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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes in vivo intracellular recording of rat lumbar motoneurons with simultaneous trans-spinal direct current stimulation. The method enables us to measure membrane properties and to record rhythmic firing of motoneurons before, during and after anodal or cathodal polarization of the spinal cord.

Abstract

Intracellular recording of spinal motoneurons in vivo provides a “gold standard” for determining the cells’ electrophysiological characteristics in the intact spinal network and holds significant advantages relative to classical in vitro or extracellular recording techniques. An advantage of in vivo intracellular recordings is that this method can be performed on adult animals with a fully mature nervous system, and therefore many observed physiological mechanisms can be translated to practical applications. In this methodological paper, we describe this procedure combined with externally applied constant current stimulation, which mimics polarization processes occurring within spinal neuronal networks. Trans-spinal direct current stimulation (tsDCS) is an innovative method increasingly used as a neuromodulatory intervention in rehabilitation after various neurological injuries as well as in sports. The influence of tsDCS on the nervous system remains poorly understood and the physiological mechanisms behind its actions are largely unknown. The application of the tsDCS simultaneously with intracellular recordings enables us to directly observe changes of motoneuron membrane properties and characteristics of rhythmic firing in response to the polarization of the spinal neuronal network, which is crucial for the understanding of tsDCS actions. Moreover, when the presented protocol includes the identification of the motoneuron with respect to an innervated muscle and its function (flexor versus extensor) as well as the physiological type (fast versus slow) it provides an opportunity to selectively investigate the influence of tsDCS on identified components of spinal circuitry, which seem to be differently affected by polarization. The presented procedure focuses on surgical preparation for intracellular recordings and stimulation with an emphasis on the steps which are necessary to achieve preparation stability and reproducibility of results. The details of the methodology of the anodal or cathodal tsDCS application are discussed while paying attention to practical and safety issues.

Introduction

Trans-spinal direct current stimulation (tsDCS) is gaining recognition as a potent method to modify spinal circuit excitability in health and disease1,2,3. In this technique, a constant current is passed between an active electrode located above selected spinal segments, with a reference electrode located either ventrally or more rostrally4. Several studies have already confirmed that tsDCS can be used in managing certain pathological conditions, such as neuropathic pain5, spasticity6, spinal cord injury<....

Protocol

All procedures connected to this protocol have been accepted by the appropriate authorities (e.g., Local Ethics Committee) and follow the national and international rules on animal welfare and management.

NOTE: Each participant involved in the procedure has to be properly trained in basic surgical procedures and has to have a valid license for performing animal experiments.

1. Anesthesia and premedication

  1. Anesthetize a rat with intraperitoneal injections.......

Representative Results

Parameters of action potentials and several membrane properties can be calculated on the basis of intracellular recordings when stable conditions of cell penetration are ensured. Figure 1A presents a typical orthodromic action potential evoked by intracellular stimulation, which meets all criteria for data inclusion (the resting membrane potential of at least -50 mV, and spike amplitude higher than 50 mV, with a positive overshoot). Action potential parameters, such as the spike amplitude, t.......

Discussion

If performed correctly, the surgical part of the described protocol should be completed within approximately three hours. One should take particular care in maintaining stable physiological conditions of an animal during the surgery, in particular body temperature and depth of anesthesia. Apart from obvious ethical considerations, a lack of proper anesthesia can result in excessive limb movements during nerve dissection or laminectomy and lead to damage to the preparation or a premature experiment termination. Upon paral.......

Acknowledgements

This work was supported by the National Science Center grant No. 2017/25/B/NZ7/00373. Authors would like to recognize the work of Hanna Drzymała-Celichowska and Włodzimierz Mrówczyński, who both contributed to the data gathering and analysis of the results presented in this paper.

....

Materials

NameCompanyCatalog NumberComments
Durgs and solutions---
Atropinum sulfuricumPolfa Warszawa--
GlucoseMerck346351-
NaHCO3Merck106329-
Pancuronium JelfaPharmaSwiss/Valeant-Neuromuscular blocker
Pentobarbital sodiumBiowet Puławy Sp. z o.o-Main anesthetic agent
Pottasium citrateChempur6100-05-06-
TetraspanBraun-HES solution
Surgical equipment---
21 BladeFST10021-00Scalpel blade
CauterizerFST18010-00-
Chest TubesMilaCT1215-
Dumont #4 ForcepsFST11241-30Muscle forceps
Dumont #5 ForcepsFST11254-20Dura forceps
Dumont #5F ForcepsFST11255-20Nerve forceps
Dumont #5SF ForcepsFST11252-00Pia forceps
ForcepsFST11008-13Blunt forceps
ForcepsFST11053-10Skin forceps
HemostatFST13013-14-
RongeurFST16021-14For laminectomy
ScissorsFST15000-08Vein scissors
ScissorsFST15002-08Dura scissors
ScissorsFST14184-09For trachea cut
ScissorsFST104075-11Muscle scissors
ScissorsFST14002-13Skin scissors
Tracheal tube--Custom made
Vein catheterVygon1261.201-
Vessel cannulation forcepsFST18403-11-
Vessel clampFST18320-11For vein clamping
Vessel Dilating ProbeFST10160-13For vein dissection
Sugrgical materials---
Gel foamPfizerGTIN 00300090315085Hemostatic agent
Silk suture 4.0FST18020-40-
Silk suture 6.0FST18020-60-
Equipment---
Axoclamp 2BMolecular devicesdiscontinuedIntracellular amplifier/ new model Axoclamp 900A
CapStar-100 End-tidal CO2 MonitorCWE11-10000Gas analyzer
Grass S-88A-M SystemsdiscontinuedConstant current stimulator
Homeothermic Blanket Systems with Flexible ProbeHarvard Apparatus507222FHeating system
ISO-DAM8AWPI74020Extracellular amplifier
Microdrive--Custom made/replacement IVM/Scientifica
P-1000 Microelectrode pullerSutter InstrumentsP-1000Microelectrode puller
SAR-830/AP Small Animal VentilatorCWE12-02100Respirator
Support frame--Custom made/replacement lab standard base 51601/Stoelting
Spinal clamps--Custom made/replacement Rat spinal adaptor 51695/Stoelting
TP-1 DC stimulatorWiNUE-tsDCS stimulator
Miscellaneous---
1B150-4 glass capillariesWPI1B150-4For microelectrodes production
Cotton wool---
flexible tubing--For respirator and CO2 analyzer connection
MicroFilWPIMF28G67-5For filling micropipettes
Silver wire--For nerve electrodes

References

  1. Angius, L., Hopker, J., Mauger, A. R. The Ergogenic Effects of Transcranial Direct Current Stimulation on Exercise Performance. Frontiers in Physiology. 8, 90 (2017).
  2. Berry, H. R., Tate, R. J., Conway, B. A.

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