Response of gilts with delayed puberty to pregnant mare serum gonadotropin or estrogen

The effect of pregnant mare serum gonadotropin (PMSG) or estradiol cyclopentylpropionate (EC) on the induction of estrus, duration of estrus, and serum progesterone concentration after estrus was evaluated in 8 gilts with delayed puberty. Four gilts were given 500 IU of PMSG IM and 4 were given 2 mg of EC, IM. The inactive status of the ovaries at the time of treatment was verified by serum progesterone values of less than 0.5 ng/ml in serial samples collected before treatment. The 4 EC-treated gilts came into estrus at a mean of 3.5 days after treatment, but 1 of the gilts did not form corpora lutea. Three PMSG-treated gilts came into estrus at a mean of 4.0 days after treatment. The remaining PMSG-treated gilt remained anestrus and did not form corpora lutea. The mean duration of estrus in EC-treated gilts was 5.25 days compared with 2.0 days for PMSG-treated gilts (P less than 0.05). Serum progesterone concentrations were higher in PMSG-treated gilts than in EC-treated gilts at 8, 11, and 17 days after treatment (P less than 0.05).     

Experimental studies on the stimulation of prenatal development in swine by PMSG treatment in early pregnancy. 1. Clinical results of embryonic development in young slaughtered sows and litter results in young and old sows after PMSG treatment on the 11th day of pregnancy

Thirty-eight gilts were slaughtered on the 25th and 39th days of pregnancy, after they had received 400 I.U. PMSG treatment on the eleventh day of pregnancy. Treated and untreated animals in a group of 140 gilts and 195 adult sows were compared with each other for post-farrowing fertility performance. Weight development of embryos obtained from the slaughtered sows depended on the number of embryos alive. The survival rate of embryos from treated sows was about 5% higher than that recorded from untreated animals. Clearly increased litter sizes which, however, were associated with lower piglet birth weights were recorded from farrowing gilts and adult sows, following PMSG treatment. The conclusion is drawn that PMSG treatment, via luteotrophic action of luteinising hormone, is capable of stabilising pregnancy-related corpora lutei, resulting in higher litter sizes. Further studies will be necessary, and emphasis will have to be laid on the problem of weight development of newborn piglets, following litter-size boosting treatment.     

The influence of exogenous pituitary growth hormone on the ovulatory response to PMSG and hCG and the LH response to estradiol benzoate in prepubertal gilts

Two experiments were performed to examine the influence of exogenous growth hormone on the reproductive axis in gilts. Experiment one employed 26 Yorkshire × Landrace prepubertal gilts, which were selected at 150 d and 86.5 ± 1.5 kg bodyweight (BW) and assigned equally to two treatments. Gilts received injections of either porcine growth hormone at 90 μg/kg BW, or vehicle buffer, from 150 to 159 d. At 154 d gilts received 500 IU PMSG, followed 96 hr later by 250 IU hCG. Gilts were slaughtered at 163 days and their ovaries recovered to determine ovulatory status. In each treatment, gilts failed to show any ovarian response to PMSG/hCG. All remaining control gilts ovulated and their ovaries appeared morphologically normal. In gilts receiving exogenous growth hormone, fewer ovaries (4/11, P<.01) appeared morphologically normal. The ovaries of all other growth hormone injected gilts had very large (12–25 mm) non-luteinized follicles. In experiment two, 20 prepubertal Yorkshire × Landrace gilts were selected at 138 days and 85 kg BW. These gilts received injections of growth hormone at 90 μg/kg BW (n=9) or vehicle (n=11) from 138 to 147 days. At 143 days, all gilts were given an injection of estradiol benzoate (EB) at 15 μg/kg BW. Blood samples were taken at the time of EB injection, at 24 and 36 hr and then at 6 hr intervals until 78 hr. All samples were assayed for serum LH concentrations. The EB induced LH peak height was lower (P<.04) in gilts receiving exogenous growth hormone than in controls. The results presented indicate that the daily injection of growth hormone at 90 μg/kg BW reduced the estradiol-induced release of LH in addition to reducing the number of corpora lutea in gonadotrophin stimulated gilts.     

