The activation of the hypothalamic–pituitary axis is critical for the initiation and maintenance of reproductive cycles in pigs and is influenced by a number of factors, such as nutrition, metabolism and gonadal steroids. Kisspeptin is a neuropeptide that is expressed in discrete regions of the porcine hypothalamus and is positioned to mediate the action of many of these factors. The expression of kisspeptin in the pig hypothalamus does not appear to be regulated by gonadal steroids in the same way as other species. It is unclear if kisspeptin is mediating nutritional or metabolic effects on gonadotropin secretion in pigs as it takes large deficits in feed intake or BW to affect hypothalamic expression of the KISS1 gene in the porcine hypothalamus. There appears to be little genetic diversity in kisspeptin or its receptor that is useful for improving reproduction in swine. Both peripheral and central injection of kisspeptin strongly stimulates the secretion of gonadotropin hormones, LH and FSH, in gilts. Similarly, synthetic analogues have been developed and showed potential promise as tools to manage reproductive cycles in gilts and sows. Review of the literature nonetheless reveals that research on kisspeptin and its function in controlling reproduction in pigs has lagged that of other livestock species.

Previous studies have established a model of atresia in preovulatory follicles after stimulation of immature rats with equine chorionic gonadotropin (eCG). This gonadotropin recruits a follicular pool and the deprivation of preovulatory luteinizing hormone (LH) surge induces the atresia in preovulatory follicles. The present study investigated the occurrence of ovulation and provided some morphological features of granulosa cell (GC) apoptosis of atretic follicles at 0, 48, 72 and 120 h after eCG stimulation. Histological sections of ovaries from untreated animals (0 h) showed primordial, primary, secondary and early antral follicles. After 48 h ovaries showed large antral follicles. Preovulatory follicles were observed at 72 h, and two out of five rats displayed cumulus–oocyte complexes (COCs) in the oviducts. All animals exhibited corpora lutea after 120 h. We observed increased estradiol (E2) levels 48 h after eCG treatment that might trigger an endogenous preovulatory gonadotropin surge. Higher progesterone (P4) level, which is the hallmark of a functional corpus luteum, was observed at 120 h. Atresia in secondary and antral follicles was observed by pyknotic granulosa cell nuclei in histology and positive immunolabelling for cleaved caspase 3. We also observed macrophages in secondary and antral follicles in atresia. Transmission electron microscopy revealed GCs with compacted chromatin against the nuclear envelope, nuclear fragmentation, cell shrinkage and fragmentation. No preovulatory follicles showed apoptosis of GCs. In conclusion, our results suggested the occurrence of an endogenous gonadotropin surge, promoting ovulation and preventing atresia of preovulatory follicles.

Gonadotropins are the key regulators of ovarian follicles development. They are applied in therapeutic practice in assisted reproductive technology clinics. In the present review we discuss the basic gonadotropic hormones – recombinant human follicle-stimulating hormone, its derivatives, luteinizing hormone and gonadotropin serum of pregnant mares, their origin, and application in ovarian follicle systems in in vitro culture systems.

Reproductive parameters of Ligula intestinalis-infected roach (Rutilus rutilus) which were held under long-tem laboratory conditions with unlimited food supply were investigated. Although uninfected and infected roach showed no difference in condition factor and both groups deposited perivisceral fat, the gonadosomatic-index was significantly lower in infected female and male roach. Quantitative histological analysis revealed that gonad development was retarded upon parasitization in both genders. In contrast to the phenotype described in the field, infected females were able to recruit follicles into secondary growth, but a high percentage of secondary growth follicles underwent atresia. In both genders, the histological data corresponded well with reduced expression of pituitary gonadotropins and lowered plasma concentrations of sex steroids, as revealed by real-time RT-PCR and ELISA, respectively. Furthermore, a reduction of vitellogenin mRNA and modulated expression of sex steroid receptors in the liver was demonstrated. Like in the field, there was a significant adverse impact of L. intestinalis on host reproductive physiology which could not be related to parasite burden. Our results show, for the first time, that maintenance under laboratory conditions can not abolish the deleterious effect of L. intestinalis on gametogenesis in roach, and indicate a specific inhibition of host reproduction by endocrine disruption.

Cumulus-enclosed or cumulus-free pig oocytes were cultured for 48 h in a serum-free maturation medium, TCM-199B containing 1 mg/ml polyvinylalcohol, supplemented with gonadotropins (PMSG + hCG) and/or epidermal growth factor (EGF), and inseminated with frozen-thawed ejaculated spermatozoa. Fourteen hours after insemination, the ability of oocytes to form male pronucleus (MPN) was examined. EGF significantly increased the ability of cumulus-enclosed oocytes to form MPN irrespective of the concentrations (1–100 ng/ml) tested. Gonadotropins had a greater effect than EGF on MPN formation in cumulus-enclosed oocytes, and a synergetic effect was observed when EGF and gonadotropins were added together. However, neither EGF nor gonadotropins exhibited a stimulatory effect on MPN formation in cumulus-free oocytes. These results indicate that the role(s) of both EGF and gonadotropins in stimulating cytoplasmic maturation of pig oocytes is mediated by cumulus.

