Abstract
Molecular pain is a relatively new and rapidly expanding research field that represents an advanced step from conventional pain research. Molecular pain research addresses physiological and pathological pain at the cellular, subcellular and molecular levels. These studies integrate pain research with molecular biology, genomics, proteomics, modern electrophysiology and neurobiology. The field of molecular pain research has been rapidly expanding in the recent years, and has great promise for the identification of highly specific and effective targets for the treatment of intractable pain. Although several existing journals publish articles on classical pain research, none are specifically dedicated to molecular pain research. Therefore, a new journal focused on molecular pain research is needed.
The word pain is thought to derive from the Latin word poena, meaning punishment. An emotional reaction to a punishment might have been what Aristotle experienced, as he defined pain as an emotional event. René Descartes, the seventeenth-century philosopher and scientist, pictured a pain pathway consisting of a thread with two ends: one end is in a peripheral part of the body, for example a toe, and the other end is a bell in the brain. According to this picture, fire touching a toe pulls the thread, and rings the bell to sound a warning in the brain. Over the past decades, and in the current Decade of Pain Control and Research (2001–2010), pain research has undergone major changes, from a system level to cellular, subcellular and molecular levels. A new era of molecular pain research is now emerging, and the journal
Recent advances in pain research are in large part due to the rapid progress in neuroscience, molecular biology, and other fields in the life sciences. Breakthroughs in bio-medical technologies have allowed us to address many important issues about pain, enriching our knowledge about the mechanisms by which sensory signals including pain are initiated, encoded, conducted, transmitted, modulated, and perceived. For example, sensory molecular biology has led to the molecular cloning and identification of a number of receptors involved in thermal, mechanical, and nociceptive signalling at the periphery, some of which have been targeted for pain management. Modern electrophysiology has been used to demonstrate the critical roles of synaptic plasticity in pain processing in the spinal cord and the brain. Long-term potentiation and long-term depression at synapses of central sensory regions have delineated the ‘memory of pain’ by neuronal circuitry along pain transmitting pathways. Functional imaging of supraspinal areas has revealed central areas related to pain processing (for example, areas coding behavioural learning and memory) and, more significantly, it has now become possible to see the alteration of these signalling pathways under chronic pain conditions. Finally, genomics and proteomics have been applied to pain research to help identify the changes in the array of molecules present in cells under chronic pain conditions. Research within all these fields will provide a better understanding of the physiological and pathological mechanisms of pain.
Pain research at the cellular, subcellular, and molecular levels has provided insights that help guide the treatment and management of intractable pain conditions including neuropathic pain, cancer pain and other chronic pain conditions. At the same time, these efforts continue to provide scientific insights into an inherently fascinating biological process. New molecules related to pain continue to be cloned and identified. It should be stressed that a ‘non-pain molecule’ under physiological conditions can become a ‘pain molecule’ under pathological conditions. This might be an underlying mechanism for spontaneous pain or pain sensation elicited by innocuous stimuli. Thus, the aims of molecular pain research should include ‘non-pain molecules'. One big task facing us is that many of the pain-related genes or proteins that have been identified are also important for other neuronal functions in the spinal cord and the brain. Pain triggers various responses in the spinal cord and the brain, including reflexes, conscious perception, cognitive learning and memory processes, emotional reaction such as depression, and drug addiction. Thus, molecules that are associated with pain are not only those located on the peripheral nerve endings for the sensing and encoding of stimuli, but also molecules that are present along sensory paths from the spinal cord to the brain for integrating and modulating sensory information. Molecular targets at different levels along sensory pathways are key to future identification of new drugs and therapies that effectively manage intractable pain conditions with low side effects. Molecular pain research will offer new opportunities for drug development in the pharmaceutical industry and improved treatment options in the clinical setting.
In our journey to explore pain mechanisms and to identify effective targets for pain management, it is important for scientists around the world to have a rapid and freely accessible forum for exchanging ideas, debating hot topics, developing collaborations, promoting science, and improving pain medicine. As an online, Open Access journal,
The launch of
Footnotes
The author(s) declare that they have no competing interests.