Blood concentrations of oxytocin equivalents after single injections of deamino-1-monocarba-[2-O-methyltyrosine]-oxytocin in lactating sows.
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Biomedical subjects
Publications and source records attributed to S Einarsson.
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Radiolabelled compounds of different molecular size were used as tracers mixed with seminal plasma to investigate whether seminal plasma enters the oviducts of inseminated gilts. The substances were 125I-labelled human serum albumin for 3 gilts, 131I-labelled polyvinylpyrrolidone plus 59Fe citrate in 2 gilts and 131I-labelled human serum albumin plus 59Fe citrate in 2 gilts. The gilts were slaughtered 1 h after insemination and the radioactivity was measured in 4 parts of the oviduct, 9 parts of the uterine horns, the body of the uterus and the cervix. Different quantities of the compounds used were found in all oviducts, but there was close agreement between the distributions of the two compounds in the genital tract after simultaneous insemination. There was a difference (60-80%) in total amount of recovered radioactivity between left and right uterine horns. It is concluded that all compounds used entered the oviducts regardless of their molecular sizes.
Radiolabelled compounds were mixed with seminal plasma and placed in the uterine lumen of anaesthetized gilts which were killed 5 min (N = 1) and 1 h (N = 2) later. After 1 h the distribution patterns of the 2 compounds placed in different horns were similar, indicating transuterine transport. Transuterine transport had begun by 5 min after deposition of seminal plasma. In all 3 gilts, the labelled substances had moved to the anterior segments of the oviduct.
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Uterine strips were collected from cows during the follicular and the luteal phases as well as from cows with ovarian cysts. The strips were mounted in organ baths and the motility was recorded by a polygraph. After the spontaneous motility of the strips had reached a steady state the test substances PGF2 alpha and oxytocin were added to the bath at three different concentrations. Frequency, amplitude and duration of the spontaneous uterine concentrations were irregular in all strips recorded independent of reproductive stage. The spontaneous activity was most pronounced during the follicular phase. The variation between animals was greatest for cystic cows. PGF2 alpha always increased the activity of the uterus but the response was not dose related above a certain level (50 ng per ml bath fluid). Oxytocin on the other hand had a linear stimulatory effect for increasing doses (0.25, 2.5 and 25 mIU per ml bath fluid).
Human chorionic gonadotrophin (HCG) combined with oestradiol benzoate was tested for induction and synchronization of heat in gilts. Judging from the progesterone levels in the blood, several of the gilts were already exhibiting spontaneous oestrous cyclicity on the day of treatment. Only gilts with low blood progesterone levels on the day of treatment showed standing oestrus within the expected time. On the basis of the results a second trial was carried out to elucidate the influence of the hormone compound on the ovarian activity in gilts during the luteal phase.
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The contractile actions of oxytocin and its analog 1-desamino-1-monocarba-[2-Tyr(OMe)]-oxytocin were compared on in vitro (experiment 1) and in vivo (experiment 2) preparations of porcine uterine horns. In both experiments, sows in estrus were selected for maximal sensitivity. Despite the loss of peak amplitude associated with the substitution at sequence position 2 of O-methyltyrosine for tyrosine, the two remaining alterations (N-terminal desamination and replacement of the 1-6 S-S bridge by CH2S) prolonged the action of single-dose presentations. Thus, instead of having a response lasting minutes when the parent hormone is given, an IV dose of about 5 micrograms of the analog/kg of body weight in the intact anesthetized sow resulted in a response lasting two hours.
The purpose of the present investigation was to study the clinical symptoms of agalactic sows post partum in randomly selected swine herds. The study comprised 71 sows affected with agalactia post partum and 71 healthy sows from the same herds used as controls. Average morbidity of the disease in these 50 herds, consisting of an average of 25 sows, was 12.8%. Sixty-three per cent of the agalactic sows were affected within one day after farrowing. There was no difference in gestation length between healthy sows and agalactic sows. The body temperature was significantly higher for affected than for healthy sows. Mastitis was diagnosed in 35 out of 71 agalactic sows. The criteria for mastitis were swelling and herdening of one or several udder glands. Vaginal discharge was recorded for affected sows (55/57) as well as for healthy sows (51/58) and is therefore not significantly associated with agalactia. The temperament of the agalactic sows was moderately or severely affected in 62 out of 71 agalactic sows. Constipation was recorded for 13/59 agalactic sows and for 3/57 normal sows. The agalactic sows had significantly higher number of piglets per litter at birth while the litter size was higher for healthy sows at weaning. Numerically, more sows were culled among agalactic sows (16/48) than among normal sows (6/42). Moreover, sows affected with agalactia at the previous parturition were more inclined to meet with the disease at the next parturition. Further studies comprising large groups of animals are, however, necessary for evaluation of this question.
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The present study was made in order to develop the freezing method of Crabo & Einarsson (1971) into a practicable deep-freezing method for boar spermatozoa. Semen was concentrated before dilution and a dosewise thawing procedure for the pellet-frozen semen was utilized. Two fertility tests on altogther 68 gilts were performed. In the first trial the insemination doses contained 6x10(9) spermatozoa and the dilution rate before cooling was 3:2 with a total dilution before freezing of 3:7. In the second trial the insemination doses contained 4.5x10(9) spermatozoa, primary dilution was 3:3 and final dilution 3:7. The pregnancy rate in trial 1 was 53% and in trial 2 72%. Mean litter size in pregnant gilts was 6.5 in trial 1 and 9.7 in trial 2. The difference in ratio of foetuses to c.l. in pregnant gilts between the trials was highly significant. The different dilution procedures are discussed and the lower fertility of semen frozen in trial 1 is suggested to be due to a shortened fertile life of spermatozoa so treated. The freezing method utilized in trial 2 is considered to be practically acceptable and the results are concluded to be satisfactory. A detailed description of the method and the equipment utilized can be requested from the authors.
This trial was performed within one large piglet producing herd in Sweden during June-August 1976. One hundred and sixty sows were randomly assigned to one of the following treatments: (1) 15 mg PGF2alpha i.m., (2) 20 mg PGF2alpha i.m., (3) two injections of 10 mg PGF2alpha i.m. at c. 8 h interval, (4) untreated countrol sows. PGF2alpha was administered in the morning of days 111, 112 or 113 of pregnancy. Of the PGF2alpha-treated sows, 83--85% farrowed within 48 h after treatment. No effect of day of treatment was found. Nor was any difference between groups observed. Neither of the treatments had a significantly negative influence of the viability of the piglets born. A numerically lower incidence of agalactia post partum was demonstrated in sows treated once with 15 mg or 20 mg PGF2alpha. A possible effect of PGF2alpha for prevention of agalactia post partum is discussed.