Fredrik Hultén

Effect of repeated ACTH-stimulation on early embryonic development and hormonal profiles in sows

This study was conducted to evaluate the effect of adrenal stimulation by synthetic adrenocorticotrophic hormone (ACTH) on the first 2 days of pregnancy in 22 multiparous sows. The experiment was performed during the second oestrus after weaning and the sows were divided into one control (C-group) and one experiment group (E-group). To determine the time of ovulation, transrectal ultrasonographic examination was performed. E-group sows were treated repeatedly with 0.1 mg/kg bodyweight of synthetic ACTH (tetracosactide) i.v. 4-8h after ovulation and continuing every 6h, until slaughter. Blood samples were collected every second hour from about 12h before expected ovulation until slaughter and were analyzed for cortisol, prostaglandin F(2 alpha) -metabolite, and progesterone (P(4)). All sows were slaughtered approximately 48 h after ovulation and the isthmic part of the oviduct was divided into three equally long segments and flushed separately with phosphate buffered saline (PBS). The uterine horns were also flushed with PBS. The embryos of the E-group sows tended (P=0.056) to have a lower cleavage rate than the embryos of the C-group sows but there was no difference between groups in oviductal transport rate of the embryos. In the E-group, significantly (P<0.05) more sows had only embryos with <20 spermatozoa attached to the ZP compared with the C-group. The plasma concentration of cortisol was significantly higher (P<0.0001) in the E-group sows during the time of treatment while the baseline level of prostaglandin F(2 alpha) -metabolite was significantly lower. The baseline level of progesterone increased in both groups after ovulation but there was no significant difference between the groups. Repeated ACTH-stimulation (1) had no effect on the oviductal transport rate of the embryos, (2) had a negative effect on the embryo development, (3) and caused a changed endocrine profile that might have changed oviductal milieu affecting embryo development.

Impact of Postovulatory Food Deprivation on the Ova Transport, Hormonal Profiles and Metabolic Changes in Sows

The effect of food deprivation on ova transport, hormonal profiles and metabolic changes was studied in 20 crossbred multiparous sows during their second oestrus after weaning. To determine the time of ovulation, transrectal ultrasonographic examination was performed. The sows were divided into 2 groups, one control group (C-group), which was fed according to Swedish standards, and one experimental group (E-group). The E-group sows were deprived of food from the first morning meal after ovulation until slaughter. Blood samples were collected every second hour from about 12 h before expected ovulation in the second oestrus after weaning until slaughter and were analysed for progesterone, prostaglandin F2α-metabolite, insulin, glucose, free fatty acids and triglycerides. All sows were slaughtered approximately 48 h after ovulation and the genital tract was recovered. The isthmic part of the oviduct was divided into 3 equally long segments and flushed separately with phosphate buffered saline (PBS). Uterine horns were also flushed with PBS. A significantly greater number of ova were found in the first and second part of the isthmus in the E-group (p = 0.05) while in the C-group most of the ova were found in the third part of the isthmus or the uterus (p = 0.01). The level of prostaglandin F2α-metabolite was significantly higher in the E-group compared with the C-group. The concentration of progesterone increased in both groups after ovulation but there were no significant differences between the groups. The other blood parameters showed that the food-deprived sows were in a catabolic state. The 48 h period of fasting results, directly or indirectly in an delayed ova transport, which may be due to a delayed relaxation in the smooth circular muscle layer of the isthmus.SammanfattningEffekten av fasta direkt efter ovulationen på äggens transporthastighet genom äggledaren, hormonprofiler och metaboliska förändringar hos suggor.Effekten av fasta direkt efter ovulering studerades på 21 korsningssuggor under deras andra brunst efter avvänjning. Suggorna delades in i 2 grupper, en kontrollgrupp och en försöksgrupp. För att fastställa ovulationstidpunkten gjordes rektal ultraljudsundersökning var fjärde timme från visad ståbrunst fram tills dess att inga folliklar kunde ses. Suggorna i försöksgruppen fastades från första morgonmålet efter ovulationen och fram till slakt medan kontrolldjuren utfodrades i enlighet med svensk norm. Blodprov togs varannan timme och användes för analys av progesteron, prostaglandin F2α- metabolit, insulin, glukos, fria fettsyror och triglycerider. Alla suggorna slaktades ungefär 48 timmar efter ovulering då livmodern togs ut tillsammans med äggledare och äggstockar för vidare undersökning. Istmus delades i tre lika långa delar, dessa spolades sedan med fosfatbuffertlösning (PBS). De nedre delarna av livmoderhornen spolades också med PBS. Signifikant (p = 0.05) fler ägg hittades i den första och andra delen av istmus hos försökssuggorna medan suggorna i kontrollgruppen hade de flesta äggen i den tredje delen av istmus och i livmodern (p = 0.01). Försöksgruppen hade signifikant högre nivåer av prostaglandin F2α-metaboliten än kontrollgruppen. Koncentrationen av progesteron steg i båda grupperna efter ovulationen, men det var ingen signifikant skillnad mellan grupperna. Blodparametrarna visade även att försökssuggorna, men inte kontrollsuggorna, hade en katabol metabolism under försöksperioden. Fasta under 48 timmar resulterade således i en fördröjd transport av äggen genom äggledaren vilket kan bero på en fördröjd minskning av kontraktionen hos de cirkulära lagren av glatt muskulatur i istmus.

