Reproductive Hormone Secretion Research Articles

Effects on Testosterone, LH and Cortisol Concentrations, and on Testicular Ultrasonographic Appearance of Induced Testicular Degeneration in Bulls

It is well known that heat stress has a detrimental effect on testicular functions. In addition to the alteration of semen quality and testicular damage, reproductive hormone secretion can be altered. The objective of this study was to describe changes in plasma concentrations of testosterone, LH and cortisol, as well as in testicular ultrasonographic appearance after induced testicular degeneration. Four Swedish Red and White bulls, aged 3 years, were used. They were fed according to Swedish standards. The scrotum was covered with an insulation device during 96 h. Semen was collected weekly 3 times before and up to 4 months after insulation. Testicular ultrasonography and clinical genital examination were performed with the same intervals. Heparinized blood samples were taken from the jugular vein at 2 h interval during 24 h every 2 weeks during the study. Blood samples were tested for the content of testosterone, LH and cortisol. Data were analysed, using one way analysis of variance of seminal data, clinical examination data as well as 24 h hormonal output data as percentage of mean individual pretreatment values. The use of a 5 MHz B-mode ultrasound unit did not contribute with an objective estimation of the degree of testicular degeneration. In 3 of the bulls testosterone levels had a tendency to decrease and LH to increase during the time of severe degeneration, whereas an opposite trend was seen during the regenerative phase, changes becoming significant 15 weeks after scrotal insulation. Variation between animals was big. Cortisol levels had a decreasing trend, changes being significant only in individual bulls at 10 and 15 weeks after scrotal insulation.(ABSTRACT TRUNCATED AT 250 WORDS)

Central peptidergic mechanisms controlling reproductive hormone secretion: novel methodology reveals a role for the natriuretic peptides.

A variety of neural factors can influence reproductive hormone secretion by neuromodulatory actions within the hypothalamus or neuroendocrine actions within the anterior pituitary gland. Passive immunoneutralization and antagonist administration protocols have suggested physiological roles for a number of these factors; however, both experimental approaches have severe technical limitations. We have developed novel methodology utilizing cytotoxin cell targeting with neuropeptides linked to the toxic A chain of the plant cytotoxin ricin. With this methodology we can target and destroy in vivo or in vitro cells bearing receptors for that peptide. Ricin A chain conjugated to atrial natriuretic peptide (ANP), a neuropeptide known to pharmacologically inhibit luteinizing hormone-releasing hormone (LHRH) release, was injected into the cerebroventricular system of intact, cycling rats and ovariectomized rats. Cytotoxin conjugate treatment significantly lengthened the estrous cycle. In ovariectomized rats the luteinizing hormone surge induced by steroid priming was completely inhibited. LHRH content of the median eminences of these rats was not significantly altered. These data suggest that ANP binding to clearance receptors in the hypothalamus displaces the C-type natriuretic peptide (CNP) from the shared clearance receptor, making more CNP available to inhibit LHRH release. In the absence of cells bearing the clearance receptor all available CNP binds to the ANPR-B receptor and exerts its effect via an inhibitory interneuron, since LHRH fibers are spared by this treatment.

Restoration of Pulsatile Luteinizing Hormone Secretion after Fasting in Rhesus Monkeys (Macaca mulatta): Dependence on Size of the Refeed Meal*

