Curr Pain Headache Rep. 2017 (Apr); 21 (4): 19 ~ FULL TEXT
Philip S. Kim, Michael A. Fishman
Center for Interventional Pain Spine and Ageless MD, LLC,
931 East Haverford Road, Suite 202,
Bryn Mawr, PA, 19010, USA.
PURPOSE OF REVIEW: Marijuana has been used both medicinally and recreationally since ancient times and interest in its compounds for pain relief has increased in recent years. The identification of our own intrinsic, endocannabinoid system has laid the foundation for further research.
RECENT FINDINGS: Synthetic cannabinoids are being developed and synthesized from the marijuana plant such as dronabinol and nabilone. The US Food and Drug Administration approved the use of dronabinol and nabilone for chemotherapy-associated nausea and vomiting and HIV (Human Immunodeficiency Virus) wasting. Nabiximols is a cannabis extract that is approved for the treatment of spasticity and intractable pain in Canada and the UK. Further clinical trials are studying the effect of marijuana extracts for seizure disorders. Phytocannabinoids have been identified as key compounds involved in analgesia and anti-inflammatory effects. Other compounds found in cannabis such as flavonoids and terpenes are also being investigated as to their individual or synergistic effects. This article will review relevant literature regarding medical use of marijuana and cannabinoid pharmaceuticals with an emphasis on pain and headaches.
KEYWORDS: Cannabinoids; Cannabis; Headache; Marijuana; Nociception; Pain; Tetrahydrocannabinols
The medical use of cannabis has been documented in ancient
Greece and China.  The most commonly used species of the
plant are Cannabis sativa and Cannabis indica. Each variety
has varying composition and relative concentrations of active
compounds. In the last two centuries, Cannabis has been used
and recommended by various physicians. Dr. William B.
OShaughnessy, an Irish physician, introduced Indian hemp
to Europe with reports of high rates of success for rheumatism,
rabies, cholera, tetanus, cramps, and delirium. Dr. William
Osler reported benefits of cannabis for various conditions including
migraines and menstrual cramps. The Marihuana Tax
Act of 1937 began the government intervention that lead to the
downfall of cannabis for medical use. The removal of cannabis
in 1940 from the US Pharmacopeia further compromised
its medical use. In 1970, the Controlled Substance Act made
cannabis a schedule I drug. Recently, the USA has opened the
policies for medical marijuana by allowing the States to legislate
medical marijuana laws. Currently, there are 23 states
with medical marijuana laws. Interesting, the federal government
applied for and was granted a patent on cannabinoids for
antioxidant and neuroprotectant use in 2003.
Cannabinoids and medical marijuana research follows a similar
path to other plant-derived therapy. Opium poppy
(Papaver Somniferum) led to the development of the standard
narcotic analgesic morphine. The morphine alkaloid led to the
development of various synthetic derivatives and discovery of
the endogenous endorphin systems. Like morphine, the isolation
and identification of the first cannabinoid Δ9-
tetrahyrocannabinol (THC) in 1964 by Dr. Raphael
Mechoulam led to discovery of the endogenous cannabinoid
system. Endogenous cannabinoids are natural chemicals such
as anandamide (AEA) and 2-arachidonoylglycerol (2-AG).
The basic function of the endocannabinoid system acts to
modulate the sensitivity to many other neurotransmitters such
as dopamine and serotonin in the central nervous system
(Figure 1. The human experience of pain and response to stress
involves the interaction of endocannabinoids through endorphins
and cortisol release. From a global perspective, the
endocannabinoid system functions are: relax, eat, sleep, forget,
and protect.  AEA is hydrolyzed by the enzyme fatty
acid amide hydrolase (FAAH) to arachidonic acid and ethanolamine;
2-AG is metabolized by monaoacylglycerol lipase
(MGL) into arachidonic acid and glycerol. 
FAAH and MGL, represent potential therapeutic targets to
modulate endogenous endocannabinoid levels or potential
mechanisms of dysfunction in the development of various
disease states. Currently, there are two well-defined
cannabinoid receptors CB1 (Cannabinoid receptor 1) and
CB2 (Cannabinoid receptor 2).  CB1 is a seventransmembrane
spanning G protein-coupled receptor
inhibiting cyclic AMP release.  CB1 is the primary
neuromodulatory receptor accounting for the psychopharmacological
effect of THC and most of its analgesic effects.
Presynaptic activation of CB1 acts as a synaptic circuit breaker
to inhibit neurotransmitters such as GABA (gamma-
Aminobutyric acid) or glutamate. CB2 works primarily as an
immunomodulatory receptor in the periphery. It is postulated
that CB2 modulates persistent inflammatory and neuropathic
pain conditions.  THC, the prototypical phytocannabinoid,
is a weak partial agonist of both CB1 and CB2 receptors. 