Anestrus in Pigs: Confirmation by a Solid-phase RIA for Progesterone and Subsequent Response to Treatment

All gilts not detected in estrus by eight months of age and any sows not observed in estrus by 14 days post-weaning, throughout a six month period in a University research herd, were bled on Monday and Thursday and plasma progesterone was measured by a solid-phase RIA. Basal concentrations of progesterone in both samples were considered indicative of true anestrus while one or more elevated values suggested that ovarian activity was present. Progesterone was basal in both samples from 44 of 70 gilts and all of the 23 sows tested. These anestrous animals were injected with either 400 IU PMSG plus 200 IU hCG or with 500 IU hCG plus 1 mg estradiol benzoate. The two treatments were equally effective with 60% of the injected females showing estrus and being successfully inseminated within ten days after treatment. Most of the gilts with elevated progesterone concentrations in the initial samples showed estrus within the following three weeks. The rapid solid-phase assay was able to differentiate between basal and luteal-phase levels of progesterone using unextracted plasma and could be a useful diagnostic aid for veterinarians attempting to determine major reasons for anestrus in gilts and sows.     

Effects of oestradiol benzoate injections, exposure to the boar and age on the attainment of puberty in the gilt

Thirty large white cross Landrace prepubertal gilts from five litters were allocated at random within litters to one of six treatment. All the gilts were given three daily intramuscular injections of 6 micrograms/kg liveweight of oestradiol benzoate but the first injection was given at either 100 days, 120 days, 140 days, 160 days, 180 days or 200 days old. From the time the first oestrogen injection was given, until the end of the experiment, the gilts were allowed daily contact with a boar for 20 minutes. The gilts were mated with a mature boar at the appearance of the second oestrus and they were slaughtered 20 days later. The numbers of gilts ovulating in the treatment groups were determined from plasma progesterone concentrations measured twice weekly throughout the experiment. The numbers of gilts ovulating within 10 days of the oestradiol benzoate injections were 3 of 5, 1 of 5, 0, 0, 3 of 5 and 1 of 5, respectively, in the groups first treated at 100 days, 120 days, 140 days, 160 days, 180 days and 200 days old. For those gilts which were successfully mated, no significant differences were observed between the treatment groups in the number of viable embryos per gilt.     

Clinical study results of the embryonic development in gilts and brooding performance of gilts and sows after HCG treatment on the 11th day of pregnancy

Forty-four pregnant gilts were slaughtered on the 32nd and 33rd days of pregnancy, after 30 of them had received 100 or 400 IU of HCG on the eleventh day of pregnancy. Both doses had resulted in higher number of living embryos. Embryo survival rates of treated sows were up to 14.9 percent higher than those of untreated animals. Higher numbers of embryos had no adverse effect on their mass development. Fertility was measured of 77 HCG-treated and untreated gilts as well as of 54 adult sows. The number of non-pregnant sows which returned to oestrus was higher in the group of gilts and adult sows which had received treatment. The number of pregnant animals in the treated adult sow group was seven percent higher than that in the control group. Increased litter sizes were additionally recordable from those gilts and adult sows that had received HCG injections. Yet, those higher litter sizes were associated with lower weight of live-born piglets. In further studies more attention should be given to possible stimulation of LH secretion in early gravidity.     

