SOME THINGS TO
THINK ABOUT
HEALTH - HEALING - WELLNESS
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MARIJUANA - A Medicinal Marvel
In this interview with Dr Grinspoon, many topics are discussed concerning the role of medicinal cannabis use in today's society.
J. Ray: What got you interested in marijuana/cannabis?
Dr Grinspoon: In 1967, I had some unexpected time so I thought I would look into marijuana to see what all the fuss was about. I was convinced at the time that marijuana was a terribly dangerous drug. I didn't understand why young people were ignoring the government's warnings about its danger in using it. So, I spent the next three years doing research and looking into it. I learned I had been brainwashed just like so many other citizens in the United States.
While marijuana is not harmless, it is so much less harmful than alcohol or tobacco that the only sensible way to deal with it is to make it legally available in a controlled system. We can see this with alcohol which is legally available to people over the age of 21 in the United States. I put all this together in a book called Marihuana Reconsidered. It was published in 1971 by Harvard University Press and was quite controversial at the time. It has just been republished as a classic with a new introduction, 25 years later.
JR: In your research you found marijuana/cannabis to be less harmful than tobacco or alcohol?
Dr G: I think cannabis is not harmless. There is no such thing as a harmless drug. Cannabis is, by any criterion, less harmful than either alcohol or tobacco. For example, tobacco costs the US about 425,000 lives every year; alcohol, perhaps 100,000 to 150,000 lives, not to speak of all the other problems caused by alcohol use. With cannabis there has not been a single case of a documented death due to its use. Now, of course, death is not the only toxicity. It is the most profound one and certainly a permanent one. If you look at it from the point of view of other toxicities, again it comes out much better than either alcohol or tobacco. In fact, the subject of our latest book, Marihuana, The Forbidden Medicine, looks at cannabis from the point of view of a medicine. When cannabis regains the place it once had in the US Pharmacopoeia it will be among the least toxic substances in that whole compendium.
JR: It was in the US Pharmacopoeia in the early 1900s?
Dr G: That is correct. Cannabis was a very much used drug up until 1941 when it was dropped from the US Pharmacopoeia. This was after the passage of the first of the draconian US anti-marijuana laws in 1937, the Marihuana Tax Act. This Act made it so difficult for physicians to prescribe cannabis that they just stopped using it.
JR: Cannabinoid receptors were recently discovered in the human brain. Are these cannabinoid receptors related to cannabis and its medical uses?
Dr G: Very definitely. Some years ago it was discovered by Dr Solomon Snyder that there are endogenous opioids; that is to say, substances like opium that we produce in our bodies. It followed from that, that there would be opioid receptors in our brains. It wasn't long afterwards that a woman named Candace Pert discovered this. In other words, if you consider a receptor as a kind of keyhole and the ligand or the neurotransmitter as the key that opens it, the key has to fit into that receptor to open it.
With cannabis it came about the other way: the receptor sites for cannabis were discovered first. I believe this was in 1990. From this it was implied that there had to be an endogenous cannabinoid, a ligand that would turn this receptor site on. Indeed, a couple of years later, a man named W. A. Devane and his group discovered this ligand and they gave it the name "anandamide", after the Sanskrit word ananda, which means "bliss". Now there are many studies of these receptors and anandamide. It is clear that these receptors are not just located in the brain but in various other organs in the body as well.
I think we are going to see in the future that these receptors play a very important part in the medicinal utility of cannabis. Right now the clinical evidence is empirical and anecdotal but, in my view, powerful enough to be translated into a policy which would allow people to use cannabis legally for medicinal purposes.
JR: Do these recent discoveries contradict past research that warned of brain damage from cannabis use?
Dr G: In my view, that kind of thing is in the realm of myth and misinformation about cannabis. Think about it for a minute. If the brain produces its own cannabinoid-like substances, it doesn't make much sense that it would produce a substance which is going to damage the brain. Indeed, long before it was discovered that there are endogenous cannabinoids, the empirical evidence did not demonstrate that cannabis damaged the brain.
There are a few studies which were methodically unsound that the US Government and, specifically, NIDA, the National Institute of Drug Abuse, and the DEA, the Drug Enforcement Administration, focus on.
JR: Can you tell me something about the US Drug Enforcement Administration, the DEA?
Dr G: The predecessor agency of the DEA, the Federal Bureau of Narcotics, was organized in 1930 by a man named Anslinger. Anslinger undertook what he called a "great educational campaign", which actually turned out to be a great disinformational campaign. This is symbolized by one of the flagships of that campaign: the movie, Reefer Madness. If you see the movie Reefer Madness today, even a person who is not very sophisticated about marijuana will laugh at the grossness of the exaggerations dramatised in that movie.
JR: Do you think pharmaceutical drug companies have anything to do with the government's prohibitive stand against medicinal cannabis use?
Dr G: Absolutely. The Partnership for a Drug Free America has a budget of about a million dollars a day. A lot of that money comes from drug companies and distilleries. You see, these companies and distilleries have something to lose- the distilleries for obvious reasons. The drug companies are not interested in marijuana as a medicine because the plant cannot be patented. If you can't patent it, you can't make money on it. Their only interest is a negative one. It will eventually displace some of their pharmaceutical products.