Cannabinoids can be broken down into three subgroups: endogenous
endocannabinoids, botanicals (phytocannabinoids), and
synthetic derivatives. Over 60 different phytocannabinoids have
been identified in the marijuana plant.  The principal cannabinoids
appear to be delta-9-tetrahydrocannabinol andcannabidiol (CBD). Other potential cannabinoids with medical
value include cannabigerol (CBG), Cannabinol (CBN),
cannabichromene (CBC) and tetrahydrocannabivarin (THCV).  CBG is a product of delta-9-THC oxidation and displays potent GABA reuptake inhibition activity and phospholipaseA2
modulator. [9, 10] CBD lacks detectable psychoactivity and
does not appear to bind to either CB1 or CB2 receptors in high
concentrations. Rather, it displays activity at other targets such as
ion channels, receptors and enzymes. Pre-clinical studies support
anti-inflammatory, analgesic, anti-emetic, anti-psychotic, anti-ischemic,
anxiolytic and anti-epileptiform activity. THCVacts as a
CB1 receptor antagonist and CB2 receptor partial agonist with
pre-clinical studies suggesting ant-epileptiform/anti-convulsant
In the living plant, these phytocannabinoids exist as both inactivemonocarboxylic
acids and an active decarboxylated forms.
Heating above 120 °C promotes decarboxylation and results in
biological activation.  Other constituents in cannabis with potential
medical benefit include the following: terpenes, noncannabinoid
phenols, flavonoids and vitamins. Further differences
in the chemical constituents are noted in various cannabis
species and extraction techniques. The terpenes and flavonoids
are not yet well characterized, but they are believed to have a
broad spectrum of potential anti-inflammatory, anti-oxidant, antibacterial
and anti-neoplastic actions. An example is noted in
myrecene, a terpenoid, with anti-inflammatory activity via
PGE-2 and opioid type analgesic effect blocked by naloxone.
The scientific and pharmaceutical approach to identify single
ingredients and synthesize one compound, such as THC, for
use may not offer full effect of the polypharmaceutical cannabis
plant. The many constituentsmay work by multiple mechanisms
to improve therapeutic activity either an additive or synergistic
manner and mitigate the side effects if their predominant active
ingredients.  An example is the co-administration of CBD
and THC may result in attenuation or potentiation of some of the
effects of THC through a pharmacodynamics mechanisms. 
A ratio of CBD to THC of at least 8:1 attenuates THC induced
effects, where as CBD potentiates THC at a ratio 2:1.
Potentiation of THC may be caused by inhibition of THC metabolism
in the liver.
Synthetic cannabinoids have been developed to mimic THC.
Oral dronabinol (THC) has been available as Marinol® for nausea
associated with chemotherapy and appetite stimulation with
HIV/AIDS. In the USA, it is classified as a schedule III drug. A
new liquid dronabinol formulation called Syndros® has recently
been approved for the same indication. Nabilone is another formulation
of synthetic THC marketed under the brand name
Cesamet® and available as an anti-emetic for chemotherapy-associated
nausea and is a schedule II substance. It is ten times
more potent than dronabinol. Ajulemic acid (CT3) is a synthetic
THC currently being studied in phase II randomized clinical trial
in peripheral neuropathic pain.  Other synthetic cannabinoids
are in development.
Biochemical and Neurophysiological Basis of Pain Control by Cannabinoids
Thorough reviews of pre-clinical and clinical studies support
the therapeutic effects of cannabinoids in nociception. [14, 15]
The endocannabinoid system is active in the central and peripheral
nervous system at nociception centers such as the
periaqueductal gray matter, ventroposterolateral nucleus of the
thalamus and the spinal cord. In neuropathic pain states,
endocannabinoids are involved in stress-induced analgesia,
wind-up phenomena, and central sensitization. [16, 17] The
periaqueductal gray region has also been implicated in migraine
generation.  In the peripheral nervous system, the
endocannabinoid system is active in suppressing hyperalgesia
and allodynia.  Pathological pain states such Complex
Regional Pain Syndrome (CRPS) has been postulated to arise
and at least involve a dysregulation of the endocannabinoid
An endocannabinoid deficiency is theorized to underlie the
pathophysiology of migraine or headaches.  Clinical studies
suggest that the lower concentration of anandamide is
found in the cerebral spinal fluid of migraineurs and the calcitonin
gene-related peptide (CGRP) and nitric oxide (NO)
levels are increased. [21, 22] In addition, the activity of the
anandamide-degrading enzyme, FAAH, is significantly decreased
in chronic migraineurs compared to controls.  It
is also postulated that active migraines are aggravated by release
of serotonin during migraine attacks. In one study, THC
inhibited release of serotonin from platelets in a plasma sample
taken during an active migraine episode.  The
endocannabinoid system is active in the trigeminovascular
system, which has been implicated in migraine pathogenesis
at the vascular and neurochemical level. 
