Related Experiment Videos
Cyclic nucleotide-activated channels in carp olfactory receptor cells
S S Kolesnikov1, A V Kosolapov
1Institute of Cell biophysics, Russian Academy of Sciences, Pushchino (Russian Federation).
Biochimica Et Biophysica Acta
|July 25, 1993
Summary
Cyclic nucleotides like cAMP and cGMP increase ion permeability in carp olfactory neuron membranes. These cyclic nucleotide-dependent channels show weak selectivity and are blocked by divalent cations.
Area of Science:
- Neuroscience
- Molecular Biology
- Ion Channel Physiology
Background:
- Olfactory neurons play a crucial role in detecting odors.
- Cyclic nucleotides are important second messengers in cellular signaling pathways.
Purpose of the Study:
- To investigate the effect of cyclic adenosine monophosphate (cAMP) and cyclic guanosine monophosphate (cGMP) on ion permeability in carp olfactory neuron plasma membranes.
- To characterize the properties and gating mechanisms of cyclic nucleotide-dependent (CN) channels.
Main Methods:
- Utilized inside-out patch-clamp electrophysiology on carp olfactory neuron plasma membrane.
- Applied cAMP and cGMP from the cytoplasmic side to measure changes in ion permeability.
- Analyzed dose-response relationships using Hill's equation and ion selectivity using the Goldman-Hodgkin-Katz equation.
Main Results:
- cAMP and cGMP reversibly increased ion permeability, with EC50 values of 1.3 +/- 0.6 microM and 0.9 +/- 0.3 microM, respectively.
- CN-channels exhibited weak selectivity for alkali metal cations (PNa/PK/PLi/PRb/PCs = 1:0.98:0.94:0.70:0.61) and were blocked by Ca2+ and Mg2+.
- Single channel conductance was 51 +/- 9 pS in 100 mM NaCl, with maximal open probability approaching 1.0. Dichlorobenzamil reduced open probability.
Conclusions:
- Cyclic nucleotides directly modulate ion channels in carp olfactory neurons, influencing neuronal excitability.
- The characterized CN-channels possess specific ion selectivity and gating properties, suggesting a role in olfactory signal transduction.
- A four-state kinetic model (inactivated, closed, two open states) effectively describes CN-channel gating and dose-response behavior.