Human Foetal Neuroblasts Exhibit BK Channel-Dependent Membrane Voltage Oscillations upon Depolarization. [PDF]
Primary cultures of neuroblasts isolated from the nucleus basalis of Meynert of 12‐weeks‐old human foetuses were prepared. Whole‐cell patch‐clamp recordings were performed by injecting a depolarizing stimulus current (+500 pA; 500 ms), and the membrane voltage recorded; this stimulus current evoked periodic‐like oscillations in membrane voltage ...
Coppi E +9 more
europepmc +2 more sources
Ginsenoside Re increases human coronary artery endothelial SKCa current and nitric oxide release via glucocorticoid receptor-PI3K-Akt/PKB pathway [PDF]
Background: Ginsenoside Re (Re) has been shown to activate small-conductance calcium-activated potassium (SKCa) current in human coronary artery endothelial cells (HCAECs).
Kitinat Rodthongdee +6 more
doaj +2 more sources
Colchicine alters apamin receptors, electrical activity, and skeletal muscle relaxation [PDF]
A low conductance calcium‐activated K+ channel is thought to regulate the rate of firing of several excitable cells. In skeletal muscle the expression of this channel is under nerve control. Previously, we reported that axonal flow blockade of rat nerves,
Behrens Pellegrino, María Isabel +2 more
core +2 more sources
Apamin-Conjugated Alendronate Sodium Nanocomplex for Management of Pancreatic Cancer
Pancreatic cancer has a low survival rate and has limited therapeutic options due to the peculiarity of the tumor tissue. Cancer nanotechnology provides several opportunities to resolve such difficulties as a result of the high surface-to-volume ratio of
Nabil A. Alhakamy +3 more
doaj +1 more source
A proposal for the structure of apamin [PDF]
Apamin is an octadecapeptide neurotoxin present in bee venom. It acts both centrally and peripherally, binding specifically to a protein in rat forebrain with high affinity (Kd 10-l’ M) [l] and acting as a potent noncompetitive inhibitor of a-adrenergic and purinergic agonists [2].
Hider, R.C., Ragnarsson, U.
openaire +2 more sources
The relationship between functional inhibition and binding for K(Ca)2 channel blockers. [PDF]
Small conductance calcium-activated potassium channels (KCa2.1,2.2,2.3) are blocked with high affinity by both peptide toxins (e.g. apamin) and small molecule blockers (e.g. UCL 1848). In electrophysiological experiments, apamin shows subtype selectivity
David Charles Hammond Benton +2 more
doaj +1 more source
EDNRB-dependent endothelin signaling reduces proliferation and promotes proneural-to-mesenchymal transition in gliomas. [PDF]
Glioma cells mainly express the endothelin receptor EDNRB, while EDNRA is restricted to a perivascular tumor subpopulation. Endothelin signaling reduces glioma cell proliferation while promoting migration and a proneural‐to‐mesenchymal transition associated with poor prognosis. This pathway activates Ca2+, K+, ERK, and STAT3 signalings and is regulated
Pineau D +36 more
europepmc +2 more sources
Sinus pacemaking is based on tight cooperation of intracellular Ca2+ handling and surface membrane ion channels. An important player of this synergistic crosstalk could be the small-conductance Ca2+-activated K+-channel (ISK) that could contribute to the
Gergő Bitay +6 more
doaj +1 more source
Inhibition of Small-Conductance, Ca2+-Activated K+ Current by Ondansetron
Background: Small-conductance Ca2+-activated K+ channels (SK channels) have been proposed as antiarrhythmic targets for the treatment of atrial fibrillation.
Shuai Guo +4 more
doaj +1 more source
Allosteric Block of KCa2 Channels by Apamin [PDF]
Activation of small conductance calcium-activated potassium (K(Ca)2) channels can regulate neuronal firing and synaptic plasticity. They are characterized by their high sensitivity to the bee venom toxin apamin, but the mechanism of block is not understood.
Lamy, Cédric +6 more
openaire +2 more sources

