Consistent, individual differences in the expression of maternal behaviour have been described in several species including the sheep. The neuroendocrine mechanisms underlying the onset of maternal behaviour in the sheep have been described, although the relationship between hormonal events and individual differences in behaviour has yet to be determined. In this study, we examined whether the individual differences in plasma estradiol, progesterone, oxytocin and cortisol concentrations were related to observed individual and breed differences in maternal behaviours in two breeds of sheep (Scottish Blackface and Suffolk) known to differ in maternal behavioural expression. Maternal estradiol concentration increased rapidly before parturition and was higher in Blackface ewes than Suffolk ewes. Plasma progesterone declined before parturition and was higher in Suffolk than Blackface ewes. Prepartum estradiol, but not progesterone, was related to individual differences in maternal grooming of the lamb. Plasma oxytocin did not differ between breeds in late gestation. There was a tendency for oxytocin to be higher in Blackface than Suffolk ewes immediately after birth. However, there were no significant relationships between prepartum or postpartum oxytocin and any maternal behaviours. Plasma cortisol was higher in Blackface than Suffolk ewes in the last days of pregnancy but rose in both breeds over the last 24 h before parturition and did not differ at delivery. Cortisol peripartum was negatively related to individual differences in maternal affiliative behaviours. These data suggest that estradiol, and potentially cortisol, may mediate individual differences in maternal behaviour in sheep.

To determine the effects of feed-back from a farrowing nest on periparturient behaviour, heart rate and hormones, 20 gilts housed in Schmid pens were permitted to build a nest of peat, straw and branches. Ten gilts then had their nest removed (NR) 10 h after the onset of nest-building and again every 4h until parturition, whereas 10 gilts were given sham removals (C). Based on video recordings, gilt periparturient postures and nest-building behaviour were observed from 7 h before until 6 h after the birth of the first piglet. Maternal heart rate was measured using a transmitter belt and a watch receiver and the heart rate during the last 7 h prepartum analysed. Maternal blood samples were taken via a jugular catheter every 20 min over the last 7 h prepartum and later analysed for plasma concentrations of cortisol and oxytocin.Treatment did not affect the quantity or timing of nest-building and postural behaviour prior to or during parturition. However, treatment significantly affected changes over time in heart rate and plasma cortisol as parturition approached. Heart rate (P = 0.008) and plasma cortisol (P = 0.002) increased for NR gilts, but remained constant for C gilts, although nest-building activity decreased during this period in both groups (P = 0.006). Plasma oxytocin was unaffected by treatment. The prepartum increases in plasma cortisol and heart rate in NR gilts in the absence of greater activity suggest that nest removal was stressful. The observed treatment effects could have resulted from gilts perceiving environmental novelty following nest disruption, a specific lack of feed-back from the nest or disturbance from nest removal activity per se. The results emphasise the importance of the farrowing environment and the opportunity to construct a nest on sow welfare. (C) 2003 Elsevier B.V. All rights reserved.

Domestic pigs, Sus scrofa, build a maternal nest on the day before parturition. A model for nest building has been established in pigs, in which exogenously administered prostaglandin (PG) F2α may be used to elicit nesting behaviour in cyclic, pseudopregnant and pregnant pigs. The central mechanisms mediating this response are unknown. The present study determined regional brain activity using semi-quantitative analysis of c-fos mRNA, after induction of nest-building behaviour by PGF2α in Large White pseudopregnant pigs. Oestradiol valerate injections (5 mg/day) were given on days 11–15 of the oestrous cycle to induce pseudopregnancy. The pigs were housed individually in pens (2.8×1.7 m) containing straw. On the test day (day 46 or 47 of pseudopregnancy) animals were injected with 3 ml saline (n=5) or 15 mg of PGF2α (Lutalyse, Upjohn; n=6) intramuscularly. Pigs treated with PGF2α, but not saline, displayed bouts of rooting, pawing and gathering straw, which we interpret as nest building behaviour. The pigs were killed 65 min after treatment, which was 30 min after peak nest building activity, and the brain, uterus and ovaries removed for processing using in situ hybridisation. Saline-treated pigs had elevated levels of c-fos mRNA, compared to background, in the pituitary, corpus luteum and uterus, and a lower, but elevated, level of expression in cerebellum, cortex, hippocampus and olfactory bulb. PGF2α-treated pigs had significantly higher levels of c-fos mRNA expression than saline-treated pigs in the parvocellular and magnocellular regions of the hypothalamic paraventricular nucleus, the supraoptic nucleus (including the pars dorso-medialis), the neural lobe of the pituitary gland and the cerebellum. PGF2α-treated pigs also had significantly higher c-fos induction in corpus luteum. These data show that the pattern of c-fos mRNA expression in specific brain areas is different between pigs that show PGF2α-induced nest building and saline-injected controls.

