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The effect of Gn-RH on the pregnancy rate of artificially inseminated cows.

One hundred and nine pure bred Holstein Friesians were injected intramuscularly with 0.125 mg of a synthetic Gn-RH analogue at the time of the first service to study the effect of Gn-RH on the fertility of inseminated cows. Sixty-four cows or 58.7 per cent were diagnosed as pregnant after one insemination compared to 54 animals or 49.5 per cent in the untreated control group. Total pregnancy rate of 81.65 per cent was 8.3 per cent higher than in the controls, while the services per conception rate improved from 1.49 to 1.39. Gn-RH administration at the time of oestrus could improve herd fertility through its including effect on follicular rupture and regulatory influence on ovarian function.

Animals↗

Reproductive wastage following artificial insemination of heifers.

Hereford cross beef heifers at pasture were inseminated at a detected oestrus with thawed semen and were slaughtered at the following intervals after insemination: day 3 (60 heifers); day 8 (71); day 14 (65); day 18 (78) and day 28 (29). The recovery rates of ova at days 3 and 8 were 87 and 77 per cent respectively. The percentage of heifers that were pregnant at the respective time intervals after slaughter were 81, 84, 75, 60 and 62. There was no difference in the proportion of normally developing ova or embryos between days 3 and 8, 8 and 14, 14 and 18 or 18 and 28. There were significant differences in the number of animals with variable embryos between days 3 and days 18 + 28 (P less than 0.025); 8 and 18 + 28 (P less than 0.01); and 14 and 18 + 28 (P less than 0.05). Based on the results and other data in the literature, fertilisation failure can account for up to 20 per cent of reproductive wastage. Embryonic mortality accounts for most of the remaining wastage and occurs gradually between days 8 and 18. Pregnancy rates at days 18 and 28 approximate to calving data.

Animals↗

Applications of flow cytometry to artificial insemination: a review.

Flow cytometry is a technique in which sub-populations of cells can be analysed and separated according to the staining pattern seen with various fluorescent markers. This review describes some of the ways in which flow cytometry can be applied to the investigation of sperm populations, either as a means of quality control of semen or to examine the characteristics of different sub-populations of sperm within an ejaculate. These methods can replace or augment existing subjective assessments of semen characteristics. Using this technique it is possible to produce aliquots of sexed sperm for insemination or for in vitro fertilisation. An objective assessment can be made of the effects of environmental stress on male physiology by monitoring changes in semen quality.

Animals↗

Assessment of the morphology of frozen-thawed bull sperm in relation to its cryopreservation for artificial insemination.

The morphology of sperm in raw semen was compared with that of the live sperm in semen which had been frozen and thawed. The thawed semen was stained with 6-carboxyfluorescein diacetate and propidium iodide and examined by fluorescence microscopy; smears of the raw semen were stained with eosin and nigrosin. Thirty-four ejaculates from 24 bulls of various breeds were examined. There were fewer abnormal heads, detached heads, coiled tails and proximal cytoplasmic droplets/pseudodroplets in the thawed semen than in the raw semen, there was no change in the number of bent tails, but the number of distal cytoplasmic droplets/pseudodroplets increased. There were no significant differences in morphology between ejaculates which passed or failed the osmotic resistance test after thawing, but failed batches tended to have more distal cytoplasmic droplets/pseudodroplets.

Animals↗