Rostral Agranular Insular Cortex Lesion with Motor Cortex Stimulation Enhances Pain Modulation Effect on Neuropathic Pain Model
It is well known that the insular cortex is involved in the processing of painful input. The aim of this study was to evaluate the pain modulation role of the insular cortex during motor cortex stimulation (MCS). After inducing neuropathic pain (NP) rat models by the spared nerve injury method, we made a lesion on the rostral agranular insular cortex (RAIC) unilaterally and compared behaviorally determined pain threshold and latency in 2 groups: Group A (NP + MCS; ) and Group B (NP + RAIC lesion + MCS; ). Also, we simultaneously recorded neuronal activity (NP; ) in the thalamus of the ventral posterolateral nucleus and RAIC to evaluate electrophysiological changes from MCS. The pain threshold and tolerance latency increased in Group A with “MCS on” and in Group B with or without “MCS on.” Moreover, its increase in Group B with “MCS on” was more than that of Group B without MCS or of Group A, suggesting that MCS and RAIC lesioning are involved in pain modulation. Compared with the “MCS off” condition, the “MCS on” induced significant threshold changes in an electrophysiological study. Our data suggest that the RAIC has its own pain modulation effect, which is influenced by MCS.
Neuropathic pain is a neurodegenerative disease, caused by lesion or dysfunction of the central or peripheral nervous system. It is one of the most difficult types of pain to control because it is a multidimensional clinical entity mediated by many different pathophysiological mechanisms [1–4]. Drug-refractory neuropathic pain has been treated with invasive treatments such as lesioning or electrical stimulation therapy in the central or peripheral nervous system. Because of advantages such as reversibility and adjustability, neuromodulation therapy has become more popular.
In 1991, Tsubokawa first reported the use of motor cortex stimulation (MCS) in a patient with chronic, drug-resistant neuropathic pain . MCS was initially applied to central pain secondary to thalamic stroke, but, over time, its usage expanded to various other types of neuropathic pain. The clinical literature reveals that chronic MCS shows approximate 45 to 75% of pain control rate [6–10]. Thus, the MCS procedure was accepted as a promising therapy for patients with severe drug-refractory pain. However, despite the clinical use of MCS for pain modulation, the mechanisms underlying its effects remain unclear.
There were several imaging studies and electrophysiological investigations performed to solve the mechanism of MCS, and they showed that many brain structures are activated after MCS [11–13]. MCS was found to attenuate hyperactivity of thalamic neurons . We have previously reported that MCS modulate pain-signaling pathways and suppress activation of the ventral posterolateral nucleus (VPL) . The insular cortex, although not yet extensively explored, also showed clear involvement in pain perception through imaging studies using PET or fMRI. Within the insular cortex, in animal studies, the rostral anterior insular cortex (RAIC) has extensive reciprocal corticocortical connections which shows its involvement in multiple aspects of pain behavior . Also after making a lesion in the RAIC, there were diminished pain-related behaviors in neuropathic models without lateralization, which shows clear evidence of the pain modulation role of RAIC .
The aim of this study was to evaluate the role of pain modulation in the RAIC during MCS.
2. Materials and Methods
All procedures were conducted according to the guidelines of the Ethical Committee of the International Association for the Study of Pain and approved by the Institution Animal Care and Use Committee (IACUC) of Yonsei University . Male Sprague-Dawley rats () weighing 180–200 g were used in this study. Three animals were housed per laboratory cage with food and water available ad libitum. Light was controlled under a 12 h light/dark (light on between 07:00 am and 19:00 pm) cycle. The temperature was maintained at °C and relative humidity was at %. Animals were allowed to acclimate for at least a week before surgery and behavioral testing. The behavior-based study of the MCS effect was observed in two animal groups: Group A, a neuropathic pain group (), and Group B, neuropathic pain + RAIC lesion group (). Furthermore, neuronal activity of MCS effect was measured electrophysiologically in the neuropathic pain group ().
2.2. Surgical Procedures
2.2.1. Surgical Procedures for Pain Model
To induce neuropathic pain, we used the spared nerve injury (SNI) method . Rats were deeply anesthetized with pentobarbital sodium (50 mg/kg, intraperitoneally), and the left sciatic nerve was exposed. Under a surgical microscope (Olympus, Tokyo, Japan), the three major divisions of the sciatic nerve were exposed, and the common peroneal and tibial nerves were completely ligated and transected. Hemostasis was completed, and the cut was closed with muscle and skin sutures.