Other postulated endocannabinoid-deficiency conditions
include fibromyalgia, idiopathic bowl syndrome and endometriosis.  The endocannabinoid system is also very active in
modulating nociceptive response in gastrointestinal and visceral
sites.  Endocannabinoid modulators may help restore
homeostasis and lead to normalization of function in
pathophysiological conditions. 
Clinical Studies Review
The White House Office of National Drug Control recommends
that the Institute of Medicine focus cannabis research
on the following:
Physiologic effects of synthetic and phytocannabinoids
Development of new delivery systems
Psychological effect of cannabis
Health risks of smoked marijuana 
High-quality clinical studies that are randomized, doubleblinded
and placebo controlled are limited overall with small
population and short duration of the study. Sample of these
studies are listed in Table 1. The studies are broken down on
the type of cannabinoid use with listing of type of patients. As
we have discussed in the previous section, the type of cannabinoids;
synthetic and phytocannabinoid and delivery system
can affect response for various types of chronic pains.
Clinical Evidence of Synthetic Cannabinoids
The synthetic cannabinoids are delivery in oral formulation
with mixed results for pain (see Table 1). The focus of synthetic
THC has been on nausea associated with chemotherapy
and appetite stimulation in HIV/AIDS. The studies with
dronabinol show some benefit for multiple sclerosis but no
benefit for postoperative pain. [28, 29] In the study of multiple
sclerosis patients, 24 patients received benefit with 10 mg
dronabinol compared to placebo with modest reduction of
pain p = .02.  Dronabinol was assessed in 30 patients with
chronic non-cancer pain in a double-blind cross-over single
day sessions with improvement.  These were patients on
high-dose opioids who noted 10 or 20 mg dronabinol added
additional analgesia in combination with current opioids.
Methodological issues are present where58% of patients correctly
guessed the dronabinol dose on test day and 4 placebo
patients had a positive THC assay.
Further studies were done using nabilone with mixed
results for pain (Table 1). Nabilone is a semi-synthetic
analogue of THC that is tenfold more potent and has a
long duration of action. As with dronabinol, prominent
sedation and dysphoria are noted side effects. In a postoperative
pain study of 41 patients, postoperative pain
scores actually increase compared to control group. 
A small randomized control trial with 12 patients with
spasticity showed a decrease in pain (p < .05) vs. placebo
but no improvements such as spasticity, motor function,
and activities of daily living. A double-blind randomized
crossover comparison of nabilone to dihydrocodeine in
chronic neuropathic pain, showed both drugs produced
marginal benefit with dihydrocodeine superior in efficacy
and side effect profile/  In a randomized control trial
(RCT), 40 patients noted benefit with nabilone with fibromyalgia
with decrease in pain and anxiety.  Another
fibromyalgia study compared nabilone vs. amitriptyline
and noted nabilone yielded benefit for sleep but not pain,
mood, or quality of life. 
Another synthetic THC analogue, ajulemic acid (CT3) is
under review and has been utilized in a phase II RCT in 21
patients with peripheral neuropathic pain.  Pain relief is
statistically significant (p = .02) and no major adverse side
effects were noted.
Evidence for Smoked or Vaporized Cannabis
Randomized controlled clinical trials are limited to studies
with small patient populations and limited duration. The clinical
trials in human volunteers with painful stimuli support
analgesic benefit of smoked or vaporized cannabis (Table 2).
One study shows that smoked cannabis increased pain tolerance
to pressure algometer and that experienced users had
greater effect compared to naïve users.  In a cold pressor
test, volunteers experienced equal decreases in pain sensitivity
and tolerance in smoked marijuana and 10 mg dronabinol
when compared to placebo.  The dronabinol group experienced
longer duration of effect. In a radiant heat stimulation
test, the healthy volunteers experienced a dose-dependent response
to 3.55% THC cannabis compared to placebo. [38
Naloxone administration did not alter the response to cannabis.
Finally, an intradermal capsaicin test was done on human
volunteers.  Interesting, the noxious stimulus was blunted
with smoked cannabis 4% THC only. At 2% THC, no analgesic
effect was noted and 8% THC caused increased pain
from the stimuli suggesting a therapeutic window of
Clinical trials in human patients with smoked cannabis
focus on chronic neuropathic pain and specifically the subset
of patients with HIV neuropathy (Table 3). A HIV neuropathy
group of 25 patients underwent a double blind RCT
with 3.56% THC smoked vs. placebo cigarettes over 5 days.
 The cannabis group noted a 30% reduction in VAS and
hyperalgesia. The cannabis was well tolerated with sedation
(54%), anxiety (25%) and disorientation (15%) as the most
common side effects. Similar findings were noted in another
HIV neuropathy study with a decrease in pain with cannabis
18% THC smoked.  The study was administered four
times daily over 5 days with a 2-week washout period.
These patients were considered experienced with cannabis.
The cannabis was overall well-tolerated. In two different
centers and investigators, similar methods with smoked cannabis
on chronic neuropathic pain identified a significant
analgesic response. [43, 44, ]
In the Canadian study, 23
subjects underwent a single 25 mg inhalation of various
cannabis potencies (09.4% THC) three times daily 5 days.
