Use of In Vivo Single-fiber Recording and Intact Dorsal Root Ganglion with Attached Sciatic Nerve to Examine the Mechanism of Conduction Failure

Podsumowanie

Single-fiber recording is an effective electrophysiological technique that is applicable to the central and peripheral nervous systems. Along with the preparation of intact DRG with the attached sciatic nerve, the mechanism of conduction failure is examined. Both protocols improve the understanding of the peripheral nervous system's relationship with pain.

Streszczenie

Single-fiber recording has been a classical and effective electrophysiological technique over the last few decades because of its specific application for nerve fibers in the central and peripheral nervous systems. This method is particularly applicable to dorsal root ganglia (DRG), which are primary sensory neurons that exhibit a pseudo-unipolar structure of nervous processes. The patterns and features of the action potentials passed along axons are recordable in these neurons. The present study uses in vivo single-fiber recordings to observe the conduction failure of sciatic nerves in complete Freund’s adjuvant (CFA)-treated rats. As the underlying mechanism cannot be studied using in vivo single-fiber recordings, patch-clamp-recordings of DRG neurons are performed on preparations of intact DRG with the attached sciatic nerve. These recordings reveal a positive correlation between conduction failure and the rising slope of the after-hyperpolarization potential (AHP) of DRG neurons in CFA-treated animals. The protocol for in vivo single fiber-recordings allows the classification of nerve fibers via the measurement of conduction velocity and monitoring of abnormal conditions in nerve fibers in certain diseases. Intact DRG with attached peripheral nerve allows observation of the activity of DRG neurons in most physiological conditions. Conclusively, single-fiber recording combined with electrophysiological recording of intact DRGs is an effective method to examine the role of conduction failure during the analgesic process.

Wprowadzenie

The normal transmission of information along nerve fibers guarantees the normal function of the nervous system. Abnormal functioning of the nervous system is also reflected in the electrical signal transmission of nerve fibers. For example, the degree of demyelination in central demyelination lesions can be classified via comparison of changes in nerve conduction velocity before and after intervention application¹. It is difficult to intracellularly record nerve fibers, except in special preparations such as the squid giant axon². Therefore, electrophysiological activity is only recordable via the extracellular recording of single fibers. As one of the classical electrophysiological methods, single-fiber recording has a longer history than other techniques. However, fewer electrophysiologists grasping this method despite its extensive application. Therefore, a detailed introduction of the standard protocol for single-fiber recording is needed for its appropriate application.

Although various patch-clamp techniques have dominated modern electrophysiological study, single-fiber recording still plays an irreplaceable role in recording the activities of nerve fibers, especially fibers transmitting peripheral sensation with their sensory cell body located in dorsal root ganglion (DRG). The advantage of using single-fiber recording here is that in vivo fiber recording provides a long observation time with the capacity to record responses to natural stimuli in preclinical models without disturbance of the intracellular environment^3,4.

An increasing number of studies over the last two decades has examined complex functions along nerve fibers⁵, and conduction failure, which is defined as a state of unsuccessful nerve impulse transmission along the axon, was present in many different peripheral nerves^6,7. The presence of conduction failure in our investigation served as an intrinsic self-inhibitory mechanism for the modulation of persistent nociceptive input along C-fibers⁸. This conduction failure was significantly attenuated under conditions of hyperalgesia^4,9. Therefore, targeting the factors involved in conduction failure may represent a new treatment for neuropathic pain. To observe conduction failure, the firing pattern should be recorded and analyzed on the basis of sequentially discharged spikes based on single-fiber recording.

To thoroughly understand the mechanism of conduction failure, it is necessary to identify the transmission properties of the axon, or more precisely, the membrane properties of DRG neurons, based on their pseudo-unipolar anatomical properties. Many previous studies in this field have been performed on dissociated DRG neurons^10,11, which may not be feasible for the investigation of conduction failure due to two obstacles. First, various mechanical and chemical methods are used in the dissociation process to free DRG neurons, which may result in unhealthy cells or alter the phenotype/properties of the neurons and confound the findings. Second, the attached peripheral nerves are basically removed, and conduction failure phenomena are not observable in these preparations. Therefore, a preparation of intact DRG neurons with an attached nerve has been improved to avoid the abovementioned obstacles. 