2.2.2. MCS Electrode Implant
For MCS, we used a custom-made liquid crystal polymer electrode . One week after establishing the animal model for neuropathic pain, we measured the pain threshold to determine whether the neuropathic pain had been effectively induced. A detailed description of our behavior test for measuring pain threshold is in Section 2.3.1. After the behavior test, rats that did not exhibit a neuropathic pain response were excluded from this study. To implant the MCS electrode, rats were anesthetized with pentobarbital sodium (50 mg/Kg, intraperitoneally) and fixed with a stereotaxic frame (Narishige, Tokyo, Japan). The scalp was opened and the skull was exposed. To place the electrode on the left hindlimb area of the primary motor cortex , we made a rectangular hole (2.0 mm × 2.0 mm). The coordination was from −0.2 to +1.8 mm from the Bregma and from 0.5 to 2.5 mm from the midline. The electrode was placed in the epidural space, and the electrode was firmly fixed using bolts and glue. The scalp was secured with sutures after completing all procedures.
2.2.3. RAIC Lesion
In Group B, prior to implanting the MCS electrode, we made a burr hole that allowed us to insert an electrode in the target site (RAIC, AP: anteroposterior direction: +1.0 mm from the Bregma, ML: midline: +4.5 mm right side, lateral from midline, and DV: dorsoventral direction: −6.0 mm from the dura mater) . After inserting electrodes in the target coordinates, we delivered an electrical pulse of 0.1 mA for 10 seconds for the RAIC lesioning. Then, the lesioning electrode was removed and the MCS electrode was implanted.
2.3. Behavior Tests
The time table for SNI modeling and behavioral test in the two groups is presented in Figure 1.
2.3.1. Measuring Tactile Threshold
Rats were placed inside acrylic cages ( cm) on a wire mesh grid for measuring the mechanical threshold. After 30 minutes of adaptation, a series of von Frey filaments (0.4, 0.6, 1, 2, 4, 6, 8, and 15 g of bending force) were applied to the lateral edge of the left hind paw. We calculated the tactile threshold by using the up and down method .
2.3.2. Measuring Response Latency
To measure the response latency, rats were placed in the same acrylic cages. After 30 minutes of adaptation, we applied painful stimulation to the left hindlimb, using a Plantar test unit (model 37370, Ugo Basile Biological Instruments, Comerio, VA, Italy) which measures the time by gradual application of strength automatically. When the rat initiated a withdrawal response, the Plantar test unit recorded the duration of resistance from stimulation and the value of final force. We measured the latency three times and used the average value for analysis.
2.3.3. Behavioral Test Schedule and MCS Parameters
After 30 min of adaptation in the acryl cages, MCS was turned on (biphasic pulses of 65 Hz, 210 μs, 80 μA, for 30 min) using a stimulator (Model 2100, A-M Systems, Sequim, WA, USA). Behavioral tests were conducted at the following time points: before stimulation, 30 minutes after the start of stimulation, immediately after ceasing stimulation, and 5 times every 10 min.
We simultaneously recorded neuronal activity in the VPL of the thalamus and RAIC of NP model to compare the changes before and after MCS. Rats (), confirmed NP models after behavioral tests, were anesthetized with urethane (1.3 g/kg), and a microelectrode (573220, A-M Systems, Sequim, WA, USA) was inserted into the VPL and RAIC to obtain extracellular recordings of single unit activity. Two-channel array electrodes were positioned stereotactically in the VPL (ML: +2.8 mm; AP: −2.2 mm; DV: −6.0 mm from the Bregma) and the RAIC (AP: +1.0 mm; ML: +4.5 mm; DV: −6.0 mm from the Bregma). The neuronal activities were recorded for 5 minutes. During acquisition of the neural signal, mechanical stimulation, using 300 g of von Frey hair filaments, was applied to the rats’ left hind paw area. Signals from the microelectrode were amplified (amplifier model 1700, A-M Systems, Sequim, WA, USA), and the signal was converted and transmitted to the recording system using an AD converter (Micro 1401, Cambridge Electronic Design Limited, Milton Road, Cambridge, UK). The data were stored by Spike 2 (Cambridge Electronic Design Limited, Milton Road, Cambridge, UK). Recorded waveforms were analyzed using Offline Sorter (Plexon Inc., USA), NeuroExplorer (NeuroExplorer Inc., USA).
Signal analysis was obtained for 20 sec before and after MCS. Because of firing differences in each region following MCS, the interval between the signal analyses was regulated.
2.5. Histological Verification of RAIC Lesion
To verify the RAIC lesioning after completion of our experiments, rats were intracardially perfused with normal saline and fixed with 4% paraformaldehyde in PBS (). The brain was carefully removed and prepared for frozen sectioning. Coronal sections of 30 μm thickness were obtained using a microtome with deep freezer (Figure 2). The slices were dyed using cresyl violet. Microscopy images were obtained using a microscope (Olympus, Tokyo, Japan).
