or 75% of prestarvation body weights. Vaginal smears were made to establish estrus cycling for 12 days before and 12 days during starvation. Lordosis responses to cervical probing were recorded for 4 days before starvation, 4 days during starvation and also 1 day during starvation after priming with estrogen. Though starvation did not significantly affect estrus cycling, it did significantly decrease the lordosis response; the difference was eliminated by estrogen injection. Deprivation also significantly decreased blood plasma refractive index and ovarian weight, but did not affect blood hematocrit or adrenal weight. It was suggested that food deprivation affects the lordosis response by reduction of estrogen levels.     

Effect of crowding on some physiological and behavioral variables in adult male rats

The effect of two population densities on body weight gain, food and water intake and the weight of some organs and glands was studied in adult male rats. Behavioral reactivity to open field was also assessed. Crowded rats (10 animals per cage) showed lower body weight gain than control rats (3 per cage) throughout all the experimental period. Crowding decreased food intake and increased water intake. Any effect of crowding on the weight of thymus, liver and endocrine glands (except testes) was found. Open field defecation and activity were the same in control and crowded rats. Discrepancies from earlier works could likely be due to methodological differences and these are discussed in the text.     

Sexual dimorphism in the regulation of caloric intake and body weight of rats fed different diets

Female, androgenized female (AF), and male rats were given access to 1 of 3 diets—chow (C), high-dextrose (D-chow:dextrose, 2:1), and high-fat (F-chow:Crisco, 2:1) for 2 months. Caloric intake (CI), water intake, and body weights were monitored daily. Responses to gonadectomy and a single injection of estradiol benzoate (EB) were also studied. For females, F- and C-fed rats had comparable CI's, whereas D-fed rats chronically ate much less. For males, F-fed rats overate, whereas C- and D-fed rats had comparable CI's. The pattern of CI of AF rats fed the 3 diets was intermediate between that of males and females. Male rats were less responsive to the anorexic effects of EB than were the other two groups, and the F-diet potentiated the anorexic effects of EB in all three groups. Results are discussed in terms of a sex difference in the hypothalamic regulation of feeding behavior which is modulated by gonadal hormones.     

Melatonin and estradiol effects on food intake, body weight, and leptin in ovariectomized rats

OBJECTIVE: The study in ovariectomized (Ovx) rats, as a model of menopausal status, of the effects of melatonin (M) and/or estradiol (E), associated or not with food restriction, on body weight (BW) and serum leptin levels. METHODS: Female SD rats (200-250 g) were Ovx and treated with E, M, E+M or its diluents. Control sham-Ovx rats were treated with E-M diluents. After 7 weeks being fed ad libitum, the animals were exposed for 7 more weeks to a 30% food restriction. We measured: food intake, BW, nocturnal and diurnal urinary excretion of sulphatoxymelatonin (aMT6s), leptin in midday and midnight blood samples, glucose, total cholesterol, LDL, HDL and triglycerides. RESULTS: Day/night rhythm of aMT6s excretion was preserved in all cases. The increase of aMT6s excretion in M-treated animals basically affected the nocturnal period. In animals fed ad libitum, E fully prevented Ovx-induced increase of BW, leptin and cholesterol. Melatonin reduced food intake and partially prevented the increase of BW and cholesterol, without changing leptin levels. Under food restriction, M was the most effective treatment in reducing BW and cholesterol. Leptin levels were similar in M, E or E+M treated rats, and lower than in untreated Ovx rats. CONCLUSIONS: Our result gives a preliminary experimental basis for a post-menopausal co-treatment with estradiol and melatonin. It could combine the effectiveness of estradiol (not modified by melatonin) with the positive effects of melatonin (improvement of sleep quality, prevention of breast cancer, etc.). The possible beneficial effects of melatonin which could justify its use, need to be demonstrated in clinical trials.     

Estradiol and insulin: independent effects on eating and body weight in rats.

