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.
引用
收藏
页数:12
相关论文
共 50 条
  • [41] Vitamin E as a treatment for ulcerative dermatitis in C57BL/6 mice and strains with a C57BL/6 background
    Lawson, GW
    Sato, A
    Fairbanks, LA
    Lawson, PT
    CONTEMPORARY TOPICS IN LABORATORY ANIMAL SCIENCE, 2005, 44 (03): : 18 - 21
  • [42] Hybrid C57BL/6J x FVB/NJ mice drink more alcohol than do C57BL/6J mice
    Blednov, YA
    Metten, P
    Finn, DA
    Rhodes, JS
    Bergeson, SE
    Harris, RA
    Crabbe, JC
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (11) : 1949 - 1958
  • [43] Supplementing the liquid alcohol diet with chow enhances alcohol intake in C57BL/6 mice
    Anji, Antje
    Kumari, Meena
    DRUG AND ALCOHOL DEPENDENCE, 2008, 97 (1-2) : 86 - 93
  • [44] Cocaine concentrations in fetal C57BL/6 mouse brain relative to maternal brain and plasma
    Miller, SR
    Middaugh, LD
    Boggan, WO
    Patrick, KS
    NEUROTOXICOLOGY AND TERATOLOGY, 1996, 18 (06) : 645 - 649
  • [45] Gender influences infectivity in C57BL/6 mice exposed to mouse minute virus
    Thomas, Marvin L., III
    Morse, Brent C.
    O'Malley, James
    Davis, Judith A.
    St Claire, Mark B.
    Cole, Marlene N.
    COMPARATIVE MEDICINE, 2007, 57 (01) : 74 - 81
  • [46] ALCOHOL-PREFERRING AND ALCOHOL-AVOIDING C57BL MICE
    POLEY, W
    BEHAVIOR GENETICS, 1972, 2 (2-3) : 245 - 248
  • [47] ALCOHOL INDUCED FACIAL DYSMORPHOLOGY IN C57BL/6 MOUSE MODELS OF FETAL ALCOHOL SPECTRUM DISORDER
    Anthony, B.
    Vinci-Booher, S.
    Wetherill, L. F.
    Ward, R.
    Goodlett, C.
    Zhou, F. C.
    ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2009, 33 (06) : 130A - 130A
  • [48] Early Blood Profile of C57BL/6 Mice Exposed to Chronic Unpredictable Stress
    McDonald, Lindsay T.
    Lopez, Marcelo F.
    Helke, Kristi L.
    McCrackin, M. A.
    Cray, James J., Jr.
    Becker, Howard C.
    LaRue, Amanda C.
    FRONTIERS IN PSYCHIATRY, 2019, 10
  • [49] HETEROGENEITY OF BRAIN-REACTIVE AUTOANTIBODIES IN AGING C57BL/6 MICE
    MALLICK, S
    LUEDTKE, RL
    FORSTER, MJ
    LAL, H
    FASEB JOURNAL, 1993, 7 (03): : A55 - A55
  • [50] Spontaneous Incidental Brain Lesions in C57BL/6J Mice
    Tarrant, James C.
    Savickas, Patrick
    Omodho, Lorna
    Spinazzi, Marco
    Radaelli, Enrico
    VETERINARY PATHOLOGY, 2020, 57 (01) : 172 - 182