Imagine a patient who requires cancer chemotherapy. Now he can take the best of the anti-nausea drugs, which would be ondansetron. He would pay about US$35 or $40 per 8-milligram pill and would then take three or four of them for a treatment. Normally, he would take it orally, but people with that kind of nausea often can't, so he would take it intravenously. The cost of one treatment for that begins at US$600 because he will need a hospital bed, etc. Or he can smoke perhaps half of a marijuana cigarette and receive relief from the nausea.
Currently, marijuana on the streets is very expensive. One can pay from US$200 to $600 an ounce. This is what I call the prohibition tariff. When marijuana is available as a medicine, the cost would be significantly less than other medications; it would cost about US$20 to $30 an ounce. You can't tax it in the US because it is a medicine. So that would translate out to maybe about 30 cents for a marijuana cigarette.
So our chemotherapy patient could get, many people believe, better relief from the marijuana cigarette for 30 cents. This, in comparison to the ondansetron which would cost at the very least US$160 a day and, if he had to take it intravenously, more than US$600 per treatment.
Well, if you multiply that by all of the symptoms and syndromes we discuss in the book, Marihuana, The Forbidden Medicine, then you can see that the drug companies will have something to lose here.
JR: Do you see this as a big obstacle in changing drug policy here in North America?
Dr G: Well, it is certainly playing a part. It is indirectly playing a part in the Partnership for a Drug Free America ads. To say they are inaccurate is an understatement.
JR: Are we also talking about DARE, the Drug Abuse Resistance Education program we see in many schools at this time?
Dr G: Oh yes, that is a terrible program. Again, it is miseducating children about drugs. It has now been established in a major study that it doesn't do a bit of good. We're all worried about youngsters doing drugs, but now DARE has been demonstrated not to do any good.
JR: In your book, Marihuana, The Forbidden Medicine, there are many references to the medicinal uses of cannabis. What are some of the medical problems you have seen medicinal cannabis help?
Dr G: The most common cancer treatment in the last couple of decades is with the cancer chemotherapeutic substances. A big problem with some of these is the severe nausea and vomiting. It is the kind of nausea that anybody who has not experienced it can only imagine. It is very important that this nausea be defeated so patients can be reasonably comfortable with this treatment. As I have mentioned, there are conventional drugs available; it is just that cannabis is often the best.
Then there is glaucoma which is a disorder of increased intraocular pressure in the eyes. If that pressure is not brought down, glaucoma can eventually lead to blindness. There are conventional medicines that work pretty well; but, for some people, cannabis works better and with fewer side-effects.
Epilepsy is a disorder which has been treated by cannabis for centuries. About 25 per cent of people in the US who have various forms of epilepsy don't get good relief from the conventional medicines. Many of them do get relief from one of the oldest anti-epileptic medicines, cannabis.
Multiple sclerosis affects more than two million people in the US, and one of its distressing symptoms is muscle spasm. It is very painful. Anybody who has had a cramp while swimming will know what muscle spasm pain is all about. Cannabis is very effective for the muscle spasms of not only multiple sclerosis but also of paraplegia and quadriplegia.
Furthermore, cannabis helps people with MS who may have trouble controlling their bladders. Cannabis is very helpful in reducing this kind of loss of control. Not long ago I was in London doing a TV debate on the topic of medicinal cannabis use. There was a woman in the audience who said she had come down from Leeds, two-and-a-half hours on the train, to be in the television audience. She has MS. The part that was so distressing for her was the social embarrassment of losing control over her bladder. Well, she said cannabis has restored her bladder control and she could now make the two-and-a-half-hour trip from Leeds with no trouble.
Cannabis has been used for centuries in the treatment of various kinds of chronic pain. It was used on the battlefields of the Civil War as an analgesic medicine until morphine displaced it. Morphine was much quicker for the pain and a much more powerful pain-reliever than cannabis. Cannabis cannot defeat very powerful pain. The price of using morphine was that many people suffered from what was then called "soldier's disease", which was addiction to morphine.
Cannabis is very useful in the treatment of migraine headaches. Sir William Osler, in his last textbook on medicine, describes cannabis as the best single medicine for the treatment of the pain of migraine.
The list is longer than that but I don't think you want me to go on and on about this. One of the amazing things about cannabis is its versatility. It has many uses. It is also remarkably non-toxic and it will be quite inexpensive when it is not a prohibited substance. In my opinion, cannabis will be seen as a wonder drug of the 1990s, much as penicillin was in the 1940s.
JR: In your first book on cannabis, Marihuana Reconsidered, you mentioned that the international drug-control treaties, specifically the United Nations Single Convention on Narcotic Drugs, were not a serious obstacle to the legalisation of cannabis. Do you still go along with this?
Dr G: There is no question about it. There is no serious obstacle. Treaties can be changed and I think the push to do that will come from Europe. The interest in this is growing much more rapidly in Europe than in the US. In fact, there is so much new information regarding medicinal cannabis use that Yale University Press has asked us for a second edition of Marihuana, The Forbidden Medicine. This book has been translated into 10 languages, including Japanese.
