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陈东华, 李艳东, 贾林芝, 厉小波, 王立人, 曲迪, 王群. 冷冻保护剂及预冷时间对河蟹精子体外冷冻保存的影响[J]. 水生生物学报, 2008, 32(4): 579-585.
引用本文: 陈东华, 李艳东, 贾林芝, 厉小波, 王立人, 曲迪, 王群. 冷冻保护剂及预冷时间对河蟹精子体外冷冻保存的影响[J]. 水生生物学报, 2008, 32(4): 579-585.
CHEN Dong-Hua, LI Yan-Dong, JIA Lin-Zhi, LI Xiao-Bo, WANG Li-Ren, QU Di, WANG Qun. CRYOPRESERVATI ON OF ERIOCHEIR SINENSIS SPER M S (IN VITRO)W ITH D IFFERENT CRYOPROTECTIVE SOLUTI ONS AND PREFREEZING TIM E[J]. ACTA HYDROBIOLOGICA SINICA, 2008, 32(4): 579-585.
Citation: CHEN Dong-Hua, LI Yan-Dong, JIA Lin-Zhi, LI Xiao-Bo, WANG Li-Ren, QU Di, WANG Qun. CRYOPRESERVATI ON OF ERIOCHEIR SINENSIS SPER M S (IN VITRO)W ITH D IFFERENT CRYOPROTECTIVE SOLUTI ONS AND PREFREEZING TIM E[J]. ACTA HYDROBIOLOGICA SINICA, 2008, 32(4): 579-585.

冷冻保护剂及预冷时间对河蟹精子体外冷冻保存的影响

CRYOPRESERVATI ON OF ERIOCHEIR SINENSIS SPER M S (IN VITRO)W ITH D IFFERENT CRYOPROTECTIVE SOLUTI ONS AND PREFREEZING TIM E

  • 摘要: 本文以甘油、二甲亚砜(DMSO)为冷冻保护剂,采用两步降温法,以精子存活率和DNA损伤程度为检验其冷冻效果的评价指标,研究了冷冻保护剂和预冷时间对河蟹Eriocheir sinensis精子冷冻保存效果的影响。胰蛋白酶消化法获得河蟹游离精子,液氮冷冻保存8h以上,精子保存密度为107个/mL,伊红染色法检测精子存活率,单细胞凝胶电泳(SCGE)检测精子DNA损伤。实验共设置10个组,分别为不同浓度的单一冷冻保护剂(每种保护剂的体积百分比分别为5%、10%、12.5%、15%)和两种保护剂组合(两种保护剂在同一实验组中的体积百分比含量均为5%、10%)。结果显示,12.5%甘油的保存效果最佳,精子存活率达到62.60%。在此基础上,以10%甘油作为冷冻保护剂,设置5、10、20、30、40min 5个时间梯度,研究了预冷时间对精子冷冻保存效果的影响。结果显示预冷时间的长短对精子冷冻保存效果的影响显著,当预冷时间低于20min时,精子大量死亡,且精子DNA严重损伤;当预冷时间超过30min时,精子存活率明显提高,精子DNA损伤明显减弱。

     

    Abstract: As for genetic breeding and conservation of biotic germplasm resources, the cryopreservation of sperms serves asan effective protection. However, the process of cryopreservation and cryoprotective solutions both enable to cause damageof sperms to some extent, includingDNA damage of sperms. Anyhow, serving as vectors of genetic information, the integrityof DNA is necessary for the normal development of offspring. Therefore, the extent of DNA damage caused during cryopr2eservation can be used as an important index to evaluate the cryopreservative effects. In this study, sperms of Eriocheirsinensis cryopreserved in glycerol and dimethyl sulfoxide (DMSO) (in vitro) were detected for the cryopreservation effectswith different cryoprotective solutions and prefreezing times. Viability rate and DNA damage of sperms were betaken asevaluation indices. Sperms of Eriocheir sinensiswere acquired by trypsinase digestion and cryopreserved in the liquefied ni2trogen for over 8 hourswith sperm density at 107sperm/mL. Meanwhile, viability rate of spermswas assessed by eosin stainand DNA damagewas detected by single cell gel electrophoresis(SCGE). Ten experimental groups and three control groupswere set. Those ten groupswere four glycerol and DMSO scalar solutions(for each) (5%, 10%, 1215%, 15%) and twocomposite solutions with equivalent glycerol and DMSO (5%, 10%). Results revealed that cryoprotective solution with1215% glycerolwas optimum for cryopreservation of Eriocheir sinensis sperms(in vitro), where viability rate reached to62160%. Furthermore, cryoprotective solution with 10% glycerolwas used to study its cryopreservation effectswith differ2ent prefreezing times and five time gradients(5, 10, 20, 30 and 40 min) were set. It revealed that prefreezing time had aconspicuous influence on cryopreservation effects, i. e. sperms were thorough dead with overwhelming DNA damage afterless than 20 minπprefreezing, however, viability rate of sperms ascend obviously with DNA damage decreasing distinctlywhen prefreezing time was over 30min.

     

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