Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers.

Standard

Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers. / Kirillova, Irina; Teliban, Alina; Gorodetskaya, Natalia; Grossmann, Lydia; Bartsch, Fabian; Rausch, Vanessa; Struck, Marek; Tode, Jan; Baron, Ralf; Jänig, Wilfrid.

In: PAIN, Vol. 152, No. 7, 7, 2011, p. 1562-1571.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Kirillova, I, Teliban, A, Gorodetskaya, N, Grossmann, L, Bartsch, F, Rausch, V, Struck, M, Tode, J, Baron, R & Jänig, W 2011, 'Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers.', PAIN, vol. 152, no. 7, 7, pp. 1562-1571. <http://www.ncbi.nlm.nih.gov/pubmed/21474243?dopt=Citation>

APA

Kirillova, I., Teliban, A., Gorodetskaya, N., Grossmann, L., Bartsch, F., Rausch, V., Struck, M., Tode, J., Baron, R., & Jänig, W. (2011). Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers. PAIN, 152(7), 1562-1571. [7]. http://www.ncbi.nlm.nih.gov/pubmed/21474243?dopt=Citation

Vancouver

Kirillova I, Teliban A, Gorodetskaya N, Grossmann L, Bartsch F, Rausch V et al. Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers. PAIN. 2011;152(7):1562-1571. 7.

Bibtex

@article{19b6fa7d5101447aa937c9e3a2f41096,
title = "Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers.",
abstract = "Lidocaine applied systemically or locally attenuates neuropathic pain in patients. Here we tested the hypothesis that ectopic activity in injured afferent A- or C-fibers is suppressed by lidocaine. In rats the sural nerve (skin nerve) or lateral gastrocnemius-soleus nerve (muscle nerve) was crushed. Four to 11 days after crush lesion afferent fibers were isolated from the lesioned nerves in bundles rostral to the injury site. Ongoing ectopic activity was recorded from 75 A-fibers (muscle N=43, skin N=32) and 69 C-fibers (muscle N=30, skin N=39). Most afferent fibers were functionally characterized by their responses to mechanical and thermal (mostly heat) stimuli applied at or distal to the nerve injury site. Low-threshold cold-sensitive cutaneous C-fibers were excluded from the analysis. Lidocaine was either applied to the nerve at or distal to the injury site in concentrations of 1 to 1000 ?g/mL or injected i.v. in doses of 0.09 to 9 mg/kg (skin) or 0.047 to 4.7 mg/kg (muscle). Local application of lidocaine depressed ectopic activity in A- and C-fibers dose-dependently. Depression was weaker in C- than in A-fibers. Intravenous application of lidocaine depressed ongoing ectopic activity in A- and C-fibers dose-dependently. Responses to heat or mechanical stimulation of the injured nerve were not suppressed at the highest concentrations of lidocaine. The results support the hypothesis that decrease of neuropathic pain following local or systemic application of a local anesthetic is related to decrease of ectopic ongoing activity in injured afferent nerve fibers.",
keywords = "Animals, Male, Time Factors, Disease Models, Animal, Rats, Statistics, Nonparametric, Electric Stimulation, Rats, Wistar, Drug Administration Routes, Action Potentials/drug effects, Anesthetics, Local/*administration & dosage, Blood Pressure/drug effects, Lidocaine/*administration & dosage, Nerve Fibers/drug effects/physiology, Nerve Fibers, Myelinated/drug effects, Nerve Fibers, Unmyelinated/drug effects, Pain Threshold/*drug effects, Peripheral Nervous System Diseases/*drug therapy/etiology, Reaction Time/drug effects, Skin/innervation, Animals, Male, Time Factors, Disease Models, Animal, Rats, Statistics, Nonparametric, Electric Stimulation, Rats, Wistar, Drug Administration Routes, Action Potentials/drug effects, Anesthetics, Local/*administration & dosage, Blood Pressure/drug effects, Lidocaine/*administration & dosage, Nerve Fibers/drug effects/physiology, Nerve Fibers, Myelinated/drug effects, Nerve Fibers, Unmyelinated/drug effects, Pain Threshold/*drug effects, Peripheral Nervous System Diseases/*drug therapy/etiology, Reaction Time/drug effects, Skin/innervation",
author = "Irina Kirillova and Alina Teliban and Natalia Gorodetskaya and Lydia Grossmann and Fabian Bartsch and Vanessa Rausch and Marek Struck and Jan Tode and Ralf Baron and Wilfrid J{\"a}nig",
year = "2011",
language = "English",
volume = "152",
pages = "1562--1571",
journal = "PAIN",
issn = "0304-3959",
publisher = "Elsevier",
number = "7",

}

RIS

TY - JOUR

T1 - Effect of local and intravenous lidocaine on ongoing activity in injured afferent nerve fibers.

