The history of Israel hails it as a place of intense spirituality for many religions, most notably Jewish, Christian and Islamic culture. Ironically, a much younger (counter) culture can also point to this Holy Land as a major component of its heritage: The origin of the medical marijuana movement.
In 1964, at the Weizmann Institute of Science in Rehovot, Israel, Dr. Raphael Mechoulam along with Dr. Yehiel Gaoni and Dr. Haviv Edery, succeeded in the very first isolation and elucidated of the active constituent of cannabis – Δ9-tetrahydrocannabinol, also known as THC. The discovery of the THC compound – now almost 50 years ago – started a revolution in thinking about cannabis that still carries on today.
Dr. Mechoulam is currently an Israeli professor of Medicinal Chemistry and Natural Products at the Hebrew University of Jerusalem. His total syntheses of THC, as well as other cannabinoids such as cannabidiol (CBD), are the cornerstones of the burgeoning medicinal cannabis industry. Furthermore, these major contributions in the fields of organic chemistry and the interactions between human and plant biology have lead to the discoveries of the CB receptors in the human brain and the existence of the endocannabinoid system within human bodies.
Dr. Mechoulam was kind enough to give his time for an exclusive interview with Nico Escondido and HIGH TIMES Magazine at his university laboratory in Jerusalem, Israel. It is very plausible that Dr. Mechoulam may one day win a Nobel Prize for his work and contributions in these fields. But it is his courage in introducing a previously unresearched plant to the world, a plant that is rapidly proving itself as nothing short of miraculous, that makes Dr. Raphael Mechoulam, The Man.
Let’s start at the beginning. Tell us a little bit about what the marijuana scene was like when you began working with cannabis?
It was a South American problem really. Nobody was smoking it in the U.S. except for a few musicians – a few black musicians you know. Incidentally, it seems to have something to do with, well ah, how can I explain that? Maybe understanding the music better, or hearing the music better. Especially jazz musicians. But that was it.
So then how did your research with cannabis come about exactly?
Well, when my friend [Yehiel Gaoni] and I started working on it I was 32 years old. And when I initially asked for a grant, I sent it out to the NIH [National Institute of Health] in the U.S. I asked for a research grant but they said, “No, no, no. It is not in our interest. Let us know when you have something more relevant for us.” But then, soon after we isolated THC, they decided it was relevant work.
And so when we started working, essentially nobody was working on that, and the reasons were probably legal. You couldn’t really do it in the U.S. at least, and the U.S. was, at that time, the only place that there was any serious research going on… and the U.K. The laws were such that you had to have guards all over the place. You can’t see an American professor with graduate students and having three guards around him.
So, we had just isolated THC and, to the world’s surprise, they [NIH] came over to see our work. We had 10 grams of THC isolated from hashish, so they took it back with them and most of the initial research in the U.S. was done with our THC.
And so here we had no problem working because you know here, well the laws are the same but the application of the law is a little bit different. They knew I was not going to go outside and start selling marijuana. They didn’t assume that I will do that. We were able to work on it for a couple of years, though essentially nobody else was around, so we published quite a bit and that was in the mid-60s. So, that was it.
We know that your interest lies in the connection between chemistry and biology, but what was the intent for you with cannabis? Did you think back then that there was medicinal value in cannabis?
No, no, it’s a natural product. If you look at the other illicit drugs that are throughout the world, morphine came out of opium,or poppy plants, and cocaine came out of cocoa leaves, and these were discovered 150 years ago. Morphine was isolated in the early 19th century and cocoa and cocaine from in the middle 19th century, and surprisingly the THC, the active component of cannabis was not known which seemed very strange. And I know why it was not isolated, because techniques were very complicated. See morphine and cocaine are so-called alkaloids.
Namely natural products that contain a nitrogen on the molecule, and it can give us salt. It precipitates as a salt. And so you have salt, cocaine is a salt, morphine is a salt, very easy to prepare. It turned out that THC does not have a nitrogen and it is present in a mixture of compounds – we know that there are about 60 of them now. And they didn’t have the techniques to isolate them in the past. So a few people tried here and there, actually some very good people, one of them [Lord Alexander Todd] got the nobel prize for something else. But they never succeeded in isolating the pure substance and so they never knew whether they had one compound or many compounds, and so on.
So the impetus was really that cannabis was being used and you knew of its use, yet there was no real research? I’m trying to figure out why it was cannabis that you guys went to instead of not, say, botswalia or some other plant.
Well, my interest is in natural products that have some biological activity and there are a huge number of natural products and plants that have activities. I probably have the best library, at least in Israel, with books and publications on natural products, on plants, you name it we can find it. And let’s say just for the fun of it, here is this dictionary of plants found in southern and eastern Africa – all plants with medicinal properties. So you can pick out any one of them and just open it and say, ‘Buchu’. Ok, it is a natural product. It lists some of the known herbal remedies. It’s also used for relief of rheumatism.
