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用环己酰亚胺或哇巴因处理后体外培养的绵羊胚胎中纤溶酶原激活物生成的抑制作用

Suppression of plasminogen activator production in sheep embryos in vitro after treatment with cycloheximide or ouabain.

作者信息

Menino A R, Williams J S

机构信息

Department of Animal Sciences, Oregon State University, Corvallis 97331-6702.

出版信息

J Reprod Fertil. 1994 Sep;102(1):65-71. doi: 10.1530/jrf.0.1020065.

DOI:10.1530/jrf.0.1020065
PMID:7799327
Abstract

Effects of the metabolic inhibitors cycloheximide and ouabain on development in vitro and plasminogen activator production by sheep embryos were investigated. Embryos (n = 152) from the eight-cell to the morula stage were surgically collected from naturally mated, oestrus-synchronized and superovulated Polypay ewes. In Expt 1, embryos (n = 104) were grouped by cell stage, cultured in Whitten's medium with 1.5% BSA containing 0, 0.1 or 1.0 microgram cycloheximide ml-1 for 24 h, washed and cultured in this medium for 168 h. In Expt 2, morulae (n = 48) were cultured for 48 h in Whitten's medium with 1.5% BSA transferred to the same medium containing 0 or 1.0 mmol ouabain l-1 and cultured for 24 h, and then washed and cultured in this medium for 120 h. At 24 h intervals in both experiments, the medium was recovered and analysed for plasminogen activator. In Expt 1, eight-cell embryos underwent limited development; little difference in the production of plasminogen activator due to cycloheximide treatment was therefore observed. Compared with medium without cycloheximide, treatment with 1.0 microgram cycloheximide ml-1 reduced the number of 16-cell embryos (P < 0.05) and morulae (P < 0.05) (60% versus 10% and 77% versus 8%, respectively) that began to hatch. The mean production of plasminogen activator was greatest in embryos cultured initially as morulae compared with that of 16-cell and eight-cell embryos (P < 0.05). Cycloheximide treatment suppressed the mean production of plasminogen activator in a dose-dependent manner (P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了代谢抑制剂放线菌酮和哇巴因对绵羊胚胎体外发育及纤溶酶原激活物产生的影响。从自然交配、发情同步且经超数排卵处理的波利佩母羊中,通过手术采集处于八细胞至桑葚胚阶段的胚胎(n = 152)。在实验1中,将胚胎(n = 104)按细胞阶段分组,在含1.5%牛血清白蛋白的惠滕氏培养基中培养,该培养基含有0、0.1或1.0微克/毫升放线菌酮,培养24小时,然后洗涤并在此培养基中再培养168小时。在实验2中,将桑葚胚(n = 48)在含1.5%牛血清白蛋白的惠滕氏培养基中培养48小时,转移至含有0或1.0毫摩尔/升哇巴因的相同培养基中培养24小时,然后洗涤并在此培养基中再培养120小时。在两个实验中,每隔24小时收集培养基并分析纤溶酶原激活物。在实验1中,八细胞胚胎发育有限;因此未观察到放线菌酮处理对纤溶酶原激活物产生有显著差异。与不含放线菌酮的培养基相比,用1.0微克/毫升放线菌酮处理减少了开始孵化的16细胞胚胎数量(P < 0.05)和桑葚胚数量(P < 0.05)(分别为60%对10%和77%对8%)。与16细胞和八细胞胚胎相比,最初作为桑葚胚培养的胚胎中纤溶酶原激活物的平均产量最高(P < 0.05)。放线菌酮处理以剂量依赖方式抑制纤溶酶原激活物的平均产量(P < 0.05)。(摘要截断于250字)

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