Late in 1995 we received a letter from our German publisher congratulating us on our seventh printing. They said our book has begun a "robust debate on the medicinal use of marijuana in Germany". So, the Europeans are way ahead of us, and I think the pressure will probably come from them to make the necessary legal changes so cannabis can be used as a medicine without interference. The present situation is just awful. These poor people who use it as a medicine already have some degree of anxiety regarding their disease. Another layer of anxiety is imposed on them by their government; namely, they might get arrested or have their homes confiscated because they use cannabis as a medicine.
JR: Do you think these international treaties are what keep the 'war on drugs' alive?
Dr G: I think the Single Convention is not a big obstacle, frankly. I think lots of people use that as an excuse, that we can't do anything because of the Single Convention. I'm not an expert on it, but the international lawyers I've talked to say this is not the problem. I think the war on drugs is a much bigger thing than our discussion of medicinal cannabis use. The 'war on drugs' is a much more complicated problem. If we stick to the narrow agenda of medicinal cannabis use, I think putting pressure on our government representatives and other people in powerful positions is the way.
People are learning about cannabis as a medicine. Anybody who knows a person with AIDS who is dealing with the wasting syndrome probably knows someone who has discovered that cannabis not only retards his weight-loss but maybe helps him to regain weight. People who know patients with multiple sclerosis, migraine, glaucoma who are using cannabis, begin to see that it is a very useful medicine and they begin to wonder what all the fuss is about. So I think people are getting educated.
The other thing that is happening that I think is very hopeful is that doctors are getting educated. You see, doctors usually get their drug education from drug companies or from pharmaceutical company sales people who go around to doctors' offices, as well as from journal articles, advertisements and promotional campaigns from these drug companies. There are no drug companies interested in cannabis, so doctors don't learn much about it. In my view, doctors have not only been miseducated like so many other people, but they have also been agents of that miseducation. What is happening now is doctors are learning from patients. This is a new way for doctors to learn about a new medicine. They learn lots of things from their patients, but generally not about new medicines.
An example of this would be an AIDS patient who started using cannabis for his wasting syndrome. Imagine him going into his doctor's office and getting on the scales. The doctor knows he's been losing weight all along and nothing that the doctor has given him has helped. Suddenly, the doctor sees his patient has gained weight since the last visit and he asks, "What's going on?" The patient says, "It is the cannabis I've been smoking: it has helped me put on some weight." This makes a powerful impression on a doctor who has been struggling to help his patient gain weight. Once this happens to a doctor, his attitude begins to change.
JR: How can the average person work for changes in the drug laws?
Dr G: Well, right now in the US, Congressman Barney Frank of Massachusetts has introduced a bill to do just this; to make it possible for people to use cannabis as a medicine. He needs co-sponsorship and support for this bill. People who are interested in this can contact Barney Frank or even their own representatives and ask them to support HR 2618, the Bill for medical cannabis use for those in medical need.
JR: Is this a similar bill to what Newt Gingrich and others had introduced into Congress in the early 1980s?
Dr G: It's the same bill. It is the McKinney bill. I had suggested to Congressman Frank to expand the number of symptoms and syndromes for which cannabis can be used. We know more about it than we did in 1982, but it is the same bill. Gingrich supported it then, but not now.
JR: In February 1994 you and James Bakalar wrote, "The War on Drugs: A Peace Proposal", published in The New England Journal of Medicine. In it you talk about harm-reduction strategies in the Netherlands and other countries. What do you think is holding back these governments in North America from making the changes necessary for a truce in the drug war, specifically in regards to medicinal cannabis use?
Dr G: Unfortunately, it is attitudes and fears that are unwarranted. Take one harm-reduction approach; namely, clean needles. Now, we've been saying for years that clean needles will reduce the spread of AIDS among drug users. The IV drug users are the group spreading it the most. There are people who are afraid of needle-exchange programs because they think it will cause an increase in the use of intravenous drugs. I would say this has been going on now for four or five years. Now the data is overwhelming. It clearly demonstrates that exchanging needles does cut down the spread of AIDS and it does not cause an increase in the use of these drugs. It is so convincing that some local municipalities have gone ahead with needle exchanges, but the Federal government and the President are all dead set against it. We could have saved a lot of people from AIDS by instituting this policy of clean needles early on. Even now we are dragging our feet because of this misapprehension about giving needles out. Ignorance and fear are not always corrected by data. The data on needle exchange is compelling whether it's from Australia, New Haven or wherever. There is no question. You would think when you have this kind of data it would be translated into social policy, considering the cost of AIDS in human suffering. But we're having an awful tough time persuading the authorities that we should go full steam ahead with needle exchange.
There is an attitude here in the US that the only way to treat anyone using a drug not approved of is to treat them as a criminal. Many of these people even go to jail. The costs of criminalising these people have been extreme. Since I started my work on marijuana in 1967, more than 10 million Americans have been arrested on marijuana charges in the US. In 1994, the year for which we have the latest FBI data on this, 483,000 Americans were arrested on marijuana charges. That is just extraordinary when you consider that cannabis imposes less harm on the individual and on society than either alcohol or tobacco.
