Preservation of Bull Semen at Sub-Zero Temperatures Part 3

================================================================ Storage Glycerol Sperm motility after storage (percent) temperature level -------------------------------------- (C.) (percent) 18 hours 42 hours ---------------------------------------------------------------- -79 7 61 61 -20 7 2 1 11 3 1 15 14 10 19 30 22 23 29 19 27 25 18 31 21 12 ----------------------------------------------------------------

While survival was fair over a short period of time with 19 percent glycerol at -20 C., deterioration was rapid during storage. After 18 hours of storage, the samples at -20 C. (19 percent glycerol) contained only one half as many motile sperm as were still present in the samples at -79 C. (7 percent glycerol). After 42 hours of storage, the best samples at -20 C. contained only one-third the number of motile sperm still present in the samples stored at -79 C. These trials leave little doubt that under the present system of freezing and storing, storage at ordinary deep-freeze temperatures is far inferior to storage at dry-ice temperatures.

THAWING

The importance of carefully controlled cooling and storage has been emphasized in the foregoing sections. The need for controlling thawing rates and the temperature of thawing was not clearly defined in the early work on freezing bull s.e.m.e.n. The British used a thawing temperature of 40 C., which was satisfactory. If there is a need to hold the s.e.m.e.n for a time after thawing, then a lower thawing temperature might be more desirable so that cooling again will not be necessary.

=Comparison of thawing temperatures of 5 C. and 38 C.= The effects of thawing at temperatures of 38 (body temperature) and 5 C.

(refrigerator temperature) were investigated. The first trial involved thawing as rapidly as possible by dropping gla.s.s ampules of frozen s.e.m.e.n into water baths at the two temperatures. The frozen s.e.m.e.n samples contained glycerol levels of 4, 6, 8, and 10 percent. The mean percentages of motile sperm found after thawing thirteen diluted s.e.m.e.n samples treated in this manner are shown in Figure 6.

[Ill.u.s.tration: Effect of glycerol percentage and thawing temperature on sperm motility after freezing and thawing (Fig. 6)]

The 5 C. thawing temperature resulted in a higher percentage of sperm survival at all the glycerol levels than 38 C., with the difference in favor of 5 C. becoming greater as the glycerol level increased. The reason for the interaction between glycerol level and thawing temperature is not known. It may be that the presence of the higher levels of glycerol at 38 C. brought about harmful metabolic activity.

The difference in survival of sperm in s.e.m.e.n thawed at 5 C. and at 38 C. continued during storage at 5 C. (Table 15). It was also evident that the interaction between glycerol level and thawing temperature continued during storage (Fig. 7).

[Ill.u.s.tration: Effect of thawing temperature on sperm motility during storage at 5 C. following freezing and thawing (Fig. 7)]

Table 15.--Effect of Glycerol Level, Thawing Temperature, and Storage at 5 C. After Thawing on Sperm Motility (Average of 13 e.j.a.c.u.l.a.t.es)

===================================================================== Thawing Glycerol Sperm motility (percent) temperature level ------------------------------------------- ( C.) (percent) Post- After storage at 5 C.

thawing ---------------------- Average 1 day 3 days --------------------------------------------------------------------- 38 4 28.5 17.3 5.1 17.0 6 31.5 22.4 9.2 21.1 8 33.1 15.0 4.6 17.6 10 19.5 3.6 0.8 8.0 Average 28.2 14.6 4.9 12.2

5 4 29.2 21.7 19.8 23.9 6 37.7 33.8 23.5 31.7 8 41.5 33.1 17.3 30.6 10 33.1 18.5 6.0 19.2 Average 35.4 26.8 16.6 20.6 ---------------------------------------------------------------------

It is obvious that motility falls off rapidly after the s.e.m.e.n is thawed.

In a field trial in which the initial intent was to test the effect of glycerol levels on fertility of frozen s.e.m.e.n, the s.e.m.e.n was thawed in the morning and used during the same day. Survival of the sperm with 4 percent glycerol was so poor that only a few breedings were made with these samples. Even at 7 and 10 percent, the fertility results were much lower than with s.e.m.e.n that had not been subjected to freezing. At that time it was felt that thawing the samples and using them throughout the day may have caused the low fertility results. Since then, a large-scale experiment by Cornell University investigators, in cooperation with the New York Artificial Breeders' Cooperative, has shown definitely that thawing should be delayed until a few minutes prior to breeding.[11] If the s.e.m.e.n is used immediately, a thawing temperature of either 5 or 38 C. appears to be suitable. However, there is less danger of cold shock due to recooling if 5 C is used.

