JUN 24, 2016 9:09 AM PDT

Effective, Non-Addictive Options for Chronic Pain

WRITTEN BY: Kara Marker
Nonsteroidal anti-inflammatory drugs (NSAIDS), opioids, anticonvulsants, and antidepressants are all drugs used to help treat chronic pain, a condition that afflicts more than 100 million Americans. However, half of people don’t experience pain relief from these drugs, and the half that do are at risk for opioid addiction, overdoses of which have quadrupled since 1999. These drugs aren’t the answer, but what is?
Credit: www.gizmag.com
Researchers at Drexel University College of Medicine set out to identify other ways to target and treat the causes of chronic pain. The ended up discovering a protein called MeCP2 that played a broad and complex role in causing pain. Directly targeting MeCP2 wasn’t an option though; we need to experience some degree of pain to know when our body is damaged. The other option was to instead target the genes MeCP2 regulated. The only problem? They didn’t know what these genes were.
Just like an antiviral drug might target viral machinery to prevent a pathogen from multiplying and causing infection, the Drexel researchers anticipated targeting the MeCP2-regulated genes to prevent nerve injury-induced chronic pain. MeCP2 controls the expression of these genes, meaning that the researchers don’t need to change the structure of the genes. They just need to change how they are expressed.
The science of gene expression, called epigenetics, is of growing interest in the research community. In the case of chronic pain, it seems like nerve injury causes changes in how MeCP2 binds genes and affects their expression, causing the sensation of constant, increased pain. Interestingly, a mutation in MeCP2 also causes an autism spectrum disorder called Rett syndrome. In addition to severe impairments in talking, moving, eating, and breathing, people with Rett syndrome have a higher tolerance for pain.
Was there a way to achieve a similar effect for people with chronic pain by altering the expression of certain MeCP2-regulated genes? Possibly. The next step was to pin down which genes are specifically regulated by MeCP2 that are also involved in causing chronic pain. Lead author of the Drexel study, Melissa Manners, PhD, focused on the dorsal root ganglia, a bundle of sensory neurons that transfer information between the peripheral nervous system and the spinal cord.
First, Manners and her team confirmed the role of MeCP2 in chronic pain: levels of the protein increased after nerve injury. Next, in a global study of the mouse genome in a chronic neuropathic pain state, the found that MeCP2 bound more genes coding for proteins and small non-protein coding regulatory RNA molecules when the mice were in chronic pain. Specifically, they discovered that MeCP2 binds chromatin, a complex that forms chromosomes from genetic material.
When MeCP2 binds chromatin, it influences the way certain genes are expressed, and scientists can now experiment with changing the expression of these genes. By understanding the pathway of pain centered on MeCP2, new effective and non-addictive targets for pain alleviation can be developed.
Manners’ study was recently published in Epigenetics & Chromatin.

Sources: Drexel University, Scitable by Nature Education, Yale Histology, International Rett Syndrome Foundation
About the Author
Master's (MA/MS/Other)
I am a scientific journalist and enthusiast, especially in the realm of biomedicine. I am passionate about conveying the truth in scientific phenomena and subsequently improving health and public awareness. Sometimes scientific research needs a translator to effectively communicate the scientific jargon present in significant findings. I plan to be that translating communicator, and I hope to decrease the spread of misrepresented scientific phenomena! Check out my science blog: ScienceKara.com.
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