In men and adult male rhesus monkeys brief periods of fasting (i.e. 1-2 days) can often lead to a suppression of hypothalamic-pituitary-testicular axis activity, marked by decreased circulating concentrations of LH, FSH, and testosterone. Refeeding a normal meal can rapidly restore normal secretory patterns of LH and testosterone. To learn more about the nature of the signal that links reproductive hormone secretion to nutrient intake, we examined whether the degree of restoration of pulsatile LH and testosterone secretion after a brief period of fasting is influenced by the size of the refeed meal. Adult male rhesus monkeys had indwelling venous catheters surgically implanted and were maintained on swivel/tether systems for remote collection of blood samples. Monkeys were fasted for 1 day and then on the following day they were refed one of five meals which varied in size and calorie content (i.e. 0 Cal/0 pellets Purina monkey chow; 100 Cal/5 pellets; 200 Cal/10 pellets; 300 Cal/15 pellets; or 600 Cal/30 pellets). Blood samples were collected from 0800-2400 h at 20-min intervals on the days of refeeding and assayed for LH and testosterone content. After a day of fasting, the frequency of pulsatile LH secretion the following morning was very low (0.56 +/- 0.1 pulses/3 h, measured from 0800-1100 h). When monkeys were not refed (i.e. were subjected to a second day of fasting; 0 pellet group) LH pulse frequency remained low [2.88 +/- 0.72 pulses/13 h, measured from 1100-2400 h (equivalent to 0.66 pulses/3 h)] throughout the day and evening hours. Refeeding monkeys 5, 10, 15, and 30 pellets caused a progressive stimulation of pulsatile LH secretion (3.17 +/- 0.54, 3.67 +/- 0.56, 5.5 +/- 0.67, and 6.38 +/- 0.53 pulses/13 h, respectively). Like LH pulse frequency, mean circulating LH and testosterone concentrations progressively increased as the size of the refeed meal was increased. For all three parameters (i.e. LH pulse frequency, mean LH concentration, and mean testosterone concentration) there was a significant, P less than or equal to 0.001, linear trend with increasing meal size. These findings indicate a very strong relation between the level of nutritional intake and the level of central drive to the reproductive axis during nutritional recovery from fasting, and suggest a physiological parameter that responds in a progressive fashion to increasing food intake serves as the signal to link central drive to the reproductive axis to changes in nutrient intake.(ABSTRACT TRUNCATED AT 400 WORDS)

Role of Neuropeptide Y in Reproductive Functiona

NPY acts both at the hypothalamus and the anterior pituitary gland to modulate reproductive hormone secretion. Within the hypothalamus, NPY stimulates LHRH secretion in the presence of physiological levels of estrogen and suppresses pulsatile LHRH release following ovariectomy. Intracerebroventricular injection of NPY antiserum blocks or delays the LH surge in steroid-primed ovariectomized rats, thereby adding support for a physiological role of NPY in the neuroendocrine events preceding ovulation. Blockade of alpha 2 adrenergic receptors decreases NPY-stimulated LH release in steroid-primed rats implying a potential noradrenergic mediation of NPY activity. Physiological levels of progesterone do not augment, and may actually suppress NPY-induced LHRH secretion in vitro from median eminences obtained from estrogen-primed ovariectomized rats. The physiological role of progesterone, if any, in modulating NPY effects on LHRH release remains to be determined. Little, if anything, is known about the NPY receptor in the median eminence or the intracellular mechanisms which transduce the NPY signal into activation of LHRH release in estrogen-treated ovariectomized rats although translocation of intracellular calcium is required. Equally puzzling is the mechanism of desensitization of the LHRH-releasing mechanisms of the median eminence of ovariectomized rats or the specific site of NPY suppression of pulsatile LHRH secretion. NPY is released into the hypothalamo-hypophysial portal circulation and this appears correlated with LHRH secretion before the LH surge. NPY affects LH and FSH release from anterior pituitary cells in vitro and enhances LHRH-induced LH secretion. Taken together, the studies described above suggest an important physiological role for NPY as a modulator of neuroendocrine activity which culminates in the preovulatory surge of LH.

The Olfactory Bulbs Enhance Reproductive Hormone Secretion in Male Rats on Long or Short Photoperiod

