Pain occurs as a result of injury, such as peripheral neuron damage or inflammation stemming from peripheral tissue violation. Research findings have been published on the involvement of central nervous system abnormalities in the onset of pain and sustained pain. The primary somatosensory cortex in the cerebral cortex plays an important role in identifying the strength and location of pain. Research carried out using fMRI and two-photon microscopy has shown that activity in this part of the brain is accelerated when acute pain is experienced. However, it has yet to be revealed how the functional connectivity and synchronization between neurons changes over time, and what kind of effect these alterations have on pain.
The researchers conducted experiments using inflammatory pain model mice and the results revealed that both the spontaneous activity of the neuronal population and the synchronized activity between neurons in the primary somatosensory cortex increased during acute pain. Furthermore, they discovered that when a single neuron was stimulated with holographic light, there was an increased response from the surrounding neurons. As the pain was ameliorated, the neurons gradually returned to their original state. The researchers also showed that expression levels in N-type calcium ion channels are involved in this mechanism, revealing that the pain threshold could be restored when inhibitors that blocked these channels were administered. It is hoped that these discoveries can contribute towards treatments for patients with chronic pain.
The research group included the following members: Specially Appointed Assistant Professor OKADA Takuya and Professor MIZOBUCHI Satoshi, both of the Division of Anesthesiology, Kobe University Graduate School of Medicine. Professor WAKE Hiroaki (Kobe University Organization for Advanced and Integrated Research) and Assistant Professor KATO Daisuke, both of the Department of Anatomy and Molecular Cell Biology, Nagoya University Graduate School of Medicine. Professor MATOBA Osamu (Kobe University Organization for Advanced and Integrated Research). Professor TAKIGUCHI Tetsuya (Kobe University Graduate School of System Informatics). These research findings will be published in Science Advances on March 19, 2021.
Main Points
The research group showed that when acute pain is experienced, there is an increase in both spontaneous activity and synchronized activity in neurons in the primary somatosensory cortex. Furthermore, when a single neuron was stimulated with holographic light, the response from the surrounding neurons also increased during this acute pain. The researchers also demonstrated that when the pain was ameliorated, the neurons returned to their original state. The expression levels of N-type calcium ion channels in the primary somatosensory cortex were elevated during acute pain and the researchers revealed that this pain could be ameliorated by administrating channel inhibitors (either as an intraventricular injection, or as an ointment on the surface of the primary somatosensory cortex). It is hoped that these results will contribute towards the development of treatments for patients suffering from chronic pain. Research Background
Pain occurs as a result of injury, such as peripheral neuron damage or inflammation stemming from peripheral tissue violation. It is an unavoidable sensation that everyone has experienced, however the detailed mechanism for the onset and sustention of pain has yet to be illuminated. Vital research into pain has been conducted that focuses on the activation of neurons and glial cells in the dorsal horn of the spinal cord. With the development of imaging technologies, there has been increased research into the relationship between pain and regions of the brain in recent years.
The cerebral cortex's primary somatosensory cortex (S1) is an area of the brain that plays in important role in distinguishing pain. Research conducted using imaging technologies such as fMRI and two-photon microscopy have shown that the neuronal population in S1 is aggravated during acute pain, however the detailed, underlying neural networks in S1 that are involved in generating and sustaining pain have not been clarified.
The research team used a two-photon microscope to conduct calcium imaging to track identified neurons, illuminating increases in both spontaneous neuronal activity and synchronization between S1 neurons during acute pain. Furthermore, they revealed that when a single neuron was stimulated with holographic light, there was an increased response from the surrounding neurons and as the pain was ameliorated, the neurons gradually returned to their original state. In addition, the expression of N-Type calcium ion channels was found to play a role in this mechanism, and the researchers showed that when this expression was corrected, the pain threshold could be effectively restored.
Research Methodology and Findings
The researchers conducted calcium imaging using a two-photon microscope. This method enabled them to monitor the activity of neurons in a living brain. Inflammatory pain model mice were developed by injecting Complete Freund's Adjuvant (CFA) into the hind paws. During acute pain, the spontaneous activity of neurons in the 2/3 layer of S1 increases, as does the synchronization between neurons. The research group also showed that the neurons returned to their original state once pain was ameliorated. Moreover, they discovered that the higher the level of synchronization between neurons, the lower the pain threshold (Figure 1).
