Tonic dopamine inhibition of L-type Ca2+ channel activity reduces α(1D) Ca2+ channel gene expression

Journal of Neuroscience

Volumn 19, Issue 9, 1999, Pages 3345-3352

  Fass, Daniel M ^a,c   Takimoto, Koichi ^a   Mains, Richard E ^b   Levitan, Edwin S ^a  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

D2 receptor; Dopamine; Haloperidol; L type Ca2+ channel; Melanotrope; Nimodipine; Quinpirole

Indexed keywords

BROMOCRIPTINE; BUCLADESINE; CALCIUM CHANNEL; CALCIUM ION; DOPAMINE 2 RECEPTOR; HALOPERIDOL; ION CHANNEL; MESSENGER RNA; NIMODIPINE; OMEGA AGATOXIN IVA; OMEGA CONOTOXIN MVIIC; QUINPIROLE;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; DOPAMINERGIC TRANSMISSION; DOWN REGULATION; GENE EXPRESSION REGULATION; INTRAPERITONEAL DRUG ADMINISTRATION; ION CURRENT; NEUROTRANSMISSION; NONHUMAN; PRIORITY JOURNAL;

EID: 0033135809     PISSN: 02706474     EISSN: None     Source Type: Journal    
DOI: 10.1523/jneurosci.19-09-03345.1999     Document Type: Article

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