Abstract Unlike seasonally breeding species such as the Syrian hamster, Sprague-Dawley laboratory rats do not normally respond to short photoperiod (6L18D) with reproductive regression. However, removal of the olfactory bulbs (BX) unmasks a photoperiodic response in pre-pubertal rats so that blinding or short photoperiod results in an inhibition of reproductive hormone secretion and/or a delay in pubertal development. This is apparently mediated by pineal melatonin which inhibits gonadotropin and/or prolactin secretion, but the mechanism by which BX facilitates the response to photoperiod is not clear. Experiment I was performed to determine serum levels of reproductive hormones at frequent intervals following BX and/or maintenance on short days. Twenty-three-day old male rats were BX or underwent sham BX (SH). They were thereafter maintained on a 14L:10D (long photoperiod) or 6L:18D photoperiod for the duration of the study. At 6 weeks following surgery, BX rats on either photoperiod had smaller testes than the SH groups. At week 8, the BX group on 6L:18D had smaller testes than the other three groups. There were transient reductions in serum luteinizing hormone and follicle-stimulating hormone in the BX rats on short photoperiod, but there were prolonged effects of BX decreasing prolactin levels in rats on long or short photoperiod. In SH rats, testosterone was elevated for weeks 6 through 10 of the study, and BX blocked this increase. Experiment II was performed to determine whether BX alters testosterone feedback on gonadotropin secretion. Twenty-three-day old male rats were BX or underwent SH operation and were then returned to a room on 14L10D. Six to 8 weeks later, all animals were castrated and placed on 6L18D or returned to 14L:10D. Eight weeks following castration, the rats were implanted with Silastic capsules containing 0, 10, 20 or 40mm testosterone. The post-castration increase in serum luteinizing hormone and follicle-stimulating hormone was lower in the BX than SH rats. In long photoperiod, serum luteinizing hormone and follicle-stimulating hormone were often lower in the BX rats receiving no testosterone replacement or lower doses of testosterone than in the SH group receiving similar capsules. Maintenance on short photoperiod increased the responsiveness to testosterone so that even the rats receiving low doses of testosterone had very low luteinizing hormone and follicle-stimulating hormone levels whether they were SH or BX. In summary, BX rats on long or short photoperiod had lower serum prolactin and testosterone levels than the comparable SH group and BX inhibited the post-castration increase in gonadotropin secretion. The data therefore suggest that the olfactory bulbs tonically enhance reproductive hormone secretion (especially around the time of pubertal development).

Hormonal basis of variation in oestrous cyclicity in selected strains of mice

Reproductive hormone secretion and ovarian LH receptor content were studied during the oestrous cycle of mice that differed in fertility after genetic selection. Strain variation in the secretory pattern of progesterone was observed along with differences in the timing and magnitude of prolactin release. Scatchard analysis showed similar affinities of the LH receptor for hCG in strains with increased or decreased reproductive performance, with a single order of binding sites during both pro-oestrus and dioestrus. The number of unoccupied LH receptors during pro-oestrus was greatest in mice with increased reproductive performance. These results provide evidence that trait selection can change gonadotrophin receptor concentration and the dynamics of hormone secretion during the oestrous cycle of the mouse.

Additive Effects of Atrial Natriuretic Peptide and Angiotensin II on Luteinizing Hormone and Prolactin Release in Female Rats

The present experiments were designed to assess the effects of central administration of atrial natriuretic peptide (ANP), alone or in conjunction with angiotensin II (AII), on luteinizing hormone (LH) and prolactin release in ovarian steroid-primed female rats. Intracerebroventricular injection of ANP (200 ng/2 microliters over 1 min) induced an increase in plasma LH levels without significantly affecting prolactin release. Injection of AII (50 ng/2 microliters over 1 min) also resulted in an increase in LH levels and, in addition, reduced plasma prolactin titers. Coinjection of ANP and AII did not elevate LH levels beyond that achieved by either peptide alone, but produced a further suppression in prolactin levels than that seen with AII alone. Water intake induced by AII was attenuated by coadministration of ANP. In a second protocol utilizing lower doses of the peptides delivered by infusion, either ANP (800 ng/h; 13.3 ng/min) or AII (200 ng/h; 3.3 ng/min) alone produced 100% increases in LH levels. Coinfusion of the peptides induced an additive (250%) increase in plasma LH titers. In this protocol, the release of prolactin was unaffected by infusion of the peptides, either alone or as a comixture. Water intake induced by AII infusion was attenuated by coadministration of ANP. Taken together, these experiments demonstrate that, in contrast to the antagonistic interaction of ANP and AII on water intake, the peptides affect reproductive hormone secretion in the same direction and, under particular experimental conditions, display additive effects in stimulating LH and inhibiting prolactin release.

Effect of different nocturnal illuminances on melatonin, prolactin, and gonadotropins in male rats.

