Results of the motility of bovine spermatozoa following freezing and thawing in the LDL extender and in the Tris-egg yolk extender obtained using the Hamilton Thorne image analyser (n=3).The results given are the means ± standard deviation of the motility characteristics recorded for the three bulls.
The freezing process exposes the spermatozoa to thermal shock, which results in damage to the plasma membrane and acrosome [1, 2]. Various extenders have been tested in an attempt to limit cellular injury. Egg yolk is the most widely used of these extenders by artificial insemination centres. Many demands were formulated to replace egg yolk in extenders by it’s cryoprotector factor. In recent years, centrifugation techniques have enabled the isolation of the LDL(Low Density Lipoproteins) that are responsible for the cryopreservative effect of egg yolk [3,4,5]. The incorporation of LDL in bovine extenders has given improved motility results in comparison with extenders containing egg yolk [5,6,7]. However, to extend the use of this new LDL-based extender to insemination centres, a fertility study was essential. Fertility can either be assessed in the laboratory using
1.1. Collection of semen, dilution and processing
Two extenders were used; Tris-egg yolk extender (T-EY)): 20 ml of chicken egg yolk and LDL extender: 8% LDL (w/v) in accordance with the method described by Moussa et al. (2002) (patent n° 0100292) . The extenders were thawed on the day of sampling and maintained at 37°C. Three bulls belonging to an artificial insemination centre and that had been approved for public use, were used. All three had a recorded progeny. Using the Laicophos® extender, the artificial insemination centre had a non-return rate at 60-90d of 64.7% for Bull 1, 57.2% for Bull 2, and 72.2% for Bull 3. The semen was collected using an artificial vagina. To excite the bulls, they were teased with a Normandy cow for thirty minutes prior to sampling. The semen was collected into a glass tube that had been previously warmed to 37°C. Following collection, the ejaculates were immediately placed in a water bath at 37°C. Each ejaculate was divided into two equal fractions. Each fraction was immediately diluted to 100 x 106 spz/ml with the two extenders that had been previously warmed to 37°C, and then subjected to progressive cooling from 37°C to +4°C over 1h and 30 in a refrigerated unit before being placed into straws. The semen was maintained in equilibrium for 4 hours at +4°C. The straws were held for 10 minutes at +4 cm from the surface of the liquid nitrogen (-120°C) before being immersed and then stored in liquid nitrogen (-196°C).
1.2. Semen evaluation before artificial insemination in the field
Before inseminating the cows, semen was evaluated on motility and plasma membrane integrity. The semen was analysed using the Hamilton-Thorne sperm analyser with the CEROS 12 software program, Hamilton-Thorne biosciences, Inc, Beverly, USA. The machine had been previously configured for the analysis of bovine semen. The following parameters were studied: motility (% mobile spermatozoa), straight line velocity: VSL (µm/sec.), curvilinear velocity: VCL (µm/sec.), the linearity index: LIN (= VSL/VCL x 100), amplitude of lateral head displacement: ALH (µm), and average path velocity: VAP (µm/sec). VAP, VSL, STR, and LIN provide information about the progressive movements of the spermatozoa, VCL and ALH characterise the lateral movements, and BCF (Beat Croix Frequency) provides information about the frequency of movements.
The post-thaw percentage of motile spermatozoa was greater in the LDL extender than in the Tris-egg yolk extender (table 1). The proportion of motile spermatozoa was nearly twice as high in the LDL extender, 58.3% vs. 46% in the Tris-egg yolk (table 1). To evaluate plasma membrane integrity, semen was added to an hypo-osmotic solution (100 mOsm/kg H2O). The spermatozoa was observed under a phase-contrast microscope and classified as positive or negative. Positive spermatozoa (plasma membrane intact) tail swollen and / or curled:. Negative spermatozoa (plasma membrane damaged) tail not curled. No significant difference (table 2) was found between the semen that had been frozen-thawed in the LDL and Tris-egg yolk extenders. The results of the motility analysis and plasma membrane integrity demonstrated that the semen could be used by stock breeders for artificial insemination.
2. Assesment of in vivo fertility after AI of the cows
One hundred and ninety-three females from 83 different herds were inseminated by three inseminators with 25 years of experience. The females included in the study were from dairy or suckler herds with a Calving to First Insemination Interval (CFI) of more than 60 days, heifers over 18 months old, and first inseminations only. For each insemination, the following data was recorded: date of insemination, herd number, the animal’s identification number, breed, lactation or calving index, date of the previous calving if relevant, condition score, the bull used, and the extender used. The pregnancy diagnoses were conducted by recording returns to oestrus and trans-rectal palpation between the 65th and 150th day of gestation. This data is summarised in table 3. Pregnancies can be obtained in the field following the artificial insemination of cows with semen that has been frozen and thawed in the LDL extender. However, no significant difference could be found between the LDL extender and the Tris egg yolk extender in terms of the success rates of insemination (Table 4).
