TY - JOUR
T1 - Peripheral motor axons of SOD1(G127X) mutant mice are susceptible to activity-dependent degeneration
AU - Alvarez Herrero, Susana
AU - Calin, A
AU - Graffmo, K S
AU - Moldovan, M
AU - Krarup, C
PY - 2013/6/5
Y1 - 2013/6/5
N2 - Motor neuron disorders may be associated with mitochondrial dysfunction, and repetitive electrical impulse conduction during energy restriction has been found to cause neuronal degeneration. The aim of this study was to investigate the vulnerability of motor axons of a presymptomatic late-onset, fast-progression SOD1G127X mouse model of amyotrophic lateral sclerosis to long-lasting, high-frequency repetitive activity. Tibial nerves were stimulated at ankle in 7 to 8-month-old SOD1G127X mice when they were clinically indistinguishable from wild-type (WT) mice. The evoked compound muscle action potentials and ascending compound nerve action potentials were recorded from plantar muscles and from the sciatic nerve, respectively. Repetitive stimulation (RS) was carried out in interrupted trains of 200-Hz for 3h. During the stimulation-sequence there was progressive conduction failure in WT and, to a lesser extent, in the SOD1G127X. By contrast, 3days after RS the electrophysiological responses remained reduced in the SOD1G127X but recovered completely in WT. Additionally, morphological studies showed Wallerian degeneration in the disease model. Nerve excitability testing by "threshold-tracking" showed that axons recovering from RS had changes in excitability suggestive of membrane hyperpolarization, which was smaller in the SOD1G127X than in WT. Our data provide proof-of-principle that SOD1G127X axons are less resistant to activity-induced changes in ion-concentrations. It is possible that in SOD1G127X there is inadequate energy-dependent Na+/K+ pumping, which may lead to a lethal Na+ overload.
AB - Motor neuron disorders may be associated with mitochondrial dysfunction, and repetitive electrical impulse conduction during energy restriction has been found to cause neuronal degeneration. The aim of this study was to investigate the vulnerability of motor axons of a presymptomatic late-onset, fast-progression SOD1G127X mouse model of amyotrophic lateral sclerosis to long-lasting, high-frequency repetitive activity. Tibial nerves were stimulated at ankle in 7 to 8-month-old SOD1G127X mice when they were clinically indistinguishable from wild-type (WT) mice. The evoked compound muscle action potentials and ascending compound nerve action potentials were recorded from plantar muscles and from the sciatic nerve, respectively. Repetitive stimulation (RS) was carried out in interrupted trains of 200-Hz for 3h. During the stimulation-sequence there was progressive conduction failure in WT and, to a lesser extent, in the SOD1G127X. By contrast, 3days after RS the electrophysiological responses remained reduced in the SOD1G127X but recovered completely in WT. Additionally, morphological studies showed Wallerian degeneration in the disease model. Nerve excitability testing by "threshold-tracking" showed that axons recovering from RS had changes in excitability suggestive of membrane hyperpolarization, which was smaller in the SOD1G127X than in WT. Our data provide proof-of-principle that SOD1G127X axons are less resistant to activity-induced changes in ion-concentrations. It is possible that in SOD1G127X there is inadequate energy-dependent Na+/K+ pumping, which may lead to a lethal Na+ overload.
U2 - 10.1016/j.neuroscience.2013.03.017
DO - 10.1016/j.neuroscience.2013.03.017
M3 - Journal article
C2 - 23523994
SN - 0306-4522
VL - 241
SP - 239
EP - 249
JO - Neuroscience
JF - Neuroscience
ER -