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Not Just a High: Medical Marijuana
Not Just a High: Medical Marijuana
June 19, 2010 Author: Nathan Seppa Source: Science News
In science’s struggle to keep up with life on the streets, smoking cannabis for medical purposes
stands as Exhibit A.
Medical use of cannabis has taken on momentum of its own, surging ahead of scientists’ ability to
measure the drug’s benefits. The pace has been a little too quick for some, who see medicinal
joints as a punch line, a ruse to free up access to a recreational drug.
But while the medical marijuana movement has been generating political news, some researchers
have been quietly moving in new directions — testing cannabis and its derivatives against a host of
diseases. The scientific literature now brims with potential uses for cannabis that extend beyond its
well-known abilities to fend off nausea and block pain in people with cancer and AIDS. Cannabis
derivatives may combat multiple sclerosis, Crohn’s disease and other inflammatory conditions, the
new research finds. Cannabis may even kill cancerous tumors.
Many in the scientific community are now keen to see if this potential will be fulfilled, but they haven’
t always been. Pharmacologist Roger Pertwee of the University of Aberdeen in Scotland recalls
attending scientific conferences 30 years ago, eager to present his latest findings on the
therapeutic effects of cannabis. It was a hard sell.
“Our talks would be scheduled at the end of the day, and our posters would be stuck in the corner
somewhere,” he says. “That’s all changed.”
Underlying biology
The long march to credibility for cannabis research has been built on molecular biology. Smoking
or otherwise consuming marijuana — Latin name Cannabis sativa — has a medical history that
dates back thousands of years. But the euphoria-inducing component of cannabis, delta-9-
tetrahydrocannabinol, or THC, wasn’t isolated until 1964, by biochemist Raphael Mechoulam, then
of the Weizmann Institute of Science in Rehovot, Israel, and his colleagues. Within two decades,
other researchers had developed synthetic THC to use in pill form.
The secrets of how THC worked in the body lay hidden until the late 1980s, when researchers
working with rats found that the compound binds to a protein that pops up on the surface of nerve
cells. Further tests showed that THC also hooks up with another protein found elsewhere in the
body. These receptor proteins were dubbed CB1 and CB2.
A bigger revelation came in 1992: Mammals make their own compound that binds to, and switches
on, the CB1 receptor. Scientists named the compound anandamide. Researchers soon found its
counterpart that binds mainly to the CB2 receptor, calling that one 2AG, for 2-arachidonyl glycerol.
The body routinely makes these compounds, called endocannabinoids, and sends them into action
as needed.
“At that point, this became a very, very respectable field,” says Mechoulam, now at Hebrew
University of Jerusalem, who along with Pertwee and others reported the anandamide discovery in
Science. “THC just mimics the effects of these compounds in our bodies,” Mechoulam says.
Although the receptors are abundant, anandamide and 2AG are short-acting compounds, so their
effects are fleeting.
In contrast, when a person consumes cannabis, a flood of THC molecules bind to thousands of
CB1 and CB2 receptors, with longer-lasting effects. The binding triggers so many internal changes
that, decades after the receptors’ discovery, scientists are still sorting out the effects. From a
biological standpoint, smoking pot to get high is like starting up a semitruck just to listen to the
radio. There’s a lot more going on.
Though the psychoactive effect of THC has slowed approval for cannabis-based drugs, the high
might also have brought on a serendipitous discovery, says neurologist Ethan Russo, senior
medical adviser for GW Pharmaceuticals, which is based in Porton Down, England. “How much
longer would it have taken us to figure out the endocannabinoid system if cannabis didn’t happen
to have these unusual effects on human physiology?”
Beyond the pain
Today smoked cannabis is a sanctioned self-treatment for verifiable medical conditions in 14 U.S.
states, Canada, the Netherlands and Israel, among other places. It usually requires a doctor’s
recommendation and some paperwork.
