The discovery could explain the repeated – and costly – failure over the last 20 years of clinical trials of potential pain-killing drugs that targeted the substance, known as ‘Substance P’.
Substance P is produced in both the central nervous system – the brain and spinal cord – and in our peripheral nervous system – all the other nerves and nerve cells that send signals to the brain.
The new research, by the Hebei Medical University in China and the University of Leeds in the UK, has found that, in the peripheral nervous system, Substance P makes nerve cells less responsive and excitable, thereby reducing sensations of pain. This is in direct contrast to its role in the central nervous system, where it triggers very different signals, exciting neurons and so promoting pain.
“This means that when drugs were used in trials to suppress Substance P’s action in the central nervous system, they may have also prevented it from acting as a painkiller in the peripheral system. So, although the drugs looked like they worked in the lab, when they moved to clinical trials, they failed.”
Substance P works in the peripheral system by modulating the action of certain proteins that control the ability of pain-sensing neurons to respond to ‘painful’ stimuli. In particular, Substance P makes one type of these proteins extremely sensitive to zinc, so that natural trace levels of zinc in circulation are enough to dampen their activity and suppress the neuronal responses.
Professor Gamper – who is also a visiting professor at Hebei Medical University – believes this discovery could open the door to new drugs that don’t have the negative side effects currently associated with stronger painkillers.
“Drugs such as morphine hijack the body’s natural painkilling mechanisms, such as those used by endorphins. But because they act within the central nervous system, they can affect other brain cells that use similar pathways, leading to side effects such as addiction or sleepiness,” Professor Gamper added.
“If we could develop a drug to mimic the mechanism that Substance P uses, and ensured it couldn’t pass the blood brain barrier into the central nervous system, so was only active within the peripheral nervous system, it’s likely it could suppress pain with limited side effects.”
The study – which looked at the action of Substance P within nerve cells in the lab and in animal models – focused on acute pain, but Professor Gamper aims to look at its role within chronic pain as well.
The research was funded by the Medical Research Council in the UK and by the National Basic Research Program and the National Natural Science Foundation of China. It is published in Antioxidants and Redox Signalling.
Professor Chris Peers, one of the paper’s co-authors is available for interview.
Media contact: Peter Le Riche, University of Leeds press office on 0113 343 2049 or email firstname.lastname@example.org
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