How different types of cannabis affect the brain

07 Mar 2015

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New research from Universi College London (UCL) reveals the positive and negative effects of different types of cannabis on the human brain.

"Our cannabis research over the last six years has highlighted how different types of cannabis can have different effects,'' explains Professor Val Curran, director of the UCL Clinical Psychopharmacology Unit, who led the study.

''The cannabis plant contains around 100 unique ingredients called 'cannabinoids'. The two most prominent of these are THC (tetrahydrocannabinol) and CBD (cannabidiol). THC is the stuff that makes you stoned. Our previous research suggests that CBD may be a kind of antidote to some of the harmful effects of THC.''

In the study, the team compared the effects of two different types of cannabis. One type has high levels of THC (~13 per cent) but virtually no CBD and is often referred to as 'skunk'. The other type, sometimes called 'hash', generally has a lower level of THC (~6.5 per cent) and substantial amounts of CBD (~8 per cent).

Each of the 21 volunteers went to the laboratory on three separate days and inhaled the placebo, high-potency or low-potency cannabis which had been evaporated into a balloon. Volunteers were given twice as much low-potency cannabis so that the dose from both types of cannabis was about 5mg THC (about a third of a standard 'spliff'). After inhaling the cannabis or placebo, volunteers were asked to perform various tasks, some inside an MRI scanner.

Both types of cannabis were found to significantly increase brain activity when people were listening to music that they enjoyed. People's desire to listen to music rose 55 per cent on cannabis compared with placebo.

Cannabis also made participants twice as likely to report hearing voices in random white noise, with 94 per cent participants on cannabis hearing speech compared with 47 per cent of participants on placebo.

Cannabis significantly impaired memory, tested by asking people to listen to and repeat short passage

The high-potency cannabis impaired connectivity in the brain's salience network, which helps to focus different parts of the brain on important tasks. This network is thought to underpin the motivation to turn ideas into action and get things done. These changes may explain why people on high-potency cannabis also performed worse in a test of motivation, which asked them to choose whether they would put in more effort for greater rewards.

Participants reported more enhanced sound perception on the low-potency cannabis than when on high-potency cannabis or placebo. They had more brain activation in the visual cortex on low-potency cannabis than on placebo, when looking at pictures that they were asked to memorise. They also made fewer errors in remembering those pictures than when on high-potency cannabis.

Blood pressure also varied across the different types, with a mean diastolic blood pressure of 70 for placebo, 74 for low-potency cannabis and 79 for high-potency cannabis.

''We confirmed that CBD helps to counteract some of the negative effects of THC, and for many participants led to a more pleasant experience,'' says Professor Curran. ''People use cannabis for different reasons, but many of the effects that people enjoy are still present in low-potency varieties without some of the harms associated with the high-potency varieties such as skunk. In the UK, 80% of the cannabis sold nowadays is skunk, making it hard for people to access cannabis with a THC-CBD balance. 

''The increasing market dominance of skunk over the last decade has occurred alongside an increase in the numbers of people seeking treatment for cannabis addiction. About 10 per cent of cannabis users now fit clinical criteria for addiction to the drug. We are concerned that skunk may be significantly more addictive than other forms of cannabis and that it might provoke greater paranoid episodes and memory loss.''

The study forms part of an ongoing research program into the effects of drugs on human cognition, emotion and behaviour at the UCL Clinical Psychopharmacology Unit (CPU), funded primarily by the MRC with additional support from Drug Science and the Beckley Foundation.

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