People smoke the drug to alleviate pain, sleep easier and deal with nausea, lack of appetite and
mood disorders such as anxiety, stress and depression. Patients not wanting to smoke cannabis
can seek out prescriptions for FDA-approved capsules containing cannabis compounds for
treatment of some of these same problems.
Research now suggests that multiple sclerosis could join the growing list of cannabis-treated
ailments. More than a dozen medical trials in the past decade have shown that treatments
containing THC (and some that combine THC with another derivative called cannabidiol, or CBD)
not only ease pain in MS patients but also alleviate other problems associated with the disease. MS
results from damage to the fatty sheaths that insulate nerves in the brain and spinal cord.
“MS patients get burning pain in the legs and muscle stiffness and spasms that keep them awake at
night,” says John Zajicek, a neurologist at the Peninsula College of Medicine and Dentistry in
Plymouth, England. Patients can take potent steroids and other anti-inflammatory drugs, but the
effects of these medications can be inconsistent.
Pertwee has analyzed 17 trials in which MS patients received some form of cannabis or its
derivatives. Reports from the patients themselves, who didn’t know if they were getting real
cannabinoids or a placebo in most of the trials, show improvements in muscle spasticity, sleep
quality, shakiness, sense of well-being and mobility. Pertwee, who is also a consultant for GW
Pharmaceuticals — which makes a cannabinoid drug that is delivered in spray form, called Sativex
— reviewed the findings in Molecular Neurobiology in 2007.
Sativex was approved in Canada for MS in 2005 after studies (some included in Pertwee’s analysis)
showed its success in relieving symptoms of the disease.
GW Pharmaceuticals expects clearance for MS treatment in the United Kingdom and Spain this
year. Later, the company plans to seek U.S. approval of Sativex for cancer pain.
Zajicek’s team has also compared MS patients who received a placebo with patients receiving
either a capsule containing THC or one with THC and CBD. Both of the cannabis-based drugs
outperformed a placebo, and the researchers are now working on a multiyear MS trial.
Calming symptoms such as muscle spasticity and pain is useful, Zajicek says, but the true value of
cannabinoids may exceed that. “To me, the really exciting stuff is whether these drugs have a much
more fundamental role in changing the course of MS over the longer term,” he says. “We’ve got
nothing that actually slows progression of the disease.”
Fighting inflammation
CBD, the same cannabis component that proved beneficial alongside THC for MS, may also work
on other hard-to-treat diseases. Tests on cell cultures and lab animals have revealed that CBD
fights inflammation and mitigates the psychoactive effects of THC.
Crohn’s disease, which can lead to chronic pain, diarrhea and ulcerations, could be a fitting target
for CBD. In Crohn’s disease, inflammatory proteins damage the intestinal lining, causing leaks that
allow bacteria in the gut to spread where they shouldn’t. This spread leads to a vicious cycle that
can trigger more inflammation.
Karen Wright, a pharmacologist at Lancaster University in England, and her colleagues have found
that CBD inhibits this inflammation and can reverse the microscopic intestinal leakiness in lab tests
of human cells. Adding
THC doesn’t seem to boost the benefit, Wright reported in December 2009 in London at a meeting
of the British Pharmacological Society. The results bolster earlier findings by Wright’s team showing
that cannabinoids could improve wound healing in intestinal cells.
CBD’s anti-inflammatory effect may work, at least in some cases, through its antioxidant properties
— the ability to soak up highly reactive molecules called free radicals, which cause cell damage.
In the brain and eye, CBD slows the action of microglia, immune cells that can foster harmful
inflammation when hyperactivated by free radicals. Working with rats whose retinas were induced to
have inflammation, biochemist Gregory Liou of the Medical College of Georgia in Augusta and his
team found that CBD neutralized free radicals, preventing eye damage. This finding could have
implications for people with diabetes who develop vision loss.
Apart from being an anti-inflammatory and antioxidant, CBD tones down the psychoactive effect of
THC without eliminating its medical properties. CBD also mutes the occasional anxiety and even
paranoia that THC can induce. This has been welcome news to scientists, who consider the “buzz”
of cannabis little more than psychoactive baggage.