2.6. Statistical Analysis
Data are reported as mean ± SEM. Behavioral test data were analyzed using one-way and two-way analysis of variance (ANOVA) with Bonferroni’s post hoc test. Electrophysiological data were evaluated using the Friedman test followed by Dunn’s post hoc test. The values of <.05 were considered significant. All statistical analyses were performed using SPSS (Version 20, SPSS Inc., Chicago, IL, USA).
3.1. Changes of Mechanical Threshold in Groups A and B
One week after pain modeling, we measured mechanical threshold in these rats. The average mechanical threshold was significantly decreased from to g (mean ± SEM) in Group B and from to g in Group A (Figure 3). After RAIC lesioning, in Group B, we measured the mechanical thresholds after the 2nd week. The average mechanical threshold of Group B was increased to g and this was also significantly higher () than that of Group A ( g). At the 3rd week after modeling, the increased mechanical thresholds in Group B were maintained ( g), and the threshold was also significantly higher than that in Group A ( g, ).
3.2. Changes in Mechanical Thresholds in Groups A and B with MCS
To examine the effect of MCS over time in each group, we measured pain thresholds in both groups with MCS at the 3rd week when the neuropathic pain model was established. Mechanical thresholds were measured in Groups A and B at regular time intervals. In both Groups A and B, the statistical significant changes of threshold were observed only during MCS on and immediate MCS off (Table 1). Compared to prestimulation value (Pre; g), mechanical threshold values were increased in Group A during MCS on (15 minutes; g) and immediate MCS off (30 minutes; g) and 10 minutes after MCS off (40 minutes; g). Similarly, compared to prestimulation value (Pre; g), mechanical threshold values were increased in Group B during MCS on (15 minutes; g) and immediate MCS off (30 minutes; g) and 10 minutes after MCS off (40 minutes; g).
In order to investigate the effect of RAIC lesion on mechanical thresholds over time, Groups A and B were compared at each time point. Statistically significant differences in threshold values between Groups A and B were observed at time points of 15, 30, and 40 minutes (Figure 4).
We measured pain response latency at 3 weeks after SNI modeling in both Groups A and B. In Group A, the baseline mechanical latency was sec, and the latency was significantly increased by MCS on, sec, which was statistically significant (). In Group B, the baseline latency was sec, and it increased to sec during MCS on, which was also statistically significant ().
In Group B without MCS, the latency showed significant increase compared with Group A without MCS. These findings were also noted after MCS on (Figure 5). Also, two-way analysis of variance showed significant interaction between MCS and RAIC lesion factors on withdrawal latency (Figure 5). Therefore, MCS with additional lesioning of the RAIC (Group B with MCS on) was more effective for pain suppression than MCS alone.
3.4. Neuronal Activity in the VPL and RAIC with MCS
Neuronal firing rate was rapidly increased in both VPL (%) and RAIC (%) upon mechanical pain stimulation and showed typical postdischarge patterns of neuropathic pain (Figures 6(a) and 6(b)). Without MCS, in both VPL and RAIC, percentage changes in spontaneous activity were not significantly different between pain stimulation (30–50 s; pain) and after discharge (60–80 s; after). Firing rates were significantly reduced in the postdischarge zone (60–80 s) with MCS on in both VPL (%) and RAIC (%) compared to firing rates during pain stimulation (30–50 s) with MCS off (VPL: %; RAIC: %; Figures 6(c) and 6(d)).
The purpose of our study was to investigate the pain modulatory effect of MCS on the insular cortex, especially in the RAIC. The mechanism of MCS-induced pain modulation has still not been elucidated despite its clinical use. One of the most widely accepted hypotheses to explain the antinociceptive effect following MCS is that pain is modulated by descending inhibitory systems [2, 22–24]. The corticospinal tract from the motor cortex descends through the internal capsule and, after decussating in caudal medulla, reaches the spinal cord neurons in the anterior and posterior horn . Because of a lack of direct projection from the primary motor cortex (M1) to superficial layers or the marginal zone of the dorsal horn, MCS may indirectly inhibit nociceptive inputs in the spinal cord . Moreover, the motor cortex has diverse efferent projections to widely distributed cortical and subcortical areas. These structures include the thalamic nuclei, which receive strong projections from the motor cortex, an important site for sensory modulation . The periaqueductal gray (PAG) system, coupled with the rostral ventromedial medulla (RVM), exhibits descending antinociceptive effects by activating the opioid system, and these two structures are connected with descending tracts . Another MCS antinociception mechanism could be modulated by an ascending inhibitory system. The thalamus, activated by MCS, could inhibit nociceptive processing, but the specific nuclei affected by MCS and the source of altered inhibition are still debatable . In an animal study of MCS, Cha et al. reported an enhanced inhibitory and antinociceptive input from the nucleus of zona incerta to the posterior thalamus .