We studied the role of nocturnal illuminance as a possible regulatory factor in the production and secretion of reproductive hormones. Adult male rats were kept under artificial lighting conditions (LD 12/12 hours) where the daily illuminance was 520-550 lx and the nocturnal illuminance 0, less than 0.1, or 1-1.5 lx. After a 7 day adaptation period, the pineal contents of melatonin, the serum levels of LH, FSH, and prolactin, and the pituitary contents of these hormones were measured by radioimmunoassay in samples taken 4 and 7 hours after the onset of light and onset of darkness. When the rats were kept in full darkness or under the minimal nocturnal iluminance (less than 0.1 lx), the patterns of pineal melatonin were equal. When nocturnal illuminance was 1-1.5 lx, the pineal melatonin contents at night were lower than in complete darkness. However, this illuminance level did not totally abolish the nocturnal increase of melatonin synthesis. The serum levels of LH, FSH, and prolactin were all affected by the increase of nocturnal illuminance so that the difference between the daytime and nighttime levels increased (higher values during the night). The variation of nocturnal illuminance did not change the pituitary contents of gonadotropins. The effects on pituitary prolactin were negligible as well. The results are interpreted to support the concept that nocturnal illuminance levels may regulate the secretion of the studied hormones in male rats.

Effect of short-term starvation on reproductive hormone gene expression, secretion and receptor levels in male rats

The effects of 4-6 days of food deprivation on the pituitary-testicular function of adult male rats were studied. Fasting decreased body weights on average by 23% (P less than 0.01) and those of seminal vesicles by 55% (P less than 0.01) in 4 days. No consistent changes were found in testicular and ventral prostate weights. The pituitary levels of gonadotrophin-releasing hormone (GnRH) receptors decreased by 50% (P less than 0.01). Serum and pituitary levels of LH, FSH and prolactin decreased by 25-50% (P less than 0.01 for all). Testicular and serum levels of testosterone decreased by 70-80%, testicular LH receptors by 26%, those of prolactin by 50% (P less than 0.01 for all), but those of FSH remained unaffected. Acute (2 h) stimulation by a GnRH agonist (buserelin, 10 micrograms/kg i.m.) resulted in similar LH, FSH and testosterone responses in the fasted and control animals, and human chorionic gonadotrophin (hCG) stimulation (30 IU/kg i.m.) in similar increases in testosterone. A 42% decrease was found in pituitary content of mRNA of the common alpha subunit (P less than 0.05), but the mRNAs of the LH- and FSH-beta chains and prolactin were unaffected by fasting for 4 days. When the same mRNAs were measured after 6 days of fasting, the decrease of the mRNA of FSH-beta also became significant (50%, P less than 0.01). In contrast, the mRNA of LH-beta was increased twofold (P less than 0.01) at this time and serum LH levels were similar in control and starved animals.(ABSTRACT TRUNCATED AT 250 WORDS)

Conference on “Brain-Gut Peptides and Reproductive Hormone Secretion”

Conference on “Brain-Gut Peptides and Reproductive Hormone Secretion”

Conference on Brain-Gut Peptides and Reproductive Hormone Secretion

Conference on Brain-Gut Peptides and Reproductive Hormone Secretion

Patterns of reproductive hormone secretion in hibernating Turkish hamsters.

Changes in gonadal state and in circulating reproductive hormones [follicle-stimulating hormone (FSH), prolactin (PRL), and testosterone] were studied for 30 wk in male Turkish hamsters (Mesocricetus brandti) induced to hibernate by exposure to a short-day, cold environment [10:14-h light-dark (LD) cycle, 6 +/- 1 degree C]. Similar measures were compared in hamsters maintained under short-day warm conditions (10:14-h LD, 21 +/- 2 degrees C). A decrease in testicular size and in hormone levels was observed after 9-12 wk of short-day exposure in all animals. After 24 wk, hormone levels rose again, accompanied by testicular recrudescence, in short-day warm hamsters and in hamsters that failed to hibernate in the cold. For animals that hibernated the temporal pattern of endocrine and gonadal changes differed only slightly in comparison. Testicular recrudescence of hibernators lagged approximately 3 wk behind that of short-day warm hamsters. Hormone levels were generally lower in hibernators sampled during bouts of torpor than during bouts of spontaneous arousal from torpor. A marked elevation of serum FSH was observed in aroused hibernators well before the end of the hibernation season (at 21 wk of short-day exposure). Mean testosterone and PRL values had increased by wk 27, after hibernation was terminated in the majority of animals. These results indicate that testosterone may not be essential for the termination of the hibernation season. The data also suggest that an endogenous timing mechanism, resistant to the decreased body temperature experienced during torpor, may function to trigger a resurgence of the neuroendocrine-gonadal axis at the end of the winter season.