But CBD has paid a price for this anti-upper effect. “CBD has essentially been bred out of North
American black market drug strains,” Russo says. People growing cannabis for its recreational
qualities have preferred plants high in THC, so people lighting up for medical purposes, whether to
boost appetite in AIDS patients or alleviate cancer pain, may be missing a valuable cannabis
component.
Cannabis versus cancer
With or without CBD, cannabis may someday do more for cancer patients than relieve pain and
nausea. New research suggests THC may be lethal to tumors themselves.
Biochemists Guillermo Velasco and Manuel Guzmán of Complutense University in Madrid have
spent more than a decade establishing in lab-dish and animal tests that THC can kill cancer of the
brain, skin and pancreas.
THC ignites programmed suicide in some cancerous cells, the researchers reported in 2009 in the
Journal of Clinical Investigation. The team’s previous work showed that THC sabotages the process
by which a tumor hastily forms a netting of blood vessels to nourish itself, and also keeps cancer
cells from moving around.
THC achieves this wizardry by binding to protein receptors on a cancerous cell’s surface. Once
attached, the THC induces the cell to make a fatty substance called ceramide, which prompts the
cell to start devouring itself. “We see programmed cell death,” Velasco says. What’s more,
noncancerous cells don’t make ceramide when they come into contact with THC. The healthy cells
don’t die.
Many compounds kill cancer in a test tube and even in animals, but most prove useless because
they cause side effects or just don’t work in people. The Madrid team is now seeking funding to test
whether cannabis derivatives can kill tumors in cancer patients. In an early trial of nine brain cancer
patients whose disease had worsened despite standard therapy, the scientists found that THC
injections into tumors were safe to give.
Early reports from other research groups suggest that THC also fights breast cancer and leukemia.
“I think the cancer research is extremely promising,” Russo says. “Heretofore, the model for cancer
was to use an agent that’s extremely toxic to kill the cancer before it kills you. With cannabinoids,
we have an opportunity to use agents that are selectively toxic to cancer cells.”
Looking ahead
Testing of cannabis and its derivatives has also begun on type 1 diabetes, rheumatoid arthritis,
stroke, Tourette syndrome, epilepsy, depression, bipolar disorder and schizophrenia. Pertwee is
particularly optimistic that cannabis will help people with post-traumatic stress disorder. Experiments
in rats show that THC “speeds up the rate at which the animals forget unpleasant experiences,” he
says. And a recent study in people with PTSD showed that THC capsules improved sleep and
stopped nightmares.
Despite these heady beginnings, medical cannabis still faces an uphill climb. Although some states
have sanctioned its use, no smoked substance has ever been formally approved as a medicine by
U.S. regulatory agencies. Smoking cannabis can lead to chronic coughing and bronchitis, and
smoking renders a drug off-limits for children, Mechoulam notes.
THC pills don’t have these downsides, but the drugs have received only lukewarm acceptance.
Despite smoking’s drawbacks, “it is seen as better because you can regulate the amount of THC
you’re getting by not puffing as much,” says pharmacologist Daniele Piomelli of the University of
California, Irvine. Capsules can cause dizziness and make it hard to focus. “Patients suffering from
neuropathic pain or depression don’t want to be stoned — they want relief,” he says.
Controlled, randomized trials that seek to clarify whether smoked cannabis delivers on its medical
promise — with acceptable side effects — have been hard to come by. But scientists in California
have recently concluded several studies in which patients with severe pain received actual
cannabis cigarettes or cannabis cigarettes with the cannabinoids removed.
In one trial, researchers randomly assigned 27 HIV patients to get the real thing and 28 to get fake
joints. All the patients had neuropathic pain, in which neurons can overreact to even mild stimuli.
About half of the people getting real cannabis experienced a pain reduction of 30 percent or
greater, a standard benchmark in pain measurement. Only one-quarter of volunteers getting the
placebo reported such a reduction.
