Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat

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Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat. / Moldovan, Mihai; Krarup, Christian.

In: Journal of Physiology, Vol. 560, No. Pt 3, 2004, p. 795-806.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Moldovan, M & Krarup, C 2004, 'Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat', Journal of Physiology, vol. 560, no. Pt 3, pp. 795-806. https://doi.org/10.1113/jphysiol.2004.069476

APA

Moldovan, M., & Krarup, C. (2004). Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat. Journal of Physiology, 560(Pt 3), 795-806. https://doi.org/10.1113/jphysiol.2004.069476

Vancouver

Moldovan M, Krarup C. Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat. Journal of Physiology. 2004;560(Pt 3):795-806. https://doi.org/10.1113/jphysiol.2004.069476

Author

Moldovan, Mihai ; Krarup, Christian. / Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat. In: Journal of Physiology. 2004 ; Vol. 560, No. Pt 3. pp. 795-806.

Bibtex

@article{0ff910a074c211dbbee902004c4f4f50,
title = "Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat",
abstract = "The purpose of our study was to assess by threshold tracking internodal and nodal membrane excitability during the maturation process after tibial nerve crush in cat. Various excitability indices (EI) were computed non-invasively by comparing the threshold of a submaximal compound motor potential at different stimulation durations (strength-duration relationship), after a conditioning nerve impulse (recovery of excitability), or during the application of a polarizing current (threshold electrotonus). Four months after the lesion, regenerated nerves showed a higher rheobase, shorter chronaxie, shorter refractory period and higher than normal threshold variations during threshold electrotonus (TE). A partial recovery was observed during the first 2 years of maturation. The recovery to depolarizing TE seemed complete but all other EI remained abnormal even after 5 years of regeneration, the most pronounced being the 157 +/- 8% (mean +/- S.E.M.) increase in threshold during hyperpolarizing TE compared with 94 +/- 4% in controls. These EI abnormalities are consistent with increased input impedance. Nevertheless, the time course of maturation and incomplete recovery of EI could only be partially explained by changes in fibre morphology. The highly abnormal response to hyperpolarizing but not to depolarizing TE suggests that voltage-dependent membrane function also remained abnormal, possibly due to membrane hyperpolarization.",
author = "Mihai Moldovan and Christian Krarup",
note = "Keywords: Action Potentials; Animals; Axons; Cats; Motor Neurons; Nerve Regeneration; Tibial Nerve",
year = "2004",
doi = "10.1113/jphysiol.2004.069476",
language = "English",
volume = "560",
pages = "795--806",
journal = "The Journal of Physiology",
issn = "0022-3751",
publisher = "Wiley-Blackwell",
number = "Pt 3",

}

RIS

TY - JOUR

T1 - Persistent abnormalities of membrane excitability in regenerated mature motor axons in cat

AU - Moldovan, Mihai

AU - Krarup, Christian

N1 - Keywords: Action Potentials; Animals; Axons; Cats; Motor Neurons; Nerve Regeneration; Tibial Nerve

PY - 2004

Y1 - 2004

N2 - The purpose of our study was to assess by threshold tracking internodal and nodal membrane excitability during the maturation process after tibial nerve crush in cat. Various excitability indices (EI) were computed non-invasively by comparing the threshold of a submaximal compound motor potential at different stimulation durations (strength-duration relationship), after a conditioning nerve impulse (recovery of excitability), or during the application of a polarizing current (threshold electrotonus). Four months after the lesion, regenerated nerves showed a higher rheobase, shorter chronaxie, shorter refractory period and higher than normal threshold variations during threshold electrotonus (TE). A partial recovery was observed during the first 2 years of maturation. The recovery to depolarizing TE seemed complete but all other EI remained abnormal even after 5 years of regeneration, the most pronounced being the 157 +/- 8% (mean +/- S.E.M.) increase in threshold during hyperpolarizing TE compared with 94 +/- 4% in controls. These EI abnormalities are consistent with increased input impedance. Nevertheless, the time course of maturation and incomplete recovery of EI could only be partially explained by changes in fibre morphology. The highly abnormal response to hyperpolarizing but not to depolarizing TE suggests that voltage-dependent membrane function also remained abnormal, possibly due to membrane hyperpolarization.

AB - The purpose of our study was to assess by threshold tracking internodal and nodal membrane excitability during the maturation process after tibial nerve crush in cat. Various excitability indices (EI) were computed non-invasively by comparing the threshold of a submaximal compound motor potential at different stimulation durations (strength-duration relationship), after a conditioning nerve impulse (recovery of excitability), or during the application of a polarizing current (threshold electrotonus). Four months after the lesion, regenerated nerves showed a higher rheobase, shorter chronaxie, shorter refractory period and higher than normal threshold variations during threshold electrotonus (TE). A partial recovery was observed during the first 2 years of maturation. The recovery to depolarizing TE seemed complete but all other EI remained abnormal even after 5 years of regeneration, the most pronounced being the 157 +/- 8% (mean +/- S.E.M.) increase in threshold during hyperpolarizing TE compared with 94 +/- 4% in controls. These EI abnormalities are consistent with increased input impedance. Nevertheless, the time course of maturation and incomplete recovery of EI could only be partially explained by changes in fibre morphology. The highly abnormal response to hyperpolarizing but not to depolarizing TE suggests that voltage-dependent membrane function also remained abnormal, possibly due to membrane hyperpolarization.

U2 - 10.1113/jphysiol.2004.069476

DO - 10.1113/jphysiol.2004.069476

M3 - Journal article

C2 - 15297575

VL - 560

SP - 795

EP - 806

JO - The Journal of Physiology

JF - The Journal of Physiology

SN - 0022-3751

IS - Pt 3

ER -

ID: 68786