돼지정자의 동결융해 후 활력 및 생존성에 대한 보존액, 동해보호제, 예비동결 및 동결처리시간의 영향 Effect of Cryodiluents, Cryoprotectants, Pre-freezing Method and Total Time Required for Freezing on Post-thaw Viability of Boar Spermatozoa원문보기
본 연구는 동결융해 후 정자의 생존성에 영향을 미치는 요인을 찾기 위하여 수행하였다. 동결융해 후 생존성에 대한 요인으로써 동결보존액, 동해보호제, 예비동결법 및 동결소요시간을 비교하였다. 동결과정중 정액의 질을 평가하기 위하여 활력, NAR 및 생존율을 조사한 결과는 다음과 같다. 돼지정액을 BF5, LYE, Soejima 및 modified Soejima 보존액으로 동결하였을 때 동결융해 후 정자활력은 M-Soejima 보존액이 44.5$\pm$6.4%로 다소 높았다. M-Soejima 보존액의 2차 회석액에 caffeine(2mM), heparin(l00 ${\mu}\ell$/$m\ell$) 및 caffeine＋heparin 를 첨가하였을 때 동결융해 후 활력은 caffeine 첨가구가 61.7% 로 가장 높았으며, 단독 혹은 혼합첨가가 첨가하지 않은 대조구보다 유의적으로 높은 활력을 나타내었다 (p＜0.05). M-Soejima 보존액에 동해보호제로서 glycerol(Gly), ethylene glycol(EG), propylene glycol(GP), Gly＋EG 및 Gly＋PG을 첨가하였을 때 동결융해 후 활력 및 NAR 율은 Gly＋PG의 혼합첨가시 (31.3%/39.5%) 가 다른 첨가구보다 다소 높았으며 생존율은 Gly＋EG 첨가구가 21.2% 로 다른 첨가구보다 다소 높았다. BE5와 M-Soejima 보존액으로 straw 및 pellet 동결법으로 동결하는 동안 dry ice-pellet, dry ice-straw 및 L$N_2$vapor-straw 법으로 예비동결하였을 때 각각 22.8, 47.5, 52.5% 및 42.5, 47.5, 57.5% 의 활력을 나타내었다. 또한 M-Soejima 보존액의 straw 법으로 l차 희석부터 동결완료까지 소요되는 시간을 2, 5 및 7시간으로 하였을 때 동결융해 후 활력 및 생존율은 처리간에 큰 차이가 없었으나, NAR 율은 처리시간이 길어질수록 다소 높은 경향을 나타내었다. 이러한 결과로 미루어 볼 때 동결융해 후 활력, NAR 및 생존율을 높이기 위해서는 caffeine 이 첨가된 M-Soejima 보존액에 동해보호제로 glycerol과 propylene glycol 또는 ehtylene glycol 을 사용하여 2시간 동안 빠르게 동결처리된 정액이 다소 유리할 것으로 사료되었다.
본 연구는 동결융해 후 정자의 생존성에 영향을 미치는 요인을 찾기 위하여 수행하였다. 동결융해 후 생존성에 대한 요인으로써 동결보존액, 동해보호제, 예비동결법 및 동결소요시간을 비교하였다. 동결과정중 정액의 질을 평가하기 위하여 활력, NAR 및 생존율을 조사한 결과는 다음과 같다. 돼지정액을 BF5, LYE, Soejima 및 modified Soejima 보존액으로 동결하였을 때 동결융해 후 정자활력은 M-Soejima 보존액이 44.5$\pm$6.4%로 다소 높았다. M-Soejima 보존액의 2차 회석액에 caffeine(2mM), heparin(l00 ${\mu}\ell$/$m\ell$) 및 caffeine＋heparin 를 첨가하였을 때 동결융해 후 활력은 caffeine 첨가구가 61.7% 로 가장 높았으며, 단독 혹은 혼합첨가가 첨가하지 않은 대조구보다 유의적으로 높은 활력을 나타내었다 (p＜0.05). M-Soejima 보존액에 동해보호제로서 glycerol(Gly), ethylene glycol(EG), propylene glycol(GP), Gly＋EG 및 Gly＋PG을 첨가하였을 때 동결융해 후 활력 및 NAR 율은 Gly＋PG의 혼합첨가시 (31.3%/39.5%) 가 다른 첨가구보다 다소 높았으며 생존율은 Gly＋EG 첨가구가 21.2% 로 다른 첨가구보다 다소 높았다. BE5와 M-Soejima 보존액으로 straw 및 pellet 동결법으로 동결하는 동안 dry ice-pellet, dry ice-straw 및 L$N_2$vapor-straw 법으로 예비동결하였을 때 각각 22.8, 47.5, 52.5% 및 42.5, 47.5, 57.5% 의 활력을 나타내었다. 또한 M-Soejima 보존액의 straw 법으로 l차 희석부터 동결완료까지 소요되는 시간을 2, 5 및 7시간으로 하였을 때 동결융해 후 활력 및 생존율은 처리간에 큰 차이가 없었으나, NAR 율은 처리시간이 길어질수록 다소 높은 경향을 나타내었다. 이러한 결과로 미루어 볼 때 동결융해 후 활력, NAR 및 생존율을 높이기 위해서는 caffeine 이 첨가된 M-Soejima 보존액에 동해보호제로 glycerol과 propylene glycol 또는 ehtylene glycol 을 사용하여 2시간 동안 빠르게 동결처리된 정액이 다소 유리할 것으로 사료되었다.
