Rahman M Mahfujur, Ali M Rahmat, Sarder M Rafiqul Islam, Mollah M Fazlul Awal, Khan Najmus Sakib
Department of Fisheries Biology and Genetics, Bangladesh Agriculture University, Mymensingh, 2202, Bangladesh.
Cryobiology. 2016 Dec;73(3):316-323. doi: 10.1016/j.cryobiol.2016.10.004. Epub 2016 Oct 13.
The study was conducted to develop sperm cryopreservation protocol for the endangered spiny eel, Mastacembelus armatus as well as to use the cryopreserved sperm in breeding. Activation of sperm was evaluated by observing motility in different osmolalities of NaCl solution (48-319 mOsmol/kg) and found that sperm motility decreased with increasing osmolality of the NaCl solution and it was totally inhibited at 319 mOsmol/kg. The highest motility and swimming duration of sperm were observed as 14.5 ± 0.5 min and 4.75 ± 0.25 min at 128 mOsmol/kg and 67 mOsmol/kg, respectively. The concentration of sperm was found to be 1.75 × 10 to 2.25 × 10 cells/ml. Evaluation of toxicity of cryoprotectants of dimethyl sulfoxide (MeSO) and methanol to sperm was performed at 5, 10 and 15% concentrations during 5-30 min incubation period and found that cryoprotectants with 5 and 10% concentrations produced better motility up to 10 min incubation. In the selection of suitable diluent for cryopreservation of sperm, Alsever's solution with 10% MeSO performed best producing 91.67 ± 1.67% and 65 ± 2.89% equilibration and post-thaw motility, respectively. In breeding trials, sperm preserved with Alsever's solution plus MeSO produced more or less similar fertilization (82.25 ± 4.46%) and hatching (12 ± 0.65%) to those preserved with 0.9% NaCl solution plus MeSO as 79.88 ± 4.67% and 11 ± 0.46% fertilization and hatching respectively. Fresh sperm used as control produced 87.63 ± 3.6% and 14 ± 0.5% fertilization and hatching respectively. Both cryopreserved and fresh sperm-derived fry performed well but the control fry showed a significantly better (P < 0.05) growth. Fry derived from four diluents did not show any significant (P > 0.05) growth difference but Alsever's solution plus MeSO produced better results.
本研究旨在为濒危物种多刺鱼芒(Mastacembelus armatus)制定精子冷冻保存方案,并将冷冻保存的精子用于繁殖。通过观察精子在不同渗透压的氯化钠溶液(48 - 319毫摩尔/千克)中的活力来评估精子的激活情况,发现随着氯化钠溶液渗透压的增加,精子活力下降,在319毫摩尔/千克时完全被抑制。在128毫摩尔/千克和67毫摩尔/千克时,精子的最高活力和游动持续时间分别观察到为14.5±0.5分钟和4.75±0.25分钟。精子浓度为1.75×10至2.25×10个细胞/毫升。在5 - 30分钟的孵育期内,对二甲基亚砜(MeSO)和甲醇这两种冷冻保护剂对精子的毒性进行了评估,浓度分别为5%、10%和15%,发现浓度为5%和10%的冷冻保护剂在孵育10分钟内产生更好的活力。在选择适合精子冷冻保存的稀释剂时,含10% MeSO的阿尔塞弗溶液表现最佳,平衡和解冻后活力分别为91.67±1.