Related Experiment Video
Updated: Aug 17, 2026

Bladder Smooth Muscle Strip Contractility as a Method to Evaluate Lower Urinary Tract Pharmacology
Published on: August 18, 2014
Activation and blockage of a calcium-sensitive cation-selective pathway in the apical membrane of toad urinary
I Aelvoet1, D Erlij, W Van Driessche
1Laboratorium voor Fysiologie, KU Leuven, Campus Gasthuisberg, Belgium.
Abstract:
1. The properties of cation movements through a previously described Ca2+-sensitive oxytocin-stimulated pathway in the apical membrane of the toad urinary bladder were further investigated. 2. In the absence of Ca2+ and other polyvalent cations in the mucosal medium, oxytocin markedly stimulated the flow of current from mucosa to serosa when the major cation in the mucosal solution was any of the following ions: Na+, K+, Rb+, Cs+ or Li+. Analysis of the current noise showed a Lorentzian component associated with the movement of these cations. 3. Ca2+ and other divalent cations in the mucosal solution depressed both the current and the Lorentzian component of the fluctuation spectra. The Michaelis-Menten constants were 2.5, 10 and 58 mumol/l for Ca2+, Sr2+ and Mg2+ respectively. 4. The dihydropyridine Ca2+ channel blockers nitrendipine (10(-5) mol/l) and nicardipine (10(-6) mol/l) inhibited the Ca2+-sensitive current. 5. Alterations of the mucosal pH showed that the current and the plateau of the Lorentzian component increased by elevating the pH from 6 to 8. The Ca2+-sensitive current was further stimulated by increasing pH to 9. However, this manoeuvre resulted in the disappearance of the Lorentzian component in the noise spectrum. 6. Increasing either mucosal [Na+] or [K+] up to 115 mmol/l did not lead to saturation of the current passing through the Ca2+-sensitive channel. In contrast the amiloride-sensitive channel showed saturating behaviour when mucosal [Na+] was increased; half-maximum current was reached when mucosal [Na+] was about 15 mmol/l. 7. When a Na+-free mucosal solution, prepared with either choline or TEA as major cation, was rapidly replaced by a solution with Na+ (115 mmol/l), the current through the Ca2+-sensitive channel increased rapidly and then remained at a nearly constant level. This behaviour is in contrast with the response of the current through the amiloride-sensitive pathway. After suddenly increasing mucosal Na+ concentration ([Na+]m), the current through this channel first increased rapidly and then declined to values of nearly 50% of the peak about 10 min after the increase in [Na+]m.(ABSTRACT TRUNCATED AT 400 WORDS)
Insights
Oxytocin stimulates cation flow through a specific channel in toad bladders, which is inhibited by calcium and dihydropyridines but not saturated by sodium or potassium. This pathway differs significantly from the amiloride-sensitive channel.
Area of Science:
- Physiology
- Membrane Transport
- Ion Channels
Background:
- Oxytocin is known to stimulate cation transport in the toad urinary bladder.
- A previously identified Ca2+-sensitive pathway in the apical membrane is investigated further.
Purpose of the Study:
- To characterize the properties of cation movements through the oxytocin-stimulated pathway.
- To compare the behavior of this pathway with the amiloride-sensitive channel.
Main Methods:
- Electrophysiological recordings of current flow and noise analysis.
- Investigation of cation (Na+, K+, Rb+, Cs+, Li+, Ca2+, Sr2+, Mg2+) effects on current.
- Use of dihydropyridine channel blockers (nitrendipine, nicardipine).
- pH-dependence studies of the mucosal solution.
Main Results:
- Oxytocin stimulated cation flow (Na+, K+, Rb+, Cs+, Li+) in the absence of Ca2+.
- Ca2+ and other divalent cations inhibited the current and reduced noise spectra, with specific Michaelis-Menten constants.
- Dihydropyridine blockers inhibited the Ca2+-sensitive current.
- Increased mucosal pH (6-9) stimulated current, but high pH abolished the noise component.
- The Ca2+-sensitive channel did not show saturation with increasing Na+ or K+, unlike the amiloride-sensitive channel.
Conclusions:
- The oxytocin-stimulated pathway exhibits distinct cation transport properties compared to the amiloride-sensitive channel.
- This pathway is sensitive to Ca2+ inhibition and dihydropyridine blockade.
- The channel's behavior suggests a different mechanism of ion permeation and regulation.
More Related Videos
Related Concept Videos
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
Antihypertensive Drugs: Action of Calcium Channel Blockers
Reabsorption and Secretion in the Loop of Henle
Physiology of the Genitourinary System II: Tubular Reabsorption and Secretion