Intramuscular injection of the naturally occurring prostaglandin F2alpha (PGF2alpha) to sexually mature female pigs induces luteolysis and rapidly elicits a behavioural response consistent with pre-partum nest-building. Intramuscular injection of the synthetic prostaglandin F2alpha (cloprostenol) also induces luteolysis but no nest-building behaviour is observed. The effects of PGF2alpha, but not cloprostenol, on nest-building behaviour may be mediated via peripheral PGF2alpha receptors (FP) or via direct action on central FP receptors. We have previously shown FP receptor mRNA to be localized in porcine paraventricular nucleus (PVN), supraoptic nucleus (SON) and pars dorso-medialis of the suproptic nucleus (SOD), suprachiasmatic nucleus, choroid plexus and anterior and intermediate pituitary lobes. In this experiment, we examined hypothalamic expression of the immediate early genes c-fos and c-jun mRNA after treatment with PGF2alpha or cloprostenol. Twenty-one 8-month-old nulliparous female pigs (gilts) were injected intramuscularly with a luteolytic dose of PGF2alpha (15 mg), cloprostenol (175 microg) or saline control, their behaviour was recorded and they were killed 60 min later. Coronal hypothalamic sections and control ovarian tissues were incubated with 45-mer oligonucleotide probes complementary to porcine c-fos and c-jun genes using standard in situ hybridization histochemistry techniques. Significantly higher c-fos and c-jun mRNA expression was found in PGF2alpha-treated compared to saline or cloprostenol-treated pigs in the PVN, SON and SOD. Significantly higher c-fos and c-jun mRNA expression was found in corpus lutea of PGF2alphaand cloprostenol-treated pigs compared to saline controls. Treatment with PGF2alpha induced nest-building behaviour whereas treatment with cloprostenol and saline did not. This suggests that PGF2alpha, or one of its metabolites, and not cloprostenol, crosses the blood-brain barrier and acts directly on hypothalamic receptors to mediate its effect on nest-building behaviour.

In the pig, nest building occurs in the day preceding parturition (gestation= 114-116 days). Nest building behaviour can be induced in pregnant, pseudopregnant and cyclic female pigs following injection of prostaglandin F2alpha. Here we investigated behaviour and endocrine changes after the administration of indomethacin, which inhibits cyclo-oxygenase enzymes and thus prostaglandin synthesis.In experiment 1, pregnant primiparous pigs (gilts) were blood sampled through jugular vein catheters every 20 min from 1000 h on day 113 of pregnancy and behaviour was recorded until birth. Two hours after pre-partum nest building began, animals received 4 mg/kg indomethacin (n = 7) or control vehicle (n = 8) intramuscularly. Indomethacin-treated animals showed less nest building than controls between 1 and 5 h after injection (P<0.05), during which time they were mostly inactive and lay down for longer than controls. From 5 h before birth until birth there was no significant treatment difference in nest building behaviour. There was a tendency for the start of birth to be delayed in indomethacin-treated animals. Plasma 13,14-dihydro-15-keto-prostaglandin F2alpha (a major metabolite of prostaglandin F2alpha rose during pre-injection nest building and then fell following indomethacin treatment, but was not significantly different between groups when behaviour differed. Plasma oxytocin, cortisol and progesterone were not significantly affected by treatment. In experiment 2, indomethacin-treated non-pregnant gilts (n = 7) did not show any changes in activity or posture compared with vehicle-treated controls (n=6) between 90 and 150 min after treatment.These results suggested that indomethacin treatment reversibly and specifically inhibits porcine pre-partum nest building by a mechanism that may involve endogenous prostaglandin F2alpha synthesis inhibition but is independent of circulating oxytocin, cortisol and progesterone concentrations.

