Literature DB >> 23644584

Experimental methods for testing the effects of neurotrophic peptide, ADNF-9, against alcohol-induced apoptosis during pregnancy in c57bl/6 mice.

Youssef Sari1.   

Abstract

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.

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Year:  2013        PMID: 23644584      PMCID: PMC3667573          DOI: 10.3791/50092

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  13 in total

1.  Complete sequence of a novel protein containing a femtomolar-activity-dependent neuroprotective peptide.

Authors:  M Bassan; R Zamostiano; A Davidson; A Pinhasov; E Giladi; O Perl; H Bassan; C Blat; G Gibney; G Glazner; D E Brenneman; I Gozes
Journal:  J Neurochem       Date:  1999-03       Impact factor: 5.372

2.  Activity-dependent neurotrophic factor: structure-activity relationships of femtomolar-acting peptides.

Authors:  D E Brenneman; J Hauser; E Neale; S Rubinraut; M Fridkin; A Davidson; I Gozes
Journal:  J Pharmacol Exp Ther       Date:  1998-05       Impact factor: 4.030

3.  A femtomolar-acting neuroprotective peptide.

Authors:  D E Brenneman; I Gozes
Journal:  J Clin Invest       Date:  1996-05-15       Impact factor: 14.808

4.  Prevention of fetal demise and growth restriction in a mouse model of fetal alcohol syndrome.

Authors:  C Y Spong; D T Abebe; I Gozes; D E Brenneman; J M Hill
Journal:  J Pharmacol Exp Ther       Date:  2001-05       Impact factor: 4.030

5.  VIP and peptides related to activity-dependent neurotrophic factor protect PC12 cells against oxidative stress.

Authors:  R A Steingart; B Solomon; D E Brenneman; M Fridkin; I Gozes
Journal:  J Mol Neurosci       Date:  2000-12       Impact factor: 3.444

6.  Differential expression of proteins in fetal brains of alcohol-treated prenatally C57BL/6 mice: a proteomic investigation.

Authors:  Youssef Sari; Min Zhang; Yehia Mechref
Journal:  Electrophoresis       Date:  2010-01       Impact factor: 3.535

7.  Vasoactive intestinal peptide (VIP) prevents neurotoxicity in neuronal cultures: relevance to neuroprotection in Parkinson's disease.

Authors:  D Offen; Y Sherki; E Melamed; M Fridkin; D E Brenneman; I Gozes
Journal:  Brain Res       Date:  2000-01-31       Impact factor: 3.252

8.  Cloning and characterization of the human activity-dependent neuroprotective protein.

Authors:  R Zamostiano; A Pinhasov; E Gelber; R A Steingart; E Seroussi; E Giladi; M Bassan; Y Wollman; H J Eyre; J C Mulley; D E Brenneman; I Gozes
Journal:  J Biol Chem       Date:  2001-01-05       Impact factor: 5.157

9.  Activity-dependent neuroprotective protein-derived peptide, NAP, preventing alcohol-induced apoptosis in fetal brain of C57BL/6 mouse.

Authors:  Y Sari
Journal:  Neuroscience       Date:  2008-11-21       Impact factor: 3.590

10.  A novel peptide, colivelin, prevents alcohol-induced apoptosis in fetal brain of C57BL/6 mice: signaling pathway investigations.

Authors:  Y Sari; T Chiba; M Yamada; G V Rebec; S Aiso
Journal:  Neuroscience       Date:  2009-09-25       Impact factor: 3.590

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