The most frequent side effects were headache, dry eyes,
burning sensation, dizziness, numbness and cough. Wilsey
et al. assessed medicinal cannabis in neuropathic pain using
double-blind randomized crossover study design. All the
Wilsey studies showed similar benefit with various concentrations
of THC. The most important methodological measure
was inclusion of specific objective neurological measures
and measured impairment in attention, learning, and
memory; most noted at 7% THC. In addition, the comparison
of various concentration of THC showed that lower
THC of 2.9 vs. 6.7% and 1.29 vs. 3.53% worked just as
well for pain with fewer side effects.
Evidence for Cannabis-Based Extracts
Cannador® is a cannabis extract available as an oral capsule
with various ratios of THC:CBD ratios. In the studies
reviewed, the ratio was 2:1. Cannador was utilized in a phase
III RCT for the treatment of spasticity. Six hundred thirty
patients were studied with a noted decrease in pain related to
spasms but no improvement in spasticity as measured by the
Ashworth scale.  Cannador was evaluated in 65 patients
with postherpetic neuralgia with no improvement.  In
postoperative pain, a slight reduction in pain was noted in a
single dose of 5, 10, and 15 mg. An incremental reduction in
pain and reduction in opioid requirements was noted. A single
case of a serious vasovagal adverse event was noted at 15 mg,
which lead to study termination.
Nabiximols (Sativex®) is a cannabis extract delivered as an
oral-mucosal spray at approximate THC:CBD ratio of 1:1.
Multiple RCT studies have demonstrated pain relief in various
chronic pain conditions. In a phase II study of 20 patients with
neurogenic pain, significant improvement was noted with
THC extract (Tetranabinex®) and THC:CBD extract
(Sativex®,) compared to placebo. The nabiximols combination
of THC and CBD offered better pain control than THC
extract alone with fewer side effects of intoxication. Similar
results were noted in another phase II study of intractable
chronic pain where  THC:CBD were superior to THC
alone.  Sixty-five patients in a phase III study of brachial
plexus avulsion injury showed pain reduction with both THC
and THC:CBD formulations. 
In a RCT study with multiple
sclerosis, THC:CBD combination improved pain control
over placebo.  Similar results were noted for pain relief in
patients with peripheral neuropathies. The equal ratio of THC
to CBD provided a reduction in dynamic and punctate
allodynia. A safety extension study in 160 multiple sclerosis
patients showed sustained improvement over the course of a
year without significant tolerance to nabiximols. Spasticity
and pain as measured by VAS were both significantly reduced.
No significant adverse effects were seen on mood or cognition.
Chronic pain related to rheumatoid arthritis also
responded to nabiximols in RCTs.  Two well-designed
RCTs showed statistically significant pain relief for intractable
cancer pain. [53, 54] Another RCT with multiple sclerosis
patient showed significant relief of bladder spasms and pain.
 Overall, Nabiximols is well tolerated with reduction in
pain but also improvement in sleep. [56 It is believed that the
sleep is improved by reduction in pain and not as a hypnotic
effect. The benign common adverse side effects of nabiximol
include the following: bad taste, oral stinging, dry mouth,
dizziness, nausea and fatigue. These side effects did not lead
to discontinuation of therapy in any of these trials.
Pharmacology, Dosing, and Side Effects
The pharmacokinetics and pharmacodynamics of cannabinoids
is complex as it on the interaction of various cannabinoids
as well as on the route of administration. The actual
temporal relationship between delta-9-THC and associated
clinical/therapeutic benefits, psychotropic, cognitive and motor
effects are not well established. Dosing for cannabis is
highly variable due multitude of factors. Each individual
may have interindividual (genetic) differences in the
endocannabinoid system, metabolism (cytochrome
P450system), previous exposure, and tolerance to cannabis.
The various strains/formulations of cannabis display an array
of potencies and other constituents that make it difficult to
have a traditional uniform dosing scheduling. The dosing of
any cannabis product is highly individualized and relies to a
great extent on titration. For cannabis-naïve patients, it is recommended
to start at the lowest dose and titrate to effect.
Surveys suggest that the majority of people using smoked or
orally ingested cannabis for medical purposes use between 10
and 20 g of cannabis per week or approximately 13 g of
cannabis per day.  The standard cannabis cigarette contains
approximately 750 mg of cannabis material.
Little is known in regard to conversion of smoked cannabis
to an equivalent oral dose.  A formula exists where the
smoked cannabis content of delta-9-THC is multiplied by 2.5
to correct for differences between the bioavailability of delta-
9-THC through smoked route (25%) vs. oral route (10%). [57,
Smoked and Vaporized Cannabis
Smoking cannabis results in a very rapid onset of action
(minutes) with higher blood levels of cannabinoids and short
duration of pharmacodynamics effects compared to oral administration.
