AbstractPalytoxin (PTX) caused K+ release from rabbit erythrocytes at a concentration as low as 10−11 M. The K+ release due to PTX at a concentration below 10−9 M was dependent on Ca2+ in medium. The effect of Ca2+ was substituted fully by Sr2+ and partially by Ba2+. W-7 (2 × 10−4 M), a known inhibitor of calmodulin, markedly inhibited the rate of K+ release due to PTX. W-5 (2 × 10−4 M), an analog of W-7 with lower affinity to calmodulin than W-7, showed weaker inhibition. Other calmodulin antagonists, such as prenylamine, chlorpromazine and compound 4880, also inhibited the PTX-induced K+ release. These results suggest that the K+ release induced by PTX involves the process(es) mediated by intracellular Ca2+ and calmodulin
AbstractThree calmodulin (CM) antagonists W-7, W-5, and trifluoperazine (TFP) were tested for abilit...
AbstractLow concentrations of the calmodulin antagonist W-7 (1-1μM) enhanced the respiratory burst (...
The calmodulin-binding properties of the rabbit skeletal muscle Ca2+ release channel (ryanodine rece...
AbstractPalytoxin (PTX) caused K+ release from rabbit erythrocytes which was dependent on the concen...
AbstractThe concentration of cytosolic free calcium was monitored in suspensions of intact human neu...
AbstractPatch-clamp recordings were performed to study the effects of three calmodulin (CaM) antagon...
A channel open on the membrane can be formed by palytoxin (PTX). Ten nanomolar PTX caused an irrever...
AbstractPalytoxin (PTX), a highly toxic and sugar-containing substance isolated from Palythoa tuberc...
1. The effects of the calmodulin antagonists, calmidazolium and fendiline were investigated on endot...
The nervous tissue-specific protein B-50 (GAP-43), which has been implicated in the regulation of ne...
Potassium channels are a diverse class of membrane proteins found in virtually all cells. The first ...
(1980). Plasma membranes prepared from human red blood cells exhibit a Ca2tactivated, Mg2t dependent...
AbstractPolymyxin B (PXB), a cyclic peptide antibiotic, in concentrations 0.1–3.0 mg/ml (0.08–4.0 mm...
Ca- and Mg-ATPase activity was measured in crude homogenates and in a subcellular particulate fracti...
To investigate whether potassium channels are involved in the signal transduction mechanisms of anti...
AbstractThree calmodulin (CM) antagonists W-7, W-5, and trifluoperazine (TFP) were tested for abilit...
AbstractLow concentrations of the calmodulin antagonist W-7 (1-1μM) enhanced the respiratory burst (...
The calmodulin-binding properties of the rabbit skeletal muscle Ca2+ release channel (ryanodine rece...
AbstractPalytoxin (PTX) caused K+ release from rabbit erythrocytes which was dependent on the concen...
AbstractThe concentration of cytosolic free calcium was monitored in suspensions of intact human neu...
AbstractPatch-clamp recordings were performed to study the effects of three calmodulin (CaM) antagon...
A channel open on the membrane can be formed by palytoxin (PTX). Ten nanomolar PTX caused an irrever...
AbstractPalytoxin (PTX), a highly toxic and sugar-containing substance isolated from Palythoa tuberc...
1. The effects of the calmodulin antagonists, calmidazolium and fendiline were investigated on endot...
The nervous tissue-specific protein B-50 (GAP-43), which has been implicated in the regulation of ne...
Potassium channels are a diverse class of membrane proteins found in virtually all cells. The first ...
(1980). Plasma membranes prepared from human red blood cells exhibit a Ca2tactivated, Mg2t dependent...
AbstractPolymyxin B (PXB), a cyclic peptide antibiotic, in concentrations 0.1–3.0 mg/ml (0.08–4.0 mm...
Ca- and Mg-ATPase activity was measured in crude homogenates and in a subcellular particulate fracti...
To investigate whether potassium channels are involved in the signal transduction mechanisms of anti...
AbstractThree calmodulin (CM) antagonists W-7, W-5, and trifluoperazine (TFP) were tested for abilit...
AbstractLow concentrations of the calmodulin antagonist W-7 (1-1μM) enhanced the respiratory burst (...
The calmodulin-binding properties of the rabbit skeletal muscle Ca2+ release channel (ryanodine rece...