AU - Kirillova, Irina

AU - Teliban, Alina

AU - Gorodetskaya, Natalia

AU - Grossmann, Lydia

AU - Bartsch, Fabian

AU - Rausch, Vanessa

AU - Struck, Marek

AU - Tode, Jan

AU - Baron, Ralf

AU - Jänig, Wilfrid

PY - 2011

Y1 - 2011

N2 - Lidocaine applied systemically or locally attenuates neuropathic pain in patients. Here we tested the hypothesis that ectopic activity in injured afferent A- or C-fibers is suppressed by lidocaine. In rats the sural nerve (skin nerve) or lateral gastrocnemius-soleus nerve (muscle nerve) was crushed. Four to 11 days after crush lesion afferent fibers were isolated from the lesioned nerves in bundles rostral to the injury site. Ongoing ectopic activity was recorded from 75 A-fibers (muscle N=43, skin N=32) and 69 C-fibers (muscle N=30, skin N=39). Most afferent fibers were functionally characterized by their responses to mechanical and thermal (mostly heat) stimuli applied at or distal to the nerve injury site. Low-threshold cold-sensitive cutaneous C-fibers were excluded from the analysis. Lidocaine was either applied to the nerve at or distal to the injury site in concentrations of 1 to 1000 ?g/mL or injected i.v. in doses of 0.09 to 9 mg/kg (skin) or 0.047 to 4.7 mg/kg (muscle). Local application of lidocaine depressed ectopic activity in A- and C-fibers dose-dependently. Depression was weaker in C- than in A-fibers. Intravenous application of lidocaine depressed ongoing ectopic activity in A- and C-fibers dose-dependently. Responses to heat or mechanical stimulation of the injured nerve were not suppressed at the highest concentrations of lidocaine. The results support the hypothesis that decrease of neuropathic pain following local or systemic application of a local anesthetic is related to decrease of ectopic ongoing activity in injured afferent nerve fibers.

AB - Lidocaine applied systemically or locally attenuates neuropathic pain in patients. Here we tested the hypothesis that ectopic activity in injured afferent A- or C-fibers is suppressed by lidocaine. In rats the sural nerve (skin nerve) or lateral gastrocnemius-soleus nerve (muscle nerve) was crushed. Four to 11 days after crush lesion afferent fibers were isolated from the lesioned nerves in bundles rostral to the injury site. Ongoing ectopic activity was recorded from 75 A-fibers (muscle N=43, skin N=32) and 69 C-fibers (muscle N=30, skin N=39). Most afferent fibers were functionally characterized by their responses to mechanical and thermal (mostly heat) stimuli applied at or distal to the nerve injury site. Low-threshold cold-sensitive cutaneous C-fibers were excluded from the analysis. Lidocaine was either applied to the nerve at or distal to the injury site in concentrations of 1 to 1000 ?g/mL or injected i.v. in doses of 0.09 to 9 mg/kg (skin) or 0.047 to 4.7 mg/kg (muscle). Local application of lidocaine depressed ectopic activity in A- and C-fibers dose-dependently. Depression was weaker in C- than in A-fibers. Intravenous application of lidocaine depressed ongoing ectopic activity in A- and C-fibers dose-dependently. Responses to heat or mechanical stimulation of the injured nerve were not suppressed at the highest concentrations of lidocaine. The results support the hypothesis that decrease of neuropathic pain following local or systemic application of a local anesthetic is related to decrease of ectopic ongoing activity in injured afferent nerve fibers.

KW - Animals

KW - Male

KW - Time Factors

KW - Disease Models, Animal

KW - Rats

KW - Statistics, Nonparametric

KW - Electric Stimulation

KW - Rats, Wistar

KW - Drug Administration Routes

KW - Action Potentials/drug effects

KW - Anesthetics, Local/administration & dosage

KW - Blood Pressure/drug effects

KW - Lidocaine/administration & dosage

KW - Nerve Fibers/drug effects/physiology

KW - Nerve Fibers, Myelinated/drug effects

KW - Nerve Fibers, Unmyelinated/drug effects

KW - Pain Threshold/drug effects

KW - Peripheral Nervous System Diseases/drug therapy/etiology

KW - Reaction Time/drug effects

KW - Skin/innervation

KW - Animals

KW - Male

KW - Time Factors

KW - Disease Models, Animal

KW - Rats

KW - Statistics, Nonparametric

KW - Electric Stimulation

KW - Rats, Wistar

KW - Drug Administration Routes

KW - Action Potentials/drug effects

KW - Anesthetics, Local/administration & dosage

KW - Blood Pressure/drug effects

KW - Lidocaine/administration & dosage

KW - Nerve Fibers/drug effects/physiology

KW - Nerve Fibers, Myelinated/drug effects

KW - Nerve Fibers, Unmyelinated/drug effects

KW - Pain Threshold/drug effects

KW - Peripheral Nervous System Diseases/drug therapy/etiology

KW - Reaction Time/drug effects

KW - Skin/innervation

M3 - SCORING: Journal article

VL - 152

SP - 1562

EP - 1571

JO - PAIN

JF - PAIN

SN - 0304-3959

IS - 7

M1 - 7

ER -