Nutritional and metabolic factors in the regulation of reproductive hormone secretion in the primate.

Nutritional and metabolic factors in the regulation of reproductive hormone secretion in the primate.

Reproductive hormone secretion and testicular growth in bull calves actively immunized against testosterone and oestradiol-17 beta.

Groups of bull calves received a primary immunization against testosterone (Group T; N = 7) or oestradiol-17 beta (Group E; N = 9) at 3 months of age and booster injections on four occasions at approximately 2 month intervals. Controls (Group C, N = 7) were immunized against human serum albumin alone using the same protocol. Immunity was achieved against both steroids as judged by the secondary antisteroid antibody titres in Group T (730 +/- 231; reciprocal of titre) and Group E (12,205 +/- 4366) bulls; however, peak antibody titres generally declined with successive booster injections. Mean plasma concentrations of LH, FSH and testosterone during the period from 3 to 10 months of age were higher (P less than 0.05) in Group T bulls than in Groups C and E. Group T bulls had larger testes compared with controls from 6 months of age onwards. At castration at 14 months of age, testes of Group T bulls were heavier (P less than 0.05) than those of Groups C and E (179 +/- 13, 145 +/- 8 and 147 +/- 6 g, respectively). At 10 months of age, there were no differences among treatment groups in LH responses to LHRH, but the testosterone responses were greater (P less than 0.05) in bulls in Group T (26.2 +/- 4.9 ng/ml) and Group E (16.6 +/- 1.8 ng/ml) compared with those in Group C (6.9 +/- 0.6 ng/ml). Testosterone responses to hCG determined at 13 months of age were also greater (P less than 0.05) in Groups T and E relative to controls. At 14 months of age daily sperm production rates per bull (X 10(-9)) were higher (P less than 0.10) in Group T bulls (2.2 +/- 0.1) than those in Groups C (1.6 +/- 0.2) and E (1.6 +/- 0.1). These results indicate that early immunity against testosterone is associated with increased gonadotrophin secretion and accelerated growth of the testes in prepubertal bulls. Also, chronic immunity against testosterone or oestradiol-17 beta enhances the steroidogenic response of bull testes to gonadotrophic stimulation. If the above responses observed in young bulls are shown to be sustained, then immunity against gonadal steroids early in life may confer some reproductive advantage in mature animals.

Age Factors Potentiating Drug Toxicity in the Reproductive Axis

Traditionally, drug toxicity in the reproductive system has been a concern only as it affects fertility and fecundity in young individuals. The purpose of this report is to address the potential problem of synergy between drug actions and abnormal secretion of reproductive hormones that together produce disease in older individuals. Thus, reproductive toxicity has different, but no less serious implications in aging individuals. During aging, the coordinated function of elements within the reproductive neuroendocrine axis degrades. This change promotes atypical secretion of hormones producing abnormal responses in target organs and thus creates a condition with pathogenic potential. Certain drugs may contribute to reproductive toxicity in aging individuals either by accelerating the process of dysregulation and/or by synergizing with hormones to stimulate pathologic changes in target tissues. The geriatric population of the world is increasing, and since it consumes a proportionately larger percentage of drugs than younger groups, this novel form of reproductive toxicity may represent a problem in drug safety that warrants serious consideration.

Age factors potentiating drug toxicity in the reproductive axis.