Boar semen can be frozen successfully. However, there is a large variability in the extent of damage boar semen samples experiences during cryopreservation. This experiment was undertaken to find out factors that affect a post-thaw viability of boar spermatozoa. For this purpose, cryodiluents(BF5, L...
Boar semen can be frozen successfully. However, there is a large variability in the extent of damage boar semen samples experiences during cryopreservation. This experiment was undertaken to find out factors that affect a post-thaw viability of boar spermatozoa. For this purpose, cryodiluents(BF5, LEY, Soejima and M-Soejima), cryoprotectants(glycerol. ethylene glycol, and propylene glycol), pre-freezing method(dryice-pellet, dryice-straw and L$N_2$vapour-st-raw) and total time required for freezing(2. 5, and 7 h) were compared as a factors. To investigate quality of semen during freezing process, motility(%), normal apical ridges(%, NAR), and proportion of living sperm(%) by flow cytometic analysis were assessed after collection, cooled, pre-frozen and post-thawing. Post-thaw motility of semen diluted with M-Soejima was 52.0%, respectively. When heparin, caffeine or heparin＋caffeine was added to 2nd cryodiluent of M-Soejima during freezing process, the highest motility after thawing was shown at the addition of caffeine (2mM), with 61.7$\pm$2.9% of motility. M-Soejima with heparin or caffeine was significantly higher than that of controI(p＜0.05). The result using glycerol(Gly), ethylene glycol(EG), propylene glycol(PG), and their mixture (Gly＋EG and Gly＋PG) as cryoprotectants, the highest motility was shown at the mixture treatment with Gly plus PG. However, the highest proportion of live spermatozoa was shown at Gly＋EG, there was no significantly difference among treatments(p＞0.05). When semen was pre-frozen with three manners(dryice-pellet, dryice-straw, and L$N_2$ vapor-straw), motility(%) of post-thaw spermatozoa was the highest in the L$N_2$ vapor-straw pre-freezing method of M-Soejima cryodiluent with 57.5% of motility, For a simple, economical and timesaving approach to freezing boar semen, total time required for freezing were 2, 5, and 7 hours, post-thaw motility were 43.8, 45.0 and 38.8%, NAR were 19.5, 22.7 and 28.5%, and viability were 20.8, 19.9 and 22.1%, respectively. This data suggests that boar semen diluted with M-Soejima cryodiluent contained caffeine, using mixture of glycerol and propylene glycol or ethylene glycol as cryoprotectants, frozen with 2 hours, can be taken better motility, NAR, and proportion of live spermatozoa.
Boar semen can be frozen successfully. However, there is a large variability in the extent of damage boar semen samples experiences during cryopreservation. This experiment was undertaken to find out factors that affect a post-thaw viability of boar spermatozoa. For this purpose, cryodiluents(BF5, LEY, Soejima and M-Soejima), cryoprotectants(glycerol. ethylene glycol, and propylene glycol), pre-freezing method(dryice-pellet, dryice-straw and L$N_2$vapour-st-raw) and total time required for freezing(2. 5, and 7 h) were compared as a factors. To investigate quality of semen during freezing process, motility(%), normal apical ridges(%, NAR), and proportion of living sperm(%) by flow cytometic analysis were assessed after collection, cooled, pre-frozen and post-thawing. Post-thaw motility of semen diluted with M-Soejima was 52.0%, respectively. When heparin, caffeine or heparin＋caffeine was added to 2nd cryodiluent of M-Soejima during freezing process, the highest motility after thawing was shown at the addition of caffeine (2mM), with 61.7$\pm$2.9% of motility. M-Soejima with heparin or caffeine was significantly higher than that of controI(p＜0.05). The result using glycerol(Gly), ethylene glycol(EG), propylene glycol(PG), and their mixture (Gly＋EG and Gly＋PG) as cryoprotectants, the highest motility was shown at the mixture treatment with Gly plus PG. However, the highest proportion of live spermatozoa was shown at Gly＋EG, there was no significantly difference among treatments(p＞0.05). When semen was pre-frozen with three manners(dryice-pellet, dryice-straw, and L$N_2$ vapor-straw), motility(%) of post-thaw spermatozoa was the highest in the L$N_2$ vapor-straw pre-freezing method of M-Soejima cryodiluent with 57.5% of motility, For a simple, economical and timesaving approach to freezing boar semen, total time required for freezing were 2, 5, and 7 hours, post-thaw motility were 43.8, 45.0 and 38.8%, NAR were 19.5, 22.7 and 28.5%, and viability were 20.8, 19.9 and 22.1%, respectively. This data suggests that boar semen diluted with M-Soejima cryodiluent contained caffeine, using mixture of glycerol and propylene glycol or ethylene glycol as cryoprotectants, frozen with 2 hours, can be taken better motility, NAR, and proportion of live spermatozoa.
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