Is it true? Is it not true? I just opened the book, I have no idea. So there are thousands of them and you have to decide what you want to work on and one has to choose something that makes sense. And here I know that this [cannabis] is something that makes sense, namely that it has a compound within the plant that has obviously active products and it turned out to be interesting.
But at that time you didn’t know about cannabinoid receptors in the human body?
No, as a matter of fact, that came much later. You see, there are mistakes in science, too. People didn’t realize that there were receptors. As a matter of fact, an excellent group in Oxford with Sir Bill Payton, Sir William – probably pharmacologist number one in the world, a good friend of mine – he had said there were no receptors and for very good reasons. Those reasons are probably too complicated to explain for a journal or a magazine.
Well, try us anyway…
Basically the reasons were, you see, when something [like a molecule] binds to a receptor, it has to have a specific stereochemistry. You have two hands, they’re identical… well, they’re not identical. If you put one on top of the other, they’re just the opposite, they are mirror images of each other, they are not identical. So it is true for many of the natural products. They can have two images – mirrored images, but only one of them is the natural product, the other probably doesn’t even exist. We could synthesize it, but it’s not the natural product. In this case the natural product [THC] has the activity. If both of them have activity then chances are it does not bind to anything biological like a receptor, an enzyme or something like that because a receptor itself is asymmetric.
So, if this is the receptor [holding up one hand], you can have only one thing binding to it but not its mirror image. Only one of them. And it turned out that both of them were active – both mirror images of THC. One of them was natural, the other one, which we had synthesized, both of them worked [as an active compound.] So, Bill said ‘No, it can’t be. There cannot be a THC receptor.’
Well, it turned out that they were not very good organic chemists. They were buying the raw material, the starting material [for their testing] that already had the two images – with the mirror image being synthetic – and you cannot separate them at that point.
So, if you have even 20 percent of the wrong stereoisomer [isometric molecules having the same molecular formula] then you end up with a completely wrong stereoisomer. So both compounds tested as active and thus they thought there would not be a human receptor.
But then we actually did some better work, I think, as we found out that it’s not true because only one mirror image was, in fact, active (laughing). So for the 20 years since we discovered the chemical material [THC], we all went along the wrong pathway! So when we discovered that only one of them was active, another good friend of mine in St. Louis finally found the first receptor.
Dr. Howlett?
Yes, correct. Dr. Allyn Howlett. And so Dr. Howlett found the receptor and basically if you have a receptor in the body it’s not because there is a plant out there. It doesn’t work that way. It works only because there is something in your body which will activate that receptor. So we went after those compounds that activated it. And we found the compound in the brain that activated it.
Anandamide.
Precisely. [Anandamide, also known as N-arachidonoylethanolamine or AEA, is an endogenous cannabinoid neurotransmitter. It was isolated and its structure was first described by Czech analytical chemist Lumír Ondřej Hanuš and American molecular pharmacologist William Anthony Devane in the Laboratory of Raphael Mechoulam, at the Hebrew University in Jerusalem, Israel in 1992. The name is taken from the Sanskrit word ananda, which means “bliss, delight”.]
We know there are so many different cannabinoids; THC, CBD, CBN, CBG, etc.; Do they all bind with the CB1 and CB2 receptors?
Only THC. And only THC is psychoactive. So as it binds to the CB1 receptor it causes the activities that are known as cannabis activities. That’s it, period. None of the others, well, at least not significantly – there are a little bit here and there – but no other compound out of the 60 or whatever they are, that binds.
There is a lot of interest now in the United States within the medical movement to find cannabis strains that are high with cannabidiol or CBD.
Well, this is something that I made a big fuss about. You see, with illicit cannabis, which is a huge, huge thing in the States, there is no interest in having anything else but very high levels of THC. Because the THC is the compound that attaches [to the receptors] and is psychoactive.
Nobody’s interested in CBD because it causes no activity. It is, from a medical point of view, very important because it’s an anti-inflammatory and does all kinds of interest in things. It even blocks some of the undesirable effects of THC.
Under THC – of course, you’ve never smoked marijuana (laughing) – but seriously, when you have not smoked and then do and the doses are high, you may have an acute loss of memory. I mean, you don’t remember everything as it should be remembered. And if you have enough CBD you block that kind of memory loss.
I was interested in cannabidiol. But if you look at the cannabis that’s being grown illicitly in the US, and it’s a small business (chuckling)… probably the #1 agricultural product, I’ve been told, in terms of money, there is little or no CBD in there.
There was a medical meeting recently in the U.S. and I went there. I gave the opening lecture and I told them you can’t [not have CBD]. You have to have CBD and that’s it. So they’re trying to get CBD now in medical marijuana, which is the right thing to do.