Experiments in biological engineering to induce puberty in young female swine. 4: Ovulation period after puberty in animals aged about 200 days, using different combinations of gonadotropic hormones

44 prepuberal gilts were treated with gonadotropic combinations and investigated for ovarian dynamics. 400 PMS + 200 HCG (Suigonan-Vemie) induced ovulations at the 4th day p.i., 100 FSH + 100 HCG resp. 200 FSH + 200 HCG at the 6th day p.i. At the 8,-11th day p.i. the PMS/HCG-treated animals showed corp. lut, in 100, the FSH/HCG-treated in 50 resp. 87% of the cases. A second injection of 250 HCG 3 days after 200 FSH + 200 HCG increased the number of animals which had ovulated. Zystic ovaries (larger than or equal to 11 mm) developed in all groups. Declaration of gonadotropins in "international units".     

Effect of the gonadotrophins treatment on morphological alterations in ovary and peripheral plasma concentrations of steroid hormones in gilts

The present study was designed to examine the influence of gonadotrophins treatment on the ovarian morphology changes and plasma concentrations of steroid hormones in peripheral blood. The experiment was performed on sexually pubertal gilts (Large White x Landrace) of similar age (7-8 months) and body mass (100-110 kg) with two controlled subsequent estrous cycles. The animals were randomly divided into four groups: two control consisting of pigs with the luteal phase (n = 9, the 10th day of the estrous cycle) and the follicular phase (n = 6, the 20th day of the estrous cycle) and two experimental ones consisting of animals with both mentioned periods (n = 7 and n = 9) treated with gonadotrophins (PMSG and hCG). The gilts in the luteal phase were injected (s.c.) with gonadotrophins at a daily dose of PMSG 400 and hCG 200 IU from the 16th to the 27th day (the 6th day of the next estrous cycle). The gilts in the follicular phase, were injected with the same dose of gonadotrophins but from the 8th to the 19th day of the estrous cycle. Plasma concentrations of P4, A4, T, E1, E2 and metabolite of PGF2 alpha-PGFM were determined by radioimmunoassay (RIA) method. Injections of PMSG and hCG in both experimental groups produced several times enlarged: weight, size and volume of ovaries and alterations in a number of structural elements as compared with those found in the control animals. The morphological elements presented in ovaries: corpora haemorrhagica, corpora lutea, regular and atretic follicles and first of all cysts by distinctly differentiation thickness of the walls are characteristic for cystic ovarian degeneration. Plasma concentrations all determined hormones after gonadotrophins treatment in experimental groups were increased except E1 (insignificant decrease) in luteal phase as compared with those found in the control groups. Statistically significant increase (p < 0.001) in plasma concentrations of P4, A4, and T in both experimental groups and E2 (p < 0.001) in luteal phase were noted. In peripheral plasma concentrations increase of E1 and E2 in follicular phase of the estrous cycle were insignificant.     

Effects of biotechnical management procedures on blood parameters in gilts. 2. Protein-bound iodine and copper

Two groups of twelve gilts each kept on platforms were synchronised in two passes over 20 days, using 100 mg Suisynchron per animal and die followed by PMS treatment (1,000 I.U. Intergonan) and HCG treatment (250 I.U.). Complement fixation occurred five days after the first hormone application and was followed twelve to 15 days later by another phase of treatment, using Gravigonan (250 I.U. follicle-stimulating hormone (FSH), 500 I.U. HCG, 1 mg oestradiol benzoate in 10 ml serum of swine). Blood samples were continuously drawn during the various phases of treatment and cycle from the above animals as well as from 20 gilts synchronised in the above way and from another 20 untreated gilts. Protein-fixed iodine and copper levels were assessed from those samples. The protein-fixed iodine and copper levels of the blood were significantly reduced (P less than 0.01) by synchronisation, using Suisynchron. None of the two parameters was particularly affected by PMS and HCG treatments. Blood-borne protein-fixed iodine and copper was increased by administration of gonabione. Both parameters went up further during full oestrus at which date they were higher in untreated animals than in synchronised. (Protein-fixed iodine: 3.50/226micrograms/100 ml; P less than 0.01; copper: 0.283/0.234 mg/100 ml; P less than 0.01).     