Traditionally, drug toxicity in the reproductive system has been a concern only as it affects fertility and fecundity in young individuals. The purpose of this report is to address the potential problem of synergy between drug actions and abnormal secretion of reproductive hormones that together produce disease in older individuals. Thus, reproductive toxicity has different, but no less serious implications in aging individuals. During aging, the coordinated function of elements within the reproductive neuroendocrine axis degrades. This change promotes atypical secretion of hormones producing abnormal responses in target organs and thus creates a condition with pathogenic potential. Certain drugs may contribute to reproductive toxicity in aging individuals either by accelerating the process of dysregulation and/or by synergizing with hormones to stimulate pathologic changes in target tissues. The geriatric population of the world is increasing, and since it consumes a proportionately larger percentage of drugs than younger groups, this novel form of reproductive toxicity may represent a problem in drug safety that warrants serious consideration.

Reproductive hormone secretion and spermatogenic function in thyroidectomized rams receiving graded doses of exogenous thyroxine.

This study aimed to obtain a better understanding of the relationship between circulating thyroxine (T4) concentrations and reproductive endocrine function in the ram. Mature Merino rams were thyroidectomized and supplemented with 0, 30, 100 and 300% of normal T4 for 10 weeks. Thyroidectomy had no apparent effect on spermatogenic function but interfered with sperm maturation, the latter being returned to normal by 30% T4 replacement. Circulating testosterone levels were reduced by thyroidectomy and restored to control levels by 30% T4; when T4 levels were supranormal (300%), circulating testosterone levels were again reduced. The lowered circulating testosterone levels in thyroidectomized rams occurred as a result of suppressed testosterone secretion from the testis, observed under basal conditions and also following LH-releasing hormone (LHRH) and human chorionic gonadotrophin injection. In thyroidectomized rams, sex hormone binding globulin (SHBG) levels were depressed without changes in testosterone clearance rate (TCR), while in rams with supranormal T4 levels, TCR was increased without changes in SHBG levels. Subnormal levels of T4 also restored to normal the reduced LH pulse frequency in thyroidectomized rams. Reduced LH pulse frequency, together with diminished LH release following LHRH injection in thyroidectomized rams, suggested effects of T4 at the hypothalamo-pituitary axis. The present study demonstrates that complete lack of thyroid hormones suppresses normal reproductive endocrine function in the ram, but that this can be restored to normal by 30% T4 replacement. The results support the theory that T4 plays a permissive rather than a regulatory role in reproductive function in males.

Effect of carbohydrate supplementation on reproductive hormones during fasting in men.

We previously demonstrated that during a 10-day fast in mildly obese men, urinary gonadotropin excretion significantly increased, and serum testosterone concentrations significantly decreased. The mechanisms by which these changes occur are unknown. We postulated that the mechanism of the gonadotropinuria might involve decreased proximal renal tubular reabsorption of gonadotropins during fasting and might be related to renal tubular reabsorption of ketones during fasting, a process that is enhanced by carbohydrate (CHO) administration. We studied the effects of CHO supplementation on ketosis, ketonuria, and reproductive hormone secretion and excretion in 14 mildly obese men, 24-54 yr old, who were 14-69% above ideal body weight. Group I (n = 6) received no CHO supplementation, group II (n = 4) received 15 g CHO, and group III (n = 4) received 45 g CHO daily during the 10-day fast (F). During the control (C) and refeeding (R) periods, all subjects received a 1500-cal diet. Daily 24-h urine collections were made for the measurement of total ketones (millimolar concentrations) and LH and FSH (expressed as international units of the Second International Reference Preparation of human menopausal gonadotropin). Values (mean +/- SE) for 3 representative days (control day 3, fasting day 8, and refeeding day 3) for all subjects are shown below: (table; see text) We also studied the effects of CHO supplementation on serum levels of pituitary gonadotropins, LH and FSH responses to exogenous LHRH stimulation, biological activity of LH, and circulating total and free testosterone levels. Neither dose of CHO prevented the decline in total and free testosterone levels. Serum LH concentrations, as measured by both the RIA and in vitro bioassay did not change significantly with fasting. Serum FSH concentrations in daily samples did not change significantly. The previously reported decline in the FSH response to LHRH stimulation with fasting was not prevented by CHO. We conclude that CHO supplementation prevents the gonadotropinuria of fasting in men. The effect appears to occur in the kidney. The mechanisms may be related to that by which CHO promotes the renal tubular reabsorption of ketones. The reduced serum testosterone level cannot be explained by a lack of biologically active LH. It appears that fasting has a direct effect on the testis, possibly by reducing its responsiveness to gonadotropic stimulation or by inhibiting steroidogenesis.

