Background
Numerous studies have shown that there are two main classes of pain sensing neurons in the skin and other peripheral tissues: myelinated Aδ and unmyelinated C nociceptor[
1,
2]. There are many distinctions between these two types of nociceptive afferents [
3,
4]. Activation of these afferents evokes distinct sensations: Aδ fiber mediated pain is typically described as rapid, pricking or sharp, and localized whereas C fiber mediated pain is usually described as a diffuse, burning or aching sensations that outlast stimulus duration[
5‐
7].
Although separate activation of Aδ and C fiber nociceptors, demonstrated electrophysiologically, has been achieved through the use of radiant skin heating in rats[
4], these methods are not optimal for testing in humans. In the last two decades human studies have often used lasers as tools for evaluation of nociception and the integrity of nociceptive pathways in experimental pain models and neurological diseases[
8‐
20,
32].
Coherent radiation, as from a laser, is not a stimulus found in nature. However, as with radiant heat, lasers provide the advantage over contact stimulators of providing a purely thermal, as opposed to mixed, stimulation. In addition, lasers allow brief pulses (μs to ms) with very fast rise time. Beyond these advantages, diode lasers provide uniform skin heating from approximately 50 to 600 μm deep and a high level of pulse repeatability. Because the surface does not need to be overheated to provide conductive heating of deeper nociceptors (as with CO2 and Thulium lasers), diode lasers provide a degree of added safety over these devices. Diode laser stimuli have been used for
in vivo cutaneous stimulation of free nerve endings in humans and rodents and for
in vitro activation of TRPV1 and TRPV2 channels in cultured dorsal root ganglia neurons and HEK273 cells[
18,
21‐
23]. These experiments have indicated that brief, high heating rate diode laser pulses can selectively activate myelinated Aδ fiber nociceptors in rats and produce pricking pain in humans, whereas low heating rate, longer pulses can preferentially activate unmyelinated C fibers in rats and produce burning pain in humans. However, it is not known whether these different pulse parameters will differentially activate Aδ or C fibers in humans. To investigate this question, we used a combination of psychophysical and electrophysiological (cortical evoked potentials) to investigate whether brief pulses would produce both singular pricking pain and a cortical activation pattern characteristic of Aδ fiber activation, as well as whether long pulses would produce singular burning pain and cortical activation consistent with C fiber activation. In addition, to provide complimentary evidence, we investigated the differential effects of topical capsaicin, which selectively sensitizes TRPV1 expressing, mostly unmyelinated nociceptors[
4].
Discussion
This study sought to investigate whether brief, intense, high heating rate pulses emitted by a diode infrared laser would evoke pain mediated selectively or preferentially and repeatedly by the activation of myelinated (Aδ) thermonociceptors, whereas lower rates of skin heating produced by lower intensity laser pulses would produce pain mediated selectively or preferentially by the activation of unmyelinated (C) thermonociceptors. We assessed psychophysical responsiveness and cortical potentials evoked by two laser skin heating parameters in human volunteers. For SP laser stimuli close to pain threshold, pain was described as monomodal and sharp or pricking, whereas LP laser stimuli were described as monomodal and burning.
This finding of monomodal pain modalities appears to be unique in the literature, as laser stimuli usually evoke double pain sensations indicative of activation of both A and C thermonociceptors [
24‐
26]. Monomodal sensation has been achieved with other lasers [
10] and with high-rate skin contact skin heating[
26], but it is not clear that the sensation perceived was pain, but rather may be monomodal warm mediated by the activation of unmyelinated warm fibers[
26]. The ability to evoke monomodal pain with an infrared diode laser is likely due to the homogenous heating of epidermal and dermal tissue (for both hairy and glabrous skin), up to 600 microns from the surface[
18]. The range of depths of (at least unmyelinated) nociceptive terminals in the skin is 40-570 μm[
27], thus fairly well matching the range of homogenous direct tissue heating of infrared diode lasers. Other lasers (e.g., CO
2) and high rate contact heating predominantly heat the surface, wherefrom surface heat is conducted to underlying tissue - a process that requires time and overheating of the surface[
24]. Simultaneous direct heating of epidermal as well as deeper nerve terminals allows for differential activation based on the activation properties of those terminals - as opposed to the conductive properties of the tissue.