JR: What kind of feedback did you receive from your June 1995 article, "Marihuana as Medicine", in JAMA?
Dr G: Well, that article caused a lot of fuss. It was published in the Journal of the American Medical Association (JAMA). This organisation has been steadfast in its opposition to marijuana for 50 years-since an editorial published in 1945. Although the AMA doesn't say so officially, I think publishing our article signals a growing change in physicians' attitudes towards medicinal cannabis. There were physicians who wrote me nasty letters. More impressive were the many physicians who shared their stories about how they learned about cannabis from seeing how it helped a particular patient. Several of them said we ought to have an organization, a physicians' organization, for the medical use of marijuana. The article created a stir not just in this country. I think JAMA is published in 33 languages. It was no small wonder that there was a lot of mail from other parts of the world as well.
JR: Was the feedback mostly positive?
Dr G: Absolutely. By far, most of it was positive. There were some nasty letters, but I have received those from the time I first published Marihuana Reconsidered. The first letter I received was a very nasty letter. As the years go on, though, the mail gets much more positive.
JR: What do you see for the future of medicinal cannabis use?
Dr G: It strikes me that there are a lot of parallels with the discovery of penicillin. Penicillin was discovered by a man named Alexander Fleming in 1928. He had gone off for summer vacation and left a Petri dish out in his laboratory. When he came back, the Petri dish was just covered with Staphylococcus, except for an area surrounding what looked like a little island of mould. He looked into it and found that the mould was giving off a substance which he called "penicillin". It was killing the Staphylococcus. Yet his discovery was ignored until 1941. For over a decade his publication was ignored, until the pressure of World War II highlighted the need for antibacterial substances other than sulphonamides. Then a couple of investigators did a study with just six patients and demonstrated it was a good antibiotic.
Penicillin became very inexpensive to produce. It was clear that penicillin was not toxic and it was very versatile as a drug. It was used in the treatment of many different kinds of infectious diseases. It became the wonder drug of the 1940s.
When cannabis can be produced as a medicine it will be very inexpensive. I have already listed some of the reasons why it can be said to be versatile, and, the government position notwithstanding, it is remarkably non-toxic. It has exactly the same three characteristics that made penicillin a wonder drug. These are some of the reasons I believe that, in the late 1990s, cannabis is going to be recognized as a wonder drug.
Grinspoon, Lester, M.D., Marihuana Reconsidered, Quick American
Archives (a division of Quick Trading Company, PO Box 429477, San Francisco,
CA 94142, USA), 1994 (ISBN 0-932551-13-0), first published by Harvard
University Press, 1971.
Grinspoon, Lester, M.D. and James B. Bakalar, Marihuana, The Forbidden
Medicine, Yale University Press, New Haven and London, 1993 (ISBN
0-300-05435-1 [cloth], ISBN 0-300-05994-9 [paperback].
Grinspoon, Lester, M.D. and James B. Bakalar, "The War On Drugs: A Peace
Proposal", New England Journal of Medicine, vol. 330, no. 5, 3
February 1994.
Grinspoon, Lester, M.D. and James B. Bakalar, "Marihuana as Medicine: A Plea
for Reconsideration", Journal of the American Medical Association (JAMA),
vol. 273, no. 23.
For more information on the DARE school programs, here is a list of
articles and world wide web addresses:
Harmon, Michele Alicia, "Reducing the Risk of Drug Involvement Among Early
Adolescents: An Evaluation of Drug Abuse Resistance Education (DARE)",
Institute of Criminal Justice and Criminology, University of Maryland,
College Park, MD 20742, USA, April 1993.
Web address:
http://turnpike.net/~jnr/dareeval.htm
"Studies Find Drug Program Not Effective", USA Today, 11 October 1993. See web site: http://turnpike.net/~jnr/dareart.htm.
"A Different Look at DARE", Drug Reform Coordination Network Topics, in-depth series. Web site address: http://drcnet.org/DARE.
Dr Lester Grinspoon is an Associate Professor of Psychiatry at the Harvard Medical School. He has published over 140 papers and 12 books. His major area of interest has been 'illicit' drugs. His first book, Marihuana Reconsidered, was published in 1971 by Harvard University Press and republished in 1994 as a classic. He has written books on amphetamines, cocaine and psychedelic drugs. In 1990 he won the Alfred R. Lindesmith Award of the Drug Policy Foundation for "Achievement in the field of drug scholarship". Marihuana, The Forbidden Medicine, Dr Grinspoon's latest book, written with James Bakalar, has been translated into 10 languages. A second edition is now in press. [Copies of Marihuana, The Forbidden Medicine, can be ordered from the Publicity Department, Yale University Press, New Haven, Connecticut, USA, phone +1 (203) 432 0971.]
Jana Ray is a freelance writer and community radio personality who works
to educate the public about humane alternatives to the global war on drugs.
