期刊文献+

人精液的冻贮研究 被引量:2

The study of cryopreservation in human spermatozoa
下载PDF
导出
摘要 目的 研究在T-G型冷冻保护剂(Cryopreservative medium, CPM)作用下,速缓冻贮法对人精子结构和功能的影响。方法 随机双盲对照, 将45份正常精液随机分组,加与不加CPM ,以速缓冷冻法分别进行冻贮,冻贮前后分别进行常规分析、低渗肿胀试验、穿卵试验、超微结构观察及精子染色体分析。结果 未加CPM组冻贮后的精液未见有精子复苏, 经冷冻保存的精子质量明显降低,缓冻法对精子的影响显著小于速冻法,精子染色体的畸变率及X/Y精子比例均未见明显变化。结论 速、缓冻贮对人精子均有负面影响,缓冻法优于速冻法,两法对精子染色体畸变率和性染色体比例未产生明显影响。 :Objective To study the effect of slow or quick freezing- storing on the function and ultrastructure of human spermatozoa with T-G type cryopreservative medium(CPM) as cryoprotectant during a longer period. Methods 45 normal semen samples were subjected to cryopreservation with or without T-G type CPM and slow or quick freezing- storing respectively. Fresh and frozen-thawed semen were examined by the routine analysis of semen and spermatozoa hypoosmotic swelling test and spermatozoa in vitro penetrate zona-free hamster ova assay and spermatozoa head ultrastructure observation and spermatozoa chromosome analysis. Results No spermatozoa in cryopreservated semen without T-G type of CPM was alive after thawed. The quality of frozen-thawed human semen by slow and quick freezing- storing methods with T-G type CPM was significantly lower than that of fresh semen(P<0.01) and the effect of slow freezing method was smaller than that of quick freezing method(P<0.01). Neither of the methods increased the rate of spermatozoa chromosome abnormalities and X/Y ratio of human spermatozoa(0.90<P<0.95). Conclusion Both cryopreservation methods have negative effect on human spermatozoa and the slow freezing method is better than the quick one. The sperm chromosome and X/Y spermatozoa ratio are not significantly affected by the two methods.
出处 《重庆医科大学学报》 CAS CSCD 2000年第4期390-392,共3页 Journal of Chongqing Medical University
关键词 冷冻保护剂 精液冻贮 精子染色体 CPM :Cryopreservative medium(CPM);Semen freezing-storing;Spermatozoa penetrate zona-free hamster ova assay;Spermatozoa chromosome;Spermatozoa ultrastructure.
  • 相关文献

参考文献1

  • 1张秀成,精子检测与分离,1993年

同被引文献18

  • 1Sallam H N,Ezzeldin F,Sallam A,et al.Sperm velocity an morphology,female characteristics,and the hypo-osmotic swelling test as predictors of fertilization potential:experience from the IVF model[J].Int J Fertil Womens Med,2003,48 (2):88-95.
  • 2Mahadevan M,Trounon A O.Effect of cryoprotective media and dilution methods on the preservation of human spermatozoa[J].Andrologia,1983,15 (4):355-366.
  • 3Lindholmer C H."Hie importance of seminal plasma for human sperm motility[J].Bio Reprod,1974,10:533-542.
  • 4Heindel J J,Lipshultz L I,Steinberger E.Stimulation of cyclic adenosine 3':5'-monophosphate accumulation in human testes in vitro by luteinizing hormone,follicle-stimulating hormone,and prostaglandins[J].Fertil Steril.1978,30(5):595-599.
  • 5Consentino M J,Emilson E B V,Cockett A T K.Prostaglandins in semen and their relationship to male fertility:a study of 145 men[J].Fertil Steril,1984,41:88-94.
  • 6Makler A,Fisher M,Murillo O,et al.Factors affecting sperm motility,IX.survival of spermatozoa in various biological media and under different gaseous compositions[J].Fertil Steril,1984,41:428-432.
  • 7Check ML, Check D J, Long R. Effect of shortened exposure time to the critical period for ice crystal formation on subsequent postthaw semen parameters from cryopreserved sperm, Arch Androl,1994,32(1) :63-67.
  • 8Okada S,Suzumori K, Yagami Y. Cytogenetic effects of crypreserration on sperm, assessment using an improved method for analyzing human sperm chromosomes, J Obslet Gynaecol, 1995,21(6) :641-647.
  • 9Pederson H, Lehech PH. Ultrastructural changes in the human spermatozoom after freezing for artificial insemination. Fertil Steril, 1971,22(2) :125.
  • 10Gopalkrishnan K, Padwal V, D souza S, et al. Semere asthenozoospermiaa structural an sperm ultrastructure. Hum Reprod, 1995,10:2295.

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部