Inhibition of human α1E subunit-mediated Ca2+ channels by the antipsychotic agent chlorpromazine

Acta Physiologica Scandinavica

Volumn 173, Issue 4, 2001, Pages 401-408

  McNaughton, N C L ^a   Green, P J ^a   Randall, A D ^a  

^a GLAXOSMITHKLINE   (United Kingdom)

Author keywords

Electrophysiology; Patch clamp; Pharmacology; Recombinant channel; Voltage gated calcium channel

Indexed keywords

CALCIUM CHANNEL; CHLORPROMAZINE; NEUROLEPTIC AGENT; CACNA1E PROTEIN, HUMAN; CALCIUM CHANNEL R TYPE; CATION TRANSPORT PROTEIN;

ARTICLE; CALCIUM CURRENT; CONCENTRATION RESPONSE; CONTROLLED STUDY; DRUG MECHANISM; HUMAN; HUMAN CELL; IC 50; MEMBRANE POTENTIAL; NERVE CELL; PRIORITY JOURNAL; CELL LINE; CELL MEMBRANE POTENTIAL; CHANNEL GATING; CYTOLOGY; DOSE RESPONSE; DRUG EFFECT; GENETIC TRANSFECTION; GENETICS; KIDNEY; METABOLISM; PATCH CLAMP;

ANTIPSYCHOTIC AGENTS; CALCIUM CHANNELS; CALCIUM CHANNELS, R-TYPE; CATION TRANSPORT PROTEINS; CELL LINE; CHLORPROMAZINE; DOSE-RESPONSE RELATIONSHIP, DRUG; HUMANS; ION CHANNEL GATING; KIDNEY; MEMBRANE POTENTIALS; PATCH-CLAMP TECHNIQUES; TRANSFECTION;

EID: 0035544091     PISSN: 00016772     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-201X.2001.00914.x     Document Type: Article

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