|Motile spermatozoa (%)||58.3 ± 16.7||46.0 ± 18.2|
|Rapid (%)||45.3 ± 14.2||27.0 ± 12.3|
|Average (%)||5.7 ± 3.1||7.7± 2.5|
|Slow (%)||7.3 ± 3.2||11.3±4.5|
|Static (%)||43.7 ± 5.5||54.0± 15.1|
|Hyperactive (%)||5.3 ± 2.1||6.3 ± 5.9|
|Progressive (%)||34.7 ± 4.0||16.0 ± 6.1|
|VAP (µm/sec.)||83.5 ± 7.7||71.0 ± 5.3|
|VSL (µm/sec.)||66.6 ± 9.2||57.3 ± 6.3|
|LIN (%)||60.7 ± 1.5||58.3± 5.5|
|STR (%)||82.0 ± 1.7||79.7± 3.2|
|VCL (µm/sec.)||104.1± 28.6||99.9 ± 5.8|
|ALH (µm)||4.3 ± 0.3||4.6 ± 1.1|
|Swollen spermatozoa (intact)|
of the population
|Tris egg yolk|
|Lactation index||Mean ± standard dev.|
|1.6 ± 1.9|
|1.5 ± 1.5|
(mean ± standard deviation)
|3.0 ± 0.2||3.0 ± 0.3|
|Calving to first insemination interval in days (mean ± standard deviation)||94 ± 25|
(1 CFI not given)
|95 ± 32|
(1 CFI not given)
3. Is there a correlation between motility and fertility?
Pregnancies were obtained following the artificial insemination of cows with semen that has been frozen-thawed in an LDL extender without any significant difference in the success rate following insemination between the 2 extenders. The initial objective was not to demonstrate the superiority of the LDL extender, but to demonstrate its efficacy in the field in terms of percentage gestation. The success rates with artificial insemination are satisfactory (table 3): 59.2% for the LDL extender and 65.3% for the Tris-egg yolk extender. In a previous study, Amirat et al.2004  demonstrated that fertility was maintained
Motility results demonstrate that the percentage of motile spermatozoa following thawing is superior in the LDL extender in comparison with the Tris-egg yolk extender. These results concur with the works of Moussa et al. (2002)  and Amirat et al. (2004) . However, inter-individual variability on the motility performances following thawing has already been reported by Farrell et al. (1998)  and Holt (2000) . The results obtained do not make it possible to relate the motility of the spermatozoa to fertility due to the insufficient number of measurements. No study has demonstrated a precise correlation between motility parameters and fertility in cows. In cattle, the percentage of mobile spermatozoa, linearity (LIN), and straight line velocity (VSL) seem to be correlated to fertility according to Budworth et al. (1988) , and Farrell et al. (1998). The average path velocity (VAP), curvilinear velocity (VCL), and the frequency of tail movements (FTM), also appear interesting . According to Liu et al. (1991) , the most interesting motility parameters in human semen are linearity (LIN), straight line velocity (VSL), and the percentage of rapid spermatozoa.
4. What parameters could influence the AI success rate?
The confirmation of pregnancies were performed by rectal palpation on average at around the 100th day. However, embryonic mortality is recorded in the same way as failure of fertilisation; this reduces the fertility results observed. Ultrasonographic pregnancy diagnosis at 30 days would have been more accurate for measuring the fertility of the semen as the impact of embryonic mortality is lower between D0 and D30 than between D0 and D150. Descoteaux et al. (2006)  thus report that 10% of cows that are given a positive pregnancy diagnosis at 28 days present with embryonic mortality at D60. Nevertheless, the cows included in the present study were selected as a function of various criteria that ensure satisfactory female fertility, which explains the difference in fertility recorded between the results of our study and those reported by Barbat et al. (2005)  and Freret et al. (2006) . These studies are based on the results of inseminations conducted over a given period by insemination centres, without any selection criteria for the cows used. Female fertility was therefore inferior to that observed in our study. The observed fertility is a combination of the fertility of the male and female.
In addition to the many different diseases that can affect fertility, other parameters may influence the fertility of cows as breed  or lactaction index . In the study described here, the lactation index did not have any significant effect on the overall AI success rate (p<0.05). However, the lactation index had an impact for the LDL extender. Superior fertility was observed in the heifers, followed by the primiparous cows. A reduction in fertility was seen in cows with a lactation index of 2 or 3. There were insufficient numbers of cows with high lactation indexes to reveal any trends (Table 6). Milk production , energy profile , post-partum pathologies , and the herd effect  are other parameters that interfere with fertility results. Amman and Pickett (1987)  show that to measure male fertility a significant number of inseminations are necessary to rule out variations caused by female fertility. Van Wagttendonk de Leeuw et al. (2000)  demonstrate that to detect a 2% difference in the non-return rate, with a confidence interval of 95% and a statistical power of 80%, 6,600 inseminations are needed per extender. A limited population of 193 cows was inseminated as it was impossible to undertake a larger scale study due to the difficulty of convincing the breeders to use semen that had been frozen and thawed in an extender that did not have proven
The inseminator did not have a significant influence on the total Insemination Success Rate, with a threshold of significance of p=0.05 (Table 5). Inseminator 3 achieved higher insemination success rates for both extenders McKenna et al. (1990)  calculated the inseminator effect at ± 9.5 points. The animals that he inseminated were on average younger with a higher proportion of heifers. Barbat et al. (2005)  reported superior fertility in heifers in comparison with cows.
|Bull 1||25.0(*). (**)||83.3(*)||72.2(**)||60.0||87.5(**)||62.5||82|
|2 and 3||37.9(*)||61.3||50.0|
Although semen fertility was difficult to measure due to the various parameters that intervene causing variations in the results, this preliminary study enabled us to demonstrate for the first time that bull semen that has been frozen then thawed in the LDL extender retains a good level of fertility since gestations were obtained following artificial insemination. The continuation of this study in a larger population would make it possible to specify the impact of the LDL extender on the success of artificial insemination.