Opposing effects of spinal nerve ligation on calcium-activated potassium currents in axotomized and adjacent mammalian primary afferent neurons

Konstantinos D. Sarantopoulos, J. Bruce McCallum, Marcel Rigaud, Andreas Fuchs, Wai Meng Kwok, Quinn H. Hogan

Research output: Contribution to journalArticle

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Abstract

Calcium-activated potassium channels regulate AHP and excitability in neurons. Since we have previously shown that axotomy decreases ICa in DRG neurons, we investigated the association between ICa and K(Ca) currents in control medium-sized (30-39 μM) neurons, as well as axotomized L5 or adjacent L4 DRG neurons from hyperalgesic rats following L5 SNL. Currents in response to AP waveform voltage commands were recorded first in Tyrode's solution and sequentially after: 1) blocking Na+ current with NMDG and TTX; 2) addition of K(Ca) blockers with a combination of apamin 1 μM, iberiotoxin 200 nM, and clotrimazole 500 nM; 3) blocking remaining K+ current with the addition of 4-AP, TEA-Cl, and glibenclamide; and 4) blocking ICa with cadmium. In separate experiments, currents were evoked (HP - 60 mV, 200 ms square command pulses from - 100 to + 50 mV) while ensuring high levels of activation of IK(Ca) by clamping cytosolic Ca2+ concentration with pipette solution in which Ca2+ was buffered to 1 μM. This revealed IK(Ca) with components sensitive to apamin, clotrimazole and iberiotoxin. SNL decreases total IK(Ca) in axotomized (L5) neurons, but increases total IK(Ca) in adjacent (L4) DRG neurons. All IK(Ca) subtypes are decreased by axotomy, but iberiotoxin-sensitive and clotrimazole-sensitive current densities are increased in adjacent L4 neurons after SNL. In an additional set of experiments we found that small-sized control DRG neurons also expressed iberiotoxin-sensitive currents, which are reduced in both axotomized (L5) and adjacent (L4) neurons. Conclusions: Axotomy decreases IK(Ca) due to a direct effect on K(Ca) channels. Axotomy-induced loss of ICa may further potentiate current reduction. This reduction in IK(Ca) may contribute to elevated excitability after axotomy. Adjacent neurons (L4 after SNL) exhibit increased IK(Ca) current.

Original languageEnglish
Pages (from-to)84-99
Number of pages16
JournalBrain Research
Volume1132
Issue number1
DOIs
StatePublished - Feb 9 2007
Externally publishedYes

Fingerprint

Afferent Neurons
Spinal Nerves
Ligation
Potassium
Calcium
Neurons
Axotomy
Diagnosis-Related Groups
Clotrimazole
Apamin
Calcium-Activated Potassium Channels
Glyburide
Cadmium
Constriction

Keywords

  • Apamin
  • Calcium-activated potassium channel
  • Clotrimazole
  • Dorsal root ganglion
  • Iberiotoxin
  • Nerve injury
  • Neuropathic pain

ASJC Scopus subject areas

  • Neuroscience(all)
  • Clinical Neurology
  • Developmental Biology
  • Molecular Biology

Cite this

Opposing effects of spinal nerve ligation on calcium-activated potassium currents in axotomized and adjacent mammalian primary afferent neurons. / Sarantopoulos, Konstantinos D.; McCallum, J. Bruce; Rigaud, Marcel; Fuchs, Andreas; Kwok, Wai Meng; Hogan, Quinn H.

In: Brain Research, Vol. 1132, No. 1, 09.02.2007, p. 84-99.

Research output: Contribution to journalArticle

Sarantopoulos, Konstantinos D. ; McCallum, J. Bruce ; Rigaud, Marcel ; Fuchs, Andreas ; Kwok, Wai Meng ; Hogan, Quinn H. / Opposing effects of spinal nerve ligation on calcium-activated potassium currents in axotomized and adjacent mammalian primary afferent neurons. In: Brain Research. 2007 ; Vol. 1132, No. 1. pp. 84-99.
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AU - Kwok, Wai Meng

AU - Hogan, Quinn H.

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N2 - Calcium-activated potassium channels regulate AHP and excitability in neurons. Since we have previously shown that axotomy decreases ICa in DRG neurons, we investigated the association between ICa and K(Ca) currents in control medium-sized (30-39 μM) neurons, as well as axotomized L5 or adjacent L4 DRG neurons from hyperalgesic rats following L5 SNL. Currents in response to AP waveform voltage commands were recorded first in Tyrode's solution and sequentially after: 1) blocking Na+ current with NMDG and TTX; 2) addition of K(Ca) blockers with a combination of apamin 1 μM, iberiotoxin 200 nM, and clotrimazole 500 nM; 3) blocking remaining K+ current with the addition of 4-AP, TEA-Cl, and glibenclamide; and 4) blocking ICa with cadmium. In separate experiments, currents were evoked (HP - 60 mV, 200 ms square command pulses from - 100 to + 50 mV) while ensuring high levels of activation of IK(Ca) by clamping cytosolic Ca2+ concentration with pipette solution in which Ca2+ was buffered to 1 μM. This revealed IK(Ca) with components sensitive to apamin, clotrimazole and iberiotoxin. SNL decreases total IK(Ca) in axotomized (L5) neurons, but increases total IK(Ca) in adjacent (L4) DRG neurons. All IK(Ca) subtypes are decreased by axotomy, but iberiotoxin-sensitive and clotrimazole-sensitive current densities are increased in adjacent L4 neurons after SNL. In an additional set of experiments we found that small-sized control DRG neurons also expressed iberiotoxin-sensitive currents, which are reduced in both axotomized (L5) and adjacent (L4) neurons. Conclusions: Axotomy decreases IK(Ca) due to a direct effect on K(Ca) channels. Axotomy-induced loss of ICa may further potentiate current reduction. This reduction in IK(Ca) may contribute to elevated excitability after axotomy. Adjacent neurons (L4 after SNL) exhibit increased IK(Ca) current.

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