“That’s about as good [a reduction] as other drugs provide,” says Igor Grant, a neuropsychiatrist at
the University of California, San Diego, who is among the scientists overseeing the trials.
While such studies provide evidence that smoked marijuana has medical benefits, future trials are
more likely to explore the benefits of cannabis derivatives that don’t carry the baggage that
smoking does.
Ultimately, the fate of medical cannabis and its derivatives will rest on the same make-or-break
requirements that every experimental medicine faces — whether it cures a disease or alleviates its
symptoms, and whether it’s tolerable.
“We have to be careful that marijuana isn’t seen as a panacea that will help everybody,” Grant
says. “It probably has a niche.… We can’t ignore the fact that cannabis is a substance of abuse in
some people.”
--------------------------------------------------------------------------------
Getting cannabis in
When most people think of medicinal cannabis, smoking comes to mind. Though smoking works
quickly and allows users to regulate their intake, it’s hardly a scientific approach: Cannabis quality
is often unknown, and inhaling burned materials is bad for the lungs. These and other drawbacks
have spawned new ways to consume medical marijuana.
Some people inhale cannabis by using a device that heats the plant without igniting it. This
vaporization unleashes many of the same cannabinoid compounds as smoking does, without the
combustion by-products, researchers say. Anecdotally, patients report that the effect is prompt, on
a par with smoking.
Because cannabis derivatives can pass through the lining of the mouth and throat, a company
called GW Pharmaceuticals has devised a spray product called Sativex. This drug contains roughly
equal amounts of two key cannabinoids — THC and CBD — plus other cannabis components in an
alcohol solution. A dose of Sativex is sprayed under the tongue; no smoking required.
In the face of these options, the “pot pill” seems almost passé. But capsules of synthetic THC exist.
One called Marinol has been approved in the United States since 1985, and another called
Cesamet was cleared more recently. Doctors can prescribe the drugs for nausea, vomiting, loss of
appetite and weight loss. Though sales of capsules have increased recently, many users complain
of psychoactive side effects and slow action.
June 19, 2010 Author: Nathan Seppa Source: Science News
In science’s struggle to keep up with life on the streets, smoking cannabis for medical purposes
stands as Exhibit A.
Medical use of cannabis has taken on momentum of its own, surging ahead of scientists’ ability to
measure the drug’s benefits. The pace has been a little too quick for some, who see medicinal
joints as a punch line, a ruse to free up access to a recreational drug.
But while the medical marijuana movement has been generating political news, some researchers
have been quietly moving in new directions — testing cannabis and its derivatives against a host of
diseases. The scientific literature now brims with potential uses for cannabis that extend beyond its
well-known abilities to fend off nausea and block pain in people with cancer and AIDS. Cannabis
derivatives may combat multiple sclerosis, Crohn’s disease and other inflammatory conditions, the
new research finds. Cannabis may even kill cancerous tumors.
Many in the scientific community are now keen to see if this potential will be fulfilled, but they haven’
t always been. Pharmacologist Roger Pertwee of the University of Aberdeen in Scotland recalls
attending scientific conferences 30 years ago, eager to present his latest findings on the
therapeutic effects of cannabis. It was a hard sell.
“Our talks would be scheduled at the end of the day, and our posters would be stuck in the corner
somewhere,” he says. “That’s all changed.”
Underlying biology
The long march to credibility for cannabis research has been built on molecular biology. Smoking
or otherwise consuming marijuana — Latin name Cannabis sativa — has a medical history that
dates back thousands of years. But the euphoria-inducing component of cannabis, delta-9-
tetrahydrocannabinol, or THC, wasn’t isolated until 1964, by biochemist Raphael Mechoulam, then
of the Weizmann Institute of Science in Rehovot, Israel, and his colleagues. Within two decades,
other researchers had developed synthetic THC to use in pill form.
