Calcium-dependent current generating the afterhyperpolarization of hippocampal neurons
Abstract
A single-electrode voltage-clamp technique was employed on in vitro hippocampal slices to examine the membrane current responsible for the slow afterhyperpolarization (AHP) in CA1 pyramidal cells. This was achieved by using conventional procedures to evoke an AHP in current clamp, followed rapidly by a switch into voltage clamp (hybrid clamp). The AHP current showed a dependence on extracellular K+, which was close to that predicted for a K+ current by the Nernst equation. The AHP current could be blocked by Cd2+ or norepinephrine. Although the AHP current showed a requirement for voltage-dependent Ca2+ entry, the current did not show any clear intrinsic voltage dependence. Once activated, AHP current is not turned off by hyperpolarizing the membrane potential. The effects of norepinephrine, Cd2+, and tetraethylammonium (TEA) were used to identify an AHP current component to the outward current evoked by depolarizing voltage commands from holding potentials that approximate to the resting potential for these cells. The AHP current can contribute significantly to the outward current during the depolarizing command. Upon repolarization it is evident as a slow outward tail current. This slow tail current had the same time constant as AHP currents evoked by hybrid clamp. Fast components to the tail currents were also observed. These were sensitive to Cd2+ and TEA. They probably represent a voltage-sensitive gKCa, sometimes termed C-current. The strong sensitivity to voltage and TEA displayed by the conventionally described gKCa (IC) are properties inconsistent with the AHP. It seems likely that the AHP current (IAHP) represents a Ca2+-activated K+ current separate from IC and that these two currents coexist in the same cell.
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AHP currents are mainly mediated by calcium-dependent potassium channels, but also partly by calcium-independent potassium channels.
“AHP currents are mainly mediated by calcium-dependent potassium channels [77, 78], but also partly by calcium-independent potassium channels [79].”
From Chronic unpredictable stress induces depression-related behaviors by suppressing AgRP neuron activity (2021) · cites this paper as [77]
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“Like the SK channels that contribute to the ImAHP, the channels underlying the IsAHP are voltage independent and K selective, and they require Ca 2 influx for activation ( Lancaster and Adams, 1986; Sah, 1996).”
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“To evoke and study in a quantitative manner the currents underlying single-spike afterhyperpolarization, a protocol based on principles outlined by Lancaster and Adams (1986) was applied.”
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“…c ϭ Ϫ30mV , 2 d ϭ d ϱ ͓͑Ca 2ϩ ͔ i ͒ c ϭ 7mV , c ϱ ͑V͒ ϭ ͕1 ϩ exp͓ Ϫ ͑V Ϫ c ͒ / c ͔͖ Ϫ1 a c ϭ 6 d ϱ ͓͑Ca 2ϩ ͔ i ) ϭ ( 1ϩa c / ͓Ca 2ϩ ͔ i ͒ Ϫ1 I sAHP , q dq / dt ϭ ͓q ϱ ͓͑Ca 2ϩ ͔ i ͒ Ϫ q͔ / q q ϭ 450 a q ϭ 2 2 q ϱ ͓͑Ca 2ϩ ͔ i ͒ ϭ ͑1 ϩ a q 4 / ͓Ca 2ϩ ͔ i 4 ͒ Ϫ1 References and comments : 1 )…”
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“large-conductance calcium-activated potassium (BK) channels (Lancaster and Adams, 1986; Lancaster and Nicoll, 1987); mAHPs are generated by SK currents (Schwindt et al.”
BackgroundAiken, S. P., Lampe, B. J., & Brown, B. S. (1995) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.1995.tb15019.x · Cited by 167 · see citing works
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Watermaze Learning Enhances Excitability of CA1 Pyramidal Neurons
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Small‐Conductance Calcium‐Activated Potassium Channels
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“In contrast, apamin-insensitive AHPs such as are seen in hippocampal pyramidal neurons, have a rising phase and then decay over several seconds.(2,4) This distinction is also seen in cells”
BackgroundCalcium‐dependent potassium conductance in guinea‐pig olfactory cortex neurones in vitro.