Relationship between two morphological types of ovaries and their follicular microscopic population before puberty and their ensuing follicular development and ovulation rates at puberty in gilts

A population of ovarian follicles was studied in 32 gilts with two morphological types at four physiological stages. Left ovaries were serially sectioned (10 microns), and follicles (greater than .19 mm) were counted and measured by histological technique. In Exp. 1, prepuberal gilts that maintained the grape-type (GT) or other-type (OT) of ovaries at 140 and 160 d of age as determined by laparoscopy had their population of follicles studied at 165 d of age and compared with that on d 3 of the first puberal estrus in gilts that maintained the same ovarian type (GT or OT) at 140, 160 and 180 d of age. In Exp. 2, gilts that maintained the same ovarian types at 140, 160 and 180 d of age were compared at d 19 and 3 of the first and second puberal estrus, respectively. At 165 d of age, OT ovaries contained a greater number of classes 3 (.63 to 1.12 mm) and 4 (1.13 to 2.00 mm) nonatretic (less than 4 pycnotic bodies) follicles than GT (P less than .01), whereas at d 3 of the first puberal estrus, their mean number became comparable between the two ovarian types (P greater than .1) and similar to 165-d GT ovaries. At 165 d of age, atretic follicles formed 19.6% and 10.7% of the population of antral follicles in OT and GT ovaries (P less than .05) whereas at puberty 17.5% and 19.6% atresia was observed in the same two groups, respectively (P greater than .10).(ABSTRACT TRUNCATED AT 250 WORDS)     

Steroid concentrations in cows with corticotropin-induced cystic ovarian follicles and the effect of prostaglandin F2alpha and indomethacin given by intrauterine injection.

In 7 instances, cystic ovarian follicles resulted when adrenocorticotropin (ACTH) was administered daily during the follicular phase of the estrous cycle in cows. Two cows given daily injections of hydrocortisone (cortisol) during the follicular phase of the estrous cycle did not develop cystic ovaries. Plasma concentrations of estradiol in cows with induced cystic ovarian follicles were similar to the peak values observed at estrus and were between 6 and 12 pg/ml. Progesterone concentrations in plasma of cows with cystic ovaries were low, between 1 and 2 ng/ml. Ovulation occurred when 2 cows were given human chorionic gonadotropin (HCG) during the period of ovarian cyst development with ACTH administration. Several days of administration of ACTH was required to cause cyst development. Ovulation occurred at the expected time in 1 cow when injections began on day 19, that is, late in the follicular period. In another cow, when treatment was stopped on day 3, after the expected time of estrus a delayed ovulation occurred. In 2 cows with induced cystic ovarian follicles, cyst atresia occurred spontaneously about day 13 to 17 of the cycle. In these cows, new follicular growth and ovulation followed (although delayed in 1 cow). The time of atresia of cystic follicles was not influenced by the intrauterine injection of 10 ml of sterile saline solution on days 8, 9, and 10 in 1 cow. When 5 mg of prostaglandin F2alpha in 10 ml of sterile saline solution was given (uterine injection) in 2 cows on days 8, 9, and 10, cyst atresia occurred earlier than the time of spontaneous atresia. Intrauterine administration of 100 mg of indomethacin in 10 ml of sterile saline solution daily for 13 or 14 days to 2 cows, starting on day 12 or 13 of the cycle, resulted in persistence of the induced cystic ovarian follicles. After cessation of indomethacin treatment, atresia of cysts followed and new follicular growth and ovulation occurred.     

Contact with oestrous female pigs stimulates and synchronises puberty in gilts.