Domestic pigs build a maternal nest in the day preceding parturition. We have shown that prostaglandin F(2alpha) (PGF(2alpha)) induces nest building behaviour in non-pregnant pigs. The aim of this experiment was to examine the effects of different environmental temperatures on PGF(2alpha)-induced nest building. Data were collected from 9 Large White (LW) and 10 Large Black (LB) 8-9-month-old nulliparous sows (gilts). The pigs were housed in social groups between experiments and tested individually in pens (1.8mx1.8m) containing straw, within an environmentally controlled chamber. Pigs were habituated to the testing pens (maintained at 17 degrees C) and tested once at each of three temperatures (low, 5 degrees C; moderate, 17 degrees C; high, 30 degrees C). During testing the temperature of the chamber was adjusted at 09.00h and had reached set point by10.00h. The pigs were injected intramuscularly with 3ml saline at 10.30h and 0.1mg/kg PGF(2alpha) (Lutalyse, Upjohn) at 11.30h. Behaviour was scored for 1h after treatment with saline and 1h after treatment with PGF(2alpha) using one/zero sampling from video recordings. Nest building behaviour (rooting, pawing and gathering straw) was induced by PGF(2alpha) at all temperatures in both LW and LB breeds. There was a significant increase in rooting behaviours with decreasing temperature. No significant effects of temperature were found on the scores for gather or paw. The pigs spent more time lying down at the high compared to the low temperature after both saline and PGF(2alpha) treatment. Other behaviours unrelated to nest building but induced by PGF(2alpha), such as scratching, were unaffected by temperature. The results show that the nest building behaviour of non-pregnant pigs can be induced by exogenous PGF(2alpha) treatment, and that some, but not all, aspects of PGF(2alpha)-induced nest building (rooting but not pawing or gathering) are altered by environmental temperature.

We studied the effects of spinal intrathecal fentanyl on oxytocin secretion in 20 healthy women prior to an elective caesarean delivery at term under spinal anaesthesia. The women were randomly allocated into two groups with respect to spinal anaesthesia. Group I (n=10) received intrathecal bupivacaine (15 mg) plus fentanyl (25 microgram), and Group II (n=10) received intrathecal bupivacaine (15 mg) alone, prior to caesarean section. The two groups were comparable demographically. Altogether, ten samples of 4.5 ml of blood (taken every 60 s) were obtained before and ten samples were obtained after the intrathecal administration of the drug and establishment of the T6 block, and plasma oxytocin concentrations were assayed for each subject. Oxytocin was measured by RIA. We found no significant differences in plasma oxytocin concentrations of individual subjects before and after intrathecal injection. In addition, there were no significant differences in plasma oxytocin concentrations between the two groups when pooled samples from the subjects were compared for the pre- and post-intrathecal injection phases. We conclude that the spinal intrathecal administration of fentanyl does not suppress oxytocin secretion in pregnant women who are not in labour at term.

Previous studies showed that prostaglandin (PG)F2alpha treatment stimulated nest building behaviors in prepartum and pseudopregnant pigs. This experiment studied behaviors of PGF2alpha-treated pseudopregnant nulliparous pigs (gilts) exposed to newborn piglets. Penned pseudopregnant gilts (days 46-53) were injected with either 10 mg PGF2alpha (n = 8) or saline (n = 8) im, and behavior was recorded for 2 h (period A). Between 2 and 6 h (period B), gilts were given two male piglets (< 12 h old) and a novelty object (house brick) and recordings continued. During period A, PGF2alpha animals showed greater frequencies of standing, pawing, rooting, lifting, and carrying straw (indices of nest building) and scratching than saline treated animals. During period B, one PGF2alpha- and two saline-treated gilts attacked piglets, which were removed from the pen and the gilts excluded from further analysis. There were no treatment differences in period B in gilt posture, nest building behavior, or interactions with piglets or novelty object, except for a reduced frequency to trap piglets beneath their bodies and an increased frequency to attempt to escape from the pen in PGF2alpha-treated animals. Piglet position relative to the gilts' head and udder was unaffected by treatment. Gilts in both groups approached and nosed piglets more within the first 30 min of period B than subsequently. PGF2alpha-induced nest building had only a weak impact upon subsequent interactions between gilts and piglets, suggesting that mechanisms controlling porcine nest building and maternal behavior in this model were not directly linked.