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“Although the membrane voltage was not precisely controlled during the depolarizing step because of the gain and space-clamp limitations, voltage control of the AHP tail current was well maintained (Lancaster and Adams, 1986; Constanti and Sim, 1987; Sah and McLachlan, 1991; Zhang et al., 1995).”
BackgroundResultLearning to learn – Intrinsic plasticity as a metaplasticity mechanism for memory formation
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“…pyramidal neurons, repetitive firing activates the slow afterhyperpolarization current (sIAHP, see Section 1.2 for adescription of the AHP, Hotson & Prince, 1980; Lancaster & Adams, 1986; Storm, 1989), which hyperpolarizes the somatic and proximal dendritic membrane potential (Sah & Bekkers, 1996).”
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“The methylsulfate anion was used because it has been shown to preserve IsAHP in a form similar to that observed with sharp electrode recordings (Lancaster and Adams, 1986).”
Cloned neuronal Ik(A) channels reopen during recovery from inactivation
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Potassium Currents during the Action Potential of Hippocampal CA3 Neurons
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“voltage-activated potassium currents in hippocampal pyramidal neurons: IA, ID, and IK (Gustafsson et al., 1982; Segal and Barker, 1984; Zbicz and Weight, 1985; Lancaster and Adams, 1986; Numann et al., 1987; Sah et al., 1988; Storm, 1988; Lancaster et al., 1991; Klee et al., 1995; Bossu et al., 1996).”
BackgroundThe Calcium Rationale in Aging and Alzheimer's Disease
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Book Review: Metabotropic Glutamate Receptors: Electrical and Chemical Signaling Properties
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“The postburst AHP is primarily comprised of an outward, calcium-activated K(1) current that modulates postsynaptic excitability of many cell types, including hippocampal and cortical pyramidal neurons (Hotson and Prince, 1980; Gustafsson and Wigström, 1981; Lancaster and Adams, 1986; Schwindt et al., 1992; Storm, 1990…”
BackgroundProtein kinase A-independent modulation of ion channels in the brain by cyclic AMP.
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Chapter 11 Chapter Membrane currents in hippocampal neurons
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“Consistent with the proposed role of BK channels in many cell types (Pennefather et al., 1985; Lancaster and Adams, 1986; Lang and Ritchie, 1987, 1990), both BK, and BK, currents contribute to action potential repolarization in chromaffin cells.”
BackgroundWong, R. K. S., & Stewart, M. (1992) · The Journal of Physiology · doi:10.1113/jphysiol.1992.sp019401 · Cited by 135 · see citing works
Quantified distribution of the noradrenaline innervation in the hippocampus of adult rat
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Apamin interacts with all subtypes of cloned small-conductance Ca 2+ -activated K + channels
Grunnet, M., Jensen, B., Olesen, S., & Klaerke, D. A. (2001) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/s004240000447 · Cited by 134 · see citing works
“In particular, in neurones, currents originating from SK channels are thought to be responsible for the slow afterhyperpolarization (sAHP) following an action potential [10, 18 , 20, 25, 26, 28, 34].”
- Authors
- Lancaster, B., & Adams, P. R.
- ORCID
- Adams, P. R.
- Venue
- Journal of Neurophysiology
- Publisher
- American Physiological Society
- Published
- 1986-06-01
- Volume
- 55
- Issue
- 6
- Pages
- 1268-1282
- ISSN
- 0022-3077 (ISSN-L)
- 1522-1598
- OpenAlex
- W1876408798
- Cited by
- 547
- References
- 0
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 4 · 2023: 4 · 2022: 2 · 2021: 5 · 2020: 4 · 2019: 8 · 2018: 6 · 2017: 5 · 2016: 4 · 2015: 3 · 2014: 1 · 2013: 7 · 2012: 11
- FWCI
- 9.16
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Journal of Neurophysiology (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Neurological Disorders and Stroke (NS18579)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Keywords
- afterhyperpolarization, calcium-activated potassium current, CA1 pyramidal neurons, tetraethylammonium sensitivity, cadmium block, norepinephrine, voltage-gated potassium channels
- MeSH terms
- Action Potentials, Animals, Calcium, Hippocampus, Ion Channels, Kinetics, Neural Conduction, Synaptic Transmission, Potassium, Rats, In Vitro Techniques
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