To verify the above results, an experiment was conducted using a combination of two-photon microscope calcium imaging and holographic stimulation. It was discovered that when a single S1 neuron in an inflammatory pain model mouse was stimulated, the response from the surrounding neurons increased during acute pain. Conversely, when pain was ameliorated, the response from the surrounding neurons decreased. In summary, it was shown that synchronization between neurons increased as a result of strengthened functional connectivity between neurons in S1 during acute pain, and that when this pain was ameliorated, this synchronization decreased.
In order to verify the relationship between the increased spontaneous activity of neurons in S1 2/3 layer and the threshold for pain, a modified human muscarinic receptor (hM3Dq) activated by clozapine-N-oxide (CNO) was used to artificially induce increased neuronal activity in the S1 of the mice. The researchers then compared the neuronal activity and pain threshold in the mice before and after CNO administration (using chemogenetics (*4)). These results showed that when S1 neuronal activity was artificially induced in mice, the synchronization between neurons increased while the pain threshold decreased.
Flow Cytometry (*5) was used to investigate the molecular mechanism relating to these results. The expression levels of each ion channel in the S1 neurons of inflammatory pain model mice that had experienced acute pain were compared with those of wild-type mice that had not been exposed to pain. The results showed that in the inflammatory pain model mice, there was increased expression in the N-type calcium channels, and that by administering calcium channel inhibitors (either as an intraventricular injection, or as an ointment on the surface of S1), the pain threshold could be restored.
Further Research
The primary somatosensory cortex (S1) is an area of the brain that plays in important role in distinguishing pain, and research up until now has shown that neuronal population activity in S1 is accelerated when acute pain is induced. The current research study revealed that not only was this activity accelerated in response to acute pain but that there is also an increase in functional connectivity and synchronized activity between the neurons.
Next, the research team is due to examine the causal relationship between neuronal activity and pain, using holographic stimulation. They will do this by first identifying and determining the features of the S1 neurons that play a large role in pain, and then applying holographic stimulation to the identified cells to investigate the causal relationship. Furthermore, the researchers plan to look into possible treatment options for acute pain, such as preventing the increase in functional connectivity between neurons.
INFORMATION:
Glossary
1. Two-photon microscope: A microscope that can be used to observe cells inside living tissues. Its infrared laser can permeate through many layers of tissue, meaning that it can even be used to observe deep regions of the brain.
2. Calcium imaging: This method for observing the activity of neurons uses a two-photon microscope to optically measure the concentrations of calcium ions inside them.
3. Holographic stimulation: Holographic technologies allow us to record light wave information pertaining to an object and then regenerate this into 3D information using a computer. By utilizing this holographic technology, it is possible to stimulate only select cells with light.
4. Chemogenetics: A method of artificially stimulating or suppressing cell activity. This is achieved by expressing a modified human muscarinic receptor in the target cell. This receptor is activated by clozapine-N-oxide (CNO), altering the cell's activity.
5. Flow Cytometry:A technique used to rapidly observe and analyze particles or cells individually. The cells or particles are separated from each other by suspending them in liquid. They are then run past a laser beam in single file.
Acknowledgements
This research received funding from the Japan Science and Technology Agency (grant number: JPMJCR1755) and the Japan Society for the Promotion of Science (18K16482).
Journal Information
Title:
Pain induces stable, active microcircuits in the somatosensory cortex that provide a new therapeutic target
DOI:TBA
Authors:
Takuya Okada, Daisuke Kato, Yuki Nomura, Norihiko Obata, Xiangyu Quan, Akihito Morinaga, Hajime Yano, Zhongtian Guo, Yuki Aoyama, Yoshihisa Tachibana, Andrew J Moorhouse, Osamu Matoba, Tetsuya Takiguchi, Satoshi Mizobuchi and Hiroaki Wake
Journal:
Science Advances
