Sari Youssef
Department of Pharmacology, College of Pharmacy and Pharmaceutical Sciences, University of Toledo, USA.
J Vis Exp. 2013 Apr 24(74):e50092. doi: 10.3791/50092.
Experimental designs for investigating the effects of prenatal alcohol exposure during early embryonic stages in fetal brain growth are challenging. This is mostly due to the difficulty of microdissection of fetal brains and their sectioning for determination of apoptotic cells caused by prenatal exposure to alcohol. The experiments described here provide visualized techniques from mice breeding to the identification of cell death in fetal brain tissue. This study used C57BL/6 mice as the animal model for studying fetal alcohol exposure and the role of trophic peptide against alcohol-induced apoptosis. The breeding consists of a 2-hr matting window to determine the exact stage of embryonic age. An established fetal alcohol exposure model has been used in this study to determine the effects of prenatal alcohol exposure in fetal brains. This involves free access to alcohol or pair-fed liquid diets as the sole source of nutrients for the pregnant mice. The techniques involving dissection of fetuses and microdissection of fetal brains are described carefully, since the latter can be challenging. Microdissection requires a stereomicroscope and ultra-fine forceps. Step-by-step procedures for dissecting the fetal brains are provided visually. The fetal brains are dissected from the base of the primordium olfactory bulb to the base of the metencephalon. For investigating apoptosis, fetal brains are first embedded in gelatin using a peel-away mold to facilitate their sectioning with a vibratome apparatus. Fetal brains embedded and fixed in paraformaldehyde are easily sectioned, and the free floating sections can be mounted in superfrost plus slides for determination of apoptosis or cell death. TUNEL (TdT-mediated dUTP Nick End Labeling; TdT: terminal deoxynucleotidyl transferase) assay has been used to identify cell death or apoptotic cells. It is noteworthy that apoptosis and cell-mediated cytotoxicity are characterized by DNA fragmentation. Thus, the visualized TUNEL-positive cells are indicative of cell death or apoptotic cells. The experimental designs here provide information about the use of an established liquid diet for studying the effects of alcohol and the role of neurotrophic peptides during pregnancy in fetal brains. This involves breeding and feeding pregnant mice, microdissecting fetal brains, and determining apoptosis. Together, these visual and textual techniques might be a source for investigating prenatal exposure of harmful agents in fetal brains.
研究胚胎早期阶段产前酒精暴露对胎儿大脑生长的影响,其实验设计颇具挑战性。这主要是因为对胎儿大脑进行显微解剖并切片以确定产前酒精暴露所致凋亡细胞存在困难。本文所述实验提供了从小鼠繁育到鉴定胎儿脑组织中细胞死亡的可视化技术。本研究使用C57BL/6小鼠作为动物模型,来研究胎儿酒精暴露以及营养肽对酒精诱导凋亡的作用。繁育过程包括一个2小时的交配窗口,以确定胚胎的确切年龄阶段。本研究采用了已建立的胎儿酒精暴露模型,以确定产前酒精暴露对胎儿大脑的影响。这包括让怀孕小鼠自由摄取酒精或成对喂食液体饮食作为唯一营养来源。文中详细描述了涉及胎儿解剖和胎儿大脑显微解剖的技术,因为后者颇具挑战性。显微解剖需要体视显微镜和超细镊子。文中以可视化方式提供了解剖胎儿大脑的分步程序。胎儿大脑从嗅球原基底部解剖至后脑底部。为了研究细胞凋亡,首先使用可剥离模具将胎儿大脑嵌入明胶中,以便用振动切片机进行切片。嵌入并固定在多聚甲醛中的胎儿大脑很容易切片,游离的切片可以安装在超低温载玻片上,用于确定细胞凋亡或细胞死亡。已使用TUNEL(TdT介导的dUTP缺口末端标记;TdT:末端脱氧核苷酸转移酶)检测法来鉴定细胞死亡或凋亡细胞。值得注意的是,细胞凋亡和细胞介导的细胞毒性以DNA片段化为特征。因此,可视化的TUNEL阳性细胞表明细胞死亡或凋亡细胞。这里的实验设计提供了有关使用既定液体饮食来研究酒精影响以及神经营养肽在孕期对胎儿大脑作用的信息。这包括繁育和喂养怀孕小鼠、显微解剖胎儿大脑以及确定细胞凋亡。总之,这些可视化和文字技术可能是研究胎儿大脑产前暴露于有害物质的一个来源。