GLYCEROL ADDITIONS

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When the British procedure for freezing bull semen was first tried in this country, many of the refinements of the technique still had not been defined. It was known that glycerol worked well in protecting sperm during freezing. The effects of glycerol on sperm at 5° C., the appropriate levels to use in freezing, and the manner of adding it were not well established. Therefore, a number of trials were conducted in an attempt to establish the best procedures.Effect of glycerol on sperm survival at 5° C. Since early work indicated the need for adding glycerol to diluted semen in order to protect the sperm during freezing, it was considered important to determine the levels of glycerol that sperm would tolerate at 5° C. Ten semen samples were extended 1:9 (semen to diluent) in a 1:1 yolk-citrate diluent (yolk to 2.9 percent sodium citrate dihydrate). Each sample was then split into 6 portions and an equal volume of citrate solution containing glycerol was added slowly to each to bring the glycerol in the final mixture to 0, 5, 10, 20, or 30 percent (by volume). These samples were stored at 5° C. and examined for motile sperm after 1, 3, and 7 days. The effects of glycerol levels on the percentage of sperm surviving and the rate (or speed) of their forward motion (0 = no forward motion; 4 = extremely rapid progressive motility) are presented in Table 8.

The percentage of motile sperm decreased slightly at the higher levels of glycerol. The most noticeable effect of the increase in glycerol level was the reduction in the rate of forward motion of the sperm. At the 30-percent level, the sperm moved slowly and could be seen to rotate as they moved forward. Some samples were checked after slowly bringing the diluent up to a level of 40 percent glycerol; the sperm seemed to be immobilized completely in this solution.Glycerol levels for freezing semen. The British procedure called for the use of 10 percent glycerol in the final mixture of semen and extender prior to freezing. Yet, as shown in Table 6, in our laboratory 5 percent glycerol resulted in the survival of a higher percentage of sperm than did 10 or 15 percent. In order to define more clearly the optimum glycerol level, several ejaculates of semen were subsampled and portions were frozen after the addition of yolk-citrate extender and glycerol in varying quantities. From Table 9 it can be seen that glycerol levels of 6 and 8 percent in the final mixture resulted in maximum sperm survival during freezing. These results were confirmed in tests on the survival of sperm at 5° C. storage for 3 days following freezing and thawing with varying glycerol levels (see Table 10).

The results shown in Tables 9 and 10 were confirmed also in later experiments. Thirty-six samples were subjected to various levels of glycerol and no significant difference in freezability was found between 6 and 8 percent. Based on these findings, a glycerol level of 7 percent was adopted for use in all experiments described in this bulletin, unless otherwise indicated. Results in a number of other laboratories have agreed with our findings regarding the use of approximately 7 percent glycerol with the yolk-citrate diluent.[5], [6], [7], [9], [10] With milk as the extender, 10 to 13 percent glycerol has been preferred by some.[5], [6], [7]

Table 9.—Effect of Glycerol Level on Sperm Motility
After Freezing to -79° C. and Thawing

Glycerol
level
(percent)
Number
of
samples
Pre-
freezing
motility
(percent)
Post-
thawing
motility
(percent)
Survival
(percent)
2 10 53 2 4
4 19 55 29 53
6 19 55 34 62
8 19 55 35 64
1 0 19 55 24 44
1 2 10 53 13 25

Table 10.—Effect of Glycerol Level and Storage
at 5° C. After Thawing on Sperm Motility

(Average of 13 ejaculates)

Glycerol
level
(percent)
Spermmotility(percent)
Post-
thawing
Afterstorageat5°C.
1 day 3 days
4 29 22 20
6 38 34 24
8 42 33 17
1 0 33 18 6

Table 11.—Effects of Temperature, Rate of Addition of Glycerol,
and Equilibration Time on Sperm Motility

(Average of 12 ejaculates)

Temperatureduringaddition
of glycerol(°C.)
Equilibration
time
(hours)
Post-thawingmotility(percent)
Glyceroladditions
5 3 1 Average
4.5 2 48 48 45 47.4
6 49 51 47 48.8
18 46 47 46 46.3
Average 47 .8 48 .6 46 .0 47.5
1 0.0 2 44 43 45 43.9
6 48 50 46 47.9
18 43 46 42 44.0
Average 45 .0 46 .5 44 .3 45.3
1 5.5 2 41 38 38 39.1
6 42 45 43 43.6
18 42 43 42 42.5
Average 42 .0 41 .8 41 .4 41.7

Rate, temperature, and method of adding glycerol. Closely associated with the question of how much glycerol should be added is that of how the additions should be made. Originally it was believed that the glycerol should be added in stages so that changes would occur gradually. However, there would be a saving in time if the entire amount could be added at once. Also, if the glycerol addition could be made soon after the dilution with egg yolk-citrate extender at room temperature, time would be gained in processing the semen for use. Since aging in vitro is known to reduce the fertilizing ability of sperm, every effort should be made to keep the processing time at a minimum. The results of an experiment involving these items, along with that of how much time should be allowed after the additions before freezing (equilibration time), are presented in Table 11. One can see that sperm survived freezing better when the diluted semen was cooled to 4.5° C. before the glycerol was added. The survival at 10° and 15.5° C. was reduced with each rise in temperature. Thus, it appears that cooling to refrigerator temperature (4-5° C.) before adding the glycerol should be a part of the routine procedure.

