It became evident that glial activation was not merely just correlated with pain, but that it was critically involved in inducing pathological pain.


Astrocytes in the brain

Suddenly glial cells are turning up in spades in Chronic Fatigue Syndrome and Fibromyalgia.  The Japanese neuroinflammation study found widespread glial cell activation in the brains of people  with ME/CFS. Younger’s leptin finding suggests the glial cells may be going bonkers in ME/CFS, does his successful low dose naltrexone study in Fibromyalgia. VanElzakker’s Vagus Nerve Infection Hypothesis proposes chronic glial cell activation near the vagus nerve is causing ME/CFS.

 “Fatigue appears to arise when some stimulus induces increased proinflammatory cytokines in the brain and/or activated microglia and increased expression of chemokines” Harrington

On the fatigue side, a 2012 paper,  “Neurobiological Studies of Fatigue”, asserted that all animal models of fatigue had one thing in common – activation of  the microglia and/or cytokine/chemokine storms in the brain.” This 48 page paper noted that treatments for fatigue are ‘scarce’ with the most effective exercise being ‘difficult to administer’ in the severely fatigued (lol).

Fortunately glial cells are getting a lot of research and treatment possibilities are popping up. It’s time to take a look at a fascinating new entry in ME/CFS and FM research.

Glial Cell Activation

How turned-on or activated the glial cells are may determine how much pain or fatigue or other symptoms you have. Watkins

Pathological pain and the neuroimmune interface. Grace PM, Hutchinson MR, Maier SF, Watkins LR. Nat Rev Immunol. 2014 Apr;14(4):217-31. doi: 10.1038/nri3621. Epub 2014 Feb 28.

Toll-like receptors in chronic pain. Nicotra L, Loram LC, Watkins LR, Hutchinson MR. Exp Neurol. 2012 Apr;234(2):316-29. doi: 10.1016/j.expneurol.2011.09.038. Epub 2011 Oct 6. Review.

Until the early 1990s pain was thought to primarily be ‘nerve-based’; i.e., it was caused by activation of the sensory nerves and could be ameliorated by drugs, mostly opioids, that affected nerve transmission in the brain. With more and more findings that non-neuronal cells called glial cells play a major role in producing chronic pain, that view no longer holds.

These non-neuronal components of the brain are abundant, outnumbering the neurons ten to one, and make up greater than 70% of all the brains cells. Two types of glial cells exist: the microglia that provide the scaffolding for the neurons in the brain, and the astrocytes which participate in several functions including formation of the blood-brain barrier and blood flow regulation in the brain.

With the glial cells it’s all about activation.  When the glia cells are inactive they’re fine but when they’re pumped they tend to turn into hairy monsters.


Many animal models have implicated glial cell activation in the production of chronic pain

Several realizations in the 1990s, two of which indirectly involve ME/CFS and FM, opened researchers’ eyes to the role glial cells play in chronic pain production.  One involved the recognition that substance P – a pain producing factor which is increased in fibromyalgia – triggers glial cell activation. The other was the understanding that glial cell activation plays a key role in inducing ‘sickness behavior’ – the fatigue, fevers, pain, etc. associated with infection.

A decade later glial cell activation in the spinal cord had been implicated in a wide array of animal pain models including trauma, inflammation, chemotherapy, multiple sclerosis, migraine, back pain, and others. Glial cells are now also known to play critical roles in immune surveillance in the brain and in cleansing the brain of unwanted substances.

Research indicates that activated glial cells release substances that trigger the neurons to release excitatory substances (proinflammatory cytokines IL-1, TNF, and IL-6; chemokines; arachidonic acids; ATP; prostaglandins; nitric oxide) that enhance pain, downregulate GABA, upregulate glutamate expression, and more.

Rapid Pace of Learning

The pace of learning in this field has been fast and furious with review papers just over the last few years showing remarkable differences.

light bulb

The pace of learning in glial cells has been fast and furious

Glial cells have been implicated in two of the most puzzling problems facing the pain research field: opioid intolerance and opioid-induced hyperalgesia. Opioid intolerance occurs when opioids provide reduced pain relief after a period of use, and opioid hyperalgesia occurs when opioids cause increased sensitivity to pain over time.

As recently as 2011 a new term — ‘central immune signaling’ — was coined to describe how the brain’s immune system affects nervous system activity. The immune findings in glial cells in turn opened up a new window on the immune system in the brain.

Enter the Toll-like Receptors (TLRs) – A Major Focus in Immune Activated Nervous System Disorders Emerges

“The abundance of TLRs in pain responsive regions makes them a critical potential component of pain signaling”

The discovery of the Toll-like immune pathway (in flies) led to the 1995 Nobel Prize in Physiology or Medicine for Edward B. Lewis, Christiane Nüsslein-Volhard, and Eric F. Wieschaus. TLRs are now understood to be the critical link between the innate immune system and central nervous system.

