Selective inhibition of M-type potassium channels in rat sympathetic neurons by uridine nucleotide preferring receptors

British Journal of Pharmacology

Volumn 124, Issue 6, 1998, Pages 1261-1269

  Boehm, Stefan ^a  

^a UNIVERSITY OF VIENNA   (Austria)

Author keywords

GTP binding protein; M currents; P2Y receptor; Rat sympathetic neurons; UDP; UTP

Indexed keywords

ADENOSINE DIPHOSPHATE; ADENOSINE TRIPHOSPHATE; AMPHOTERICIN B; CALCIUM ION; CIBACRON BLUE F3GA; GUANOSINE DIPHOSPHATE; GUANOSINE TRIPHOSPHATE; MUSCARINIC AGENT; OXOTREMORINE M; POTASSIUM CHANNEL; POTASSIUM ION; PURINE P2Y RECEPTOR; PYRIDOXAL 5 PHOSPHATE; URIDINE; URIDINE DIPHOSPHATE; URIDINE TRIPHOSPHATE;

ANIMAL TISSUE; ARTICLE; CALCIUM CURRENT; CONTROLLED STUDY; NONHUMAN; POTASSIUM CURRENT; PRIORITY JOURNAL; RAT; SYMPATHETIC NERVE CELL;

ADENINE NUCLEOTIDES; ANIMALS; CALCIUM CHANNELS; GUANINE NUCLEOTIDES; HYDROLYSIS; ION CHANNEL GATING; NEURONS; POTASSIUM CHANNEL BLOCKERS; PYRIDOXAL PHOSPHATE; RATS; RATS, SPRAGUE-DAWLEY; RECEPTORS, CELL SURFACE; SURAMIN; SYMPATHETIC NERVOUS SYSTEM; TRIAZINES; URIDINE DIPHOSPHATE; URIDINE TRIPHOSPHATE;

EID: 0031856981     PISSN: 00071188     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.bjp.0701956     Document Type: Article

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