Yelian F D, Dukelow W R
Endocrine Research Center, Michigan State University, East Lansing 48824.
Andrologia. 1992 May-Jun;24(3):167-70. doi: 10.1111/j.1439-0272.1992.tb02632.x.
DNA specific fluorochrome (Hoechst 33342 and 33258) as non-toxic stains, have been widely used to measure cell density and proliferation, detect sperm-egg fusion, and observe the development of pre-implantation embryos. It has been reported that Hoechst 33342 at a concentration of 10 micrograms ml-1 had significant inhibition on embryo cleavage. In this study, we incubated B6D2F1 mouse sperm and eggs with different concentrations of Hoechst 33258, 0, 1.0, 10.0, 20.0, 100 micrograms ml-1. We found that: (1) 100 micrograms ml-1 of H-33258 significantly decreased the sperm motility at 90 min and 4 h. (P less than 0.05), (2) 20 micrograms ml-1 and 100 micrograms ml-1 of Hoechst 33258 significantly inhibited mouse fertilization in vitro (P less than 0.05), and (3) 1.0 micrograms ml-1 and 10.0 micrograms ml-1 Hoechst 33258 had no effect on fertilization rate. But when we pre-incubated sperm at 10 micrograms ml-1 Hoechst 33258 for 90 min, and inseminated oocytes in the medium with same concentration of Hoechst 33258, the embryo cleavage was significantly inhibited.
DNA特异性荧光染料(Hoechst 33342和33258)作为无毒染色剂,已被广泛用于测量细胞密度和增殖、检测精卵融合以及观察植入前胚胎的发育。据报道,浓度为10微克/毫升的Hoechst 33342对胚胎分裂有显著抑制作用。在本研究中,我们将B6D2F1小鼠的精子和卵子与不同浓度的Hoechst 33258(0、1.0、10.0、20.0、100微克/毫升)一起孵育。我们发现:(1)100微克/毫升的H-33258在90分钟和4小时时显著降低精子活力(P<0.05),(2)20微克/毫升和100微克/毫升的Hoechst 33258显著抑制小鼠体外受精(P<0.05),(3)1.0微克/毫升和10.0微克/毫升的Hoechst 33258对受精率无影响。但是当我们将精子在10微克/毫升的Hoechst 33258中预孵育90分钟,并在含有相同浓度Hoechst 33258的培养基中对卵母细胞进行授精时,胚胎分裂受到显著抑制。