Sows intramammarily inoculated with Escherichia coli at parturition: I Functional capacity of granulocytes in sows affected or non-affected by clinical mastitis

The objective of this study was to investigate if occurrence of clinical disease was related to granulocyte traits in sows. Functional capacity of granulocytes and plasma steroid hormone concentrations were assessed before inoculation with Escherichia coli in the mammary glands in sows at parturition. Blood samples were taken for 3 days approximately 1 week before parturition, and granulocyte migration, phagocytic capacity and expression of CD 18 adhesion molecules were determined. Inoculation was done within 36 h before partus. Thereafter, daily thorough clinical examinations were performed including udder health, habitus, appetite and rectal temperature, to assess the severity of disease. Based on the clinical findings four sows were classified as affected and eight as non-affected by clinical mastitis within 48 h after parturition.No difference (p>0.10) in pre-inoculation chemotaxis, phagocytosis or CD 18 expression was found between granulocytes from the sows resisting and developing clinical mastitis, respectively. However, there was an effect by the individual sow (p=0.001) on the numbers of granulocytes and white blood cells, and on plasma concentrations of estradiol-17beta and progesterone. In conclusion, these data does not suggest that impaired chemotaxis or phagocytosis by blood granulocytes contribute to the development of clinical coliform mastitis in the periparturient sow.

The impact of induced stress during Days 13 and 14 of pregnancy on the composition of allantoic fluid and conceptus development in sows

Stress due to regrouping of breeding females is difficult to avoid completely in loose-housing systems. The effects of stress during the maternal recognition of pregnancy on fetal development and survival at Day 30 of pregnancy was, therefore, studied in 17 sows allocated into one control (C-) group, one group deprived of food during Days 13 and 14 (FD-), and one group (A-), which was treated with ACTH (0.01 mg/kg body weight of Synacthen Depot) every sixth hour during the same period. Total number of fetuses, fetal survival rate, volume of allantoic fluid, and the weight and length of total fetal unit, placentas, allantochorion and fetuses were determined. The concentrations of progesterone (P4), PGFM, PGF2, PGE, estrone-sulfate, and estradiol-17beta in the allantoic fluid were analyzed. No significant differences between groups were found for any parameter measured except for P4. Food deprivation increased P4 concentration in the allantoic fluid, and there was a positive correlation between the P4 concentration and the weight of the placenta. It is, therefore, suggested that P4 influences the placenta size among food-deprived sows.

Ovulation frequency among sows group-housed during late lactation

Ovulation frequency during late lactation was determined among 114 sows from four commercial farms that group-housed the sows from about 3 weeks of lactation until weaning (G-farms), and among 21 sows from one farm that kept the sows individually penned throughout lactation (C-farm). Ovulation frequency was determined by applying a progesterone assay on faecal samples collected at weekly intervals from time of grouping until 3 weeks after weaning. The groups consisted of 11–22 sows and boar contact was not allowed during the 5–6 week lactation period. G-farm sows were fed ad libitum while C-farm sows were provided with a restricted food ration. During the group-housing period, 28% of the G-farm sows ovulated, whereas none of the singly housed sows ovulated during the corresponding period (P = 0.005). Ovulation frequency varied considerably between sow groups (0–54%) (P = 0.004), owing partly to differences in age. Not a single primiparous sow ovulated, whereas ovulation frequency among second to fourth parity sows and older sows (fifth parity and over) was 6% and 48%, respectively (P < 0.001). At the time of grouping and weaning, neither backfat thickness nor litter size differed between the sows that ovulated and those that were anoestrous. Preweaning mammary gland atrophy, indicating that milk production had ceased, was noted in 16% of the G-farm sows that ovulated but in only one (1%) of the anoestrus sows. Only 65% of the sows showing lactational ovulation were mated within 10 days after weaning. By contrast, 87% of the G-farms sows that were anoestrus during lactation and 100% of the C-farm sows were mated within this period.