Protokół

The current protocol followed the Guide for United States Public Health Service's Policy on the Humane Care and Use of Laboratory Animals, and the Committee on the Ethics of Animal Experiments of the Fourth Military Medical University approved the protocol.

1. Animals

1. Divide 24 Sprague-Dawley rats (4-8 weeks old) into two groups. Produce complete Freund's adjuvant (CFA) model by intraplantar injection of 100 μL of CFA in one group of 14 rats and another group of 10 rats by treatment with saline.
   NOTE: All of the animals were acquired from the Animal Center of the Fourth Military Medical University. Adult male and female Sprague-Dawley rats (150-200 g) were used for all procedures, and rats were randomly assigned to cages. Two rats were housed per cage under a 12-/12-hour light/dark cycle at a constant temperature (25 ± 1 °C) with free access to food and water.

2. In Vivo Single-fiber Recording

1. Prepare and disinfect all surgical instruments (scalpel, tweezers, ophthalmic scissors, shearing scissors, glass separating needle, suture needle, bone rongeur) prior to surgery. Prepare 1 L or 2 L of normal Ringer’s extracellular solution (in mM: NaCl 124, KCl 3, MgSO₄ 1.3, CaCl₂ 2, NaHCO₃ 26, NaH₂PO₄ 1.25, glucose 15; pH 7.4 and 305 mOsm). Store at 4 °C until use.
2. Anesthetize rats. On days 3 to 7 after CFA injection, use intraperitoneal injection of a mixed solution (1% chloralose and 17% urethane, 5 mL/kg body weight) to keep the animals in a stable aesthetic condition during the experiment. Apply supplementary injection of anesthetics, if necessary, after checking pupils and the response to pain stimulation. Monitor and maintain a body temperature near 37 °C.
3. Exposure of sciatic nerve trunk for recording
   1. Cut open the skin and muscle on the dorsal part of the thigh. Perform a blunt dissection along femoral biceps. Carefully isolate the sciatic nerve trunk using ophthalmic scissors and a glass separation needle. Keep the tissue wet using Ringer's solution.
   2. Fix the animal on a homemade metal hoop (3 cm long, 2 mm wide metal hoop with an iron wire 1 mm in diameter) via sewing the skin into the slot around it. Pull the skin up slightly so as to establish a fluid bath.
   3. Expose 1 cm of sciatic nerve trunk at the proximal side. Place a small brown platform under the nerve trunk to enhance the contrast and observe the fine nerve trunk clearly. Heat liquid paraffin in a water bath to 37 °C and drop it on the top of the nerve trunk to prevent drying of the surface of the fiber. Remove the pia mater spinalis and dura mater around the sciatic nerve.
4. Recording session
   1. Select a platinum filament (29 μm in diameter) as the recording electrode. Heat over for easier molding, and create a small hook at the very end. Attach the electrode to a micromanipulator to move the electrode as required.
   2. In the bath, place a reference electrode in adjacent subcutaneous tissue. Split the spinal dura and the pia mater. Separate the sciatic nerve into a single fiber (15-20 μm in diameter) in the recording pool. Then, pick up a fine fascicle of axon and suspend the proximal end of the axon on the hook of the recording electrode under a stereoscope at 25x magnification.
      NOTE: The just-dissected filaments tend to be thicker and require further separation until a single unit may be recorded.
   3. Identify the receptive field of a single nociceptive C-fiber using a mechanical stimulus (Von Frey hairs) and thermal stimulus (small cotton ball with 50-55 °C water). Briefly, if the firing of nerve fiber respond to the mechanical stimuli and hot water, then consider it as a polymodal nociceptive C-fiber⁴. Next, insert two needle stimulus electrodes (2 mm interval) into the skin of the identified field for the delivery of electrical stimuli.
   4. Display the waveform of an action potential on oscilloscope and employ a computer A/D board with a signal sampling rate of 20 kHz to amplify and record the spikes.
   5. Collect data using data acquisition software (Table of Materials). Save data on a computer and analyze later with professional software (Table of Materials).

3. Measurement of Conduction Failure

1. Deliver the repetitive electrical stimuli (0.8 ms duration, 1.5x threshold intensity) in different frequencies (2 Hz, 5 Hz, 10 Hz) to a C-fiber for 60 s^4,8,9. Allow a 10 min interval for fiber to relax between stimuli. Calculate the ratio of the number of failures to the number of delivered repetitive stimulus pulses and multiply by 100% to obtain the degree of conduction failure.

