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着床前期暴露于乙醇的体外受精小鼠胚胎的发育:亚毒性水平下胚胎发育加速。

Development of in vitro fertilized mouse embryos exposed to ethanol during the preimplantation period: accelerated embryogenesis at subtoxic levels.

作者信息

Leach R E, Stachecki J J, Armant D R

机构信息

C.S. Mott Center for Human Growth and Development, Department of Obstetrics and Gynecology, Wayne State University School of Medicine, Detroit, Michigan 48201.

出版信息

Teratology. 1993 Jan;47(1):57-64. doi: 10.1002/tera.1420470110.

Abstract

This study examined the effects of ethanol (EtOH) on mouse preimplantation development using an in vitro culture method. Embryos at the 1-cell, 2-cell, or 4-cell stage were exposed for 24 h to medium containing EtOH, then further cultured without EtOH to determine their ability to form blastocysts and to eventually hatch from the zona pellucida. EtOH exposure either arrested or enhanced normal development, depending on dose and embryonic stage of exposure. Exposure of 1-cell and 2-cell embryos to 1.6% (w/v) EtOH decreased blastocyst formation and hatching, and exposure of 1-cell embryos to 0.4% EtOH inhibited their development. At 0.1%, EtOH had an opposite effect, causing an increase in the percent blastocyst formation of treated 1-cell and 2-cell embryos. Neither inhibition nor stimulation of blastocyst formation occurred in 4-cell embryos exposed to 0.1-1.6% EtOH. Using an in vitro outgrowth model of implantation, embryos that reached the blastocyst stage were further tested for their ability to produce differentiated trophoblast cells. Blastocysts previously exposed to 0.1% EtOH during the 1-cell stage appeared to form adhesive trophoblasts earlier than control embryos, indicating that EtOH exposure can induce precocious differentiation of the trophoblast cells. The EtOH treated blastocysts contained significantly more cells than control blastocysts. These results indicate that EtOH can alter preimplantation development by either inhibiting or accelerating cell growth and differentiation.

摘要

本研究采用体外培养方法,检测了乙醇(EtOH)对小鼠植入前胚胎发育的影响。将1细胞、2细胞或4细胞阶段的胚胎暴露于含乙醇的培养基中24小时,然后在无乙醇的条件下进一步培养,以确定其形成囊胚并最终从透明带孵化的能力。乙醇暴露对正常发育的影响取决于剂量和暴露时的胚胎阶段,可能会阻止或促进正常发育。将1细胞和2细胞胚胎暴露于1.6%(w/v)乙醇中会降低囊胚形成率和孵化率,而将1细胞胚胎暴露于0.4%乙醇中会抑制其发育。在0.1%时,乙醇产生相反的效果,使处理过的1细胞和2细胞胚胎的囊胚形成率增加。暴露于0.1 - 1.6%乙醇中的4细胞胚胎,其囊胚形成既未受到抑制也未受到刺激。利用植入的体外生长模型,对发育到囊胚阶段的胚胎进一步检测其产生分化滋养层细胞的能力。在1细胞阶段曾暴露于0.1%乙醇的囊胚,似乎比对照胚胎更早形成黏附性滋养层,这表明乙醇暴露可诱导滋养层细胞早熟分化。经乙醇处理的囊胚所含细胞明显多于对照囊胚。这些结果表明,乙醇可通过抑制或加速细胞生长与分化来改变植入前胚胎发育。

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