Exogenously administered prostaglandin (PG) F2alpha induces behaviour similar to prepartum nest building in pregnant, pseudopregnant and nonpregnant female postpubescent pigs (Sus scrofa). These effects may be regulated by PGF2alpha-induced endocrine changes within the reproductive tract, such as those that initiate luteolysis. This study investigated the short-term effects of ovariohysterectomy on PGF2alpha-induced nesting behaviour in nonpregnant females. Cyclic 9-month-old virgin female pigs (gilts) received an oral dose (20 mg/day) of a synthetic progestogen (altrenogest; Regumate porcine, Hoechst, Milton Keynes, UK) for 18-21 days to synchronize oestrus. The gilts were then ovariohysterectomized (n=8) or sham-operated (n=7) on Days 3-8 after oestrus. They were housed individually and initially subjected to a series of control behavioural tests to establish the effect of ovariohysterectomy on their responses to the experimenters, novel objects, straw bedding and space restriction. Ovariohysterectomized gilts had a shorter latency to approach the experimenters than sham-operated animals, but there were no differences in their responses to a novel object, straw bedding or space restriction. Twelve to 16 days after oestrus, corresponding to the midluteal phase in sham-operated gilts, they were treated intramuscularly with 15 mg PGF2alpha (0.12 mg/kg, dinoprost; Lutalyse, Upjohn, Crawley, UK). PGF2alpha treatment induced a significant increase in straw gathering in ovariohysterectomized but not in sham-operated gilts. Other nesting behaviours, including rooting and pawing at straw, were induced in all animals. These results show that the uterus and ovaries are not required for the expression of PGF2alpha-induced nesting behaviour and the removal of the reproductive tract appears to have facilitated increased levels of gathering. This suggests that PGF2alpha induces luteolysis and nest building separately, and that PGF2alpha or a metabolite, may act centrally to mediate directly its effects on prepartum nest building in the pig.

Sows are highly motivated to build a maternal nest on the day preceding parturition. A model for nest building has been established in pigs, in which exogenously administered prostaglandin F(2alpha) (PGF(2alpha)) may be used to elicit nesting behaviour in cyclic, pseudopregnant and pregnant pigs. The aim of this experiment was to examine the effects of deprivation of straw bedding on PGF(2alpha)-induced nest building in pseudopregnant Large White gilts. Oestradiol valerate injections (5 mg/day) were given on days 11-15 of the oestrous cycle to induce pseudopregnancy. The pigs were housed individually in a pen (2.8x1.7 m) and provided with 2-kg fresh straw each day. On the test day, on day 46 or 47 of pseudopregnancy, half of the pigs were deprived of straw (substrate effect) and they were injected intramuscularly with saline or 15 mg of PGF(2alpha) (Lutalyse, Upjohn) (treatment effect) allocated in a Latin-square design. Behaviour was recorded onto video tapes for 1 h either side of treatment for analysis using a computerised event recorder. PGF(2alpha)-treated pigs housed in bare or strawed pens showed significantly higher frequencies of pawing and rooting, and stood for longer than saline-treated controls. This treatment effect has been previously shown to be comparable to pre-partum nest building. The removal of straw significantly reduced the frequency of pawing and the duration of rooting by PGF(2alpha)-treated pigs. The results demonstrate that nesting behaviour can be initiated by exogenously administered PGF(2alpha) and is further modified by the provision of straw. This suggests that PGF(2alpha)-induced nesting behaviour is subject to environmental feedback.

In seminatural environments, prepartum sows leave the herd and construct a maternal nest (a dug out hollow lined with vegetation) prior to the birth of their piglets. The endocrine drives motivating this behavior are not understood, but may involve prostaglandin (PG) F2alpha. This study examined the effect of PGF2alpha treatment on the behavior of pseudopregnant gifts housed in a large enclosure. Pseudopregnancy was induced using 5 mg/ml estradiol valerate/day im from days 11 to 15 of the estrous cycle (first day of estrus = day 0). The gifts' behavior was recorded on a control day, during which no treatment was given, and a test day (= 45.9 +/- 0.42 days of pseudopregnancy) when gilts received either 15 mg PGF2alpha (dinoprost: Lutalyse, Upjohn, Crawley, UK, n = 11) or 0.9% saline (n = 10) im at 11.00 h. PGF2alpha-treated gilts traveled further and were more frequently >10 m from the nearest pig than saline-treated animals. In the hour following injection, PGF2alpha-treated animals also showed increased frequencies of rooting and pawing the ground and stood for longer than saline-treated animals. However, gathering and carrying nest materials were not increased. These results suggest that PGF2alpha, given as a single dose to extensively housed gilts, initiated many, but not all, of the behaviors characteristic of prepartum nest building. The dose and duration of PGF2alpha treatment may have limited the observed behaviors. In addition, environmental feedback is likely to affect the degree to which some nest building behaviors are expressed.

