文章摘要
郭锡春1 刘坤1 刘占涛1 冷凯良2 张婕1 裴彤1 高华1△.海参精囊提取物对环磷酰胺诱导生殖系统受损小鼠 生精功能的影响*海参精囊提取物对环磷酰胺诱导生殖系统受损小鼠 生精功能的影响*[J].,2014,14(17):3262-3265
海参精囊提取物对环磷酰胺诱导生殖系统受损小鼠 生精功能的影响*海参精囊提取物对环磷酰胺诱导生殖系统受损小鼠 生精功能的影响*
Effects of Holothurian Spermatophore Extracts on Spermatogenesis ofReproductive Systemin Mice Injured by Cyclophosphamide*
  
DOI:
中文关键词: 海参精囊  提取  环磷酰胺  生精功能
英文关键词: Holothurian spermatophore  Extract  Cyclophosphamide  Spermatogenesis
基金项目:国家自然科学基金项目(31171671)
作者单位
郭锡春1 刘坤1 刘占涛1 冷凯良2 张婕1 裴彤1 高华1△ 1 青岛大学药学院山东青岛2660212 中国水产科学研究院黄海水产研究所山东青岛266071 
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中文摘要:
      摘要目的:本文旨在探讨海参精囊提取物对环磷酰胺诱导的生殖系统受损小鼠生精功能的保护作用。方法:昆明小白鼠随机分 组,除正常组用生理盐水外其他各组均腹腔注射环磷酰胺(CP,28 mg/kg),每天1 次,连续5 天,复制生殖系统受损、雄激素部分缺 乏模型;同时治疗组每天灌胃不同剂量的药物1次,连续4 周,记录小鼠的体重并观察其精神状态。计算精子总数、运动率、畸形率 及睾丸组织中T-SOD 酶活力,并与模型组进行比较。结果:相较于模型组小鼠,虽海参精囊提取物高低剂量间无明显差异(P> 0.05),但治疗组小鼠的精子总数、运动率、畸形率和T-SOD酶活力均有明显的改善(P<0.01),甚至接近或高于正常水平。结论:海 参精囊提取物对环磷酰胺导致的生殖系统受损小鼠的生精功能具有一定的保护作用。
英文摘要:
      ABSTRACT Objective:To investigate the protective effects of holothurian spermatophore extracts on spermatogenesis of the mice reproductive system injured by cyclophosphamide (CP).Methods: Male Kunming mice were equally allotted to groups, and they were intraperitoneally injected with CP (28 mg/kg) once a day for 5 days to construct injured reproductive systemand partial androgen deficiency model except that the control group were intraperitoneally injected with normal saline. Mice in treatment groups orally received extracts once a day for 4 weeks. Record the changes of body weight and sprit state. Quantity, motility rate and abnormal rate of sperm and enzyme activity of T-SOD were determined and compared with those of model group. Results:Compared with that in model group, though the dose of holothurian spermatophore extracts had no obvious difference (P>0.05), the quantity, sportive rate and abnormal rate of spermand T-SOD enzyme activity were all significantly improved (P<0.01), even close to or higher than the normal level.Conclusion: Holothurian spermatophore extracts had a protective effect on the spermatogenic lesion of reproductive systemin mice injured by CP.
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