4. Preparation of Iintact DRG Attached with Sciatic Nerve

1. Prepare surgical tools and Ringer's extracellular solution as described in step 2.1.
2. Separate the DRG with the attached sciatic nerve.
   1. Anesthetize the rats as described in step 2.2 (On days 3 to 7 after CFA injection). Cut the hair on back and leg with shearing scissors, and sterilize the skin with tincture of iodine.
   2. For DRG exposure, first cut open the skin from the midline of the back at the L4 to L5 segment level. Remove muscles, the process of spine, vertebra board, and transverse process using a bone rongeur to expose the spinal cord and DRG body. Cover the exposed spinal cord and DRG with cottons infiltrated by normal Ringer's extracellular solution to maintain neural activity. Stop the bleeding and clear the blood in time.
   3. Expose the sciatic nerve from two directions: remove the L4 to S1 bone structure above the vertebral foramen using ophthalmic scissors to expose the spinal nerve connected to DRG which is at the proximal end of sciatic nerve. Cut open the skin to expose the sciatic nerve at the middle thigh. Separate and disconnect the sciatic nerve from the distal end of the nerve where it goes inside the muscle, and ligate the nerve trunk with surgical line at the end of the nerve prior to cutting.
   4. Separate the sciatic nerve from the underlying connective tissue using ophthalmic scissors via lifting of the nerve ligation point. Remove the dura from the spinal cord and separate the DRG from the underlying connective tissue via lifting the dorsal root until it reaches the adjacent part of the sciatic nerve. Thus, isolate the whole preparation of DRG with an attached sciatic nerve.
3. Clear the surface of the DRG.
   1. Carefully remove the spinal dura on the surfaces of L4−L6 DRG using tweezers under a stereoscope at 4x magnification.
   2. Place the DRG with attached sciatic nerve in a glass tube containing 1 mL of mixed enzymes (0.2% proteinase and 0.32% collagenase) and digest in a 37 °C water bath for 15 min (blow slightly with a plastic dropper at an interval of 5 min).
   3. Lift the end of the ligation line and move the preparation to a dish filled with a normal Ringer's extracellular solution to wash out the enzyme. Then transfer the digested DRG to a container (Figure 1A) filled with oxygenated Ringer's extracellular solution for recording.
4. Recording session
   1. Prepare intracellular solution (in mM: potassium gluconate 120, KCl 18, MgCl₂ 2, ethylene glycol-bis(β-aminoethyl ether)-N,N,N',N'-tetraacetic acid [EGTA] 5, HEPES 10, Na₂-ATP 5, Na-GTP 0.4, CaCl₂ 1; pH 7.2 and 300 mOsm). Keep at 0 °C until use.
   2. Stabilize ganglia using a slice anchor and connect nerve end to a suction-stimulating electrode (Figure 1A). Visualize and select a DRG neuron with a water-immersion objective at 40x magnification.
   3. Pull an electrode (Table of Materials) and fill it with intracellular solution. Insert electrode on holder and apply positive pressure in the pipette with a final resistance of 4-7 MΩ.
   4. Bring electrode close to the cell and touch it. Give a negative pressure in the pipette, once GΩ seal is reached, set the membrane potential at about -60 mV and then establish whole-cell recording mode.
   5. Deliver repetitive stimuli of 5-50 Hz to the sciatic nerve through the suction electrode to screen for conduction failure. Measure the amplitude of afterhyperpolarization potential (AHP) from baseline to peak, and the 80% AHP duration.
      NOTE: One-way analysis of variance (ANOVA; for more than two groups) or Student’s t-test (for only two groups) was used to analyze the data. Data are presented as means ± standard error of the mean (SEM). The statistical significant level was set at p < 0.05.
5. Ending the Experiment
   1. ​When the experimental task is finished while the rats are still under anaesthetic situation, rats are humanely euthanized with a intracardiac injections of overdose pentobarbital sodium. 

Wyniki

The outcome of the single-fiber recording protocol depends on the quality of the fiber dissection. The animal for in vivo experiments must be in a good situation to keep the nerve trunk healthy for easy dissection (see advice in the discussion section). A drug application bath is needed in many cases for drug delivery on fibers. Figure 1 illustrates how the in vivo single-fiber recording was operated (Figure 1A) and presents one classical recording from the sciatic nerve of ...

