Researchers from Denmark have identified a protein called sortilin as a possible target for medicinal drugs. And, as we see with a lot of research, the mice have it good. According to new research, blocking sortilin in mice prevents pain. Will this translate to humans? A study published in the journal Science Advances,concludes that “in all likelihood” it will.
The results are based on a decade of basic research, and even though studies on mice have only been done so far, the study provides hope for the development of a medicine that can help people with pain induced by nerve injury – called neuropathic pain.
Neuropathic pain may be triggered by an acute injury or a chronic disease, like diabetes, and is characterized by different sensations including burning, pricking, stinging, tingling, freezing or stabbing in a chronic and disabling way.
People with severe neuropathic pain often say that they could fill a shopping cart with pain killers ranging from local anesthetic ointments to morphine “without ever really getting any good results” as the primary author of the article, Assistant Professor Mette Richner, of the Department of Biomedicine and the DANDRITE research centre, Aarhus University, Denmark, puts it.
As Richner explains, chronic pain is triggered by overactive nerve cells, i.e. nerve cells where the regulation of their activity is not working properly. For this reason, it is necessary to gain knowledge of the changes happening at the molecular level to be able to ‘nudge things into place again’.
“And it’s here, at the molecular level, that we’ve now added a crucial piece to a larger puzzle,” says Richner, who explains that sortilin appears to ‘put the brakes on the brake’ which, at the molecular level, stops the body’s pain development.
“Once nerve damage has occurred, and the nerve cells go into overdrive, molecules are released which start a domino effect that ultimately triggers pain. The domino effect can be inhibited by a particular molecule in the spinal cord called neurotensin, and our studies show that the neurotensin is ‘captured’ by sortilin, so that the brake is itself inhibited,” explains Richner.
The research group’s hope is that the pharmaceutical industry will continue to investigate whether it is possible to block sortilin locally in the spinal cord, so that the neurotensin can move freely and get the brake to function, thereby inhibiting the pain. In connection with this, Christian Vaegteremphasises that there is obviously a way to go from mouse to human being.
“Our research is carried out on mice, but as some of the fundamental mechanisms are quite similar in humans and mice, it still gives an indication of what is happening in people suffering from chronic pain,” says Christian Vaegter.
The idea of studying the complicated pain-related puzzle in relation to the spinal cord arises from a decade’s worth of research into both pain and sortilin. The initial studies revolved around mice that lack the ability to form sortilin and were apparently pain-free despite nerve damage – and of course the studies were done in accordance with methods approved by the Danish Animal Experiments Inspectorate.
The research group could subsequently ascertain that neither did normal mice develop pain after nerve damage when the researchers blocked sortilin – and from here the hunt for the correlation began, before it was ultimately explained by the regulation of the pain inhibiting molecule neurotensin.