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Afterhyperpolarization mechanisms in cat sympathetic preganglionic neuron in vitro
Journal of Neurophysiology
|June 1, 1986
Summary
Sympathetic preganglionic neurons (SPNs) exhibit a long-lasting afterhyperpolarization (AHP) composed of fast and slow components, suggesting distinct ion channel mechanisms. This AHP regulates SPN firing rate.
Area of Science:
- Neuroscience
- Cellular Physiology
- Autonomic Nervous System
Background:
- Sympathetic preganglionic neurons (SPNs) are crucial for regulating autonomic functions.
- Action potentials in neurons are followed by afterhyperpolarizations (AHPs) that influence firing rate.
- The ionic mechanisms underlying AHPs in SPNs are not fully elucidated.
Purpose of the Study:
- To characterize the biophysical properties of the afterhyperpolarization (AHP) in cat sympathetic preganglionic neurons (SPNs).
- To investigate the ionic conductances responsible for the fast (F-AHP) and slow (S-AHP) components of the AHP.
- To determine the role of the AHP in regulating SPN excitability and synaptic input efficacy.
Main Methods:
- Intracellular recordings from SPNs in an in vitro slice preparation of the cat spinal cord.
- Induction of action potentials via antidromic stimulation or direct current injection.
- Pharmacological manipulation using calcium channel blockers (cobalt), potassium channel blockers (tetraethylammonium, cesium), and tetrodotoxin (TTX).
- Analysis of AHP amplitude, duration, voltage-dependence, and reversal potential under varying extracellular potassium concentrations.
Main Results:
- A long-lasting AHP (2.8 ± 0.3 s) with distinct fast and slow components was observed following single spikes in SPNs.
- Both F-AHP and S-AHP components were associated with increased membrane conductance and were voltage-dependent.
- The S-AHP was sensitive to calcium channel blockers, suggesting a role for calcium-activated potassium channels.
- The F-AHP showed characteristics consistent with voltage-gated potassium channels and reversed polarity at negative membrane potentials.
- The AHP persisted in the presence of TTX and was associated with a decrease in synaptic input efficacy.
Conclusions:
- The AHP in SPNs comprises two distinct components, likely mediated by different potassium conductances.
- A calcium-activated potassium conductance contributes to the slow component (S-AHP).
- The fast component (F-AHP) is likely mediated by voltage-gated potassium channels.
- The AHP plays a significant role in regulating the firing rate and synaptic integration of SPNs.