Prenatal exposure to heroin in mice elicits memory deficits that can be attributed to neuronal apoptosis

Neuroscience

Volumn 160, Issue 2, 2009, Pages 330-338

  Wang, Y ^a   Han, T Z ^a  

^a BEIJING UNIVERSITY OF POSTS AND TELECOMMUNICATIONS   (China)

Author keywords

Bax; Bcl 2; caspase 3; heroin; prenatal exposure

Indexed keywords

CASPASE 2; DIAMORPHINE; PROTEIN BAX; PROTEIN BCL 2; SODIUM CHLORIDE;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CONTROLLED STUDY; DENTATE GYRUS; ENZYME ACTIVATION; FEMALE; HIPPOCAMPUS; LEARNING DISORDER; MEMORY DISORDER; MOUSE; NERVE CELL; NONHUMAN; PRENATAL EXPOSURE; PRIORITY JOURNAL; PROTEIN EXPRESSION;

ANALYSIS OF VARIANCE; ANIMALS; APOPTOSIS; APOPTOSIS REGULATORY PROTEINS; BCL-2-ASSOCIATED X PROTEIN; CASPASE 3; FEMALE; HEROIN; HIPPOCAMPUS; MATERNAL EXPOSURE; MAZE LEARNING; MEMORY; MICE; MICE, INBRED BALB C; NARCOTICS; NEURONS; PREGNANCY; PRENATAL EXPOSURE DELAYED EFFECTS; PROTO-ONCOGENE PROTEINS C-BCL-2; REACTION TIME; RNA, MESSENGER; SPATIAL BEHAVIOR; STATISTICS, NONPARAMETRIC;

EID: 64449086186     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2009.02.058     Document Type: Article

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