Near threshold pain evoked by LP appears to be mediated by the selective activation of C fiber nociceptors; pain evoked by SP appears to be mediated by the activation of Aδ nociceptors. LP-evoked pain is monomodal "burning" and, along with cortical evoked potentials, is enhanced by topical capsaicin, and demonstrates a latency shift representative of a CV of less than 1.7 m/s - all characteristics of C fiber thermonociceptors[
3‐
5,
28,
29]. SP-evoked pain is characterized as monomodal "pricking", is not enhanced by capsaicin, and has an estimated CV of around 4.5 m/s - all characteristics of Aδ thermonociceptors[
4,
7,
28].
LEP produced by these two stimulus types were also distinct. LEP evoked by suprathreshold SP were sinusoidal, insensitive to topical capsaicin, and produced an estimated conduction velocity in the Aδ range. LEP evoked by suprathreshold LP were also sinusoidal, but were enhanced by topical capsaicin and gave a conduction velocity estimate in the C fiber range. Thus, LEP measurements agreed with psychophysics in demonstrating a fiber-selective differential activation by short vs. long pulses of infrared laser light. It is possible that warm fibers also contributed to the LEP recorded in response to LP as the threshold for warm-sensitive C fibers is reached and surpassed as the temperature rises with this stimulus ~38-40°C[
30]. In addition, the conduction velocity of C fiber warm receptors is typically in the range of 2.5 m/s, well above those measured in the current study[
31]. Interestingly, Magerl used a CO
2 laser to separate Aδ vs C fiber mediated cortical responses[
32] in volunteers. However, the stimulus used to activate C fibers (40°C) was below that typically activating C nociceptors, and the conduction velocity estimated in these studies (2.4-2.8 m/s) was close to that measured for human C warm receptors[
31] suggesting that the cortical response recorded in this study may have been mediated or dominated by warm fibers, rather than thermonociceptors.
Conclusions
The results of these experiments indicate that short, high intensity laser pulses can be used to selectively produce Aδ mediated pain and LEP in humans and that longer duration, lower intensity pulses can be used to selectively produce C mediated pain and LEP in humans. These protocols may be useful then, in evaluating differential pharmacologic effects and physiologic mechanisms of these two distinct pain types.
Methods
Subjects
After approval by the Stanford Institutional Review Board and after informed consent, 10 healthy volunteers, 5 female and 5 male, aged 21-50 (median 31) years participated in this study. All subjects gave informed consent to participate in the study, which was approved by the Stanford Institutional Review Board.
Laser stimulation
Two different infrared diode laser (Lass 10, Lasmed LLC, Mountain View, CA) settings were used: 1) a short pulse (SP): 60 ms, 0.3 mm2, heating ramp up to 600 C°/s, or 2) a long pulse (LP): 1.5 s, 40 mm2, heating ramp up to 20 C°/s were applied to 10-20 spots on the hairy skin of the dorsum of the 2nd through 5th fingers (i.e., not the thumb) of human volunteers. SP was hypothesized to preferentially activate myelinated thermonociceptors, whereas LP was hypothesized to mainly stimulate unmyelinated thermonociceptors, respectively. Baseline skin temperature was measured periodically in between stimulation and maintained at 33 ± 0.5°C using a heating pad placed on the surface of the skin between stimulus sessions and under the hand during stimulus sessions.
Laser Evoked Potentials (LEP)
EEG collection
Laser evoked potentials (LEP) were recorded using Ag-AgCl surface scalp electrodes and Acquire 4.3 software with a 36-electrode Quik-Cap (both NeuroScan Inc, El Paso, Texas). Data was acquired simultaneously from 32 EEG channels (in accordance with Enhanced 10-20 International system), and 2 EOG channels - vertical VEOU and horizontal VEOL, wth AFz as a ground electrode, and A2 as a common reference, using NuAmps 40 Channel Digital DC EEG amplifier (NeuroScan Inc, El Paso, Texas). The impedance was generally maintained below 5 kΩ. The signals were bandpass (analog 0.1-70 Hz) and notch (60 Hz) filtered in real time, and digitized at a rate of 1000 Hz.
