Researchers in Japan have revealed a previously unknown mechanism for pain control involving a newly identified group of cells in the spinal cord, offering a potential target for enhancing the therapeutic effect of drugs for chronic pain.
While neurons may be the most
well-known cells of the central nervous system, an assortment of non-neuronal
cells first discovered in the mid-nineteenth century also play a wide variety
of important roles.
Originally named after the
Greek word for “glue,” these glial cells are now known to be much more than
glue and in fact are critical elements for regulating neuronal development and
function in the central nervous system.
Among the different types of
glial cells, astrocytes are the most abundant in the central nervous system,
but, unlike neurons in different brain regions, researchers still have yet to
develop a detailed understanding of groupings of astrocytes with distinct
properties.
Now, researchers led by
Makoto Tsuda, professor at Kyushu University’s Graduate School of
Pharmaceutical Sciences, have discovered a unique population of spinal cord
astrocytes with a role in producing pain hypersensitivity.
Found in the outer two layers
of gray matter near the back of the spinal cord–a location referred to as the
superficial laminae of the spinal dorsal horn–the astrocytes are in a region
known to carry general sensory information such as pressure, pain, and heat
from around the body to the brain.
Using mice, the researchers
showed that stimulating noradrenergic (NAergic) neurons–so called for their use
of noradrenaline as a neurotransmitter–that carry signals from the locus
coeruleus (LC) in the brain down to the spinal dorsal horn activates the
astrocytes and that the astrocyte activation results in pain hypersensitivity.
These observations overturn
the prevailing view that descending LC-NAergic neurons suppress pain
transmission in the spinal dorsal horn.
“The discovery of this new
population of astrocytes reveals a new role of descending LC-NAergic neurons in
facilitating spinal pain transmission,” explains Tsuda.
Considering these findings,
suppressing signaling of these astrocytes by noradrenaline may enhance the
effect of drugs for chronic pain.
To initially test this, the
researchers genetically engineered mice in which response of astrocytes to
noradrenaline was selectively inhibited and gave them duloxetine, an analgesic
drug thought to increase levels of noradrenaline in the spinal cord by
preventing uptake by descending LC-NAergic neurons.
Indeed, the modified mice
exhibited an enhanced easing of chronic pain by duloxetine, further supporting
the researchers’ proposed role of the astrocytes.
“Although we still need more
studies with different drugs, this astrocyte population appears to be a very
promising target for enhancing the therapeutic potential of drugs for chronic
pain,” says Tsuda.
Source: https://www.kyushu-u.ac.jp/en/researches/view/184
Journal article: https://www.nature.com/articles/s41593-020-00713-4
Source: New
Mechanism of Pain Control Revealed – Scents of Science (myfusimotors.com)
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