Related Experiment Video
Updated: Sep 9, 2026

Monitoring ER/SR Calcium Release with the Targeted Ca2+ Sensor CatchER+
Published on: May 19, 2017
Inhibition of Ca2+ current in ileal cells by cyclopiazonic acid and ryanodine
H S Gagov1, D B Duridanova, K K Boev
1Institute of Physiology, Bulgarian Academy of Sciences, Sofia.
Abstract:
The effects of cyclopiazonic acid and its combination with ryanodine on the inward Ca2+ current (ICa) were investigated in smooth muscle cells isolated from the circular layer of guinea-pig ileum. The ICa of these cells exhibited two components: a low-threshold, nicardipine (5 microM)-resistant, fast-inactivating component and a high-threshold, nicardipine-blockable and slowly inactivating component. Neither cyclopiazonic acid (up to 10 microM) nor ryanodine (10 microM) was able to affect both these components of ICa, when applied separately. Cyclopiazonic acid and ryanodine combination led to total abolishment of the high-threshold component, leaving the low-threshold component unaffected. The data presented suggest a process of Ca(2+)-dependent inactivation of the high-threshold component, elicited by an increase in the subplasmalemmal Ca2+ concentration due to Ca2+ released from the sarcoplasmic reticulum. It is considered that the combination of cyclopiazonic acid and ryanodine can be used as a valuable method to study the calcium sensitivity of both components of the ICa.
Related Concept Videos
G-Protein Gated Ion Channels
Sensory organs,...
Feedback Regulation of Calcium Concentration
Various transmembrane receptors, such as G protein-coupled receptors (GPCRs), elicit a response to extracellular signals by increasing cytosolic calcium. Activated GPCRs...
Calmodulin-dependent Signaling
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
Ligand-Gated Ion Channel Receptor: Gating Mechanism
Relaxation of Skeletal Muscles
When an action potential reaches the axon terminal, it depolarizes the membrane and opens voltage-gated sodium channels. Sodium ions enter the cell, further depolarizing the presynaptic membrane. This depolarization causes voltage-gated calcium channels to open.
Antihypertensive Drugs: Action of Calcium Channel Blockers