Harm-reduction strategies, legal medicinal cannabis use, drug law reform and
the preservation of everyone's human rights are fundamental principles
guiding her work. Since 1992, Jana has been an active member of the British
Columbia Anti-Prohibition League which represents various west Canadian
groups. BCAPL advocates public/government recognition of the individual's
natural, human and legal right to determine personally his/her own religion,
lifestyle and consumption.
Extracted from Nexus Magazine, Volume 3.
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From Matthew message February 14, 2010,
With thanks to all who wrote about the medicinal effects of marijuana, I see the error in my reply [in the January 11, 2010 message] to readers who asked if certain enjoyments, including “social drugs,” could delay spiritual evolution or prevent physical ascension with Earth. In my “Yes” answer, I was thinking of heroin, cocaine and the assortment of synthetic drugs that cause adverse effects on body, mind and spirit. Marijuana does indeed offer medical benefits, and there are no damaging effects from its moderate use in a social setting. Legal consequences, yes, so I surely am not encouraging its use without medical prescription! I am simply stating that with the sensible use I mentioned, marijuana is not among the drugs that form a barrier between the consciousness and the soul and prevent the absorption of light.
Pot Chemical Significantly Reduces Chronic Pain In Humans
Hannover, Germany 10-8-03: Administration of the CT-3 cannabinoid significantly reduces chronic pain in humans compared to placebo, according to the results of clinical trial data published in the current issue of the Journal of the American Medical Association (JAMA).
The results of the study indicate that "CT-3 may be an effective analgesic for poorly controlled resistant neuropathic pain," researchers at the Hannover Medical School in Germany concluded. Neuropathic pain is often resistant to standard pain medications, including opioids.
Twenty-four patients with chronic neurpoathic pain in places such as the foot, arm, face and head participated in the randomized, placebo controlled trial. Volunteers were administered two daily doses of either CT-3, a nonpsychoactive cannabinoid that has previously demonstrated anti-inflammatory properties in animals, or placebo. Researchers found CT-3 to be more effective than placebo at diminishing pain, and noted "no major adverse side effects" of the drug.
Although anecdotal reports regarding marijuana's pain-mitigating effects are abundant, few clinical human trails have been conducted. Nevertheless, after reviewing a series of animal trails on cannabinoids in pain in 1997, the US Society for Neuroscience concluded that "substances similar to or derived from marijuana ... could benefit the more than 97 million Americans who experience some form of pain each year."
In an email interview for this story, the Madrid researcher said he had heard of the Virginia study, but had never been able to locate literature on it. Hence, the Nature Medicine article characterizes the new study as the first on tumor-laden animals and doesn't cite the 1974 Virginia investigation.
"I am aware of the existence of that research. In fact I have attempted many times to obtain the journal article on the original investigation by these people, but it has proven impossible." Guzman said.
In 1983 the Reagan/Bush Administration tried to persuade American universities and researchers to destroy all 1966-76 cannabis research work, including compendiums in libraries, reports Jack Herer, who states, "We know that large amounts of information have since disappeared."
Guzman provided the title of the work -- "Antineoplastic activity of cannabinoids," an article in a 1975 Journal of the National Cancer Institute -- and this writer obtained a copy at the University of California medical school library in Davis and faxed it to Madrid.
The summary of the Virginia study begins, "Lewis lung adenocarcinoma growth was retarded by the oral administration of tetrahydrocannabinol (THC) and cannabinol (CBN)" -- two types of cannabinoids, a family of active components in marijuana. "Mice treated for 20 consecutive days with THC and CBN had reduced primary tumor size."
The 1975 journal article doesn't mention breast cancer tumors, which featured in the only newspaper story ever to appear about the 1974 study -- in the Local section of the Washington Post on August 18, 1974. Under the headline, "Cancer Curb Is Studied," it read in part:
"The active chemical agent in marijuana curbs the growth of three kinds of cancer in mice and may also suppress the immunity reaction that causes rejection of organ transplants, a Medical College of Virginia team has discovered." The researchers "found that THC slowed the growth of lung cancers, breast cancers and a virus-induced leukemia in laboratory mice, and prolonged their lives by as much as 36 percent."
Guzman, writing from Madrid, was eloquent in his response after this writer faxed him the clipping from the Washington Post of a quarter century ago. In translation, he wrote:
"It is extremely interesting to me, the hope that the project seemed to awaken at that moment, and the sad evolution of events during the years following the discovery, until now we once again Œdraw back the veil‚ over the anti-tumoral power of THC, twenty-five years later. Unfortunately, the world bumps along between such moments of hope and long periods of intellectual castration."
News coverage of the Madrid discovery has been virtually nonexistent in this country. The news broke quietly on Feb. 29, 2000 with a story that ran once on the UPI wire about the Nature Medicine article. This writer stumbled on it through a link that appeared briefly on the Drudge Report web page. The New York Times, Washington Post and Los Angeles Times all ignored the story, even though its newsworthiness is indisputable: a benign substance occurring in nature destroys deadly brain tumors.
Raymond Cushing is a journalist, musician and filmmaker. This article was named by Project Censored as a "Top Censored Story of 2000."