Dyskusje

Although recent studies have achieved calcium imaging of DRG neurons in vivo¹⁶, performing in vivo patch-clamp recording from individual DRG nociceptors remains extremely challenging. Therefore, an in vivo single-fiber approach for the pain field is of continuing importance. Single-fiber recording in the present protocol allow objective observation of conduction failure phenomena, and the combination of this technique with the ex vivo preparation developed in the current study allows examination o...

Materiały

Name	Company	Catalog Number	Comments
Instruments and software used in single fiber recording
Amplifier	Nihon kohden	MEZ-8201	Amplification of the electrophysiological signals
Bioelectric amplifier monitor	ShangHai JiaLong Teaching instrument factory	SZF-1	Monitor firing process via sound which is transformed from physiological discharge signal
Data acquisition and analysis system	CED	Spike-2	Software for data acquisition and analysis
Electrode manipulator	Narishige	SM-21	Contro the movement of the electrode as required
Hairspring tweezers	A.Dumont	5#	Separate the single fiber
Isolator	Nihon kohden	SS-220J
Memory oscilloscope	Nihon kohden	VC-9	Display recorded discharge during
Experiment
Stereomicroscope	ZEISS	SV-11	Have clear observation when separate the local tissue and single fiber
Stimulator	Nihon kohden	SEZ-7203	Delivery of the electrical stimuli
Von Frey Hair	Stoelting accompany		Delivery of the mechanical stimuli
Water bath	Scientz biotechnology Co., Ltd.	SC-15	Heating paroline to maintain at 37 °C
Instruments and software used in patch clamp recording
Amplifier	Axon Instruments	Multiclamp 700B	Monitors the currents flowing through the recording electrode and also controls the stimuli by sending a signal to the electrode
Anti-vibration table	Optical Technology Co., Ltd.		Isolates the recording system from vibrations induced by the environment
Camera	Olympus	TH4-200	See the neurons in bright field; the controlling software allows to take pictures and do live camera image to monitor the approach of the electrode to the cell
Clampex	Axon	Clampex 9.2	Software for data acquisition and delivery of stimuli
Clampfit	Axon	Clampfit 10.0	Software for data analysis
Electrode puller	Sutter	P-97	Prepare recording pipettes of about 2μm diameter with resistance about 5 to 8 MΩ
Glass pipette	Sutter	BF 150-75-10
Micromanipulator	Sutter	MP225	Give a precise control of the microelectrode
Microscope	Olympus	BX51WI	Upright microcope equipped with epifluorescence for clearly observe the cells which would be patched
Origin	Origin lab	Origin 8	Software for drawing picture
Perfusion Pump	BaoDing LanGe Co., Ltd.	BT100-1J	Perfusion of DRG in whole-cell patch clamp
Other instruments
Electronic balance	Sartorius	BS 124S	Weighing reagent
pH Modulator	Denver Instrument	UB7	Adjust pH to 7.4
Solutions/perfusion/chemicals
Calcium chloride	Sigma-Aldrich	C5670	Extracellular solution
Chloralose	Shanghai Meryer Chemical Technology Co., Ltd.	M07752	Mixed solution for Anesthesia
Collagenase	Sigma-Aldrich	SLBQ1885V	Enzyme used for clearing the surface of DRG
D (+) Glucose	Sigma-Aldrich	G7528	Extracellular solution
Liquid Paraffin	TianJin HongYan Reagent Co., Ltd.		Maintain fiber wetting
Magnesium sulfate	Sigma-Aldrich	M7506	Extracellular solution
Potassium chloride	Sigma-Aldrich	P3911	Extracellular solution
Protease	Sigma-Aldrich	62H0351	Enzyme used for clearing the surface of DRG
Sodium bicarbonate	Sigma-Aldrich	S5671	Extracellular solution
Sodium chloride	Sigma-Aldrich	S5886	Extracellular solution
Sodium phosphate monobasic	Sigma-Aldrich	S0751	Extracellular solution
Sucrose	Sigma-Aldrich	S0389	Extracellular solution
Urethane	Sigma-Aldrich	U2500	Mixed solution for Anesthesia