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Neurochem Res ; 25(12): 1629-35, 2000 Dec.
Article in English | MEDLINE | ID: mdl-11152392

ABSTRACT

The characteristics of the inhibitory effect of calcium ion (Ca2+)/calmodulin (CaM) on specific [125I]-omega-conotoxin GVIA (125I-omega-CTX) binding and on the labeling of 125I-omega-CTX to crude membranes from chick brain were investigated. The inhibitory effect of Ca2+/CaM depended on the concentrations of free Ca2+ and CaM. The IC50 values for free Ca2+ and CaM were about 2.0 x 10(-8) M and 3.0 microg protein/ml, respectively. The inhibitory effect of Ca2+/CaM was attenuated by the CaM antagonists W-7, prenylamine and CaM-kinase II fragment (290-309), but not by the calcineurin inhibitor FK506. Ca2+/CaM also inhibited the labeling of a 135-kDa band (which was considered to be part of N-type Ca2+ channel alpha1 subunits) with 125I-omega-CTX using a cross-linker. These results suggest that Ca2+/CaM affects specific 125I-omega-CTX binding sites, probably N-type Ca2+ channel alpha1 subunits, in crude membranes from chick whole brain.


Subject(s)
Brain/metabolism , Calcium Channel Blockers/metabolism , Calmodulin/pharmacology , omega-Conotoxin GVIA/antagonists & inhibitors , Animals , Animals, Newborn , Calcium/metabolism , Calcium Channels, N-Type/drug effects , Calcium Channels, N-Type/metabolism , Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitors , Calcium-Calmodulin-Dependent Protein Kinases/pharmacology , Calmodulin/antagonists & inhibitors , Chickens , Enzyme Inhibitors/pharmacology , Iodine Radioisotopes , Isoenzymes/pharmacology , Male , Membranes/metabolism , Peptide Fragments/pharmacology , Prenylamine/pharmacology , Rats , Rats, Wistar , Sulfonamides/pharmacology
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