Oxytocin plays an important role at parturition due to its involvement in uterine contractions, foetal expulsion and the onset of maternal behaviour. The role of the related neurohypophysial hormone, vasopressin, is less clear; however, there is some evidence that it is also involved in maternal behaviour and its role in osmotic regulation is well established. The aim of this study was to investigate the inhibitory effects of endogenous opioids on these hormones during the expulsive phase of parturition in the pig, and to examine how opioid restraint interacts with environmental restriction. The subjects of this study were 31 Large Whitex Landrace primiparous sows (gilts). An indwelling jugular catheter was implanted under general anaesthesia at 12 days before the expected parturition day (EPD). From 5 days before the EPD 15 of the gilts were individually housed in a restrictive parturition crate without straw and 16 were individually housed in a straw-bedded pen. Blood samples were taken with increasing frequency towards and during parturition through a catheter extension to reduce disturbance. At 7.5 min after the birth of the first piglet half of the gilts in each environment received a dose of the opioid receptor antagonist naloxone (1 mg/kg, i.v.) with the remaining gilts receiving saline as a control. Overall, there was no effect of environment on either circulating oxytocin or vasopressin. However, both oxytocin and vasopressin were inhibited by endogenous opioids during the expulsive phase. The inhibitory effects of opioids on these hormones did not appear to have any adverse effects on the progress of parturition as judged by cumulative piglet birth intervals. The regulation of the opioid inhibition of oxytocin and vasopressin during parturition is discussed in relation to other neurotransmitters and whether opioid inhibition of these neurohypophysial hormones is part of the 'normal' physiological response to parturition or whether it is stress-induced.

This experiment tested the hypothesis that opioid antagonists could influence the timing of the onset and progress of parturition in the pig. Primiparous pigs (gilts) received a jugular catheter on Days 104 to 106 of pregnancy. At 1400 h on Day 112 the gilts received 10 mg PGF2alpha, im to induce parturition. At 1000 h on Day 113 (i.e., 20 h later) gilts received either saline (n = 6), 1 mg/kg, iv naltrexone (n = 4) or 1 mg/kg, iv naloxone (n = 5). Blood samples were taken daily from Days 108 to 116. On Day 113, blood samples were taken hourly from 0500 to 0900 h and then every 30 min until 2400 h, or until the birth of the last piglet (BLP) (whichever was sooner) and assayed for progesterone, oxytocin (OT), cortisol and PRL. Additional blood samples for OT and cortisol assay were taken every minute from 0930 to 1100 h on Day 113 and for 30 min during parturition. Naloxone, but not naltrexone, delayed the onset of parturition relative to saline controls (by 14 h 21 min; P < 0.05). Duration of parturition and rate of births were not significantly affected by treatment. Mean plasma OT increased in the 4 h following naloxone but not saline treatment, during which time OT plasma pulse amplitude was reduced in naloxone and naltrexone-treated animals relative to saline treated controls. The PRL secretion rose following treatment in saline treated animals, consistent with approaching parturition, but failed to rise in opioid antagonist treated animals. Progesterone concentrations remained elevated in naloxone-treated animals for longer than in the other groups. These data suggest that a rapid change in overall effect of parenteral administration of naloxone to parturient pigs occurs from delaying its onset when administered as in these experiments, to facilitating its progress when given during parturition (earlier experiments). The delay of onset of parturition may be mediated by interference with hypothalamic control of OT or PRL release. (C) 2000 by Elsevier Science Inc.

This study investigated the effect of different doses (0–1.25 mg/kg IM) of prostaglandin (PG) F2α on the behavior of female pigs (Sus scrofa). Six-month-old cyclic nulliparous sows (gilts) were housed and tested individually in strawed pens (2.8 × 1.7 m). All doses of PGF2α induced rooting, pawing at the ground, and gathering straw. In the hour following treatment the frequency of pawing increased with increasing dose to reach a maximum level with the highest dose given. The frequency to gather straw was highest in pigs treated with the lowest dose (0.008 mg/kg). The frequency of oronasal contact with the floor and pen walls was unaffected by dose. Scratching, locomotion, and changes in body posture were highest following treatment with the three highest doses of PGF2α. Many of the behaviors observed following PGF2α treatment are characteristic of prepartum nesting behavior in pregnant sows. We conclude that two key components of maternal nest-building behavior, pawing, and gathering straw, are affected differentially by different doses of PGF2α. The implications of these results on the mechanisms underlying maternal nest building in pigs are discussed.