=Thawing rate in plastic and in gla.s.s.= Gla.s.s ampules transmit cold or heat more readily than plastic ones. The temperature rise is rapid in both gla.s.s and plastic when samples are taken from the storage box at -79 C. and placed in water at 5 C. However, complete thawing occurs more rapidly in gla.s.s than in plastic ampules. The changes in temperature that occurred when gla.s.s and plastic ampules were thawed in a water bath at 5 C. are shown in Figure 8. The initial temperature rise for the first minute or two was about the same, then the rate of warming in the plastic slowed and actual melting of the frozen sample occurred a little over a minute later in the plastic than it did in the gla.s.s. Both were thawed in less than four minutes.

[Ill.u.s.tration: Warming rates of diluted s.e.m.e.n samples in plastic vials and in gla.s.s ampules (Fig. 8)]

EFFECTS OF FREEZING PROCEDURES ON METABOLIC ACTIVITY OF BULL SPERM

By finding how methods of handling affect the sperm cells, one can sometimes improve the procedures to avoid harmful effects. Some attempts have been made in this laboratory to determine the effects of the freezing procedures on the metabolic activity of bull spermatozoa. These investigations have been limited in scope, involving the measurement of oxygen-consumption and estimates of sperm motility during and after incubation at 37 C. in a Warburg apparatus.

=Effect of glycerol additions on oxygen uptake of diluted s.e.m.e.n at 37 C.= The effect of adding glycerol to diluted s.e.m.e.n on oxygen consumption of the sperm was tested in a Warburg apparatus, using s.e.m.e.n diluted with an extender consisting of one part egg yolk and one part 2.9 percent sodium citrate dihydrate. The yolk-citrate extender was added to the s.e.m.e.n at a rate which brought the sperm concentration in 0.5 milliliter to 200 million to 500 million. An exact count was used to calculate the oxygen uptake per 10^{8} sperm per hour (ZO_{2}).

[Ill.u.s.tration: Effect of glycerol additions on oxygen consumption of sperm at 37 C. (Fig. 9)]

Glycerol in various percentages in 2.9 percent sodium citrate dihydrate solution was placed in the sidearm of the Warburg flasks. The diluted s.e.m.e.n was held in the main compartment. After a 60-minute preliminary run, in which the rate of oxygen uptake of the sperm in yolk-citrate diluent was determined, the contents of the sidearm were tipped into the main compartment. The resulting glycerol percentages after mixing the sidearm and main compartment contents were 0, 4, 8, and 12 percent. Ten samples of s.e.m.e.n were subsampled and the oxygen uptake of each was determined at all four levels of glycerol.

Oxygen uptake was increasingly stimulated during the first 20-minute interval by each increase in the amount of glycerol added (Fig. 9).

After the first 20 minutes, the rate of oxygen utilization decreased at the two higher levels of glycerol but persisted at 4 percent. The rate of oxygen consumption for the first 20-minute period at the 4-percent glycerol level was 130 percent that of the control to which only sodium citrate had been added. At 8 and 12 percent the values for the period were 144 and 192 percent, respectively, of the control rate.

[Ill.u.s.tration: Effect of glycerol and glycerol-plus-catalase additions on sperm motility during incubation at 37 C. (Fig. 10)]

With each increase in glycerol level, motility was reduced during the incubation period. This is shown in Figure 10 along with the effect on motility of adding catalase, which is discussed in the next section.

=Effect of glycerol-plus-catalase on oxygen uptake of diluted s.e.m.e.n.= Certain bacteria have been shown to break glycerol down, forming hydrogen peroxide as follows:

Glycerol + oxygen --> lactic acid + hydrogen peroxide.

Hydrogen peroxide is known to be detrimental to sperm. The addition of glycerol to diluted s.e.m.e.n first increased oxygen uptake and then reduced it. Since a reduction in sperm survival followed, some harmful action must have taken place with the addition of glycerol at 37 C. To test whether this action could be due to the release of hydrogen peroxide as occurs in certain bacteria, glycerol with catalase--the enzyme which breaks down hydrogen peroxide--was added to a portion of 8 diluted s.e.m.e.n samples and the oxygen uptake was recorded. Comparison of the resulting oxygen uptake with glycerol and with glycerol plus catalase is shown in Figure 11.

