Summary: A new study reveals cannabinoid medications may not reduce pain itself, but instead make pain feel less unpleasant and more tolerable.
Source: Syracuse University.
Researchers in the College of Arts and Sciences have determined that cannabinoid drugs do not appear to reduce the intensity of experimental pain, but, instead, may make pain feel less unpleasant and more tolerable.
Martin De Vita G’17, a doctoral candidate in the clinical psychology program, is the lead author of a highly anticipated paper on the subject in JAMA Psychiatry (American Medical Association, 2018).
The paper, whose publication coincides with “Pain Awareness Month,” represents the first systematic review of experimental research into the effects of cannabis on pain.
“Cannabinoid drugs are widely used as analgesics [painkillers], but experimental pain studies have produced mixed findings,” says De Vita, who studies interactions between substance use and co-occurring health conditions. “Pain is a complex phenomenon with multiple dimensions that can be affected separately.”
Cannabinoids are chemical compounds that give the Cannabis plant its medical and recreational properties. Marijuana–a mixture of dried, crumbled parts from the plant–contains hundreds of these compounds, of which Tetrahydrocannabinol, or THC, is the best known.
“THC is the primary psychoactive compound in marijuana and, along with CBD [also known as cannabidiol, a naturally occurring constituent of cannabis] has been the focus of most medicinal use and research,” says Associate Professor Emily Ansell, the study’s senior author and director of the University’s Research Lab on Personality, Addiction and Trauma (REPEAT).
When ingested, THC binds to receptors in the brain that control pleasure, time perception and pain. This activity boasts the production of dopamine–what Ansell calls the “feel-good chemical,” resulting in euphoria or relaxation.
Although the use of cannabis for medical purposes is legal in more than 30 states, the U.S. Drug Enforcement Administration still considers it a Schedule I drug, with no accepted medical use and a high potential for abuse. This classification, De Vita says, poses a significant challenge to researchers interested in cannabis’ therapeutic effects.
Thus, high-quality evidence supporting the effectiveness of cannabis in treating chronic pain has yet to be established.
“Patients reliably endorse the belief that cannabis is helpful in alleviating pain; however, its analgesic properties are poorly understood,” says De Vita, also a student therapist in the Syracuse VA Medical Center’s PTSD clinic and a graduate researcher in the University’s REPEAT Lab and Alcohol Research Lab. “Experimental pain studies of cannabinoid analgesia in healthy adults have produced mixed results.”
De Vita and his co-authors in the Department of Psychology–doctoral candidate Dezarie Moskal, Professor Stephen Maisto and Ansell–initially identified more than 1,830 experimental studies on cannabis that had been conducted in North America and Europe over a 40-year period. They whittled the group down to 18 studies, and extracted data from more than 440 adult participants.
The team found that cannabinoid drugs were associated with modest increases in experimental pain threshold and tolerance, no reduction in the intensity of ongoing experimental pain, reduced perceived unpleasantness of painful stimuli and no reduction of mechanical hyperalgesia.
“What this means is that cannabinoid analgesia may be driven by an affective, rather than a sensory component. These findings have implications for understanding the analgesic properties of cannabinoids,” De Vita says.
Adds Ansell: “The studies predominantly focused on THC varieties, so it is unclear whether or not other cannabinoids may have resulted in different experimental effects on pain.”
The first meta-analytic review of its kind, Syracuse’s study closely followed published guidelines for conducting and reporting systematic reviews, as well as a pre-registered protocol to enhance transparency. Two independent reviewers also examined the data separately.
“The mean quality and validity score across the studies was high, and analyses did not suggest publication bias,” De Vita says.
Whereas the study was limited to experimental (i.e., laboratory induced) pain, the group hopes to expand their line of research into clinical and neuropathic pain.
Clinical pain usually is associated with a progressive, non-malignant disease; neuropathic pain is synonymous with disease or damage to the nervous system, resulting in tissue injury.
The researchers also are interested in studying dynamic pain processes, different types and doses of cannabinoids, and the role of recreational cannabis use.
“The cumulative research synthesized in our review has helped characterize how cannabis and cannabinoids affect different dimensions of pain reactivity,” De Vita adds. “It may underlie the widely held belief that cannabis relieves pain. For now, we still have much to learn.”