The secrets of how THC worked in the body lay hidden until the late 1980s, when researchers
working with rats found that the compound binds to a protein that pops up on the surface of nerve
cells. Further tests showed that THC also hooks up with another protein found elsewhere in the
body. These receptor proteins were dubbed CB1 and CB2.
A bigger revelation came in 1992: Mammals make their own compound that binds to, and switches
on, the CB1 receptor. Scientists named the compound anandamide. Researchers soon found its
counterpart that binds mainly to the CB2 receptor, calling that one 2AG, for 2-arachidonyl glycerol.
The body routinely makes these compounds, called endocannabinoids, and sends them into action
as needed.
“At that point, this became a very, very respectable field,” says Mechoulam, now at Hebrew
University of Jerusalem, who along with Pertwee and others reported the anandamide discovery in
Science. “THC just mimics the effects of these compounds in our bodies,” Mechoulam says.
Although the receptors are abundant, anandamide and 2AG are short-acting compounds, so their
effects are fleeting.
In contrast, when a person consumes cannabis, a flood of THC molecules bind to thousands of
CB1 and CB2 receptors, with longer-lasting effects. The binding triggers so many internal changes
that, decades after the receptors’ discovery, scientists are still sorting out the effects. From a
biological standpoint, smoking pot to get high is like starting up a semitruck just to listen to the
radio. There’s a lot more going on.
Though the psychoactive effect of THC has slowed approval for cannabis-based drugs, the high
might also have brought on a serendipitous discovery, says neurologist Ethan Russo, senior
medical adviser for GW Pharmaceuticals, which is based in Porton Down, England. “How much
longer would it have taken us to figure out the endocannabinoid system if cannabis didn’t happen
to have these unusual effects on human physiology?”
Beyond the pain
Today smoked cannabis is a sanctioned self-treatment for verifiable medical conditions in 14 U.S.
states, Canada, the Netherlands and Israel, among other places. It usually requires a doctor’s
recommendation and some paperwork.
People smoke the drug to alleviate pain, sleep easier and deal with nausea, lack of appetite and
mood disorders such as anxiety, stress and depression. Patients not wanting to smoke cannabis
can seek out prescriptions for FDA-approved capsules containing cannabis compounds for
treatment of some of these same problems.
Research now suggests that multiple sclerosis could join the growing list of cannabis-treated
ailments. More than a dozen medical trials in the past decade have shown that treatments
containing THC (and some that combine THC with another derivative called cannabidiol, or CBD)
not only ease pain in MS patients but also alleviate other problems associated with the disease. MS
results from damage to the fatty sheaths that insulate nerves in the brain and spinal cord.
“MS patients get burning pain in the legs and muscle stiffness and spasms that keep them awake at
night,” says John Zajicek, a neurologist at the Peninsula College of Medicine and Dentistry in
Plymouth, England. Patients can take potent steroids and other anti-inflammatory drugs, but the
effects of these medications can be inconsistent.
Pertwee has analyzed 17 trials in which MS patients received some form of cannabis or its
derivatives. Reports from the patients themselves, who didn’t know if they were getting real
cannabinoids or a placebo in most of the trials, show improvements in muscle spasticity, sleep
quality, shakiness, sense of well-being and mobility. Pertwee, who is also a consultant for GW
Pharmaceuticals — which makes a cannabinoid drug that is delivered in spray form, called Sativex
— reviewed the findings in Molecular Neurobiology in 2007.
Sativex was approved in Canada for MS in 2005 after studies (some included in Pertwee’s analysis)
showed its success in relieving symptoms of the disease.
GW Pharmaceuticals expects clearance for MS treatment in the United Kingdom and Spain this
year. Later, the company plans to seek U.S. approval of Sativex for cancer pain.
Zajicek’s team has also compared MS patients who received a placebo with patients receiving
either a capsule containing THC or one with THC and CBD. Both of the cannabis-based drugs
outperformed a placebo, and the researchers are now working on a multiyear MS trial.