The influence of photoperiod on body weight gain, body composition, nutrient intake and hormone secretion.

Increasing daily light exposure from 8 to 16 h increases average daily body weight gains of sheep and Holstein cattle but reduces gains of white-tailed doe fawns. Some of these effects on average daily gain in sheep are the result of increased gut fill and pelt weight. Increasing daily exposure to light increases feed intake when sheep or cattle are fed ad libitum. However, increased feed intake is not a prerequisite for the anabolic effects of long duration exposures to light because increased growth occurs in the animals given 16 h light:8 h dark (16L:8D) even when feed intake is restricted. The anabolic effects of increased duration photoperiods in sheep are independent of the gonads, whereas in cattle they are dependent on the gonads. Consistent increases in average daily gains of cattle in response to longer duration photoperiods have not always been achieved. The lack of consistency may be associated with sexual maturity or rate of fattening of the animal. For example, the stimulatory effects of 16L:8D photoperiods on live weight gain are not readily manifested in immature prepubertal heifers, but occur primarily during the peripubertal period. Short days are conducive to deposition of fat, which may account for the stimulatory effects of short days on live weight gain of white-tailed doe fawns and excessively fattened Holsteins. In contrast, long duration photoperiods stimulate protein accretion in cattle. The hormonal signals that mediate the anabolic effects of increasing exposure to light are not associated with change in insulin, thyroxine or growth hormone concentrations in the blood. Glucocorticoid concentrations in serum decrease with longer duration photoperiods which is consistent with an anabolic effect. Increasing daily light exposure to 16 h/d hastens the increase in concentrations of progesterone and testosterone in sera of peripubertal heifers and prepubertal bulls, respectively. Thus, change in secretion of reproductive hormones in the peripubertal period of cattle may be associated with the anabolic effects previously described and is consistent with gonad dependency. Prolactin concentrations in serum increase in sheep and cattle as duration of light exposure increases. But, there is no irrefutable proof that prolactin is responsible for the increased rates of gain or change in carcass composition associated with longer exposures to light. Thus, the hormonal mechanisms involved in photoperiod-induced alterations in growth remain to be established.

Environmental and endocrine control of reproduction in the song sparrow, Melospiza melodia: I. Temporal organization of the breeding cycle

Endocrinologic investigations of free-living populations of song sparrows, Melospiza melodia, have revealed temporal patterns of secretion of reproductive hormones that differ from those of other monogamous avian species. Males arrive in the breeding area in March whereas females arrive 1–2 weeks later. In males the periods of territory establishment and attraction of a mate are characterized by high circulating levels of luteinizing hormone (LH) and testosterone (T), whereas testis mass is low, and growth of the cloacal protuberance (CPL) is just beginning. In April, testes and CPL develop rapidly reaching a peak in early May when females are laying eggs, and when most copulations occur. Plasma LH and T decline in early April, but increase for a second time in late April and early May coincident with the egg-laying period. Thereafter, circulating LH and T decline during the parental phase, but not to basal levels. Although there is an increase in LH during the egg-laying period for the second clutch, there is no change in T levels. Testis mass, CPL, plasma LH, and T all decline to basal levels simultaneously in late July and August. The high levels of LH and T in March, followed by a temporary decline and resurgence in April and May, indicate that environmental factors in addition to the well known effects of increasing day length can regulate secretion of these hormones. In females, plasma levels of T and dihydrotestosterone (DHT) are also elevated in March and early April, and decline to low levels as the nesting phase progresses. A further decline to basal levels, occurs in August during the molt. LH and estradiol (E 2) titers in females show two peaks coincident with the egg-laying periods for each clutch. Plasma levels of corticosterone (B) increase during the breeding season in males, but not females. In both sexes B levels are basal during the moult and increase in October after moult is completed. Body mass and fat depot decline in males as the nesting phase progresses, and then increase dramatically after breeding is terminated. As expected, females show two peaks of body mass and fat depot coincident with the two periods of egg laying. The postbreeding increases in body mass and fat depot are much less pronounced in females than in males.