Transport of fertilised and unfertilised ova in sows

Transport of fertilised and unfertilized ova was studied in 22 crossbred (Landrace x Yorkshire) multiparous sows. Sows in the inseminated group (I-group, n=11) were inseminated once with 100ml of BTS extended semen from two fertile boars with a total of 10 x 10 (9) spermatozoa during the second oestrus after weaning between 18 and 8h prior to estimated time of ovulation, as estimated from the first oestrus after weaning. All the sows were slaughtered between 36 and 48 h after ovulation in the second oestrus after weaning by stunning and bleeding. After slaughter, the reproductive tract was immediately recovered, the isthmus was divided into three equal segments, and the number of ova was determined in each segment and in the upper third of the uterine horn from the UTJ. There were no significant differences (P>0.05) either in the intervals from ovulation to slaughter (42.3+/-6.2h versus 43.2+/-5.4h) or in the numbers of corpora lutea (CL) (18.2+/-5.5 versus 15.9+/-3.5) between the non-inseminated (N-group) and the inseminated groups (I-group), respectively. Ova recovery rate was 92.5% in the N-group and 82.9% in the I-group (P>0.05). In the I-group, ova had passed 2.2+/-0.3 segments whereas in the N-group, ova had passed 2.6+/-0.3 segments (P=0.38). It can be concluded that there is no difference in the transportation of either fertilised or unfertilized ova in the reproductive tract of pigs.

Reproductive endocrinology and postweaning performance in the multiparous sow. Part 2. Influence of nursing behavior

The reason for variation in postweaning reproductive performance among multiparous sows is to a large extent unknown. In the present study, the influence of nursing behavior was explored. Blood samples were collected during lactation and after weaning from 18 multiparous sows for cortisol, LH, estradiol-17beta (E2), and progesterone analysis. Sow and piglet behavior was videotaped. The sows were fed according to litter size and slaughtered after the second postweaning estrus. The sows were divided into two groups based on average values for the different behavioral parameters. Sows with a long average nursing duration (long group) had lower average and basal LH levels on Day 14 and 21 of lactation as compared to the sows having a short average nursing duration (short group). In the long group, concentrations of E2 were lower the day after weaning, but on Day 15 and 21 of lactation no differences were noted between the two groups. Postweaning performance seemed impaired in the long group, though, differences were not significant. The sows in the long group were heavier and tended to lose less weight during lactation. To conclude, nursing duration seems to influence the extent to which reproductive functions are inhibited during lactation.

THE INFLUENCE OF INHIBITED PROSTAGLANDIN BIOSYNTHESIS ON POST-OVULATORY OVIDUCTAL OVA TRANSPORT IN SOWS

Changes in prostaglandin and progesterone concentrations after ovulation seem to affect reproductive functions in the sow. The influence of lowered prostaglandin levels on ova transport velocity through the isthmus part of the oviduct, and on progesterone concentrations, was studied during the second estrus after weaning in thirteen purebred Yorkshire multiparous sows. To determine the time of ovulation transrectal ultrasonographic examination was performed. In the second estrus, six sows were given intravenous injections of flunixin meglumine (2.2 mg/kg body weight) every sixth hour from 4 to 8 h after time of ovulation until about 48 h after ovulation, at which time the sows were slaughtered. Blood samples were collected every second hour from about 12 h before ovulation until slaughter. Progesterone and prostaglandin F2alpha (PGF2alpha) metabolite levels were determined. Immediately after slaughter the isthmus part of the oviducts were cut into 3 equally long segments and the number of ova in each segment, and in the upper part of the uterine horns, was determined. Before start of treatment, PGF2alpha metabolite levels were similar in the 2 groups (P=0.84). In the treatment group, PGF2alpha values dropped to below the detection limit immediately after start of treatment, whereas in the control group the concentrations were quite stable throughout the sampling period (P=0.005). Ova recovery rate was 94% in the treatment group and 95 % in the control group. At time of slaughter, in the treatment group ova had on average passed 2.1 segments whereas in the control group the ova had passed 2.5 segments (P=0.57). The progesterone levels increased continuously in both groups after ovulation but there was no difference in the mean progesterone concentrations between the two groups before (P=0.96) or after (P=0.58) ovulation. It can be concluded that the transport of ova through the isthmus part of the oviduct is unaffected by an inhibition of prostaglandin synthesis immediately after ovulation. Furthermore, the post-ovulatory progesterone profile seems unaffected by lowered PGF2alpha levels.