Three experiments, using a total of 132 pre-pubertal gilts, were carried out to investigate the influence of contact with oestrous female pigs on the attainment of puberty by gilts. Experiment 1 compared the effect of removing the gilts from their groups as they reached puberty in response to exposure to a boar, with leaving the gilts in their groups for five to 15 days after puberty or five to 15 days after second oestrus. All the groups exposed to boars reached puberty significantly earlier than controls (P less than 0.05) but there was no difference between these groups in their mean age at puberty. However, the synchrony of puberty was significantly greater among the gilts which remained in their groups after puberty (P less than 0.01) or second oestrus (P less than 0.001) than among the gilts which were removed at puberty. Experiment 2 investigated the influence of housing pre-pubertal gilts with penmates induced into puberty with injections of oestradiol benzoate. Puberty was significantly advanced by the presence of penmates regularly exhibiting oestrous periods. Experiment 3 compared the effect of daily exposure to an anoestrous ovariectomised sow, an oestrous ovariectomised sow or a boar, on the attainment of puberty by gilts. Gilts exposed to either an oestrous sow or a boar were significantly younger at puberty than isolated control animals (P less than 0.05) whereas the mean age at puberty of gilts exposed to an anoestrous sow was not significantly different from that of controls.(ABSTRACT TRUNCATED AT 250 WORDS)     

使用PMSG、HCG调节繁殖末期母蓝狐发情和产仔效果的试验研究

为了提高乏情母狐的利用率,第1年对50只没有发情表现的青年母蓝狐同时一次注射PMSG200IU/只,5d后再注射HCG100IU/只,有42只出现明显发情症状并接受公狐爬跨,发情率84%。对发情母狐实施子宫内输精,结果无一产仔;第2年对50只非典型发情的青年母蓝狐同时一次注射PMSG200IU/只,5d后再注射HCG100IU/只,全部出现明显的发情症状并接受交配。对其实施子宫内输精3次,结果有24只产仔,产仔率48%。试验结果表明,在母狐繁殖末期,联合使用PMSG和HCG对没有发情表现的青年母蓝狐有促使其发情的作用,但不能使其产仔;对有发情表现但不明显的青年母蓝狐有促进其发情并能使其部分怀孕和产仔的作用。     

Possibilities of ovulation synchronization in puberty-induced gilts

Puberty was induced in 39 clinically prepuberal gilts (two groups of three sub-groups each) by parallel but locally separated application of 500 IU PMSG ("Maretropin") and 250 IU HCG ("Gonadex"), with the view to testing ways to synchronise ovulation. Seventy-two hours were allowed to elapse, before 24 animals received another application of 500 IU HCG and 15 animals 250 IU HCG. The animals were slaughtered in consecutive groups of study ovulation and histolotically examined to disclose endometrial processes. Ovulations were found to be well synchronised in the recipients of a second injection of 500 IU HCG. Only sub-threshold effects with no synchronised ovulation were recorded from the animals that had received a second dose of 250 IU HCG. A second injection of 500 IU HCG should be given not until something between 78 and 82 hours after puberty induction for optimum follicle maturation and adequate proliferation of the endometrium.     

Effect of age and physical or fence-line boar exposure on estrus and ovulation response in prepubertal gilts administered PG600