A lot of the people that we meet around the world are searching for these CBD-rich strains. Now with the lab testing going on in the medical community, you know with gas chromatography machines and mass spectrometers, people are really trying to look closely at it. But after THC, the CBD and CBN results are usually negligible. The CBD is always less than one percent. However, they’ve now found two or three strains that have around 8% CBD.
What do you mean they have to find the strains? I mean, in Lebanon they have been growing cannabis for the last, I don’t know, 300, 400 years or whatever. Lebanese hashish contains five percent THC and about five percent CBD. So go to Lebanon, take a strain from there and period. Why make a fuss? We isolate cannabidiol from hashish. We don’t synthesize it, we isolate it. We do a lot of work on CBD.
So we go to the police, we pick up a couple of kilos of hashish – not marijuana. We pick up several kilos of hashish, isolate the cannabidiol and get a nice crystalline product. THC is an oil. CBD is nicely crystally. And then we make all kinds of things from CBD. So why make a fuss? Go to Lebanon and buy a few strains. Or in India, there are a lot of strains in India.
And where does the CBD bind to if not the CB1 and CB2 receptors?
Oh no, it does not bind… Well, it’s more complicated, it does not bind to the cannabinoid receptors. It does all kinds of other things. It prevents adenosine from – that’s another compound in the brain – from going where it should go. It also acts on something else, on serotonin. We have seen, for example, some work we did here on a disease which has a nice name but its a sinful disease, hepatic encephalopathy. Now hepatic encephalopathy, if you are drunk – really seriously drunk – then you have hepatic encephalopathy. Alcoholics can destroy the liver and liver failure then causes central nervous system changes. They have destroyed their liver and after destroying the liver, they start destroying the brain. That’s hepatic encephalopathy.
Now, we can cause hepatic encephalopathy to mice [in lab tests] and then see the changes that happen in the brain. They can’t walk well and all kinds of other things. We give them CBD and it improves their conditions tremendously. And that was through one of the serotonin receptors. Now serotonin is a nice compound, it has 15 or 16 receptors, maybe more, but this receptor we used was serotonin receptor 1A.
So it works in a variety of ways and, surprisingly, it has no side effects. Very strange. I would have assumed that something that has so many pathways to it, then it will have some side effects. And it has no side effects. As a matter of fact, it is completely non-toxic. One of the least toxic compounds that I’ve seen is cannabidiol. Very strange.
Many years ago, NIH thought that they should look at the toxicity of CBD because people were smoking both THC and CBD, both of which are present in marijuana. Well, we know a little bit about THC. We know nothing about cannabidiol. Does it cause anything, I don’t know, destroy the brain, or whatever? And so they did a very thorough study of the toxicity of CBD and found essentially none… which is very positive.
NIH is probably one of the best institutions in the world. They really do excellent work and I can only admire the people who decided to set up NIH, I don’t know, 30, 40 years ago.
Then what would be your guess as to why, with the NIH being in the United States, why the United States has such a hard time getting federal regulation for medicinal cannabis? Because right now it’s only state-by-state and the federal government is very adamant about not allowing marijuana to become legal for medicine yet, like you said, there is all this great research going on over there, they are on the forefront of a lot of this so where is the gap here?
There is a huge amount of research going on. But I’m not sure because many of the States do have regulations for medical marijuana. And the president actually made some noise that he wants to do it, to allow the federal government to do it. Now why didn’t he? Probably he didn’t have enough power to do it because chances are that these regulations have to go through the various committees and so on he was not sure he could get enough support.
Every administration has people where Mr. A does that and Mr. B does this and then they have a fight. Mr. B is the person that wins, and that’s it, it’s like all administrations. I was head of the University, many years ago, I know that that’s the way it works.
Politics…
Yes, exactly.
But wasn’t it the politicians who were responsible for all of this? Didn’t one politician spur the NIH’s decision to give you the research grants after you first isolated THC?
Yeah, well they [NIH] didn’t have a single grant on cannabis at that time, but the national Institute of Mental Diseases did, I think. As I said earlier, the NIH wrote to me that they don’t want to, they won’t give me money, because it’s not interesting or relevant. And then all of a sudden I get a phone call from the head of the pharmacology at NIH and they’re now interested. So, I asked him, “What happened all of a sudden? You have great interest.” Well, it turned out that a Senator had called NIH, his son had smoked pot and he wanted to know whether it would destroy his mind!
And just like that the government got NIH to change direction. They don’t want to fight the senators because they need their support, and they looked around and ah ha! They don’t support grants on marijuana, so they asked me if I was still working, we had just isolated THC and that was it.
Do you remember the name of the Senator? We can send him flowers.
No, but even if I did… I wouldn’t tell you. Anyway, he’s probably dead by now.