 The amount of delta-9-THC is variable depending
upon the composition of plant material and composition
of the cigarette.  The level of inhalation, puff duration
and breath hold make the bioavailability estimated at 256%.  Overall, about 2527% of the total amount of
delta-9-THC is absorbed in the body. 
One of the concerns about smoked cannabis is the intoxication
due to rapid absorption. Cannabis also presents with similar
concerns as with cigarette smoking, including chronic
cough and bronchitis symptoms.  Of equal concern is that
cannabis smoke contains similar carcinogens and mutagens as
tobacco smoke, including carbon monoxide, ammonia, benzene,
acetaldehyde, polycyclic aromatic hydrocarbons, aromatic
amines, and hydrogen cyanide. However, population-based
studies have failed to show increased risk of chronic pulmonary
disease or lung cancer associated with smoking cannabis. 
Nevertheless, the concerns of the carcinogens and mutagens
with combustion of cannabis have led to the development
of alternative routes of delivery. Vaporization is where
cannabis is heated to a lower temperature that volatilizes THC
and other components while mitigating the production of carbon
monoxide, polycyclic aromatic hydrocarbons, and tar.
The pharmacokinetics of vaporized cannabis is considered
the same as smoked cannabis but further research is needed
to completely elucidate this. 
Oral and Oral-Mucosal Cannabis
Oral THC has a wide variability due to gastric degradation,
first-pass pharmacokinetics, and liver metabolism. 
Studies suggest oral bioavailability may be 520%. 
Oral cannabidiol is reported to be about 1319% bioavailable
. Compared to smoked cannabis, the peak plasma concentration
of THC is 34 h, with duration of effect variable up
to 8 h. Variable duration of effects is noted with all oral preparations
of synthetic or phytocannabinoids. Interpretation of
delta-9-THC levels is complicated by the presence of active
psychoactive metabolites, such 11-hydroxy THC, which are
found in higher concentrations after oral administration compared
to inhalation . In addition, a study on simulated
gastric fluid shows cannabidiol can be converted to delta-9-
THC and delta-8-THC .
The effect of cannabis varies amongst different patient populations.
One study suggest female patients with high estrogen
levels are more sensitive to medical cannabis in regard to pain,
behavior, and reward . Long-term use may be related to
lower levels of luteinizing hormones, follicle-stimulating hormones,
prolactin, and growth hormone. One retrospective
study compared the analgesic, subjective and physiological
effects of active cannabis (3.565.60% THC) and inactive
cannabis in male and female cannabis smokers during a cold
pressor test (CPT) . Male smokers exhibited greater
cannabis-induced analgesia compared to women.
Side Effects of Cannabis
The most common acute effects of cannabis use are impairments
in memory, motor coordination, altered judgment, and
in high doses, paranoia and psychosis . In patients with
cardiovascular conditions, an increased in heart rate, cardiac
variability, and orthostatic hypotension has been reported.
Precautions should be taken with vulnerable patients. Other
physical effects can include conjunctival injection, decreased
lacrimation, headache, nausea, and vomiting. Similar side effects
are noted with use of the synthetic cannabinoids
(dronabinol, nabilone and nabiximols) with the most common
side effects reported including sedation, nausea, vomiting, dry
mouth, and dizziness. Special precaution is necessary with
concomitant administration of opiates, anti-depressants, benzodiazepines,
and anti-psychotics as decreased alertness and
over sedation may occur .
Death has not been associated with cannabis use, and the
data on this is clear. Unlike opioids, the endocannabinoid system
is not expressed in the respiratory center of the brain.
Perhaps that explains why the LD-50 (the lethal dose in 50%
of the population) for cannabis is high. In rats, the LD-50 of
oral THC is 8001900 mg/kg and in monkeys it is 9000 mg/kg
. For an average 70 kg man, that means taking 6300 tablets
of dronabinol (10 mg) or smoking 6300 joints (each joint
is 1000 mg).
The chronic use of cannabis has been associated with development
of dependence, chronic bronchitis, and increased
risk of chronic psychotic disorders . Multiple studies
demonstrate that chronic cannabis use is associated with poor
neuropsychological performance, especially in the areas of
learning and memory recall . The difficulty in long
studies is differentiating from the effects of associated tobacco
and/or alcohol use  When used in early adolescence,
long-term and/or heavy cannabis use has been associated with
altered brain development, poor educational outcomes, and
cognitive impairment . These same concerns can be applied
to fetal development and early child development with
cannabis use during pregnancy. It is also noted that chronic
long-term use of cannabis may lead to decreased sperm count,
motility, and abnormal sperm morphology .
effects of cannabis on the lungs have the same concerns as
tobacco as it relates to increased risk of bronchitis, emphysema,
airflow obstruction, and carcinogen exposure [74, 75].