Mating has been shown in many species to provoke the release of oxytocin (OT). In our study, various stimuli were applied to mares to study release of OT and prostaglandin F(2alpha) (PGF(2alpha)) associated with mating. Blood samples were collected from mares around the time of teasing both in oestrus and dioestrus and at mating. For comparison, blood samples were also collected at the time of manual manipulation of the genital tract and after intrauterine infusion of 500 ml phosphate buffered saline (PBS). Additional samples were collected 16 to 18 h after mating. Mating caused a significant increase in OT in all mares and teasing caused a significant OT response in 6 of 10 oestrous and 3 of 5 dioestrous mares. However, mating and teasing had no significant effect on concentrations of 15-keto-13,14-dihydro-PGF(2alpha) (PGFM). Manual manipulation of the clitoris, vagina and cervix caused significant OT release in all mares and intrauterine infusion of 500 ml PBS caused significant OT release in three of the five mares. However, only one mare had a significant PGF(2alpha) response during manual manipulation and only one responded positively to intrauterine infusion of 500 ml PBS. We concluded that events around mating, including stimulation of the genital tract and uterine distension, often caused an increase in circulating concentrations of OT but only rarely in PGFM.

This study examined the role of oestrogen supplementation on PGF2alpha-induced nest-building in pseudopregnant gilts. Oestradiol valerate (5 mg/day) injections were given on Days 11-15 of the oestrous cycle to induce pseudopregnancy. A further series of injections of either oestradiol valerate (5 mg/day) or vehicle were given on days 44-46 of pseudopregnancy to reflect more closely the hormone profile seen in pregnancy. Nest-building was induced by a single intramuscular injection of 15 mg of PGF2alpha (Lutalyse) on Day 47 of pseudopregnancy. The gilts were housed in pens (2.8 x 1.7 m) containing straw in experiment 1 or chronically confined in crates (0.6 x 1.7 m) that did not contain straw on days 44-48 of pseudopregnancy for experiment 2. Oestrogen supplemented gilts had significantly higher concentrations of circulating 17beta-oestradiol on day 47 of pseudopregnancy but there were no significant differences between treatments for circulating levels of prolactin, progesterone, cortisol or oxytocin, or for any behavioural measure in either experiment. These results indicate that there is no direct effect of supplementing already pseudopregnant gilts with oestradiol valerate on PGF2alpha-induced nest-building. The results also show that the pre-partum environment has a pronounced effect on nest-building behaviours and that non-pregnant pigs might be a useful model for pre-partum nest-building in this species.

Moving gilts from a strawed pen to a crate during farrowing profoundly inhibits oxytocin, probably as a result of a stress-induced opioid-inhibition of hypothalamic oxytocin release (Lawrence et al., 1992). Other work suggests that confinement of gilts in crates for 5 days prior to farrowing protects the gilt against stressinduced inhibition of oxytocin. As producers introduce gilts and sows into farrowing crates at variable times prior to farrowing it is important to identify the minimal period of exposure to crates required to confer adaptation. This work tested whether only a short period of adaptation (1 day) to farrowing crates prior to expected farrowing date (EFD) would be sufficient to prevent stress-induced inhibition of oxytocin.

Nest-building behaviour occurs 6-24 h before parturition in pigs (gestation = 116 days). Pseudopregnancy in pigs (induced with oestradiol valerate injections) lasts 50-80 days. We have shown that prostaglandin F2 alpha (PG) administration on day 47 of pseudopregnancy induces nest-building and changes to plasma prolactin, oxytocin, cortisol and progesterone similar to those seen before normal parturition, Peripheral prolactin has been proposed as a modulator of nest-building. This study assessed nest-building behaviour in prolactin-deprived gilts. Jugular vein catheters were inserted on day 39 of pseudopregnancy and blood samples collected daily from days 40-48. Animals were injected im with either 40 mg bromocriptine in 2 ml 70% ethanol (n = 8) or vehicle (n = 7) at 17.00 h on day 46 and 09.00 h on day 47 of pseudopregnancy. PG (15 mg Lutalyse: Upjohn) was injected im at 11.00 h on day 47. Blood and behavioural samples were taken from 90 min before PG to 6 h post-PG. Plasma prolactin increased in control but not bromocriptine treated animals following PG (P < 0.05). Elevations in oxytocin, cortisol and progesterone (P < 0.05) above pre-PG concentrations were also seen, but of these only progesterone showed between group differences [greater (P < 0.05) in control gilts on both days 47 and 48]. PG significantly (P < 0.05) increased both the rate and proportion of total time spent performing straw/floor-directed behaviours not including foraging (an index of nesting behaviour) in both treatment groups with no significant differences between groups. There were also no significant differences between groups in time spent performing pen fixture directed activities before or after PG. Bromocriptine suppressed the rise in prolactin concentrations after PG without suppressing nest-building behaviour. We conclude that peripheral prolactin is not an essential component of the nest-building complex in pigs.

