Hu Jingmei, Zhao Shidou, Xu Chengyan, Zhang Lin, Lu Shaoming, Cui Linlin, Ma Jinlong, Chen Zi-Jiang
Center for Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, People's Republic of China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Jinan, People's Republic of China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, Jinan, People's Republic of China; Shandong Provincial Key Laboratory of Reproductive Medicine, Jinan, People's Republic of China.
Center for Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong University, Jinan, People's Republic of China; National Research Center for Assisted Reproductive Technology and Reproductive Genetics, Jinan, People's Republic of China; The Key Laboratory for Reproductive Endocrinology of Ministry of Education, Jinan, People's Republic of China; Shandong Provincial Key Laboratory of Reproductive Medicine, Jinan, People's Republic of China.
Fertil Steril. 2015 Nov;104(5):1253-7.e1-2. doi: 10.1016/j.fertnstert.2015.07.1140. Epub 2015 Aug 4.
To compare the differences in the characteristics of post-thaw human sperm after storage in either liquid nitrogen (LN2; -196 °C) or LN2 vapor (-167 °C).
Experimental study.
University hospital.
PATIENT(S): Thirty healthy volunteers who agreed to donate their normal semen samples for infertility or research were included in the study.
INTERVENTION(S): Semen samples (n = 30) were divided into eight aliquots and frozen. Four aliquots of each human semen sample were stored in LN2 (-196 °C), and the other four aliquots were stored in LN2 vapor (-167 °C). After 1, 3, 6, or 12 months, samples were thawed and analyzed.
MAIN OUTCOME MEASURE(S): The motility was evaluated by the manual counting method. The viability was estimated by eosin staining. The morphology was analyzed by Diff-Quik staining. The sperm DNA integrity was determined with acridine orange fluorescent staining, and acrosin activity was assayed by the modified Kennedy method.
RESULT(S): The characteristics of post-thaw human sperm, including motility, viability, morphology, DNA integrity, and acrosin activity, showed no significant difference between LN2 and LN2 vapor storage for the different time periods.
CONCLUSION(S): LN2 vapor was comparable to LN2 in post-thaw sperm characteristics, suggesting that LN2 vapor may be substituted for LN2 for the long-term storage of human sperm.
比较人类精子在液氮(LN2;-196°C)或液氮蒸汽(-167°C)中储存后解冻后特征的差异。
实验研究。
大学医院。
30名同意捐献其正常精液样本用于不育症研究或其他研究的健康志愿者被纳入研究。
精液样本(n = 30)被分成八等份并冷冻。每份人类精液样本的四等份储存在液氮(-196°C)中,另外四等份储存在液氮蒸汽(-167°C)中。在1、3、6或12个月后,样本解冻并进行分析。
通过手工计数法评估精子活力。通过伊红染色评估精子存活率。通过Diff-Quik染色分析精子形态。用吖啶橙荧光染色法测定精子DNA完整性,并用改良的肯尼迪法测定顶体酶活性。
在不同时间段,解冻后人类精子的特征,包括活力、存活率、形态、DNA完整性和顶体酶活性,在液氮和液氮蒸汽储存之间没有显著差异。
在解冻后精子特征方面,液氮蒸汽与液氮相当,这表明液氮蒸汽可替代液氮用于人类精子的长期储存。