EEG Processing
EEG data then were imported and pre-processed in EEGLAB, a free open-source toolbox running under MatLab environment. Continuous data was bandpass-filtered from 0.5 to 20 Hz, and epochs containing LEP (1000 ms prior to stimulus and 4000 ms post-stimulus) were subsequently extracted and baseline corrected to 1 s before stimulus onset. High-amplitude noise contaminated channels and epochs were rejected upon visual inspection. In order to remove ocular artifacts while preserving useful signal, we used independent component analysis (ICA) to decompose EEG into a number of statistically independent components, and then subtract noise from the original data [
5]. For better results two runs of ICA were performed: first epochs containing non-stereotype artifacts were identified and rejected [
2], then ocular artifacts were removed from the data. Cz channel data were extracted from each data set, and indexed with a custom database. LEP waveforms were computed by averaging epochs pulled from the database per request.
Repeatability
To test for repeatability of laser stimuli, threshold stimulus intensities (measured in supplied current) for evoking pain were measured for both pulse types (in a randomly order). Then, LEPs were recorded while each subject received 20 stimuli of either SP or LP, set at 15% above the threshold stimulus intensity, and separated by an approximately 30 s interstimulus interval. After each successive pulse, subjects were asked to give a forced-choice between descriptors (sharp or burning; monomodal or multimodal) as well as a pain rating on a 0-10 scale (0 = no pain, 1 = threshold level pain, 10 = intolerable pain).
Intensity response
Pain threshold was determined using a random staircase method of assessment of pain thresholds. The laser current necessary to evoke a pain rating of 1 on an 11 point NRS scale was measured at 10-20 sites on the dorsal skin surface of the 2nd, 3rd, 4th, and 5th fingers (i.e., not the thumb) of each volunteer. The average of laser currents necessary to produce a rating of "1" was used to establish the pain threshold. To determine an intensity-effect relationship, both randomly selected SP and LP were then applied with increasing stimulus intensities to different areas of the dorsum of on hand with at least 30 s between stimuli while LEPs were recorded. Subjects were asked to rate the pain immediately after each stimulus. Stimulus intensities were increased in 100 mA (~ 300 mW) increments and each stimulus intensity was presented 4 times within a session. Intensity increases were continued until the subject reached a level of strong pain (rating > 3). Intensity response relationships were then determined for both evoked pain and LEP.
Capsaicin Sensitization
To provide evidence of nociceptor selectivity for pain evoked by LP or SP, changes in LEP and pain sensitivity were tested after topically applying 30 μl of capsaicin (1% in H2O/Ethanol, 50/50 v/v), to the finger of 7 subjects after establishing baseline pain thresholds. 20 minutes after applying capsaicin, thresholds were re-established and subjects were asked to rate the level of pain evoked by the pretreatment threshold current. Significant sensitization was determined by using a one-tailed t test to compare pain thresholds and LEP amplitudes before and after treatments, as well as pain levels evoked by a given stimulus level (pretreatment threshold).
Non-parametric statistics were used to determine whether there was a significant change in descriptors between those given after the first 5 stimuli and those given after the last 5. Analyses of variance were used to detect a significant shift in the average pain rating and LEP amplitude following the first 5 and the last 5 stimuli.
Conduction Velocity
In order to determine conduction velocity and thus provide additional evidence for selective activations of Aδ versus C fibers, in some subjects, after applying 15 SP or LP stimuli, set at a power that was 15% above threshold, the same stimuli were applied to the elbow, while LEP were recorded. The latency from stimulus onset to LEP peak were measured and used to calculate an estimated conduction velocity of the sensory fibers underlying responses to these stimuli.
Competing interests
MIN is the CEO of LasMed, LLC, manufacturer of the laser used in this study. None of the other authors declare competing interests.
Authors' contributions
AT contributed to the data analysis and manuscript preparation; MK contributed to the EEG data processing and data analysis; SC-H collected much of the data and aided in initial analysis; MIN provided expertise in laser stimulation and to the analysis of data; MSA contributed to the design and analysis of the study; DCY provided overall guidance to the project, contributed to data analysis and manuscript preparation. All authors read and approved the manuscript.