Neuroprotective peptide ADNF-9 in fetal brain of C57BL/6 mice exposed prenatally to alcohol

被引:4
|
作者
Sari, Youssef [1 ]
Segu, Zaneer M. [2 ]
YoussefAgha, Ahmed [3 ]
Karty, Jonathan A. [2 ]
Isailovic, Dragan [4 ]
机构
[1] Univ Toledo, Coll Pharm & Pharmaceut Sci, Dept Pharmacol, Toledo, OH 43606 USA
[2] Indiana Univ, Dept Chem, Bloomington, IN USA
[3] Indiana Univ, Dept Appl Hlth Sci, Bloomington, IN 47405 USA
[4] Univ Toledo, Dept Chem, Toledo, OH 43606 USA
关键词
DEPENDENT NEUROTROPHIC FACTOR; ETHANOL EXPOSURE; HISTONE ACETYLATION; BASAL GANGLIA; GROWTH; CHILDREN; DECREASE; DEFICITS; NEURONS; PROTEIN;
D O I
10.1186/1423-0127-18-77
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: A derived peptide from activity-dependent neurotrophic factor (ADNF-9) has been shown to be neuroprotective in the fetal alcohol exposure model. We investigated the neuroprotective effects of ADNF-9 against alcohol-induced apoptosis using TUNEL staining. We further characterize in this study the proteomic architecture underlying the role of ADNF-9 against ethanol teratogenesis during early fetal brain development using liquid chromatography in conjunction with tandem mass spectrometry (LC-MS/MS). Methods: Pregnant C57BL/6 mice were exposed from embryonic days 7-13 (E7-E13) to a 25% ethanol-derived calorie [25% EDC, Alcohol (ALC)]diet, a 25% EDC diet simultaneously administered i.p. ADNF-9 (ALC/ADNF-9), or a pair fed (PF) liquid diet. At E13, fetal brains were collected from 5 dams from each group, weighed, and frozen for LC-MS/MS procedure. Other fetal brains were fixed for TUNEL staining. Results: Administration of ADNF-9 prevented alcohol-induced reduction in fetal brain weight and alcohol-induced increases in cell death. Moreover, individual fetal brains were analyzed by LC-MS/MS. Statistical differences in the amounts of proteins between the ALC and ALC/ADNF-9 groups resulted in a distinct data-clustering. Significant upregulation of several important proteins involved in brain development were found in the ALC/ADNF-9 group as compared to the ALC group. Conclusion: These findings provide information on potential mechanisms underlying the neuroprotective effects of ADNF-9 in the fetal alcohol exposure model.
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页数:12
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