The development of a homologous radioimmunoassay (RIA) for the measurement of serum hamster prolactin (PRL) has facilitated our studies on monitoring the secretion patterns of this hormone during different states of reproduction. Four salient findings emerge from the present studies. First, rapid cardiac puncture without anesthesia does not affect serum PRL levels during selected times in the estrous cycle or during pregnancy. Second, serum PRL levels during the estrous cycle describe a daily rhythm of PRL release with maximum serum concentrations each day occurring in the afternoon and the highest of these occurring on proestrus (day 4 of cycle). Third, PRL release during pregnancy is characterized by a single surge each day; although the time of maximum PRL release varies, levels increase during the hours of darkness and decline to basal during the light. Fourth, the amount of PRL released during pregnancy diminishes with time; on day 15 the total amount of PRL in the serum is less than 10% of that measured on day 5.
Daily rhythms of LH and FSH release commence on day 16 or 17 of age in the prepubertal female golden hamster, 2-3 weeks before regular 4-day oestrous cycles begin. We tested the hypothesis that the daily surges of gonadotrophin regulate, at least in part, rate of sexual maturation and, hence, age at puberty. We predict that an advance or a delay in the initiation of the daily rhythm should result in a corresponding advance or delay in the day of puberty. In the first test, the onset of daily gonadotrophin surges was advanced by gonadotrophin-releasing hormone (GnRH) injections; in the second test, the onset was delayed by daily injection of phenobarbital sodium (PB). The day of the first of at least three consecutive post-ovulatory vaginal discharges was used as an index of the age at puberty. Gonadotrophin-releasing hormone (50 ng/0.1 ml saline per animal) was injected at 16.30 h on days 8-17 of age. These injections initiated a daily mid-afternoon surge of LH about 8 days before the onset of the daily rhythm of gonadotrophins in saline-injected controls and the day of first vaginal discharge was advanced by 4 days compared with saline-injected controls (32.0 +/- 1.8 days vs 36.3 +/- 1.0 days; P less than 0.001). Phenobarbital sodium (100 mg/kg body wt), injected at 13.30 h from 16 to 25 days of age, blocked daily surges of gonadotrophin observed in controls by day 18.(ABSTRACT TRUNCATED AT 250 WORDS)
We hypothesized that rhythms in hypothalamic serotonergic activity were permissive to daily and estrous cyclerelated rhythms of LH, FSH and prolactin (PRL). In the Syrian hamster, proestrus (PRO) is characterized by a surge of LH, FSH and PRL; diestrus (DIE) by low LH and FSH and a small surge of PRL, while in photoperiodinduced anestrous (PIA) animals there is a surge of LH and FSH and low PRL. Turnover rates of serotonin (5HT) in four brain areas were determined for the three reproductive states at 2-h intervals. Turnover in the preoptic area and arcuate nuclei did not change, indicating that 5HT projections to these regions probably do not control LH, FSH or PRL release. Serotonin turnover in the median eminence (ME) was elevated at 0600 h in PIA females, at 0600 h, 0800 h, and 1400 h on DIE and at 0600 h and 2200 h on PRO. Since the pattern of 5HT turnover in the ME is different during each of the three reproductive states, 5HT in this area is likely not crucial to the control of LH, FSH and PRL. Turnover of 5HT also did not change in the suprachiasmatic nuclei (SCN) of PRO or PIA animals. However, 5HT turnover rates in the SCN were elevated at 1200 h, 2000 h, and 2400 h on DIE. The correlation of high 5HT turnover in the SCN of DIE but not PRO and PIA animals suggested that elevated serotonergic activity in the SCN is part of the mechanism by which the gonadotropin surge is prevented on DIE. To test this, PRO and DIE hamsters were injected with 5HT receptor ligands. Administration of a 5HT agonist attenuated the PRO surge of LH and blocked the surge of PRL. In contrast, administration of two 5HT antagonists failed to elicit a surge of LH in DIE and phenobarbital-blocked PRO females, an indication that other mechanisms also contribute to inhibition of gonadotropin and PRL surges.
In male Syrian hamsters, short days induce regression of the reproductive system, but eventually spontaneous recrudescence occurs ensuing from refractoriness to the inhibitory photoperiod. Although the photoperiod of 12 L:12 D (12 h light:12 h dark) may act like a short day by inducing the testicular cycle outlined above, it may fail to evoke the increase of circulating concentrations of prolactin that accompanies testicular recrudescence. This photoperiod may fail to induce photorefractoriness, as indicated by the prolonged low concentrations of prolactin in the blood. Herein, hamsters were exposed to either 8 L:16 D or 12 L:12 D from weaning and by 28 weeks exposure to either photoperiod, the hamsters had large testes following recrudescence from a photoperiod induced-regression). Transfer to 8 L:16 D from 12 L:12 D at 28 weeks resulted in a second testicular regression and recrudescence. In a second experiment, the testes of hamsters moved to 8 L:16 D from 12 L:12 D after 29 weeks exposure to the latter photoperiod similarly regressed and then regrew. Serum concentrations of prolactin decreased in these males after transfer to the shorter daylength but also decreased in hamsters kept under 12 L:12 D both groups were usually below those of hamsters moved to 14 L:10 D. These results show that exposure for 28 or 29 weeks to 12 L:12 D was insufficient to induce photorefractoriness, despite the recrudescence of the testes following involution.
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