INFORMATION:
This research was supported by: The Canadian Institutes of Health Research, the Canada Research Chairs Program, Brain Canada, the Krembil Foundation and the Anne and Max Tanenbaum Chairs Program.
About the Canadian Neuroscience Meeting
The Canadian Association for Neuroscience is holding its 9th Annual Meeting in Vancouver, May 24 to 27 2015. Held yearly since 2007, it brings together researchers working in all fields of neuroscience research. Organized by neuroscientists and for neuroscientists, it highlights the best and most novel neuroscience research in Canada every year.
About the Canadian Association for Neuroscience:
The Canadian Association for Neuroscience is the largest association dedicated to the promotion of all fields of neuroscience research in Canada. The association has been organizing a yearly annual meeting since 2007. Learn more about our meeting at:
http://can-acn.org/meeting2015
About The Hospital for Sick Children
The Hospital for Sick Children (SickKids) is recognized as one of the world's foremost paediatric health-care institutions and is Canada's leading centre dedicated to advancing children's health through the integration of patient care, research and education. Founded in 1875 and affiliated with the University of Toronto, SickKids is one of Canada's most research-intensive hospitals and has generated discoveries that have helped children globally. Its mission is to provide the best in complex and specialized family-centred care; pioneer scientific and clinical advancements; share expertise; foster an academic environment that nurtures health-care professionals; and champion an accessible, comprehensive and sustainable child health system. SickKids is proud of its vision for Healthier Children. A Better World. For more information, please visit http://www.sickkids.ca.
New findings about mechanisms underlying chronic pain reveal novel therapeutic strategies
Michael Salter, from The Hospital for Sick Children (SickKids), uncovers a critical role for microglia in pain
2015-05-26
(Press-News.org) Chronic pain affects hundreds of millions of people worldwide and is a major cause of disability, causing more disability than cancer and heart disease. Canadian researchers, including Michael Salter at SickKids are shedding light on the molecular dynamics of chronic pain. They have uncovered a critical role for a class of cells present in the brain and spinal cord, called microglia, in pain. They have found microglia-to-neuron-signaling to be crucial in the development of pain hypersensitivity after injury, but also for one of the paradoxical effects morphine and other opioids sometimes produce, called hyperalgesia, which is an increase in pain sensitivity. The identification of these key players in the development of chronic pain helps identify important targets for the development of novel therapeutic avenues. Dr. Salter presented his latest results at the 9th Annual Canadian Neuroscience Meeting, on May 26th 2015 in Vancouver, British Columbia.
"We're developing a new understanding of the control of microglia-neuron interactions that may be critical for individualizing pain therapies" said Salter.
Pain is a complex experience. The International Academy for the Study of Pain, IASP defines it as, "an unpleasant sensory and emotional experience associated with actual or potential tissue damage, or described in terms of such damage." While acute pain can be useful, as a signal that protects us from injury or even death, and inflammatory pain can protect us during healing, chronic neuropathic pain, which is a disease of the nervous system, is pain that persists after an injury is healed, serves no useful function and is a major cause of disability.
Work done in Dr. Salter's laboratory has helped to gain understanding of the changes in the nervous system, and to uncover the key molecules that form the cascade of events that lead to chronic pain. A class of cells called microglia play a central role in this cascade. Microglia constitute about 10% of the cells of the adult brain and spinal cord (also known as the central nervous system). Initially thought to have simply a role in supporting neurons (the term glia derives from the same root as glue), microglia were later shown to have an important role in the spinal response that follows nerve injury.
"Exciting new discoveries indicate that microglia not only play a critical role in disease states but also in the normal development and functioning of the brain and spinal cord," Salter explained. "We are looking at these cells in an entirely new light."
More recently, microglia have been shown to have a much more active role in the healthy central nervous system, and to be highly active in surveillance and rapid response - microglia monitor and control the activity of neurons in the healthy nervous system. Within the dorsal horn of the spinal cord, the area through which pain signals travel to the brain, microglia block the inhibition of pain transmitting neurons, making transmission of the pain signal more efficient. This can lead to allodynia, which is defined as pain due to a stimulus that does not normally provoke pain.
Nerve injury activates a receptor on microglia, called P2X4, which, in turn causes the release of a molecule called Brain Derived Neurotrophic Factor, or BDNF. BDNF has been shown to have a role in learning in the motor cortex, where its release results in enhanced motor performance. Dr. Salter proposes that when microglia-derived BDNF facilitates the output of the dorsal horn pain-transmitting network, the result is enhanced pain. When BDNF facilitates this network, it is as if neurons had "learned" pain, and they become more efficient in the transmission of pain signals.
Morphine and other opioids are sometimes prescribed to treat chronic pain when other treatments do not work. While these drugs can be very efficient to relieve pain, some patients develop a paradoxical effect, called hyperalgesia. Paradoxical hyperalgesia is an increase in pain caused by drugs prescribed to alleviate pain. Dr. Salter's research shows that microglia-to-neuron-communication is crucial for the development of this effect.
Research done by Dr. Salter and his colleagues shows how the experience of pain can change the nervous system to make it more sensitive to further painful experiences, to feel pain in response to events that do not cause pain in most people, and how opioids can paradoxically cause more pain. Dr. Salter anticipates that by targeting the signaling pathways identified in these studies new therapeutic strategies for chronic pain will be developed
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[Press-News.org] New findings about mechanisms underlying chronic pain reveal novel therapeutic strategiesMichael Salter, from The Hospital for Sick Children (SickKids), uncovers a critical role for microglia in pain