Oregon Health & Science University
OHSU research suggests an avenue for developing treatments for
chronic pain that harness the medicinal properties of cannabis while minimizing
the threat of addiction.
The study, conducted in a rodent model, provides additional
rationale for the development of therapeutics using cannabinoid receptors to
treat chronic pain, which afflicts about 30 percent of the U.S. population.
OHSU investigators studied the function of two forms of cell
membrane receptors that bind cannabinoids that occur naturally within the body,
called endocannabinoids.
"It may be an avenue where we can get better pain
medications that are not addictive," said senior author Susan Ingram,
Ph.D., an associate professor of neurosurgery in the OHSU School of Medicine.
Ingram and colleagues report the treatment of chronic pain has
challenged the medical system, with medications that are ineffective or create
serious side effects: "However, emerging data indicate that drugs that
target the endocannabinoid system might produce analgesia with fewer side
effects compared with opioids."
The body's endocannabinoid system comprises receptors, endocannabinoid molecules and enzymes that make and degrade the endocannabinoids located in the brain and throughout the central and peripheral nervous system.
The research team focused on two cannabinoid receptors, known as
CB1 and CB2, in the rostral ventromedial medulla -- a group of neurons located
in the brainstem known to modulate pain.
The study is the first to examine CB1 and CB2 receptor function
at the membrane level in late adolescent and adult neurons.
The researchers observed that chronic inflammatory pain
increased activity of CB2 receptors and decreased CB1 activity. Cannabis
activates both CB1 and CB2 receptors equally.
The study suggests that selective activation of CB2 receptors
contributes to the medicinal benefit of cannabis while minimizing the
propensity of the other cannabinoid receptor, CB1, to induce tolerance and
withdrawal.
Ingram said the next phase of the research will further explore
this area of brain circuitry, which ultimately could lead to the development of
a new class of pain medications.
Co-authors include lead author Ming-Hua Li, Ph.D., and Katherine
L. Suchland, both with the Department of Neurological Surgery, OHSU School of
Medicine.
The study was funded by grants from the National Institutes of
Health (DA035316 and R56NS093894) and American Heart Association
(13SDG14590005, MH.L.).
