Neomycin inhibits histamine and thapsigargin mediated Ca2+ entry in DDT1 MF-2 cells independent of phospholipase C activation

European Journal of Pharmacology

Volumn 305, Issue 1-3, 1996, Pages 207-212

  Sipma, Henk ^a   Van Der Zee, Lucie ^a,b   Den Hertog, Adriaan ^a   Nelemans, Adriaan ^a  

^a UNIVERSITY OF GRONINGEN   (Netherlands)

^b MAASTRICHT UNIVERSITY   (Netherlands)

Author keywords

Ca2+ entry; Histamine H1 receptor; Neomycin; Phospholipase C

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); CALCIUM; CALCIUM CHANNEL; CALCIUM CHLORIDE; HISTAMINE; HISTAMINE H1 RECEPTOR; INOSITOL 1,4,5 TRISPHOSPHATE; LANTHANUM CHLORIDE; NEOMYCIN; PHOSPHOLIPASE C; PHOSPHOLIPASE C INHIBITOR; THAPSIGARGIN;

ANIMAL CELL; ARTICLE; CALCIUM CELL LEVEL; CALCIUM TRANSPORT; CELL CULTURE; CONTROLLED STUDY; DRUG INHIBITION; DRUG MECHANISM; NONHUMAN; PRIORITY JOURNAL; SMOOTH MUSCLE FIBER;

ANIMALS; ARACHIDONIC ACID; CALCIUM; CALCIUM-TRANSPORTING ATPASES; CELLS, CULTURED; CRICETINAE; ENZYME ACTIVATION; HISTAMINE; HISTAMINE H1 ANTAGONISTS; LANTHANUM; MALE; MESOCRICETUS; MUSCLE, SMOOTH; NEOMYCIN; PHOSPHOLIPASE C; PROTEIN SYNTHESIS INHIBITORS; RECEPTORS, HISTAMINE H1; THAPSIGARGIN; VAS DEFERENS;

EID: 0029950887     PISSN: 00142999     EISSN: None     Source Type: Journal    
DOI: 10.1016/0014-2999(96)00167-7     Document Type: Article

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