Robeck T R, O'Brien J K
SeaWorld Texas, San Antonio, Texas 78251, USA.
Biol Reprod. 2004 May;70(5):1340-8. doi: 10.1095/biolreprod.103.025304. Epub 2004 Jan 7.
Research was conducted to develop an effective method for cryopreserving bottlenose dolphin (Tursiops truncatus) semen processed immediately after collection or after 24-h liquid storage. In each of two experiments, four ejaculates were collected from three males. In experiment 1, three cryopreservation methods (CM1, CM2, and CM3), two straw sizes (0.25 and 0.5 ml), and three thawing rates (slow, medium, and fast) were evaluated. Evaluations were conducted at collection, prefreeze, and 0-, 3-, and 6-h postthaw. A sperm motility index (SMI; total motility [TM] x % progressive motility [PPM] x kinetic rating [KR, scale of 0-5]) was calculated and expressed as a percentage MI of the initial ejaculate. For all ejaculates, initial TM and PPM were greater than 85%, and KR was five. At 0-h postthaw, differences in SMI among cryopreservation methods and thaw rates were observed (P < 0.05), but no effect of straw size was observed. In experiment 2, ejaculates were divided into four aliquots for dilution (1:1) and storage at 4 degrees C with a skim milk- glucose or a N-tris(hydroxymethyl)methyl-2-aminoethane sulfonic acid (TES)-TRIS egg yolk solution and at 21 degrees C with a Hepes-Tyrode balanced salt solution (containing bovine albumin and HEPES) (TALP) medium or no dilution. After 24 h, samples were frozen and thawed (CM3, 0.5-ml straws, fast thawing rate) at 20 x 10(6) spermatozoa ml(-1) (low concentration) or at 100 x 10(6) spermatozoa ml(-1) (standard concentration). The SMI at 0-h postthaw was higher for samples stored at 4 degrees C than for samples stored at 21 degrees C (P < 0.001), and at 6-h postthaw, the SMI was higher for samples frozen at the standard concentration than for samples frozen at the low concentration (P < 0.05). For both experiments, acrosome integrity was similar across treatments. In summary, a semen cryopreservation protocol applied to fresh or liquid-stored semen maintained high levels of initial ejaculate sperm characteristics.
开展了一项研究,旨在开发一种有效的方法,用于冷冻保存宽吻海豚(Tursiops truncatus)刚采集后或经过24小时液体储存后的精液。在两项实验中,分别从三只雄性宽吻海豚采集了四份射精精液。在实验1中,评估了三种冷冻保存方法(CM1、CM2和CM3)、两种细管规格(0.25毫升和0.5毫升)以及三种解冻速率(慢速、中速和快速)。在采集时、冷冻前以及解冻后0小时、3小时和6小时进行评估。计算精子活力指数(SMI;总活力[TM]×% 前进活力[PPM]×活力评级[KR,0 - 5级]),并表示为初始射精精液MI的百分比。对于所有射精精液,初始TM和PPM均大于85%,KR为5。在解冻后0小时,观察到冷冻保存方法和解冻速率之间SMI存在差异(P < 0.05),但未观察到细管规格的影响。在实验2中,将射精精液分成四份进行稀释(1:1),并分别用脱脂奶 - 葡萄糖溶液或N - 三(羟甲基)甲基 - 2 - 氨基乙烷磺酸(TES) - TRIS蛋黄溶液在4℃下储存,以及用含有牛血清白蛋白和HEPES的Hepes - Tyrode平衡盐溶液(TALP)培养基在21℃下储存或不进行稀释。24小时后,将样本冷冻并解冻(CM3,0.5毫升细管,快速解冻速率),精子浓度为20×10⁶精子/毫升(低浓度)或100×10⁶精子/毫升(标准浓度)。解冻后0小时,在4℃下储存的样本的SMI高于在21℃下储存的样本(P < 0.001),解冻后6小时,以标准浓度冷冻的样本的SMI高于以低浓度冷冻的样本(P < 0.05)。对于两项实验,各处理间顶体完整性相似。总之,应用于新鲜或液体储存精液的精液冷冻保存方案能维持初始射精精液精子特征的高水平。