Sows are routinely housed in behaviourally restrictive crates when giving birth. In the UK there has been considerable public concern over the use of these parturition (or farrowing) crates. In attempting to objectively assess the stress experienced by sows in farrowing crates it has been necessary to consider the potential inter-relationships between behaviour, stress and the physiology associated with parturition. Evidence from behaviour and the hypothalamic-pituitary-adrenal (HPA) axis suggests that farrowing crates elicit a stress response, indicated by raised plasma cortisol, by interfering with pre-parturient maternal behaviour (nest-construction). Cortisol concentrations, however, also rise during parturition irrespective of whether sows are housed in crates or in pens that allow greater behavioural freedom, which may indicate that parturition itself has stress-inducing aspects. The hormone oxytocin, released from the posterior pituitary is fundamentally involved in the parturition process. Recently it has become apparent that opioids play a significant role in regulating oxytocin release both centrally and at the level of the pituitary. The interaction between opioids and the oxytocin system allows for the possibility that stress can influence oxytocin release. An acute mid-partum stress is highly effective at restraining oxytocin and slowing delivery rate in rats and pigs, an effect that appears largely opioid-mediated. The work reviewed here suggests that opioids also strongly regulate oxytocin release in pigs farrowing under undisturbed conditions as the opioid-antagonist naloxone elevates oxytocin in sows farrowing in crates and pens. The function of this opioid-restraint of oxytocin during normal deliveries remains unclear. The crate environment itself appears to be associated with a weak opioid-restraint of oxytocin during the late delivery phase, which may reflect a mild adverse response to giving birth in the crate. Overall, the results suggest that crates do not act to strongly elevate hypothalamic-opioid tone to inhibit posterior pituitary release of oxytocin. By inference the evidence suggests that farrowing crates are not a potent source of stress for sows during actual delivery.

We have previously shown that prostaglandin F2alpha (PG) is capable of inducing nest-building behaviour in pseudopregnant gilts and established a protocol. This experiment examined which reproductive endocrine systems might mediate these behavioural responses, in the presence or absence of a space restriction stress. Pseudopregnancy was induced with 5 mg/day i.m. (intramuscular) injections of oestradiol valerate (OV) on Days 11-15 of the oestrous cycle, jugular vein catheters were placed on Day 39 of pseudopregnancy, and blood samples were collected daily from Day 40 to Day 48. On Day 42, gilts were either space restricted to farrowing crates 1.6 x 0.6 m (C: n = 11) or left in pens 2.8 x 1.74 m (P: n = 11). On Day 47, blood samples were collected from all animals every 15 min from 90 min prior to a single i.m. injection of 15 mg of prostaglandin F2alpha (PG: Lutalyse, Upjohn, Crowley, West Sussex) to 120 min post-PG and then hourly for 4 h and assayed for oxytocin, prolactin, progesterone, and oestradiol. Results showed that mean daily concentrations of prolactin and progesterone were significantly lower (p < 0.05 respectively) in C than P gilts from Day 42 to Day 46 of pseudopregnancy. There were no significant differences in mean daily concentrations of oxytocin and oestradiol between C and P gilts during this time. For both groups, oxytocin, prolactin, and progesterone concentrations increased significantly (p < 0.05) post-PG when compared to their respective pre-PG values. However, for both groups, oestradiol concentrations were unaffected by PG injection. The prostaglandin-induced increases in oxytocin, prolactin, and progesterone concentrations did not differ between groups. We conclude that coincident changes in oestradiol secretion does not influence nesting behaviour and that space restriction stress associated with nest-building does not influence secretion of oxytocin, prolactin, oestradiol, or progesterone.