Looking at the observational studies is difficult given the high
level of concomitant use of tobacco by many patients. One
longitudinal study of 20 years looked at the association of
cannabis and tobacco use with a variety of physical health
indices . The only major concern noted was periodontal
disease. Interesting, in comparison to tobacco use, cannabis
has a limited effect on pulmonary function, systemic inflammation,
and metabolic health. One of the major concerns is the
risk of dependence and addiction with cannabis. Comparative
epidemiology of dependence showed that cannabis users had
the lowest dependence (9%) compared to other drugs such as
tobacco (32%), alcohol (15%), prescription drugs (9%), cocaine
(17%), and heroin (23%) .
Cannabinoid Interaction with Opioids
Opioid use with cannabis has the potential to decrease alertness
and cause cognitive effects. At the same time, suggested
studies support a synergistic analgesic effect. The putative
mechanism is the stimulation of beta-endorphins by THC
and potential inhibition of opioid tolerance and withdrawal
[78, 79]. One supportive clinical study shows that cannabinoids
and opioids may act synergistically . Twenty-one
individuals with chronic pain on a regimen of morphine or
oxycodone were treated with vaporized cannabis and noted
a decrease in pain with no significant increase in plasma levels
of oxycodone or morphine. At the same time, patients experienced
increased quality and duration of high with inhalation
of cannabis. The combination may allow opioid treatment
at lower doses with fewer side effects. Opioid analgesic overdose
mortality has risen, driven by increases in prescribing for
chronic non-cancer pain. State medical cannabis laws in the
USA have been associated with significantly lower opioid
overdose mortality rates of 24.8% when compared to states
without medical cannabis laws during the period of 1999 to
2010 . A more specific retrospective survey of 244 medical
cannabis patients found an associated 64% decrease in
opioid use, decrease in side effects of medications and improved
quality of life in 45% of patients . More research
is needed to validate these findings.
Medical cannabis has been used for centuries and recent evidence
for pain and spasticity has lead to a resurgence of interest.
The strongest clinical evidence in support of cannabinoids
appears to be for cancer-related pain. Evidence has grown for
use in neuropathic pain states such as HIV neuropathy and
multiple sclerosis. Evidence for acute pain is mixed with no
improvement to mild improvement. Chronic pain beyond neuropathic
conditions has promise as seen with rheumatoid arthritis.
The benefit appears to extend beyond analgesia, with
notable improvements in sleep and quality of life. Headache
and migraine clinical studies are lacking with anecdotal evidence
and historical accounting of cannabis use for headache
by Drs. Osler and OShaughnessy.
The study of cannabis as a whole plant versus selective
cannabinoids such as THC is complex. The identification of
multiple active ingredients which can interact in a synergistic
or non-synergistic way may lead to variations in the effects as
seen in studies. Cannabinoids such as cannabidiol and terpenes
are agents that have analgesic benefit without the psychoactive
effects of THC. Antioxidants such as flavonoids
may play a role in mitigating tumor genesis from carcinogens
released in the combustion of cannabis. The route of delivery
of cannabis may also play a role in the analgesic effect and
side effect profile. The strain of cannabis may also play a role
as a wide variability is noted in the relative concentrations and
types of cannabinoids and other substances. Ideal dosing for
one patient to population of patients is unclear and may be
difficult given a patient tolerance and pharmacokinetics may
play a role in proper dose.
Further research is needed to evaluate the risks and benefits
of medical cannabis. Policy and patients are forcing the US
federal government to allow more medical research and alter
the scheduling of marijuana from schedule I. Our current understanding
is that the long-term effects of cannabis need to be
addressed with rigorous analysis through the lens of the current
opioid epidemic to ensure that medical use of cannabis
today does not lead to an analogous situation in the futureWe
should not simply replace one controlled substance with another
without further analysis.
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Villalon CM, Olesen J. The role of CGRP in the pathophysiology of migraine and efficacy of CGRP receptor antagonists as acute antimigraine drugs. Pharmacol Ther. 2009;124(3):30923.
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Volfe Z, Dvilansky A, Nathan I. Cannabinoids block release of serotonin from platelets induced by plasma from migraine patients. Int J Clin Pharmacol Res. 1985;5(4):2436.
Akerman S, Holland PR, Goadsby PJ. Cannabinoid (CB1) receptor activation inhibits trigeminovascular neurons. J Pharmacol Exp Ther. 2007;320(1):6471.
Izzo AA, Sharkey KA. Cannabinoids and the gut: new developments and emerging concepts. Pharmacol Ther. 2010;126(1):2138. New concepts in the role of cannabinoids in gastrointestinal diseases.
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Buggy DJ, Toogood L, Maric S, Sharpe P, Lambert DG, Rowbotham DJ. Lack of analgesic efficacy of oral delta-9-tetrahydrocannabinol in postoperative pain. Pain. 2003;106(12):16972.
Beaulieu P. Effects of nabilone, a synthetic cannabinoid, on postoperative pain. Can J Anaesth. 2006;53(8):76975.