Boar exposure has been used for estrus induction of prepubertal gilts, but has limited effect on estrus synchronization within 7 d of introduction. In contrast, PG600 (400 IU of PMSG and 200 IU of hCG; Intervet, Millsboro, DE) is effective for induction of synchronized estrus, but the response is often variable. It is unknown whether boar exposure before PG600 administration might improve the efficiency of estrus induction of prepubertal gilts. In Exp. 1, physical or fence-line boar contact for 19 d was evaluated for inducing puberty in gilts before administration of i.m. PG600. Exp. 2 investigated whether 4-d boar exposure and gilt age influenced response to PG600. In Exp. 1, 150-d-old prepubertal gilts were randomly allotted to receive fence-line (n = 27, FBE) or physical (n = 29, PBE) boar exposure. Gilts were provided exposure to a mature boar for 30 min daily. All gilts received PG600 at 169 d of age. Estrous detection continued for 20 d after injection. In Exp. 2, prepubertal gilts were allotted by age group (160 or 180 d) to receive no boar exposure (NBE) or 4 d of fence-line boar exposure (BE) for 30 min daily before receiving PG600 either i.m. or s.c. Following PG600 administration, detection for estrus occurred twice-daily using fence-line boar exposure for 7 d. Results of Exp. 1 indicated no differences between FBE and PBE on estrus (77%), age at puberty (170 d), interval from PG600 to estrus (4 d), gilts ovulating (67%), or ovulation rate (12 corpora lutea, CL). Results from Exp. 2 indicated no effect of age group on estrus (55%) and days from PG600 to estrus (4 d). A greater (P < 0.05) proportion of BE gilts expressed estrus (65 vs. 47%), had a shorter (P < 0.05) interval from PG600 to estrus (3.6 vs. 4.3 d), and had decreased (P < 0.05) age at estrus (174 vs. 189 d) compared with NBE. Ovulation rate was greater (P < 0.05) in the BE group for the 180-d-old gilts (12.7 vs. 11.9 CL) compared with the NBE group. However, age group had no effect on ovulation (77%) or ovulation rate (12 CL). Collectively, these results indicate that physical boar contact may not be necessary when used in conjunction with PG600 to induce early puberty. The administration of PG600 to 180-d-old gilts in conjunction with 4 d prior fence-line boar exposure may improve induction of estrus, ovulation, and decrease age at puberty.     

The dose precision of PMSG in young and old sows in the process of biotechnical ovulation synchronization. 1. Comparison of diagnostic laparotomy

Treatment was applied, on two farms, to 272 gilts and 169 adult sows, 24 hours after discontinuation of Suisynchron application to the gilts or weaning of piglets of adult sows. Included were 600, 800 or 1,000 IU of PMSG for the gilts and 750, 1,000 oder 1,250 IU of the same batch (Pregmagon-Dessau) for the adult sows for ovarian stimulation. This was followed by application of 500 IU of HCG to the gilts or 300 micrograms Gn-RH vet. "Berlin-Chemie" + 300 IU HCG to the adult sows for synchronised ovulation. Laparotomy was performed on the gilts on the fifth day from PMSG application and on the adult sows on the fourth day. Average ovariotropic stimulation was "mild" in response to lower doses (14.8 follicles in gilts and 20.4 follicles in adult sows) but was "pronounced" in response to medium doses (19.4 or 22.7 follicles, respectively). The pharmacological concept of "mild" exogenic ovarian stimulation by low dosage at the threshold of effectiveness should deserve more attention, last but not least, for breeding aspects. The two groups of animals on both farms differed considerably from one another with regard to reactivity, which cannot be etiologically interpreted for the time being.     

Ovarian response to pregnant mare serum gonadotropin and porcine pituitary extract in gilts actively immunized against gonadotropin releasing hormone

Two experiments were conducted to determine the effect of exogenous gonadotropins on follicular development in gilts actively immunized against gonadotropin releasing hormone (GnRH). Four gilts, which had become acyclic after immunization against GnRH, and four control gilts were given 1,000 IU pregnant mare serum gonadotropin (PMSG), while four additional control gilts were given saline. Control animals were prepuberal crossbred gilts averaging 100 kg body weight. Control gilts given saline had ovaries containing antral follicles (4 to 6 mm in diameter). Control gilts given PMSG exhibited estrus and their ovaries contained corpora hemorrhagica and corpora lutea. PMSG failed to stimulate follicular growth in gilts immunized against GnRH, and ovaries contained regressed corpora albicantia and small antral follicles (less than 1 mm in diameter). Concentrations of luteinizing hormone (LH) and estradiol-17 beta (E2) were non-detectable in gilts immunized against GnRH and given PMSG. In the second experiment, five gilts actively immunized against GnRH were given increasing doses of PMSG every third day until unilateral ovariectomy on d 50. PMSG failed to stimulate follicular growth, and concentrations of follicle stimulating hormone (FSH), E2 and LH were not detectable. Six weeks later, gilts were given a booster immunization and then were given 112 micrograms LH and 15 micrograms FSH intravenously every 6 h for 9 d. The remaining ovary was removed on d 10. Although LH and FSH concentrations were elevated, administration of gonadotropins did not stimulate follicular growth or increase E2 concentrations. These results indicate that neither PMSG or exogenous LH and FSH can induce E2 synthesis or sustain follicular development in gilts actively immunized against GnRH.     

