Hepcidin treatment modulates the expression of divalent metal transporter-1, ceruloplasmin, and ferroportin-1 in the rat cerebral cortex and hippocampus

Biological Trace Element Research

Volumn 143, Issue 3, 2011, Pages 1581-1593

  Li, Lin ^a   Holscher, Christian ^b   Chen, Bing Bing ^a   Zhang, Zhi Feng ^a   Liu, Yue Ze ^a  

^a SHANXI MEDICAL UNIVERSITY   (China)

^b UNIVERSITY OF ULSTER   (United Kingdom)

Author keywords

Alzheimer's disease; Iron uptake; Neurodegeneration; Neurotoxicity; Parkinson's disease

Indexed keywords

CERULOPLASMIN; FERROPORTIN 1; HEPCIDIN; IRON; MESSENGER RNA; NATURAL RESISTANCE ASSOCIATED MACROPHAGE PROTEIN 2;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BRAIN CORTEX; BRAIN LEVEL; CONTROLLED STUDY; GENE EXPRESSION; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; MALE; NONHUMAN; POLYMERASE CHAIN REACTION; PROTEIN DETERMINATION; PROTEIN EXPRESSION; PROTEIN LOCALIZATION; PROTEIN MODIFICATION; PROTEIN PROTEIN INTERACTION; QUANTITATIVE ANALYSIS; RAT; REGULATORY MECHANISM; RNA ANALYSIS;

ANIMALS; ANTIMICROBIAL CATIONIC PEPTIDES; BASE SEQUENCE; CATION TRANSPORT PROTEINS; CEREBRAL CORTEX; CERULOPLASMIN; DNA PRIMERS; HIPPOCAMPUS; IMMUNOHISTOCHEMISTRY; MALE; POLYMERASE CHAIN REACTION; RATS; RATS, WISTAR; RNA, MESSENGER;

RATTUS;

EID: 82455192361     PISSN: 01634984     EISSN: 15590720     Source Type: Journal    
DOI: 10.1007/s12011-011-8967-3     Document Type: Article

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