[Ill.u.s.tration: Effect of additions of glycerol-plus-catalase on oxygen consumption of sperm at 37 C. (Fig. 11)]

Oxygen consumption was increased by the presence of added catalase at all glycerol levels and in the control. Sperm survival during the 3-hour period at 37 C. also was improved by the presence of catalase (Fig.

10). However, the general trend in oxygen consumption produced by the addition of glycerol was not changed greatly. The higher levels of glycerol still stimulated oxygen uptake during the first 20-minute period after the additions and then slowed the rate of oxygen utilization. The rate of utilization was generally higher during the test period in the presence of catalase than without added catalase. It appeared that a part of the harmful effect of glycerol might be due to the formation of hydrogen peroxide. Still, the detrimental effects of the higher levels of glycerol were not completely removed.

Table 16.--Effect of Freezing Procedures on Oxygen Utilization of Bull Sperm in Yolk-Citrate Extender

(Average of 5 e.j.a.c.u.l.a.t.es)

===================================================================== Microliters of oxygen s.e.m.e.n sample tested utilized per 10^{8} sperm -------------------------- First hour Second hour --------------------------------------------------------------------- Fresh diluted s.e.m.e.n 10.3 8.1 Fresh diluted s.e.m.e.n glycerol tipped in at end of first hour 9.7[L] 12.9[L]

Aged 20 to 24 hours at 5 C. 11.2 8.3 Aged 20 to 24 hours at 5 C. glycerol tipped in at end of first hour 11.8[L] 12.9[L]

After 20 hours equilibration with glycerol 11.7[L] 7.8[L]

After freezing and thawing 9.7 6.3 --------------------------------------------------------------------

[L] Average of 3 e.j.a.c.u.l.a.t.es.

=Effect of freezing procedures on oxygen utilization by sperm.= Limited data have been obtained on the effects of some of the freezing procedures on the oxygen utilization of bull sperm. The results obtained in these experiments confirmed the earlier findings that tipping glycerol directly into the diluted s.e.m.e.n at 37 C. caused an increase in oxygen consumption (Table 16). All other steps in the freezing procedure had little effect on oxygen consumption by the sperm. Except where glycerol was added during the determination, the rate of oxygen utilization was lower the second hour than during the first. The oxygen uptake of s.e.m.e.n that had been frozen and thawed seemed to drop faster than that of unfrozen samples.

=Effect of freezing procedures on methylene-blue reduction time.= The methylene-blue reduction test has been used as a means of measuring s.e.m.e.n quality and is dependent on the metabolic activity of the sperm.

The effects of various freezing procedures on the ability of samples to decolorize methylene blue were determined with 10 s.e.m.e.n samples. Sperm numbers were standardized to 300 10^{6} cells per milliliter and the time required for these cells to reduce a 1:40,000 solution of methylene blue was determined on freshly diluted s.e.m.e.n, after the addition of glycerol, after equilibration, and after freezing and thawing. Portions of each diluted sample were tested at these stages of the procedure with glycerol alone added and with glycerol and various sugars added.

A marked increase in the time required for the sperm to reduce methylene blue occurred when the glycerol was added (Table 17). This increase was greatest in the portions with glycerol alone and with glycerol and glucose. The time increase was less p.r.o.nounced in the presence of the three pentose sugars used. Following equilibration, the samples regained the ability to reduce methylene blue at a rate only slightly slower than when they were fresh. Freezing and storage of s.e.m.e.n resulted in slower reduction of the methylene blue than was shown after equilibration with glycerol. Since freezing usually kills some of the sperm, a slowing of the reduction time after freezing would be expected.

Table 17.--Effect of Freezing Procedures on the Methylene-Blue Reduction Time of Bull s.e.m.e.n With and Without the Addition of Sugars[M]

(Average of 10 e.j.a.c.u.l.a.t.es)

====================================================================== Methylene-blue reduction time (minutes) ------------------------------------------------ Glycerol Glycerol Glycerol Glycerol Glycerol only and and and and glucose arabinose xylose rhamnose ---------------------------------------------------------------------- Fresh s.e.m.e.n 5.2 5.2 5.2 5.2 5.2 After glycerolization 26.4 25.2 17.3 14.3 19.4 After 18 hours equilibration 7.4 6.5 6.4 5.3 6.2 Thawed immediately after freezing 11.5 10.5 9.4 9.0 9.4 Thawed 48 hours after freezing 14.3 10.2 11.3 10.1 9.5 ----------------------------------------------------------------------

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

PRACTICAL FREEZING PROCEDURE