Svendsen KB, Jensen TS, Bach FW. Does the cannabinoid dronabinol reduce central pain in multiple sclerosis? Randomised double blind placebo controlled crossover trial. BMJ. 2004;329(7460):253.
Narang S, Gibson D, Wasan AD, Ross EL, Michna E, Nedeljkovic SS, et al. Efficacy of dronabinol as an adjuvant treatment for chronic pain patients on opioid therapy. J Pain. 2008;9(3):25464.
Wissel J, Haydn T, Muller J, Brenneis C, Berger T, Poewe W, et al. Low dose treatment with the synthetic cannabinoid Nabilone significantly reduces spasticity-related pain : a double-blind placebo-controlled cross-over trial. J Neurol. 2006;253(10):133741.
Frank B, Serpell MG, Hughes J, Matthews JN, Kapur D. Comparison of analgesic effects and patient tolerability of nabilone and dihydrocodeine for chronic neuropathic pain: randomised, crossover, double blind study. BMJ. 2008;336(7637):199201.
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Ware MA, Fitzcharles MA, Joseph L, Shir Y. The effects of nabilone on sleep in fibromyalgia: results of a randomized controlled trial. Anesth Analg. 2010;110(2):60410.
Milstein SL, MacCannell K, Karr G, Clark S. Marijuana-produced changes in pain tolerance. Experienced and non-experienced subjects. Int Pharmacopsychiatry. 1975;10(3):17782.
Cooper ZD, Comer SD, Haney M. Comparison of the analgesic effects of dronabinol and smoked marijuana in daily marijuana smokers. Neuropsychopharmacology. 2013;38(10):198492.
Greenwald MK, Stitzer ML. Antinociceptive, subjective and behavioral effects of smoked marijuana in humans. Drug Alcohol Depend. 2000;59(3):26175.
Wallace M, Schulteis G, Atkinson JH, Wolfson T, Lazzaretto D, Bentley H, et al. Dose-dependent effects of smoked cannabis on capsaicin-induced pain and hyperalgesia in healthy volunteers. Anesthesiology. 2007;107(5):78596.
Abrams DI, Jay CA, Shade SB, Vizoso H, Reda H, Press S, et al. Cannabis in painful HIVassociated sensory neuropathy: a randomized placebo-controlled trial. Neurology. 2007;68(7):51521.
Ellis RJ, Toperoff W, Vaida F, van den Brande G, Gonzales J, Gouaux B, et al. Smoked medicinal cannabis for neuropathic pain in HIV: a randomized, crossover clinical trial. Neuropsychopharmacology. 2009;34(3):67280.
Ware MA, Wang T, Shapiro S, Robinson A, Ducruet T, Huynh T, et al. Smoked cannabis for chronic neuropathic pain: a randomized controlled trial. CMAJ. 2010;182(14):E694701.
Wilsey B, Marcotte T, Tsodikov A, Millman J, Bentley H, Gouaux B, et al. A randomized, placebo-controlled, crossover trial of cannabis cigarettes in neuropathic pain. J Pain. 2008;9(6):50621. One many studies support cannabis for neuropathic pain.
Wilsey B, Marcotte TD, Deutsch R, Zhao H, Prasad H, Phan A. An exploratory human laboratory experiment evaluating vaporized cannabis in the treatment of neuropathic pain from spinal cord injury and disease. J Pain. 2016;17(9):9821000.
Wilsey B, Marcotte T, Deutsch R, Gouaux B, Sakai S, Donaghe H. Low-dose vaporized cannabis significantly improves neuropathic pain. J Pain. 2013;14(2):13648.
Zajicek JP, Sanders HP, Wright DE, Vickery PJ, Ingram WM, Reilly SM, et al. Cannabinoids in multiple sclerosis (CAMS) study: safety and efficacy data for 12 months follow up. J Neurol Neurosurg Psychiatry. 2005;76(12):16649. One of many studies supporting cannabis for multiple sclerosis.
Ernst G, Denke C, Reif M, Schnelle M, Hagmeister H. Standarized cannabis extract in the treatment of postherpetic neuralgia: a randomized, double blind, placebo-controlled cross-over study. Leiden: International Associatin for Cannabis as Medicine; 2005.
Wade DT, Makela P, Robson P, House H, Bateman C. Do cannabis-based medicinal extracts have general or specific effects on symptoms in multiple sclerosis? A double-blind, randomized, placebo-controlled study on 160 patients. Mult Scler. 2004;10(4):43441.
Notcutt W, Price M, Miller R, Newport S, Phillips C, Simmons S, et al. Initial experiences with medicinal extracts of cannabis for chronic pain: results from 34 N of 1 studies. Anaesthesia. 2004;59(5):44052.
Berman JS, Symonds C, Birch R. Efficacy of two cannabis based medicinal extracts for relief of central neuropathic pain from brachial plexus avulsion: results of a randomised controlled trial. Pain. 2004;112(3):299306.