A protocol for the incubation of Centropristis striata ovarian follicles in vitro from females that spawn repeatedly under laboratory conditions was developed. Isolated follicles underwent maturation after 15–24 h of incubation at 25 °C in 75% Leibovitz L-15 medium, containing relatively low doses of human chorionic gonadotropin (hCG) or homologous pituitary extract (50% response with approximately 2 IU/ml and 0.02 pituitary equivalents/ml, respectively). During maturation in vitro, follicles underwent a remarkable volume increase (about 340%) that was correlated with proteolysis of primarily the largest yolk proteinin the oocyte. The maturation response of follicles to hCG was size-dependent within a range from 400 to 600 m in diameter, with a maximum response displayed by 530–600 m follicles. The response of these follicles to hCG was not inhibited within a range of incubation temperatures from 15 to 28 °C, but the length of time required for the follicles to achieve 50% maturation was negatively correlated with increasing temperatures (r2 = 0.97; p ≤ 0.01). However, the largest follicles (530–600 μm) did not undergo maturation in response to high doses (1 μg/ml) of the major maturation-inducing steroids (MISs) known in teleosts, 17.20-dihydroxy-4-pregnen-3-one (17.20β) and 17.20β.21-trihydroxy-4-pregnen-3-one (20βS), even after a previous incubation period of follicles with 10 IU/ml hCG for 1.3 or 6 h. These observations indicate that C. striata follicles are very sensitive to increasing doses of gonadotropin, and that their responsiveness to this hormone is highly size-dependent within a very narrow range. The preliminary results also suggest that 17.20β and 20βS are not the MIS in this species.

The effectiveness of different gonadotropin releasing hormone analogues (GnRHa) and/or pimozide for inducing ovulation in Arctic charr was investigated at two different temperatures: 5 °C, a temperature suitable for spontaneous ovulation in Arctic charr and 10 °C, a temperature which inhibited ovulation in Arctic charr. At 5 °C all the different GnRH analogues tested were able to induce and synchronize ovulation. At 10 °C a sustained release preparation of D-tryptophan6 luteinizing hormone releasing hormone (D-Trp6LH-RH) at 20 μg.kg−1 and an acute release preparation of D-arginine6salmon GnRH (D-Arg6 sGnRH) at 100 μg.kg−1 were able to induce ovulation in 80% of the females within 15 days (versus 2% in controls). Pimozide alone or in combination with a low dose of D-Arg6sGnRH was able to induce some ovulation at 10 °C, suggesting that a dopamine inhibition of gonadotropin secretion could occur at 10 °C. Egg survival in groups receiving GnRHa at 5 °C was comparable to controls (73%) except in the group receiving GnRHa in combination with pimozide (45%). At 10 °C, egg survival was significantly lower than controls at 5 °C, except for the group receiving pimozide alone. At both temperatures, egg survivals of each spawn were negatively correlated with the plasma gonadotropin (GtH2) level of the reproducing females except in groups receiving a sustained release preparation of D-Trp6LH-RH.

As in the female (Breton et al., 1988), plasma gonadotropin levels (GtH) in male roach were always the lowest the day of aggregation on the spawning areas, eventhough they were elevated 3 daysearlier. The levels increased during spawning and remained at a high level in most of the animalscaptured out of the visible spwaning areas, 3 weeks after the beginning of the spawning activity. During the same period the GnRH contents did not significantly vary in the hypothalamic lobes, the di-met-and myelencephalon. On the contrary there were marked variations in the pituitary gland and the telencephalon in which the GnRH levels were the highest the day of aggregation when GtH plasma levels were the lowest. In these two structures they decreased during spawning in correlation with the increase of the plasma GtH levels. These results are discussed in comparison with those obtained in the female and in relation with the possible endocrine and paracrine roles of the GnRH in these structures and mainly in the telencephalon.

Plasma and pituitary gonadotropin (GtH) levels, and the gonadotropin releasing hormone (GnRH) in differents areas of the brain, were measured using radioimmunoassays during the prespawning and the spawning period in a wild population of roach (Rutilus rutilus). GtH pituitary levels did not vary. On the contrary GtH plasma levels showed variations during the prespawning period and were minimum on the day of arriva1 on the spawning areas, Do. During spawning they increased in ovulated females but also in unovulated animals and returned to low values, 1 month after. During this period GnRH varied inversely in all brain structures and was always negatively correlated with the blood plasma GtH levels. This suggests that all the brain GnRH would be involved in the control of the GtH secretion during spawning. This was not the case during the prespawning period, during which only hypothalamic and pituitary GnRH levels were correlated with GtH. There were also marked variations in the telencephalic GnRH extra hypothalamic GnRH. It is hypothetized that it could be a link between environmental factors and the hypothalamo-pituitary cornplex.