NewScientist.com news service, Gaia Vince
Cannabis-based drugs could offer treatment hope to sufferers of inflammatory bowel disease, UK researchers report.
Cannabis smokers with inflammatory bowel disease (IBD) have often claimed that smoking a joint seems to lessen their symptoms. So a group of researchers from Bath University and Bristol University, both in the UK, decided to explore the clinical basis for the claims.
“There is quite a lot of anecdotal evidence that using cannabis seems to reduce the pain and frequency of Crohn’s disease and ulcerative colitis, so we decided to see if we could find out what was going on there,” says Karen Wright, a pharmacologist at Bath University. “Historically, it was smoked in India and China centuries ago for its gastrointestinal properties.”
The chronic conditions, known collectively as IBD, are caused by an over-active immune system which produces severe inflammation in areas of the gastrointestinal tract. Up to 180,000 people in the UK are thought to have colitis or Crohn’s disease and suffer symptoms of pain, urgent diarrhoea, severe tiredness and loss of weight. Repeated attacks can lead to scarring of the colon and fibrosis to the extent that the bowel narrows to form a stricture, for which a colonectomy – the surgical removal of the bowel – is the only cure.
Reports that cannabis eased IBD symptoms indicated the possible existence of cannabinoid receptors in the intestinal lining, which respond to molecules in the plant-derived chemicals. Wright and colleagues grew sections of human colon and examined them in vitro.
To their surprise, the team discovered CB1 cannabinoid receptors – which are known to be present in the brain – in the endothelial cells which line the gut. “I think they must be involved in repairing the lining of the gut when it is damaged,” Wright says.
She deliberately damaged the cells to cause inflammation of the gut lining and then added synthetically produced cannabinoids. “The gut started to heal: the broken cells were repaired and brought back closer together to mend the tears,” she told New Scientist.
Wright believes that in a healthy gut, natural endogenous cannabinoids are released from endothelial cells when they are injured, which then bind to the CB1 receptors. The process appears to set off a wound-healing reaction. “When people use cannabis, the cannabinoids bind to these receptors in the same way,” she said.
Previous studies have shown that CB1 receptors located on the nerve cells in the gut respond to cannabinoids by slowing gut motility, therefore reducing the painful muscle contractions associated with diarrhoea.
But Wright and her team also discovered another cannabinoid receptor, CB2, in the guts of IBD sufferers, which was not present in healthy guts. These receptors, which also respond to chemicals in cannabis, appear to be associated with apoptosis – programmed cell death – and may have a role in suppressing the overactive immune system and reducing inflammation by moping up excess cells, she suggests.
“Ideally we would want to be able to stimulate the body’s own endogenous cannabinoid system, which might become dysregulated during long-term inflammation. Knowing more about how this system actually works will help us to look for therapeutic targets,” Wright says. “We are not advocating cannabis use, particularly as smoking tobacco exacerbates Crohn's disease and many smokers of cannabis use tobacco as well.”
“Anything that offers hope is good news for sufferers of IBD,” says a spokesperson from the National Association for Colitis and Crohn’s Disease, commenting on the research.
Journal reference: Gastroenterology
Cancer Chemotherapy
The drugs used to treat cancer are among the most powerful, and most toxic, chemicals used in medicine. They kill both cancer cells and healthy cells, producing extremely unpleasant and dangerous side effects. The most common is days or weeks of vomiting, retching, and nausea after each treatment. The feeling of loss of control is highly depressing, and patients find it very difficult to eat anything, and lose weight and strength. People find it more and more difficult to sustain the will to live, and many chose to discontinue treatment, preferring death to treatment.
Cannabis can be used as an antiemetic, a drug which relieves nausea and allows patients to eat and live normally. It is safer, cheaper and often more effective than standard synthetic antiemetics. Smoking cannabis is more effective than taking it orally (or its synthetic derivatives such as Marinol) as patients it difficult to keep anything down long enough for it to have an effect. Smoking cannabis produces an immediate effect, and patients find it easier to control the doseage. Additionally the euphoric properties act as an anti-depressant, and the hunger and enjoyment of food properties ('the munchies') make weight gain easy, and these increase the chances of recovery.
Scientific Evidence
Vincigeurra et al. found that 78% of 56 patients with nausea who were resistant to standard drugs became symptom free through inhaling cannabis. Chang et al. found that smoking cannabis rather than ingesting it seemed more effective.
Doblin & Kleiman sent a questionaire to US oncologists (cancer specialists). 44% of the respondents had recommended illegal use of cannabis and half of them would prescribe it if it were legal.
Links:
Cannabis
Sativa v Marinol - A Patient's Story
This is a detailed personal testimony by a testicular cancer patient who
underwent 13 cycles of chemotherapy. He discovered that smoking cannabis made
his constant nausea manageable, and allowed him to eat normally. He also used
Marinol, and discovered that although it stopped his nausea, it also knocked him
unconscious, and he couldn't eat while he was sleeping. So he began to take
half his Marinol dose and top it up with cannabis, and was able to lead a normal
life between chemotheraphy sessions.