Calming symptoms such as muscle spasticity and pain is useful, Zajicek says, but the true value of
cannabinoids may exceed that. “To me, the really exciting stuff is whether these drugs have a much
more fundamental role in changing the course of MS over the longer term,” he says. “We’ve got
nothing that actually slows progression of the disease.”
Fighting inflammation
CBD, the same cannabis component that proved beneficial alongside THC for MS, may also work
on other hard-to-treat diseases. Tests on cell cultures and lab animals have revealed that CBD
fights inflammation and mitigates the psychoactive effects of THC.
Crohn’s disease, which can lead to chronic pain, diarrhea and ulcerations, could be a fitting target
for CBD. In Crohn’s disease, inflammatory proteins damage the intestinal lining, causing leaks that
allow bacteria in the gut to spread where they shouldn’t. This spread leads to a vicious cycle that
can trigger more inflammation.
Karen Wright, a pharmacologist at Lancaster University in England, and her colleagues have found
that CBD inhibits this inflammation and can reverse the microscopic intestinal leakiness in lab tests
of human cells. Adding
THC doesn’t seem to boost the benefit, Wright reported in December 2009 in London at a meeting
of the British Pharmacological Society. The results bolster earlier findings by Wright’s team showing
that cannabinoids could improve wound healing in intestinal cells.
CBD’s anti-inflammatory effect may work, at least in some cases, through its antioxidant properties
— the ability to soak up highly reactive molecules called free radicals, which cause cell damage.
In the brain and eye, CBD slows the action of microglia, immune cells that can foster harmful
inflammation when hyperactivated by free radicals. Working with rats whose retinas were induced to
have inflammation, biochemist Gregory Liou of the Medical College of Georgia in Augusta and his
team found that CBD neutralized free radicals, preventing eye damage. This finding could have
implications for people with diabetes who develop vision loss.
Apart from being an anti-inflammatory and antioxidant, CBD tones down the psychoactive effect of
THC without eliminating its medical properties. CBD also mutes the occasional anxiety and even
paranoia that THC can induce. This has been welcome news to scientists, who consider the “buzz”
of cannabis little more than psychoactive baggage.
But CBD has paid a price for this anti-upper effect. “CBD has essentially been bred out of North
American black market drug strains,” Russo says. People growing cannabis for its recreational
qualities have preferred plants high in THC, so people lighting up for medical purposes, whether to
boost appetite in AIDS patients or alleviate cancer pain, may be missing a valuable cannabis
component.
Cannabis versus cancer
With or without CBD, cannabis may someday do more for cancer patients than relieve pain and
nausea. New research suggests THC may be lethal to tumors themselves.
Biochemists Guillermo Velasco and Manuel Guzmán of Complutense University in Madrid have
spent more than a decade establishing in lab-dish and animal tests that THC can kill cancer of the
brain, skin and pancreas.
THC ignites programmed suicide in some cancerous cells, the researchers reported in 2009 in the
Journal of Clinical Investigation. The team’s previous work showed that THC sabotages the process
by which a tumor hastily forms a netting of blood vessels to nourish itself, and also keeps cancer
cells from moving around.
THC achieves this wizardry by binding to protein receptors on a cancerous cell’s surface. Once
attached, the THC induces the cell to make a fatty substance called ceramide, which prompts the
cell to start devouring itself. “We see programmed cell death,” Velasco says. What’s more,
noncancerous cells don’t make ceramide when they come into contact with THC. The healthy cells
don’t die.
Many compounds kill cancer in a test tube and even in animals, but most prove useless because
they cause side effects or just don’t work in people. The Madrid team is now seeking funding to test
whether cannabis derivatives can kill tumors in cancer patients. In an early trial of nine brain cancer
patients whose disease had worsened despite standard therapy, the scientists found that THC
injections into tumors were safe to give.
Early reports from other research groups suggest that THC also fights breast cancer and leukemia.
“I think the cancer research is extremely promising,” Russo says. “Heretofore, the model for cancer
was to use an agent that’s extremely toxic to kill the cancer before it kills you. With cannabinoids,
we have an opportunity to use agents that are selectively toxic to cancer cells.”
