Study paves way to more efficient non-addictive treatment for chronic pain
· News-MedicalResearchers at Karolinska Institutet in Sweden have developed a new comprehensive mapping of genetic activity for understanding the causes of chronic pain. The study, published in Nature Communications, opens way to more efficient non-addictive treatment for chronic pain and potentially headache disorders.
Researchers have long struggled to understand the complex mechanisms behind neuropathic pain after nerve injury - a global problem affecting millions of people. Current treatment often relies on opioids, which are associated with limited effectiveness and numerous side effects, including the risk of addiction.
Although new medications are being tested in clinical trials, they generally focus on targeting a single pathway within a broader and complex pain phenotype.
The scientists behind the new study have developed an innovative atlas of the somatosensory system during neuropathic pain called iPain, focusing on the dorsal root ganglia and trigeminal ganglia.
"Our atlas combines data from multiple sources and various chronic pain models. This comprehensive approach allows us to analyse how cells of the somatosensory system change throughout the development of chronic pain condition", says Saida Hadjab, Principal Scientist at the Department of Neuroscience, Karolinska Institutet, who led the study.
Now available on CellxGene (iPain), this atlas offers valuable resources for future pain research.
"Using our atlas, we identified different pain-related phenotypic states of nociceptors (pain-sensitive nerve cells) that are consistent across different pain models", says Prach Techameena, PhD student in neurobiology in the Hadjab Lab at KI.
The findings led to the discovery of a specific state that marks the persistence of pain in all chronic pain models analyzed.
Saida Hadjab, Principal Scientist at the Department of Neuroscience, Karolinska InstitutetWe found that this lasting pain state is associated with gene sets in nociceptors typically found in senescent cells, suggesting that senescence, commonly associated with aging, plays a novel role in chronic nervous system disorders, even in young individuals."
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