In the condition known as MS the normal functioning of the nerves in the brain and spinal cord is disrupted. Dibilitating attacks, which last for weeks, come and go unpredictably, with gradual deterioration and eventual disability. Because the central nervous system controls the entire body, the effects may appear anywhere. Common symptoms include tingling, numbness, impaired vision, difficulty in speaking, painful muscle spasms, loss of co-ordination and balance, fatigue, weakness or paralysis, loss of bladder control, urinary tract infections, constipation, skin ulcerations and severe depression.
There is no known effective treatment. The standard drugs used to treat the muscle spasms are addicitve, have severe short-term side effects and worryingly damaging long-term side effects. Many MS sufferers find that they don't even work.
Cannabis has a startling and profound effect on the symptoms of MS. It stops muscle spasms, reduces tremors, restores balance, restores bladder control and restores speech and eyesight. Many wheelchair-bound patients report that they can walk unaided when they have smoked cannabis. Patients also report that they find smoked herbal cannabis better at controlling their symptoms that synthetic derivatives. According to Marijuana - The Forbidden Medicine cannabis may even retard the progression of the disease.
Scientific Evidence
In 1995 Mills reviewed all the scientific evidence of MS treatment using cannabis, and discussed all the surrounding issues. He concluded that the evidence is sparse and of poor quality and that a proper clinical trial of smoked cannabis for MS, was needed. Dr Roger Pertwee of the Department of Biomedical Sciences at Aberdeen University wants to carry out such a study. Unfortunately he still needs proper funding and a source of legal cannabis.
In 1997 Dr Pertwee, along with Consroe et al. carried out a survey of MS patients who are using cannabis to see how cannabis helped their condition. The patients reported that cannabis helped the following conditions: spasticity, chronic pain of extremities, acute paroxysmal phenomenon, tremor, emotional dysfunction, anorexia/weight loss, fatigue states, double vision, sexual dysfunction, bowel and bladder dysfunctions, vision dimness, dysfunctions of walking and balance, and memory loss (these results are ranked in order, 97% of the patients said cannabis helped the first condition, spasticity, down to 30% reporting the last condition, memory loss.
Although there has never been a clinical trial of MS patients, that used smoked herbal cannabis, there is some direct evidence of cannabis' effect on tremor. Both Clifford and Meinck et al. reported that cannabis reduced tremors and provided graphic evidence of this, in the form of before and after tremor recordings and handwriting samples.
During the 80's there were three trials of oral synthetic THC in small numbers of MS patients. All were placebo-controlled, and involved various doses of THC from 2.5 to 15 mg daily. Many of the patients claimed to get a beneficial effect from THC, but the doctors, looking on objectively could find no effect in most of them - perhaps cannabis has a psychological benefit rather than a muscular one. Petro & Ellenberg found that THC improved spasticity compared with placebo, and that half their 8 patients had a "substantial" improvement. Clifford found that 7 of his 9 patients claimed a benfefit, but doctors could only confirm that 2 patients had benefited. Ungerleider et al. studied 13 patients with MS that proved untreatable with standard drugs. Although the patients said their spasticity had improved significantly, the doctors couldn't spot an improvement. Large THC doses were poorly tolerated by the patients, with weakness, dry mouth, dizziness and psychoactive effects the common complaints - interestingly none of the patients asked to keep a supply of THC after the trial ended.
A recent letter in the Lancet from Martyn et al. reports synthetic cannabinoid, nabilone being of benefit in a single patient study. Weeks of placebo and nabilone were alternated, and muscle spasm, general well-being and sleep all improved when cannabis was given.
There is also evidence from animal experiments. EAE is an artificial disease that has been used as a laboratory model of MS in guinea pigs. Lyman et al. reported that when animals were exposed to the disease and treated with a placebo, they all developed severe EAE and 98% died. The animals that were treated with THC had no or mild symptoms and 95% survived.
The human eyeball is filled with fluid, which exerts pressure to keep the eyeball spherical. Glaucoma is a condition where the channels through which the fluid flows gradually become blocked, and the intraocular pressure gradually increases, causing increasing damage to the optic nerve, and gradual deterioration of vision. Glaucoma is the second-largest cause of blindness, and affects 1.5 % of 50-year olds and 5 % of seventy-year olds.
Standard treatments have unpleasant or dangerous side effects, and have little effect on intraocular pressures in end-stage glaucoma. Cannabis however lowers intraocular pressures dramatically, with none of the serious side effects. Patients who find that standard medicines do not help their conditions report that smoking cannabis quickly restores their vision. Many long-term glaucoma patients have successfully maintained their sight using cannabis for 20 or 25 years, and avoided the gradual painfull deterioration to blindness that is otherwise enevitable.
However older generations, who are most at risk of glaucoma do not appreciate the euphoric side effects of smoked or ingested cannabis. There is also concern about the effects on the cardio-vasculat system. There is hope that a cannabis-containing eyedrop could be developed in the future which would have no side effects but this is made difficult since cannabinoids are not water soluble.
Ironically the discovery that cannabis lowers intraocular pressure was made accidentally during a police experiment. They were trying to discover if cannabis caused pupil dilation in users, so that they could detect and arrest them more easily!
