cloprostenol and Birth-Weight

This study investigated the effect of altrenogest treatment on the farrowing development of sows, and birth weight (BW) and piglet survival until the third day of life. Three control groups were used: (i) sows that farrowed spontaneously before 114 day of gestation (CONT <114); (ii) sows that spontaneously farrowed at ≥114 day of gestation (CONT ≥114); (iii) sows that farrowed at ≥114 day with cloprostenol treatment (CONTCLOPR). Other sows were treated with altrenogest (Regumate(®) ) for 3 days (days 111, 112 and 113 of gestation): one group gave birth spontaneously (ALT) and the other group received altrenogest until day 113 and cloprostenol on day 114 (ALTCLOPR). There were no differences (p > 0.05) in farrowing duration, BW, coefficient of variation (CV) of BW, stillborn piglets, mummified foetuses, percentage of light piglets and survival until Day 3 between sows with and without cloprostenol treatment, in both control (CONT ≥114 vs CONTCLOPR) and altrenogest-treated sows (ALT vs ALTCLOPR). Further comparisons were performed taking into account three groups: sows with early delivery (CONT <114 - farrowing before 114 days of gestation; n = 56), sows with longer gestation (CONT ≥114 - with and without cloprostenol treatment sows; n = 103) and ALT sows (with and without cloprostenol treatment; n = 105). Gestation length of CONT ≥114 and ALT sows was similar (p > 0.05), but higher than in CONT <114 sows. There were no differences (p > 0.05) between groups in farrowing duration, CV of BW, and percentages of stillborn piglets and mummified foetuses. Sows of CONT <114 group had a larger litter size and a lower BW than sows of the other two groups (p < 0.05). Sows of CONT <114 group had a higher percentage of lighter piglets and a lower piglet survival rate (p < 0.05) than ALT sows. In conclusion, altrenogest treatment proved to be an efficient method to avoid early parturition in 3-5 parity sows resulting in heavier piglets at birth.

Topics: Animals; Birth Weight; Cloprostenol; Female; Labor, Induced; Luteolytic Agents; Pregnancy; Pregnancy Outcome; Premature Birth; Progestins; Swine; Trenbolone Acetate

At birth, the physiological role of prostaglandins in bitches is unclear. Bitches were treated before parturition with either saline, the prostaglandin analogue, sodium cloprostenol, or the prostaglandin synthetase inhibitor, flunixin meglumine. The animals were examined regularly to determine the onset of parturition and a series of blood samples were taken to define the hormonal profiles before, during and after birth. Animals treated with cloprostenol whelped earlier than did controls. In addition, the prostaglandin F2 alpha metabolite surge and decrease in plasma progesterone concentration and rectal temperature were earlier than in controls. Flunixin meglumine disrupted the normal 13,14-dihydro-15-keto prostaglandin F2 alpha profile but did not abolish prostaglandin synthesis completely or delay the onset of labour in treated animals. This study confirms that prostaglandins induce luteolysis and the onset of labour in the bitch. However, the partial inhibition of prostaglandin synthesis does not prevent parturition.

Topics: Analysis of Variance; Animals; Area Under Curve; Birth Weight; Body Temperature; Clonixin; Cloprostenol; Cyclooxygenase Inhibitors; Dinoprost; Dogs; Drinking; Female; Labor Onset; Luteolysis; Pregnancy; Progesterone; Prostaglandins, Synthetic

A study was undertaken on a commercial swine farm to investigate methods of reducing perinatal mortality. During a 12-wk period, 251 sows and gilts were assigned randomly to one of four treatment groups in a 2 x 2 factorial design: 1) supervised/induced, 2) supervised/non-induced, 3) unsupervised/induced, and 4) unsupervised/non-induced. Supervised groups of sows and their litter were observed constantly for a minimum of 3 h before and until 3 d after farrowing. The onset of farrowing was induced with 250 micrograms of cloprostenol administered into the vulvo-vestibular mucosa. There was an increase (P = .012) in the number of pigs weaned from supervised (10.17 pigs/litter) relative to unsupervised group (9.44 pigs/litter). This increase was due to a reduction (P = .001) in both the number of stillborn pigs and the mortality of live-born pigs (P = .026). The latter resulted from fewer pigs that died (P = .003). Induction did not influence the mortality of pigs in the perinatal period in unsupervised groups. Induced sows farrowed an average of .43 d earlier than non-induced sows (P = .029). The mean interval from prostaglandin treatment to farrowing was 23.87 h (SD = 10.96). The results of this study suggest that a controlled farrowing system, coupled with good supervision, can improve pig survival. Financial analyses, based on improvements in pig survival resulting from additional labor in the farrowing house, suggested that this method of reducing preweaning mortality is a viable option for improving the profitability of commercial pig farms.

Topics: Animal Husbandry; Animals; Animals, Newborn; Birth Weight; Cloprostenol; Female; Labor, Induced; Mortality; Perinatal Care; Pregnancy; Prostaglandins E, Synthetic; Random Allocation; Swine

Parturition was induced in 112 gilts and sows on day 111,, 112, and 113 of gestation by means of a single intramuscular injection of 175 mcg of a prostaglandin F2 alpha analogue (Cloprostenol, I.C.I 80996). No side effects were detected immediately after injection and the course of the induced parturition was normal. The interval between injection and parturition was approximately 28 hours. Induction of parturition on day 113 resulted in a significant shortening of this interval as compared with day 111, and 112. The average weights of the piglets at birth and at 5 weeks were within the normal range. The percentage of stillbirths and the loss of piglets up to weaning did not differ significantly between control and experimental groups. The practical applications of induction of parturition are discussed.

Topics: Animals; Birth Weight; Cloprostenol; Female; Labor, Induced; Litter Size; Pregnancy; Prostaglandins F, Synthetic; Swine