Dopamine depletion induced up-regulation of HCN3 enhances rebound excitability of basal ganglia output neurons

Neurobiology of Disease

Volumn 34, Issue 1, 2009, Pages 178-188

  Meurers, Bernhard H ^a,b   Dziewczapolski, Gustavo ^c   Bittner, Anton ^b   Shi, Tao ^b   Kamme, Fredrik ^b   Shults, Clifford W ^c  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b JOHNSON AND JOHNSON PHARMACEUTICAL RESEARCH AND DEVELOPMENT   (United States)

^c UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Basal ganglia; Entopeduncular nucleus; HCN3; Microarray; Parkinson's disease; Rebound excitability

Indexed keywords

CATION CHANNEL; DOPAMINE; HYPERPOLARIZATION ACTIVATED CYCLIC NUCLEOTIDE GATED CATION CHANNEL 3; MESSENGER RNA; UNCLASSIFIED DRUG;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BASAL GANGLION; CONTROLLED STUDY; MALE; MOUSE; NERVE CELL; NERVE CELL EXCITABILITY; NONHUMAN; PARKINSON DISEASE; PRIORITY JOURNAL; PROTEIN EXPRESSION; RAT; UPREGULATION;

ANIMALS; BASAL GANGLIA; CYCLIC NUCLEOTIDE-GATED CATION CHANNELS; DISEASE MODELS, ANIMAL; DOPAMINE; GENE EXPRESSION; MALE; MEMBRANE POTENTIALS; MICE; MICE, INBRED C57BL; NEURONS; OXIDOPAMINE; PARKINSONIAN DISORDERS; POTASSIUM CHANNELS; PYRIMIDINES; RATS; RATS, SPRAGUE-DAWLEY; RNA, MESSENGER; UP-REGULATION;

EID: 62149142458     PISSN: 09699961     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.nbd.2009.01.007     Document Type: Article

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