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Neuro-Inflammation and Chronic Pain Link Established: Authors Call for Treatment Trials

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Reprinted with the kind permission of Cort Johnson and Health Rising.

…the present findings offer clinical implications that may serve to guide future studies of the pathophysiology and management of a variety of persistent pain conditions.” Loggia et. al.

Chronic pain was thought for many years to be mostly a neuronal problem. Over or underactive neurons in the spinal cord or neuronal pathways in the brain were creating problems with pain processing – causing an overly robust pain response.

A new player, the microglia, entered the pain field about ten years ago. Among other activities the microglia direct the immune response in the brain and spinal cord. In the past ten years numerous animal studies have incontrovertibly determined that over-active microglia play a critical role in producing chronic pain states.

Studies indicating that a nerve injury causes the microglia to proliferate tremendously suggest that an initial nervous system insult could, in some people, produce a kind of microglial infrastructure for pain and fatigue. By pumping out pro-inflammatory factors that activate pain producing pathways, the microglia could be the spark that keeps the fire, to speak, burning in the brain. Microglial activation by itself is able to induce allodynia in laboratory animals. Animal studies suggest that reducing microglial activation could delay or even prevent the formation of nerve pain.

Despite the great promise that microglial (and astrocyte) activation has shown in helping to explain how chronic pain occurs no one has been able to validate the role they play in producing chronic pain in humans.

The problem has been technological; until recently the technology to detect microglial activation without an autopsy simply wasn’t available. The development of molecules or ligands that bind to proteins associated with microglial (and astrocyte) upregulation is enabling researchers to get a hand on microglial activation. (Astrocytes – a form of glial cell – may be as important as the microglia in the production of chronic pain).

The molecule used in this study – TSPO – is increased in a wide variety of neurological disorders including multiple sclerosis, HIV encephalitis, ischemia and some types of arthritis. TSPO, a microglial inhibitor, is believed to reflect the brain’s attempts to rein in the microglia.

Jarred Younger has noted that the technology is not perfect. Last year we saw Japanese researchers using an older version of the same molecule to assess microglial activation in ME/CFS. (They are using the newer molecule in their present study – thanks to Simon McGrath for reporting that). Younger is attempting to use scanning techniques that can assess the degree of neuroinflammation present by measuring the temperature of the brain.)

In this study – the first of its kind done in humans – U.S. researchers examined microglial activation across the brain and cytokine levels in the blood in nine people with low back pain and nine healthy controls to determine if and where microglial activation might be causing pain.


Demonstrating glial activation in chronic pain suggests that these cells may be a therapeutic target, and the consistency with which we found glial activation in chronic pain patients suggests that our results may be an important step towards developing biomarkers for pain conditions,” Marco Loggia

Microglial activation was found most prominently in the thalamus and the somatosensory cortices. Consistently upregulated microglial activity in the thalamus suggested that this important relay center for pain and other sensory signals played a particularly prominent role in the production of chronic pain.

The Japanese research effort found evidence of neuroinflammation in ME/CFS in several of the same brain regions (cingulate cortex, thalamus) plus some new ones ( hippocampus, amygdala, midbrain, and pons). With microglial activation in the thalamus associated with reduced cognition and increased pain in ME/CFS, inflammation in the thalamus may play an important role in both ME/CFS and low back pain.

One study has found increased thalamic activity in ME/CFS and depressed patients with ME/CFS demonstrated more thalamic activity. Several studies suggest the thalamus may play a role in fibromyalgia as well.

Other areas of increased microglial activation included a variety of brain regions often associated with ME/CFS and fibromyalgia including the insula, prefrontal cortex, cingulate cortices, the supplementary motor area and the basal ganglia.


By showing that levels of an inflammation-linked protein are elevated in regions known to be involved in the transmission of pain, the study … paves the way for the exploration of potential new treatment strategies and identifies a possible way around one of the most frustrating limitations in the study and treatment of chronic pain — the lack of an objective way to measure the presence or intensity of pain.” Mass General Hospital

The authors – from Harvard and Duke Universities – asserted that now that microglial activation has been associated with chronic pain production in human that clinical trials of microglial inhibitors should begin immediately. Known microglial inhibitors have been FDA approved for other conditions.

The first drug they pointed to, interestingly enough, was none other than low dose naltrexone, a known glial cell inhibitor that two Younger studies have shown can reduce pain in fibromyalgia. They noted that two other putative microglial inhibitors (propentophylline, minocycline) have not panned out in two chronic pain trials but, pointing out that it’s easier to prevent microglial activation than knock it out, they asserted that the trials may have been too short (8 days to 4 weeks) to show efficacy.

This study should start the ball rolling on increased efforts to reduce chronic pain by reducing microglial activation. A surprising finding that the patients with the highest TSPO levels had reduced pain added TSPO enhancing drugs to the list of new possibilities for reducing pain. Younger’s Neuroinflammation, Pain and Fatigue Lab is currently testing how effective botanicals are at reducing microglial activation in Gulf War Syndrome. Younger has elicited some surprise at how effective some of the botanicals may be.

More on Possible Microglial Inhibitors

The microglial field – already a hot one – should heat up more now that pain has been linked in human studies to microglial activation. Many labs are engaged in finding ways to accurately assess microglial activation and neuroinflammation. At least three studies testing markers of microglial activation (GEH120714 (18F)), ([18F]DPA-714), [C11]PK-1195 PET) are underway. Ultimately scanning techniques should be able to pinpoint patients for whom reducing neuroinflammation makes sense.

The authors asserted that treatment trials using microglial inhibitors should begin now. Only minocycline, however, shows up in a search of the Clinical Trials database. As noted earlier, Younger is examining the efficacy of botanicals in a Gulf War Illness study.

With microglial inhibition, Dr. Pridgen’s antiviral approach to Fibromyalgia, immune therapies and brain stimulation all on the table now, researchers are getting more creative in their approach to reducing chronic pain.


About the Author: Cort Johnson has had ME/CFS for over 30 years. The founder of Phoenix Rising and Health Rising, Cort has contributed hundreds of blogs on chronic fatigue syndrome, fibromyalgia and their allied disorders over the past 10 years. Find more of Cort’s and other bloggers’ work at Health Rising.

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3 thoughts on “Neuro-Inflammation and Chronic Pain Link Established: Authors Call for Treatment Trials”

  1. Aliviah says:

    I certainly would be on board in a clinical trial. I believe this to be authentic and relate to it in my life.

  2. IanH says:

    the CoQ10 (any form) 200 mg daily.

  3. fibrogo says:

    I would like to participate in one of your studies re: fibromyalgia and chronic pain, as well as, osteoporosis, Can you inform me if this is possible and how I would be able to do so.
    Thank you,
    Dianne Tchir

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