Scientific Evidence
The effect of cannabis on intraocular pressure (IOP) in normal subjects has been well studied, however the effect on glaucoma patients is less well known, with only a handful of patients studied. Only one study used herbal cannabis, the rest have used cannabinoids.
Hepler & Frank (1971) found that oral or smoked cannabis reduced intraocular pressures in normal subjects for about 4 to 5 hours with "no indications of any deleterious effects ... on visual function or ocular structure". They concluded that cannabis may be more useful than conventional medications and probably works by a different mechanism.
Almost all of the studies using cannabinoids have been double-blind and placebo controlled. Two studies were of the effects of oral or smoked THC on IOP in normal subjects. Hepler et al. (1976) reported that the drop in IOP was dose-related. Jones et al. (1981) found that tolerance to the effects quickly built up, and there was a rebound in IOP to above baseline levels when treatment was stopped. Another two studies used intravenous infusions of various cannabinoids. Perez-Reyes et al. (1976) found that only the cannabinoids that had psychoactive effects produced a drop in IOP. Cooler & Gregg (1977) reported a drop in IOP but increased anxiety. The effects of cannabinoids on IOP were confirmed in numerous animal experiments, reviewed by Adler & Geller (1986).
The few studies on glaucoma patients all involve small numbers of patients. Hepler et al. (1976) found that when THC was smoked for months at a time by glaucoma patients, the effect on intraocular pressure stayed constant and there was no deterioration of vision. However only 7 of the 11 patients showed the effect. Merrit et al. (1980) carried out a double-blind and placebo controlled study on 18 patients and found a significant reduction in IOP but unwanted cardio-vascular and pyschoactive side-effects.
Applying cannabinoids directly to the eyes should remove the side-effects but is proving difficult since they are not water-soluble. Merrit et al. (1981) applied THC to only one eye in 8 patients, but found an effect on IOP in both eyes suggesting that the THC had been adsorbed into the bloodstream, rather than acting topically. However his patients reported no pyschoactive side-effects.
Source: National Organization for the Reform of Marijuana Laws (NORML), from the web at http://www.norml.org/index.cfm?Group_ID=3391, last accessed Jan. 4, 2006, and the Marijuana Policy Project (MPP), from the web at http://www.mpp.org/RI_number_11.html, last accessed Jan. 4, 2006.
Source: Janet E. Joy, Stanley J. Watson, Jr., and John A Benson, Jr., "Marijuana and Medicine: Assessing the Science Base," Division of Neuroscience and Behavioral Research, Institute of Medicine (Washington, DC: National Academy Press, 1999).
Source: Janet E. Joy, Stanley J. Watson, Jr., and John A Benson, Jr., "Marijuana and Medicine: Assessing the Science Base," Division of Neuroscience and Behavioral Research, Institute of Medicine (Washington, DC: National Academy Press, 1999).
Source: Janet E. Joy, Stanley J. Watson, Jr., and John A Benson, Jr., "Marijuana and Medicine: Assessing the Science Base," Division of Neuroscience and Behavioral Research, Institute of Medicine (Washington, DC: National Academy Press, 1999).
Source: Janet E. Joy, Stanley J. Watson, Jr., and John A Benson, Jr., "Marijuana and Medicine: Assessing the Science Base," Division of Neuroscience and Behavioral Research, Institute of Medicine (Washington, DC: National Academy Press, 1999).
Source: Abrams, Donald I., MD, et al., "Short-Term Effects of Cannabinoids in Patients with HIV-1 Infection - A Randomized, Placebo-Controlled Clinical Trial," Annals of Internal Medicine, Aug. 19, 2003, Vol. 139, No. 4 (American College of Physicians), p. 258.
Source: Abrams, Donald I., MD, et al., "Short-Term Effects of Cannabinoids in Patients with HIV-1 Infection - A Randomized, Placebo-Controlled Clinical Trial," Annals of Internal Medicine, Aug. 19, 2003, Vol. 139, No. 4 (American College of Physicians), p. 264.
Source: Grant, Igor, et al., "Non-Acute (Residual) Neurocognitive Effects Of Cannabis Use: A Meta-Analytic Study," Journal of the International Neuropsychological Society (Cambridge University Press: July 2003), 9, pp. 687-8.
Source: The Controlled Substances Act of 1970, 21 U.S.C. §§ 801 et seq.
Source: The Controlled Substances Act of 1970, 21 U.S.C. §§ 801 et seq.; Common Sense for Drug Policy, Compendium of Reports, Research and Articles Demonstrating the Effectiveness of Medical Marijuana, Vol. I & Vol. II (Falls Church, VA: Common Sense for Drug Policy, March 1997).
Source: The Controlled Substances Act of 1970, 21 U.S.C. §§ 801 et seq.
Source: US Department of Justice, Drug Enforcement Agency, "In the Matter of Marijuana Rescheduling Petition," [Docket #86-22] (September 6, 1988), p. 57.
Source: US Department of Justice, Drug Enforcement Agency, "In the Matter of Marijuana Rescheduling Petition," [Docket #86-22], (September 6, 1988), p. 57.
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