Looking ahead
Testing of cannabis and its derivatives has also begun on type 1 diabetes, rheumatoid arthritis,
stroke, Tourette syndrome, epilepsy, depression, bipolar disorder and schizophrenia. Pertwee is
particularly optimistic that cannabis will help people with post-traumatic stress disorder. Experiments
in rats show that THC “speeds up the rate at which the animals forget unpleasant experiences,” he
says. And a recent study in people with PTSD showed that THC capsules improved sleep and
stopped nightmares.
Despite these heady beginnings, medical cannabis still faces an uphill climb. Although some states
have sanctioned its use, no smoked substance has ever been formally approved as a medicine by
U.S. regulatory agencies. Smoking cannabis can lead to chronic coughing and bronchitis, and
smoking renders a drug off-limits for children, Mechoulam notes.
THC pills don’t have these downsides, but the drugs have received only lukewarm acceptance.
Despite smoking’s drawbacks, “it is seen as better because you can regulate the amount of THC
you’re getting by not puffing as much,” says pharmacologist Daniele Piomelli of the University of
California, Irvine. Capsules can cause dizziness and make it hard to focus. “Patients suffering from
neuropathic pain or depression don’t want to be stoned — they want relief,” he says.
Controlled, randomized trials that seek to clarify whether smoked cannabis delivers on its medical
promise — with acceptable side effects — have been hard to come by. But scientists in California
have recently concluded several studies in which patients with severe pain received actual
cannabis cigarettes or cannabis cigarettes with the cannabinoids removed.
In one trial, researchers randomly assigned 27 HIV patients to get the real thing and 28 to get fake
joints. All the patients had neuropathic pain, in which neurons can overreact to even mild stimuli.
About half of the people getting real cannabis experienced a pain reduction of 30 percent or
greater, a standard benchmark in pain measurement. Only one-quarter of volunteers getting the
placebo reported such a reduction.
“That’s about as good [a reduction] as other drugs provide,” says Igor Grant, a neuropsychiatrist at
the University of California, San Diego, who is among the scientists overseeing the trials.
While such studies provide evidence that smoked marijuana has medical benefits, future trials are
more likely to explore the benefits of cannabis derivatives that don’t carry the baggage that
smoking does.
Ultimately, the fate of medical cannabis and its derivatives will rest on the same make-or-break
requirements that every experimental medicine faces — whether it cures a disease or alleviates its
symptoms, and whether it’s tolerable.
“We have to be careful that marijuana isn’t seen as a panacea that will help everybody,” Grant
says. “It probably has a niche.… We can’t ignore the fact that cannabis is a substance of abuse in
some people.”
--------------------------------------------------------------------------------
Getting cannabis in
When most people think of medicinal cannabis, smoking comes to mind. Though smoking works
quickly and allows users to regulate their intake, it’s hardly a scientific approach: Cannabis quality
is often unknown, and inhaling burned materials is bad for the lungs. These and other drawbacks
have spawned new ways to consume medical marijuana.
Some people inhale cannabis by using a device that heats the plant without igniting it. This
vaporization unleashes many of the same cannabinoid compounds as smoking does, without the
combustion by-products, researchers say. Anecdotally, patients report that the effect is prompt, on
a par with smoking.
Because cannabis derivatives can pass through the lining of the mouth and throat, a company
called GW Pharmaceuticals has devised a spray product called Sativex. This drug contains roughly
equal amounts of two key cannabinoids — THC and CBD — plus other cannabis components in an
alcohol solution. A dose of Sativex is sprayed under the tongue; no smoking required.
In the face of these options, the “pot pill” seems almost passé. But capsules of synthetic THC exist.
One called Marinol has been approved in the United States since 1985, and another called
Cesamet was cleared more recently. Doctors can prescribe the drugs for nausea, vomiting, loss of
appetite and weight loss. Though sales of capsules have increased recently, many users complain
of psychoactive side effects and slow action.