Source: Daryl A Lovell – Syracuse University
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Open access research for “Association of Cannabinoid Administration With Experimental Pain in Healthy Adults: A Systematic Review and Meta-analysis” by Martin J. De Vita, MS; Dezarie Moskal, MS; Stephen A. Maisto, PhD; and Emily B. Ansell, PhD in JAMA Psychiatry. Published September 19 2018.
[cbtabs][cbtab title=”MLA”]Syracuse University”Cannabinoid Medications Make Pain Feel Less Unpleasant and More Tolerable.” NeuroscienceNews. NeuroscienceNews, 19 September 2018.
<https://neurosciencenews.com/pain-tolerance-cannabinoid-9890/>.[/cbtab][cbtab title=”APA”]Syracuse University(2018, September 19). Cannabinoid Medications Make Pain Feel Less Unpleasant and More Tolerable. NeuroscienceNews. Retrieved September 19, 2018 from https://neurosciencenews.com/pain-tolerance-cannabinoid-9890/[/cbtab][cbtab title=”Chicago”]Syracuse University”Cannabinoid Medications Make Pain Feel Less Unpleasant and More Tolerable.” https://neurosciencenews.com/pain-tolerance-cannabinoid-9890/ (accessed September 19, 2018).[/cbtab][/cbtabs]
Association of Cannabinoid Administration With Experimental Pain in Healthy Adults: A Systematic Review and Meta-analysis
Cannabinoid drugs are widely used as analgesics, but experimental pain studies have produced mixed findings. The analgesic properties of cannabinoids remain unclear.
To conduct a systematic review and meta-analysis of the association between cannabinoid drug administration and experimental pain outcomes in studies of healthy adults.
Design, Setting, and Participants
A systematic search of PubMed, EMBASE, MEDLINE, PsycINFO, and CINAHL was conducted from the inception of each database to September 30, 2017. Studies were eligible for inclusion if they met criteria, including healthy participants and an experimentally controlled administration of any cannabinoid preparation in a quantified dose. Studies that used participants with chronic pain were excluded. Data extracted included study characteristics, cannabinoid types and doses, sex composition, and outcomes. Study quality was assessed using a validity measure previously established in published reviews. Random-effects meta-analyses were used to pool data and generate summary estimates.
Main Outcomes and Measures
Experimental pain threshold, pain tolerance, pain intensity, pain unpleasantness, and mechanical hyperalgesia.
Eighteen placebo-controlled studies (with 442 participants) were identified. Of the 442 participants, 233 (52.7%) were male and 209 (47.3%) were female. For sample ages, 13 (72%) of the 18 studies reported a mean sample age (26.65 years), 4 (22%) reported a range, and 1 (6%) reported a median value. The search yielded sufficient data to analyze 18 pain threshold comparisons, 22 pain intensity comparisons, 9 pain unpleasantness comparisons, 13 pain tolerance comparisons, and 9 mechanical hyperalgesia comparisons. Cannabinoid administration was associated with small increases in pain threshold (Hedges g = 0.186; 95% CI, 0.054-0.318; P = .006), small to medium increases in pain tolerance (Hedges g = 0.225; 95% CI, 0.015-0.436; P = .04), and a small to medium reduction in the unpleasantness of ongoing experimental pain (Hedges g = 0.288; 95% CI, 0.104-0.472; P = .002). Cannabinoid administration was not reliably associated with a decrease in experimental pain intensity (Hedges g = 0.017; 95% CI, −0.120 to 0.154; P = .81) or mechanical hyperalgesia (Hedges g = 0.093; 95% CI, −0.059 to 0.244; P = .23). The mean quality rating across studies was good.
Conclusions and Relevance
Cannabinoid drugs may prevent the onset of pain by producing small increases in pain thresholds but may not reduce the intensity of experimental pain already being experienced; instead, cannabinoids may make experimental pain feel less unpleasant and more tolerable, suggesting an influence on affective processes. Cannabis-induced improvements in pain-related negative affect may underlie the widely held belief that cannabis relieves pain.