The effects of ovariectomy and estradiol replacement were determined in streptozotocin-diabetic female rats maintained on daily injections of protamine zinc insulin. Similar changes in food intake and body weight in these animals and in nondiabetic control animals indicate that the effects of estradiol on these measures are probably not dependent on changes in pancreatic insulin secretion. Acute and chronic insulin challenges in ovariectomized rats maintained on estradiol benzoate, nafoxidine or oil were also examined. The effects of insulin were not attenuated by prior estrogen conditioning, and there was no evidence of insulin resistance. These experiments suggest that the effects of estradiol on body weight and food intake in female rats are not dependent upon altered insulin levels nor attenuation of the effects of insulin. Estradiol may exert its influence on eating and body weight via separate and possibly more direct pathways. The data also are consistent with the suggestion that ovariectomy-induced and hypothalamic obesities are separate phenomena.     

Food intake, body weight and lordosis in male and female mongolian gerbils: effects of ovarian steroids

The effects of gonadectomy and ovarian hormone treatment on food intake, body weight, and lordosis in male and female Mongolian gerbils were examined. In female gerbils, a significant decrease in food intake and body weight was observed after ovariectomy, with estradiol benzoate (1, 10, or 100 micrograms/day) increasing food intake in a dose dependent fashion. However, the dose of estrogen (1 microgram) that restored food intake and body weight to control levels in ovariectomized animals was lower than that required to elicit maximal sexual receptivity. Progesterone, when given in conjunction with estrogen, significantly facilitated the effect of estrogen on food intake without further altering body weight. In male gerbils, castration produced a significant but transient increase in body weight and a delayed increase in food intake. Unlike female gerbils, male gerbils exhibited no significant alterations in food intake, body weight, or lordosis in response to treatment with ovarian steroids. The present results are compared to those obtained in other species.     

The desensitization effect of progesterone on female rat sexual behavior is not due to interference with estrogen priming

In order to determine if progesterone interferes with estradiol's priming action on progesterone-facilitated sexual behavior, we tested the responsiveness of progesterone-desensitized female rats to the serotonin receptor antagonist, methysergide, and the neuropeptide, luteinizing hormone-releasing hormone. Threshold doses of both compounds were established. Progesterone treatment, which caused a decrease in the lordosis rating in response to a moderate dose of progesterone did not inhibit responsiveness to threshold doses of methysergide or luteinizing hormone-releasing hormone. The results of this study support the notion that progesterone does not interfere with estradiol's priming action on progesterone-facilitated sexual receptivity. Furthermore, they suggest that progesterone's desensitization effect is specific to progesterone-facilitated lordosis.     

Effect of guanethidine sympathectomy on intake and body weight of intact and LHA-lesioned rats

The present study investigated the role of direct sympathetic nervous system innervation of the viscera in the reduced body weight levels maintained by animals bearing lesions of the lateral hypothalamic area (LHA). Adult, male rats with, and without, electrolytic lesions of the (LHA) were treated with guanethidine sulphate (25 mg/kg IP daily for 6 weeks) to produce destruction of the peripheral sympathetic nervous system. LHA-lesioned rats displayed the expected reduced body weight compared to intact rats. Sympathectomy in lesioned rats resulted in an identical pattern of effects to that seen in intact rats. Transitory reductions in intake were effected and weight was significantly depressed by one week of guanethidine treatment. However, weight had recovered to control levels in both intact and lesioned drug-treated groups by the end of the experiment. The reduced body weight level maintained by LHA-lesioned rats was not altered by guanethidine sympathectomy. The major conclusions are (1) the reduced body weights maintained following LHA lesions are not dependent upon an intact sympathetic nervous innervation of visceral organs, and (2) peripheral sympathectomy in intact adult rats has no chronic effects on either body weight or food and water intake.     

Preoptic implants of estradiol increase wheel running but not the open field activity of female rats

In order to localize the neural substrate for estrogen induction of increases in activity, bilateral implants of dilute estradiol (in concentrations of 1:10, 1:100, and 1:250) were made into the medial preoptic area (n = 5), the anterior hypothalamus (n = 8), the ventromedial hypothalamus (n = 6), and the posterior hypothalamus (n = 4) of ovariectomized female rats housed in running wheels. The same animals were also tested for open field activity and lordosis. The preoptic area was the most effective site tested for estrogenic stimulation of running wheel activity, with 3/5 animals responding consistently to estradiol application. 3/8 animals with cannulae in the anterior hypothalamus (AHA) responded with increases in activity measured in the running wheel on at least two out of three estradiol treatments. No animals with cannula placements posterior to the AHA exhibited consistent running wheel responses to estradiol. No estrogen-induced increase in open field activity was found, regardless of cannula location or concentration of estradiol; however, there was a tendency for the number of squares entered during the later tests to decrease in the ventromedial hypothalamic nucleus group and in the subgroup of animals not showing estrogen-sensitive wheel running in the anterior hypothalamic area group. Only the ventromedial hypothalamic estradiol treatments stimulated lordosis behavior. These results support earlier reports suggesting that the medial preoptic area (and possibly the adjacent anterior hypothalamic area) is the critical brain site for estrogenic stimulation of running wheel activity.(ABSTRACT TRUNCATED AT 250 WORDS)     

