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* These authors contributed equally
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.
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.
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<....
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
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.......
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.......
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.
....Name | Company | Catalog Number | Comments |
Durgs and solutions | - | - | - |
Atropinum sulfuricum | Polfa Warszawa | - | - |
Glucose | Merck | 346351 | - |
NaHCO3 | Merck | 106329 | - |
Pancuronium Jelfa | PharmaSwiss/Valeant | - | Neuromuscular blocker |
Pentobarbital sodium | Biowet Puławy Sp. z o.o | - | Main anesthetic agent |
Pottasium citrate | Chempur | 6100-05-06 | - |
Tetraspan | Braun | - | HES solution |
Surgical equipment | - | - | - |
21 Blade | FST | 10021-00 | Scalpel blade |
Cauterizer | FST | 18010-00 | - |
Chest Tubes | Mila | CT1215 | - |
Dumont #4 Forceps | FST | 11241-30 | Muscle forceps |
Dumont #5 Forceps | FST | 11254-20 | Dura forceps |
Dumont #5F Forceps | FST | 11255-20 | Nerve forceps |
Dumont #5SF Forceps | FST | 11252-00 | Pia forceps |
Forceps | FST | 11008-13 | Blunt forceps |
Forceps | FST | 11053-10 | Skin forceps |
Hemostat | FST | 13013-14 | - |
Rongeur | FST | 16021-14 | For laminectomy |
Scissors | FST | 15000-08 | Vein scissors |
Scissors | FST | 15002-08 | Dura scissors |
Scissors | FST | 14184-09 | For trachea cut |
Scissors | FST | 104075-11 | Muscle scissors |
Scissors | FST | 14002-13 | Skin scissors |
Tracheal tube | - | - | Custom made |
Vein catheter | Vygon | 1261.201 | - |
Vessel cannulation forceps | FST | 18403-11 | - |
Vessel clamp | FST | 18320-11 | For vein clamping |
Vessel Dilating Probe | FST | 10160-13 | For vein dissection |
Sugrgical materials | - | - | - |
Gel foam | Pfizer | GTIN 00300090315085 | Hemostatic agent |
Silk suture 4.0 | FST | 18020-40 | - |
Silk suture 6.0 | FST | 18020-60 | - |
Equipment | - | - | - |
Axoclamp 2B | Molecular devices | discontinued | Intracellular amplifier/ new model Axoclamp 900A |
CapStar-100 End-tidal CO2 Monitor | CWE | 11-10000 | Gas analyzer |
Grass S-88 | A-M Systems | discontinued | Constant current stimulator |
Homeothermic Blanket Systems with Flexible Probe | Harvard Apparatus | 507222F | Heating system |
ISO-DAM8A | WPI | 74020 | Extracellular amplifier |
Microdrive | - | - | Custom made/replacement IVM/Scientifica |
P-1000 Microelectrode puller | Sutter Instruments | P-1000 | Microelectrode puller |
SAR-830/AP Small Animal Ventilator | CWE | 12-02100 | Respirator |
Support frame | - | - | Custom made/replacement lab standard base 51601/Stoelting |
Spinal clamps | - | - | Custom made/replacement Rat spinal adaptor 51695/Stoelting |
TP-1 DC stimulator | WiNUE | - | tsDCS stimulator |
Miscellaneous | - | - | - |
1B150-4 glass capillaries | WPI | 1B150-4 | For microelectrodes production |
Cotton wool | - | - | - |
flexible tubing | - | - | For respirator and CO2 analyzer connection |
MicroFil | WPI | MF28G67-5 | For filling micropipettes |
Silver wire | - | - | For nerve electrodes |
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