Potential treatments for anestrus in gilts and sows

Pregnant mares' serum gonadotrophin (400 IU) combined with human chorionic gonadotrophin (200 IU) was administered to anestrous gilts (n=31) and sows (n=20) in commercial herds. Two-thirds of the treated animals were mated successfully within seven days and, although no control animals were included, the response indicated that this hormone combination would be useful in herds with anestrous problems. A second experiment was conducted to evaluate the occurrence of estrus and/or ovulations in prepuberal gilts (n=eight/treatment) following injection with pregnant mares' serum gonadotrophin/human chorionic gonadotrophin or other hormones that might stimulate ovarian activity. The pregnant mares' serum gonadotrophin/human chorionic gonadotrophin combination and follicle-stimulating hormone produced estrus within ten days of injection in at least half of the treated gilts but the response was lower with gonadotrophin-releasing hormone and a prostaglandin analogue. Combinations of human chorionic gonadotrophin with small amounts of estradiol benzoate stimulated estrus and ovulation in most of the treated gilts.     

不同日龄北京黑猪卵巢发育的研究

对30～180日龄北京黑猪母猪卵巢形态学和组织学的研究结果表明,在60日龄以前卵巢体积缓慢增长,60日龄以后直到120日龄迅速增长,150～180日龄之间增长速度减慢。90日龄卵巢切片上,首先观察到有腔卵泡。卵泡总数随日龄增加而减少,闭锁率增高。一半180日龄母猪卵巢上有成熟黄体。根据实验结果,提出北京黑猪母猪初情期在170日龄左右。     

Administration of pregnant mare serum gonadotropin to Japanese quail (Coturnix coturnix japonica): dose response over seven days and comparison of delivery by daily injection or osmotic pump

AIMS: This study is part of a research programme that aims to develop a method of hormone treatment to stimulate breeding in female birds. The aims of this study were to compare dose rates and two different delivery methods, daily injection or osmotic pump, for hormone treatment of Japanese quail (Coturnix coturnix japonica) with pregnant mare serum gonadotropin (PMSG). METHODS: PMSG (0, 5, 10, 20, 40 and 80 IU PMSG/day) was administered to 6-week-old Japanese quail housed under short-day, cool-temperature conditions (8L:16D at 7-10 degrees C) by daily injections or osmotic pump for 7 days. Three additional groups were untreated: one group was dissected at Day 0, and two groups were maintained under either short-day, cool-temperature or long-day, warm-temperature (16L:8D, 20 degrees C) conditions for 7 days. Cloacal diameter was measured daily, and ovarian and oviductal mass and plasma oestradiol concentrations measured at the end of the treatment period. RESULTS: PMSG treatment stimulated ovarian and oviductal growth. After 7 days of treatment with 10-20 IU PMSG, ovarian and oviductal mass were similar to those in birds moved from short to long days. Females treated with the highest doses of PMSG (40 or 80 IU) had significantly larger cloacal diameters and ovarian and oviductal mass than other treated birds or birds maintained under long-day, warm-temperature conditions. Daily injections and osmotic pumps were equally effective methods of delivery. However, there was considerable variation in response to PMSG among individual birds and this was particularly obvious at the higher doses (20-80 IU PMSG). There were no differences in plasma oestradiol concentrations between groups treated using daily injections or osmotic pumps. CONCLUSIONS: A dose of 10 IU PMSG/day was chosen for use in future experiments with Japanese quail, for the first 7 days of treatment. The delivery method of choice for future studies will depend on the practical considerations of the research in question.