Sex differences in the activational effects of gonadal hormones on food intake and body weight

Estrogens have been shown to decrease, and androgens to increase body weight (BWt) of guinea pigs (GPs). The magnitude of the BWt sex difference shown by intact adult GPs is due primarily to these concurrent, or activational, effects of gonadal steroids. However, a small but significant sex difference in BWt persists in animals gonadectomized at birth, indicating that early hormonal exposure may permanently influence certain steroid sensitive weight regulatory mechanisms in the two sexes. Three experiments were therefore designed to investigate the short term effects of estradiol and testosterone on food intake (FI) and BWt of gonadectomized adult male and female GPs. In the first experiment, GPs gonadectomized in adulthood were given a single injection of 6 micrograms estradiol benzoate (EB). Although EB treatment reduced FI and BWt of both females and males, significantly larger reductions occurred in females. In the second experiment, GPs gonadectomized at birth received treatments of oil or 2 micrograms EB for 7 days. EB treatment also produced significantly larger effects on FI and BWt in the neonatally gonadectomized females. The third experiment involved GPs gonadectomized as adults who were injected with either oil or 1 mg/day testosterone propionate in oil (TP) for 32 days. Compared to changes in oil injected controls, TP produced significantly larger increases in male BWt than female BWt. Therefore, although GPs show only minor sex differences in BWt which might relate to prenatal gonadal hormonal exposure, significant sex differences remain in their responsiveness to the activational effects of gonadal steroids on FI and BWt in adulthood.     

Ovarian influences on food intake and body weight regulation in lactating rats

In the following experiments, an attempt was made to determine the role of the ovary in the control of food intake and body weight regulation during lactation. In the first study, it was found that concentrations of estradiol benzoate effective in suppressing food intake and body weight in nonlactating animals were not effective during lactation. In the second experiment, ovariectomy during lactation was shown not to produce the usual increases in food intake and body weight or change in meal patterns known to occur after ovariectomy in the nonlactating rat. These results suggested that lactating animals behave the as though functionally ovariectomized and that the removal of the ovaries is of no additional consequence. The further observation that animals nursing small litters gained weight considerably more rapidly than animals nursing large litters led to the prediction that these animals would also be more responsive to the suppressive effects of EB. In the third study, EB in concentrations which are not effective in suppressing body weight in animals nursing large litters was found to suppress body weight in mothers with small litters. However, since these animals also showed a decline in milk yield, a number of alternative interpretations of these results were considered. These results, together with data concerning levels of ovarian hormones during gestation and lactation led to the hypothesis that pregnant and lactating animals undergo an elevation in body weight set-point, similar in magnitude and quality to elevations following ovariectomy in the nonlactating animal.     

Ovarian influences on the meal patterns of female rats.

A series of experiments examined the effects of estrous cycles, ovariectomy, and estradiol-replacement on free-feeding meal patterns of female rats maintained on a liquid diet. The proestrous decrease in food intake was accomplished by a decrease in meal size and a less than fully compensatory increase in meal frequency. The hyperphagia induced by ovariectomy was reflected in an increase in meal size and a decrease in meal frequency. When food intake returned to preoperative levels, meal size remained elevated while frequency decreased further. Estradiol benzoate (2 μg/day) permanently decreased meal size in long-term ovariectomized rats. The subsequent return to food intake levels of controls was due primarily to an increase in meal frequency. These results suggest that the transient changes in food intake caused by estradiol withdrawal and replacement are accomplished by permanent changes in meal size followed by compensatory changes in the number of meals consumed per day. They suggest that the decrease in meal size at proestrus is due to a direct effect of estradiol on the mechanisms that terminate short-term food intake and are not secondary to changes in the level of total daily food intake.