Stepholidine protects against H2O2 neurotoxicity in rat cortical neurons by activation of Akt

Neuroscience Letters

Volumn 383, Issue 3, 2005, Pages 328-332

  Zhang, Lei ^a   Zhou, Rulun ^a   Xiang, Guoqiang ^a  

^a UNIFORMED SERVICES UNIVERSITY OF THE HEALTH SCIENCES   (United States)

Author keywords

PI3 K Akt; SPD; SZ

Indexed keywords

2 MORPHOLINO 8 PHENYLCHROMONE; HYDROGEN PEROXIDE; PHOSPHATIDYLINOSITOL 3 KINASE; PROTEIN KINASE B; PROTEIN SERINE THREONINE KINASE; STEPHOLIDINE; 2,3,4,5 TETRAHYDRO 7,8 DIHYDROXY 1 PHENYL 1H 3 BENZAZEPINE; 2-(4-MORPHOLINYL)-8-PHENYL-4H-1-BENZOPYRAN-4-ONE; AKT1 PROTEIN, RAT; BERBERINE; CHROMONE DERIVATIVE; DOPAMINE RECEPTOR BLOCKING AGENT; DRUG DERIVATIVE; ENZYME INHIBITOR; HALOPERIDOL; MORPHOLINE DERIVATIVE; NEUROPROTECTIVE AGENT; ONCOPROTEIN; SK&F 83566;

ANIMAL CELL; APOPTOSIS; ARTICLE; BRAIN CELL; CELL DEATH; CELL SURVIVAL; CONTROLLED STUDY; ENZYME ACTIVATION; ENZYME INHIBITION; EXCITOTOXICITY; IMMUNOCYTOCHEMISTRY; NERVE CELL CULTURE; NEUROPROTECTION; NEUROTOXICITY; NONHUMAN; PRIORITY JOURNAL; PROTEIN PHOSPHORYLATION; PROTEIN SYNTHESIS INHIBITION; RAT; WESTERN BLOTTING; ANIMAL; CELL COUNT; CELL CULTURE; COMPARATIVE STUDY; CYTOLOGY; DOSE RESPONSE; DRUG EFFECT; DRUG INTERACTION; GENE EXPRESSION REGULATION; METABOLISM; METHODOLOGY; NERVE CELL; PHYSIOLOGY; PREFRONTAL CORTEX; TIME;

2,3,4,5-TETRAHYDRO-7,8-DIHYDROXY-1-PHENYL-1H-3-BENZAZEPINE; ANIMALS; BERBERINE; BLOTTING, WESTERN; CELL COUNT; CELL DEATH; CELLS, CULTURED; CHROMONES; DOPAMINE ANTAGONISTS; DOSE-RESPONSE RELATIONSHIP, DRUG; DRUG INTERACTIONS; ENZYME INHIBITORS; GENE EXPRESSION REGULATION; HALOPERIDOL; HYDROGEN PEROXIDE; MORPHOLINES; NEURONS; NEUROPROTECTIVE AGENTS; PREFRONTAL CORTEX; PROTEIN-SERINE-THREONINE KINASES; PROTO-ONCOGENE PROTEINS; PROTO-ONCOGENE PROTEINS C-AKT; RATS; TIME FACTORS;

EID: 20444408385     PISSN: 03043940     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neulet.2005.04.016     Document Type: Article

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