Rog DJ, Nurmikko TJ, Friede T, Young CA. Randomized, controlled trial of cannabis-based medicine in central pain in multiple sclerosis. Neurology. 2005;65(6):8129.
Blake DR, Robson P, Ho M, Jubb RW, McCabe CS. Preliminary assessment of the efficacy, tolerability and safety of a cannabis-based medicine (Sativex) in the treatment of pain caused by rheumatoid arthritis. Rheumatology (Oxford). 2006;45(1):502.
Johnson JR, Burnell-Nugent M, Lossignol D, Ganae-Motan ED, Potts R, Fallon MT. Multicenter, double-blind, randomized, placebo-controlled, parallel-group study of the efficacy, safety, and tolerability of THC:CBD extract and THC extract in patients with intractable cancer-related pain. J Pain Symptom Manag. 2010;39(2):16779. Support cannabis for cancer related pain.
Portenoy RK, Ganae-Motan ED, Allende S, Yanagihara R, Shaiova L, Weinstein S, et al. Nabiximols for opioid-treated cancer patients with poorly-controlled chronic pain: a randomized, placebo-controlled, graded-dose trial. J Pain. 2012;13(5):43849.
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Abrams DI, Couey P, Shade SB, Kelly ME, Benowitz NL. Cannabinoid-opioid interaction in chronic pain. Clin Pharmacol Ther. 2011;90(6):84451. Good explanation on where opioids and cannabinoids interact in a close relationship.
Ohlsson A, Lindgren JE, Wahlen A, Agurell S, Hollister LE, Gillespie HK. Plasma delta-9 tetrahydrocannabinol concentrations and clinical effects after oral and intravenous administration and smoking. Clin Pharmacol Ther. 1980;28(3):40916.
Borgelt LM, Franson KL, Nussbaum AM, Wang GS. The pharmacologic and clinical effects of medical cannabis. Pharmacotherapy. 2013;33(2):195209. Good review on cannabis side effects and complications.
Cone EJ, Johnson RE, Paul BD, Mell LD, Mitchell J. Marijuana-laced brownies: behavioral effects, physiologic effects, and urinalysis in humans following ingestion. J Anal Toxicol. 1988;12(4):16975.
Merrick J, Lane B, Sebree T, Yaksh T, ONeill C, Banks S. Identification of psychoactive degradants of cannabidiol in simulated gastric and physiological fluid. Cannabis Cannabinoid Res. 2016;1(1):10212.
Cooper ZD, Haney M. Sex-dependent effects of cannabis-induced analgesia. Drug Alcohol Depend. 2016;167:11220.
Volkow ND, Compton WM, Weiss SR. Adverse health effects of marijuana use. N Engl J Med. 2014;371(9):879. Up to date review of side effects and complication of cannabis.
Zullino DF, Delessert D, Eap CB, Preisig M, Baumann P. Tobacco and cannabis smoking cessation can lead to intoxication with clozapine or olanzapine. Int Clin Psychopharmacol. 2002;17(3):1413.
Grotenhermen F. Pharmacokinetics and pharmacodynamics of cannabinoids. Clin Pharmacokinet. 2003;42(4):32760.
Solowij N, Battisti R. The chronic effects of cannabis on memory in humans: a review. Curr Drug Abuse Rev. 2008;1(1):8198.
Rossato M, Pagano C, Vettor R. The cannabinoid system and male reproductive functions. J Neuroendocrinol. 2008;20 Suppl 1:903.
Tetrault JM, Crothers K, Moore BA, Mehra R, Concato J, Fiellin DA. Effects of marijuana smoking on pulmonary function and respiratory complications: a systematic review. Arch Intern Med. 2007;167(3):2218. Review on impact of cannabis on the pulmonary systems.
Mehra R, Moore BA, Crothers K, Tetrault J, Fiellin DA. The association between marijuana smoking and lung cancer: a systematic review. Arch Intern Med. 2006;166(13):135967.
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Manzanares J, Corchero J, Romero J, Fernandez-Ruiz JJ, Ramos JA, Fuentes JA. Chronic administration of cannabinoids regulates proenkephalin mRNA levels in selected regions of the rat brain. Brain Res Mol Brain Res. 1998;55(1):12632.
Cichewicz DL, Martin ZL, Smith FL, Welch SP. Enhancement mu opioid antinociception by oral delta9-tetrahydrocannabinol: doseresponse analysis and receptor identification. J Pharmacol Exp Ther. 1999;289(2):85967.
Bachhuber MA, Saloner B, Cunningham CO, Barry CL. Medical cannabis laws and opioid analgesic overdose mortality in the United States, 19992010. JAMA Intern Med. 2014;174(10):166873. Report of the impact on cannabis on the opioid epidemic.
Boehnke KF, Litinas E, Clauw DJ. Medical cannabis use is associated with decreased opiate medication use in a retrospective cross-sectional survey of patients with chronic pain. J Pain. 2016;17(6):73944.
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