The role they play in producing pathological pain was verified when researchers were able to reverse the most difficult pain to treat in the human body — neuropathic pain — in rodent models simply by using two TLR4 inhibitors, naloxone and naltrexone. These receptors dot the surface of the glial cells.

Infection Possible But Not Needed

These receptors respond to indicators of cellular stress and damage termed ‘endogenous danger signals’ or ‘alarmins’ (fibronectin, β-defensins, high mobility group box-1 HMGB1, ATP, heat shock proteins) produced during inflammation and injury. Increased levels of these alarmins have been implicated in a variety of central nervous system disorders including Alzheimer’s disease, stroke, and chronic pain.


Are alarmins prompting the glial cells to produce neuroinflammation in FM and ME/CFS?

The TLR4 response to environmental factors indicates that damage, not infection, is the key element. Of course, infection could cause damage, but infection is not necessary to produce the so-called ‘alarmins’ that TLR4s respond to.

Some evidence suggests alarmins may be present in FM and ME/CFS. Five studies have now found evidence of small-fiber neuropathy in fibromyalgia — a potential trigger for TLR4s. Several studies have found increased heat shock proteins in ME/CFS — another potential trigger for TLR4s. The Lights’ studies suggest small amounts of ATP and other indicators of cellular stress associated with muscle damage may be upregulating gene expression in ME/CFS, and ATP has been shown to activate glial cells.

ATP also binds to some of the same purinergic receptors (P2X4/P2X7) that studies of gene expression following exercise suggest are increased in ME/CFS. This means these triggers could be turning on the production of pro-inflammatory cytokines in ME/CFS.

The Opioid Connection

Interestingly, opioid drugs trigger glial cell activation via the TLR4 receptors. This means the drugs most commonly used to reduce pain can, in some people, trigger an immune response that increases pain, leading to either opioid tolerance or opioid-induced hyperalgesia (increased sensitivity to pain).

Jekyll and Hyde Cells

Recent evidence suggests the microglia have a Jekyll and Hyde-like nature; they can pump out neuron damaging pro-inflammatory factors or they can pump out anti-inflammatory factors that are neuroprotective. Turning the microglia back into their neuroprotective form could be the key to resolving chronic pain and other states.

High Cytokine Levels in the Body NOT Required Either

Increased cytokine levels in the body do clearly cause fatigue, pain, and other symptoms in some people with Fibromyalgia and ME/CFS, but it may also be that the glia have become so sensitized to immune system signals that only small alterations are required to set them off.

VanElzakker’s Vagus Nerve Infection Hypothesis (VNIF) and Broderick’s and Younger’s findings suggest that slight elevations of immune factors in the periphery may be all that’s needed to spark a cytokine storm in the brain. The big cytokine increases for some patients may occur in the brain.

‘Hairy Monsters’ Stuck in Hyperexcitable Mode

panic button

Could glial cells stuck in ‘panic mode’ be contributing to the pain and fatigue in FM and ME/CFS?

This is most likely to occur when glial cells get stuck in ‘hyperexcitable mode’. It’s now known that injury and environmental stressors can cause the microglial cells to become ‘stuck’ in a kind of panic-ridden defensive state. Once in this state, even mild stimuli can cause them to begin releasing proinflammatory cytokines that tweak the neurons to produce symptoms of ‘sickness behavior’.

Once neurons become activated they, in turn, can produce factors (substance P, glutatmate, nitric oxide and ATP) that keep the microglia whipped into a frenzy.

The Problem of Female Pain

The increased risk of chronic pain women face is at least partly due to sex hormones. Pain sensitivity in girls and boys prior to puberty is equal, and the sensitivity increases in females after puberty, and then it nears parity again after menopause. Some studies suggest increased estrogen levels are responsible. Estrogen in vivo has been found to increase pro-inflammatory cytokine gene expression by the microglia.


Glial cell dysregulation presents a fascinating possibility for people with Chronic Fatigue Syndrome and Fibromyalgia. Given the possible connections and the abundant research being done on them it’s a bit surprising they haven’t been connected to these disorders before. Given the role they play in producing chronic pain it would be remarkable if they were not implicated in Fibromyalgia.  Treatment possibilities seem pretty abundant but clinical trials are only beginning to swing into gear.

Depending on how the neuroinflammation studies turn out we may be hearing much more about glial cells in the future.

  • Coming up shortly – Glial Cell Inhibitors


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