Melzack and Casey suggested that the pain experience reflected interacting sensory, affective, and cognitive dimensions, which could influence each other . In some imaging studies, attempts were made to determine the mechanism underlying the MCS. For example, using positron-emission tomography (PET), researchers have found that MCS was associated with increased blood flow in the orbitofrontal, subgenual anterior cingulate cortex, midcingulate cortex, insula cortices, thalamus, and brainstem [11–13]. Another PET study showed that the anterior midcingulate cortex and PAG were significantly correlated with the degree of clinical outcome of MCS, showing that these structures exhibited decreased exogenous ligand binding because of increased endogenous opioid secretion .
From previous imaging studies, one might infer that MCS could influence the insular cortex. However, there were no other experimental studies to implicate the role of the insular cortex in chronic stimulation of the motor cortex. The insular cortex is known as a multidimensional neuroanatomical convergence site for the integration of pain. By direct connection from the thalamoinsula pathway, pain information could be received at this site for sensory and affective integration. Historically, pain related to the insular cortex was only noted by asymbolia and pseudothalamic pain syndrome [33, 34]. Other evidence was from electrical stimulation of the posterior insula cortex, which produced pain with thermal stimuli in distinct sites on contralateral locations . In animal studies, the RAIC showed somatic afferent pathways in relation to nociceptive input [15, 36, 37]. In addition, Coffeen et al. showed diminishment of neuropathic pain-related behaviors after lesioning in the RAIC of neuropathic model which was not in sham lesion, similar to our study. However, the MCS effect on the RAIC had not yet been demonstrated. Therefore, we used two groups of animals, each with an established neuropathic pain model, either without RAIC lesioning (Group A) or with lesioning (Group B), and compared their pain thresholds behaviorally and electrophysiologically. Upon mechanical stimulation, pain thresholds were significantly lower in Group A, which was what we expected from previous research. However, when we added MCS to both groups, Group B showed significant increase in threshold compared to Group A. These findings were also noted in pain latency from paw withdrawal tests. Therefore, we could assume that RAIC has its own pain modulation effect, and when adding MCS, the additional pain modulation effect could be shown. But, in our electrophysiological study, the percentages of changes in spontaneous activity were increased in both VPL and RAIC after mechanical stimulation with 300 g von Frey filament. Compared to the MCS off state, the changes of percentages after MCS on were noted in both regions (VPL and RAIC), which means the RAIC is also influenced by MCS. However, the quantitative influence of MCS on insular cortex is limited from our results. And though the RAIC has related to not only pain behavior but also anxiety behavior, we could make conclusion cautiously as above when we coupled it with our electrophysiological study.
In human studies, direct electrical stimulation of insular cortex during depth stereotactic EEG showed some degree of somatotopic organization . But, in animal studies, the somatotopy related to pain process is not fully understood. Jasmin et al. showed a unique property of RAIC in that it could respond as both analgesic and hyperalgesic responses by selective modulation of GABA receptors . The RAIC has multiple reciprocal connections with pain structures, such as orbital, infralimbic, and anterior cingulate cortices, rostroventral medulla, and periaqueductal gray matter . In addition, caudal granular insular cortex (CGIC), about 4 mm caudal to RAIC, is also known as having a role in long term alleviation of allodynic pain modulation . In this study, we did not compare the MCS effect on both the RAIC and the CGIC, so our findings have limitations on the information about MCS effect on the whole insular cortex. Additionally, the centromedian/parafascicular (CM/Pf) nuclei, which receive dense projection from the motor cortex, were inhibited by MCS, and these nuclei have interconnection with the limbic system. Therefore, our electrophysiological results could be the result of direct response to MCS or from indirect through CM/pf nuclei . To clarify the source of the effect of MCS on RAIC, we will need to block the CM/Pf effect, which could also demonstrate the amount of MCS effect on RAIC.
The results in this work suggest that the RAIC is influenced by MCS and that lesioning RAIC could produce more pain reduction. Along with previous data, our findings may contribute to a better understanding of MCS effect and the role of RAIC in pain modulation.
The authors report no conflict of interests.
Hyun Ho Jung and Jaewoo Shin contributed equally to this work as co-first authors.
This study was supported by the grant from CABMC (Control of Animal Brain Using MEMS Chip) funded by Defense Acquisition Program Administration (UD140069ID).
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