Chronic pain is a common complaint affecting millions of people worldwide. Because it is often a non-specific symptom, proper treatment strategies are more like 'keep doing things until something works'.
A new study has identified a cellular mechanism in the brain of mice that contributes to the development of chronic pain, which the authors believe can lead to a novel pharmacological treatment strategy for chronic pain.
Thomas Nevian and
Mirko Santello
from the Department of Physiology at the University of Bern investigated the modification of neurons by chronic pain in a brain region called Gyrus Cinguli, which is associated with the emotional aspects of pain. In this context the establishment of a «pain memory» plays an important role, as Nevian explains. "The neurons are constantly activated by a noxious stimulus, thus building a memory trace for pain that becomes irreversible. Our idea was to understand this mechanism better to derive potential new treatment strategies."
Pain is perceived by electrical impulses in the neurons. Therefore, the two researchers were searching for changes in the electrical properties of neurons in the limbic system. They found that neurons were more excitable in the Gyrus Cinguli. This was attributable to a down regulation of a specific ion channel, a protein in the cell membrane that determines the electrical properties of the cell. This led to an increased number of nerve impulses in these cells and thus to an increased perception of pain.
Serotonin receptors can alleviate pain
Santello and Nevian tried to manipulate this ion channel to reestablish its functionality. By activating a specific receptor sensitive to the neuromodulator serotonin they succeeded in reestablishing a normal function of the neuron. This reduced the pain perception in an animal model.
"It has been known for some time that serotonin can modulate pain perception and the function of some drugs is based on this," Nevian says. "Nevertheless, what is new in our study now is that we were able to identify a specific subtype of serotonin receptor that reduced the perception of pain more efficiently. This is an important result, which might help to treat chronic pain more efficiently in the future."
The results of the study suggest a novel mechanism how established drugs of the tryciclic class of antidepressants work. So far it was assumed that these drugs act in the periphery on nociceptors and in the spinal cord. The two scientists demonstrated that these drugs can also act directly on the perception of pain in the brain. However, Thomas Nevian emphasizes that "even though we made an important step forward now, it will take some time before novel drugs will be designed based on our results."
Citation: Santello M, Nevian T. Dysfunction of cortical dendritic integration in neuropathic pain reversed by serotoninergic neuromodulation. Neuron, 2015 (in press)
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