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一种利用牛脂肪冷表面冷冻保存公羊和公牛精子的新型颗粒技术。

A new pellet technique for cryopreserving ram and bull spermatozoa using the cold surface of cattle fat.

作者信息

Awad M M, Graham J K

机构信息

Department of Animal Production, Faculty of Agriculture, Suez Canal University, 41522 Ismailia, Egypt.

出版信息

Anim Reprod Sci. 2004 Aug;84(1-2):83-92. doi: 10.1016/j.anireprosci.2003.12.001.

Abstract

A technique for freezing ram and bull spermatozoa in pellet form, using the cold surface of cattle fat was compared to other freezing procedures. Three freezing methods were compared to cryopreserve ram spermatozoa: 0.25 ml straws, pellets frozen on the cold surface of paraffin wax and pellets frozen on the cold surface of cattle fat. In addition, two cryoprotectants, glycerol or sucrose, in an egg yolk-Tris diluent were compared. Ram spermatozoa frozen as pellets on cattle fat exhibited higher percentages of motile cells after thawing (54%) than spermatozoa frozen in straws (49%) or as pellets on paraffin wax (42%, S.E.M. = 1; P < 0.05). However, the percentages of acrosome intact cells were similar for spermatozoa frozen as pellets (49%) and spermatozoa frozen in straws (48%; P > 0.05), but higher than for spermatozoa frozen as pellets on paraffin wax (39%, S.E.M. = 1; P > 0.05). Ram spermatozoa exhibited higher percentages of motile cells after thawing when the cryoprotectant was sucrose (51%) compared to glycerol (46%; P < 0.05). Similarly, acrosomal integrity was greater with sucrose (49%) than with glycerol (42%; P < 0.05). Bull spermatozoa exhibited higher percentages of motile cells after thawing, when cells were frozen in straws (47%) than in the pellet form, regardless of the surface on which the pellets were frozen (31-37%, S.E.M. = 3; P < 0.05). However, bull spermatozoa exhibited higher percentages of motile cells when frozen as pellets on the surface of cattle fat (66%) or dry ice (61%), than when frozen on paraffin wax (53%, S.E.M. = 4; P < 0.05). In conclusion, although bull spermatozoa survive cryopreservation more effectively in straws, ram spermatozoa can be cryopreserved as pellets on the cold surface of cattle fat using sucrose as the cryoprotectant. This technique is simple, requires little equipment, is less expensive than using straws and may prove useful for cryopreserving ram and possibly bull spermatozoa in developing countries.

摘要

将一种利用牛脂肪冷表面以颗粒形式冷冻公羊和公牛精子的技术与其他冷冻方法进行了比较。比较了三种冷冻方法来冷冻公羊精子:0.25毫升细管、在石蜡冷表面冷冻的颗粒以及在牛脂肪冷表面冷冻的颗粒。此外,还比较了在蛋黄 - 三羟甲基氨基甲烷稀释液中使用的两种冷冻保护剂,甘油或蔗糖。在牛脂肪上以颗粒形式冷冻的公羊精子解冻后具有活力的细胞百分比(54%)高于在细管中冷冻的精子(49%)或在石蜡上以颗粒形式冷冻的精子(42%,标准误 = 1;P < 0.05)。然而,以颗粒形式冷冻的精子(49%)和在细管中冷冻的精子(48%;P > 0.05)顶体完整细胞的百分比相似,但高于在石蜡上以颗粒形式冷冻的精子(39%,标准误 = 1;P > 0.05)。当冷冻保护剂为蔗糖时,解冻后公羊精子具有活力的细胞百分比(51%)高于甘油(46%;P < 0.05)。同样,蔗糖组(49%)的顶体完整性高于甘油组(42%;P < 0.05)。公牛精子解冻后,当细胞在细管中冷冻时具有活力的细胞百分比(47%)高于以颗粒形式冷冻时,无论颗粒在何种表面冷冻(31 - 37%,标准误 = 3;P < 0.05)。然而,公牛精子在牛脂肪表面(66%)或干冰上以颗粒形式冷冻时具有活力的细胞百分比高于在石蜡上冷冻时(53%,标准误 = 4;P < 0.05)。总之,尽管公牛精子在细管中冷冻保存时存活效果更好,但公羊精子可以使用蔗糖作为冷冻保护剂在牛脂肪冷表面以颗粒形式冷冻保存。这种技术简单,所需设备少,比使用细管成本低,可能对发展中国家冷冻公羊甚至公牛精子有用。

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