A comparison of the results from adding the glycerol in 5, 3, and 1 equal portions is given also in Table 11. Little difference in survival during freezing was noted between the three rates of addition. Using 3 equal additions resulted in slightly better results, but the advantage was not statistically significant. While little difference was evident from adding the glycerol in 3 portions as compared to 1, many still use 3 additions in the hope of obtaining a slightly better sperm survival. In fact, some have gone to a procedure of adding the glycerol dropwise with constant gentle agitation. This method has not been tested in this laboratory.Allowing sperm to equilibrate with the glycerol. Allowing sperm to stand in the presence of glycerol is considered by some to be necessary in order that the glycerol penetrate the sperm heads before freezing. From the first successful attempts at freezing bull sperm came the practice of allowing 12 to 20 hours for this process of equilibration. A long equilibration time results in aging the sperm. Data from a number of sources indicate that a drop of approximately 5 percent in fertility in the field occurs with each 24 hours of aging in the test tube. Thus it would seem desirable to reduce the equilibration time to a minimum commensurate with good freezability in order to reduce the effects of aging (at 5° C.). Results of attempting to reduce equilibration time are given in Table 11. At 4.5° C., little variation in motility following freezing and thawing was found after equilibration times of 2, 6, and 18 hours. At the higher temperatures of 10° and 15.5° C., the shortest equilibration time—2 hours—was slightly more detrimental with the differences significant at the 5-percent level at 15.5° C. For all temperatures combined, 6 hours was significantly better than 2 or 18 hours.Sugar additions and equilibration time. Early in their experiences in freezing semen, the Australian workers found a short equilibration time—30 minutes—to be satisfactory if sugars were added to the diluent.[5] This protective action of sugars during the equilibration period was confirmed in our investigations. The results of one phase of this study are shown in Table 12. From these data it can be seen that the presence of glucose or rhamnose at a level of 1.25 percent improved sperm survival during the period of equilibration. In another trial these sugars and two others, arabinose and xylose, were tested for their protective action in freezing semen. The percentages of surviving sperm remaining after the various steps in the freezing procedure with and without the presence of these sugars are shown in Table 13.

Table 12.—Effect of Adding Sugars to Yolk-Citrate Diluent
on Sperm Motility During Equilibration With Glycerol[J]

Stagewhenobserved Spermmotility(percent)
Glycerol
only
Glycerol
and
glucose
Glycerol
and
rhamnose
Freshdilutedsemen 56 56 56
Afterglycerolization 54 54 54
Afterequilibration
2 hours 51 53 53
6 hours 48 52 53
12 hours 46 50 51
18 hours 40 46 46

[J] Glycerol level in the final frozen mixture was 7 percent. Sugars were added to a level of 1.25 percent.

Three of the sugars—glucose, arabinose, and rhamnose—protected the sperm during equilibration and freezing. Xylose was less effective, but its addition resulted in slightly better sperm survival than glycerol alone. It was found also that the methylene-blue reduction time (metabolic test for semen quality) was faster in samples to which the sugars had been added—after glycerolization, after equilibration, and after freezing the samples. This is confirming evidence for the presence of more living and actively metabolizing sperm in the portions to which sugars had been added.

Table 13.—Effect of Adding Sugars to Yolk-Citrate Diluent
on Sperm Motility During the Freezing Procedures[K]

(Average of 10 ejaculates)

Stageof
observation
Spermmotility(percent)
Glycerol
only
Glycerol
and
glucose
Glycerol
and
arabinose
Glycerol
and
xylose
Glycerol
and
rhamnose
Fresh diluted semen 63 63 63 63 63
After glycerolization 54 55 54 57 60
After 18 hours equilibration 39 43 44 39 46
After freezing to -79° C. and
immediate thawing
28 34 34 29 24
After 4 days at -79° C. 23 26 26 25 27

[K] Glycerol level in the final frozen mixture was 7 percent. Sugars were added to a level of 1.25 percent.

Substitutes for glycerol. Since glycerol was so effective in protecting sperm during freezing, many have assumed that related compounds might be even better. Several compounds, some related to glycerol and some not, have been tried as substitutes for glycerol in the freezing procedure. They include ethylene glycol, propylene glycol, trimethylene glycol, mannitol, sorbitol, dextrans, and seminal-plasma proteins. None of these materials has been as effective as glycerol in protecting sperm during freezing. In fact, several of the materials proved to be injurious to sperm prior to attempts to freeze the samples. While the work in our laboratory with these substances as glycerol substitutes was by no means finally conclusive, because of the many possible interactions of experimental conditions, sufficient data were gathered to lead us to abandon further study until greater promise of success might be evident.


                                                                                                                                                                                                                                                                                                           

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