by Seshata on 10/07/2014 | Uncategorized

The neuroprotective effects of cannabis

Following on from our recent article on the relationship between cannabis use and stroke, we now investigate the role of cannabinoids in mitigating brain damage caused by traumatic brain injury and ischemic stroke. There is mounting evidence to suggest that their various properties have great therapeutic potential.

Following on from our recent article on the relationship between cannabis use and stroke, we now investigate the role of cannabinoids in mitigating brain damage caused by traumatic brain injury and ischemic stroke. There is mounting evidence to suggest that their various properties have great therapeutic potential.

Antioxidative & anti-inflammatory properties

In recent years the evidence for the antioxidative and anti-inflammatory properties of various cannabinoids has become well-established, and our understanding of the role they play in modulating neurotransmission too has grown. Thus, serious consideration is now being given to their potential as neuroprotective agents. Cannabinoids have been shown to prevent neuronal death in acute neuronal injury, including ischemic stroke and traumatic brain injury, as well as provide symptomatic relief in multiple sclerosis, Huntington’s disease, and other chronic neurodegenerative diseases.

Data gathered both in vitro and in vivo suggest that the endocannabinoid receptor agonists anandamide and 2-AG, as well as various synthetic cannabinoids and phytocannabinoids, have neuroprotective effects following traumatic brain injury (TBI). It is well-known that TBI leads to the release of harmful compounds that cause secondary brain damage; now, researchers are finding that neuroprotective mediators are also released, and that the final outcome is determined by the balance between the two classes of compounds.

Inhibition of damage-causing compounds

A study published in 2002 (Mechoulam et al) demonstrated that production of anandamide and 2-AG increased in the brain following TBI, and that production of substances known to cause neural damage—tumour necrosis factor-a and reactive oxygen species (ROS)—was inhibited by their presence. It is thought that the endocannabinoid system’s role in inhibiting release of neurotransmitters such as glutamate (the main transmitter in glutamatergic synaptic transmission, which plays a major role in nervous impulse modulation as well as in cognitive functions such as learning and memory), as well as in modulating the inflammatory response, is significant in this context.

Various studies have confirmed these findings. Another study published in 2002 by Mechoulam et al demonstrated that endogenous levels of anandamide and 2-AG also increase following TBI in mice and rats; when both compounds were administered after TBI, the extent of brain damage was reduced. Reductions in the extent of brain oedema (accumulation of fluid leading to swelling), infarct volume (extent of tissue necrosis), and hippocampal cell death were all noted, along with a generally-improved clinical recovery.

2-AG may counteract vasoconstriction

Traumatic brain injury is a major cause of death and ongoing neurological complications

It was also noted that 2-AG was more effective when administered with similar compounds in the fatty acid glycerol ester class. 2-AG is known to play a significant role in vascular modulation which may increase its effectiveness following TBI—by counteracting vasoconstriction (narrowing of blood vessels) caused by release of endothelins (21-amino acid compounds, which are the most potent vasoconstrictors known), it may help to restore the blood supply to the affected area. This relationship also corresponds to the idea of a balance between harmful and beneficial compounds that determines the overall outcome.

The abundance of existing evidence has provided the basis for several clinical trials investigating neurodegenerative conditions and neuronal injury and their response to cannabinoid compounds. However, our understanding of the complex relationship between the endocannabinoid system and the various other signalling systems of the body is far from complete, and must improve greatly if we are to make effective use of their potential in neuroprotection following TBI.

Cannabinoids in post-stroke recovery

THC, CBD and various other cannabinoids have been repeatedly demonstrated to exert a neuroprotective influence during and following occurrence of ischemic stroke (IS). While there are various studies indicating that cannabis use can increase risk of stroke, it appears that this phenomenon is limited to a small subset of susceptible individuals. For the majority, cannabinoid therapies appear to have great potential in mitigating inflammation and oxidative stress due to IS.

CBD has been the subject of much investigation as a neuroprotectant for IS. It has been shown to increase cerebral blood flow following IS and thereby aid in mitigating infarct volume; unlike THC, which exhibits a tendency to decrease in effectiveness with repeated doses, it remains effective even after fourteen days of repeated treatment. For this reason, it is seen as having greater therapeutic potential than THC in this area of research. CBD has also been shown to reduce inflammation caused by release of interleukin-1, nitric oxide, and tumour necrosis factor-a following IS.

Just as with TBI, much of the damage subsequent to IS is due to oxidative stress, which is caused by the build-up of ROS due to excessive glutamatergic signalling. Both THC and CBD have been shown to be effective antioxidants that inhibit glutamatergic signalling and thereby reduce the extent of ROS build-up following ischemic stroke; however, CBD again shows greater effectiveness as an antioxidant and therefore has greater therapeutic potential than THC.

Glutamate signalling and cannabinoids

Brain damage following an acute event such as IS or TBI occurs in part due to inflammation (Mahesh Kumar)
Brain damage following an acute event such as IS or TBI occurs in part due to inflammation (Mahesh Kumar)

The interactions between various cannabinoids and the glutamatergic signalling system were investigated further in a study entitled Neuroprotective Antioxidants from Marijuana, published in 2000. In this study, cannabidiol and several other cannabinoids were investigated for their neuroprotective potential in rats in vitro, in neuron cultures exposed to toxic levels of glutamate.

It is known that high glutamate levels induce neurotoxicity (particularly mediated by the NMDA, AMPA and kainate glutamate receptors) and lead to the formation of secondary damage-causing compounds such as ROS and tumour necrosis factor-a. It is also known that glutamate activity is reduced by the presence of antioxidants; as CBD and THC are well established as antioxidants, the basis for further investigation was clear.

Cannabinoid receptor-independent mechanism

The research demonstrated that both THC and CBD increased neuroprotection and reduced NMDA, AMPA and kainate receptor neurotoxicities. Furthermore, the level of neuroprotection was not increased by the action of specific cannabinoid receptor antagonists, indicating that the mechanism of action was independent of the cannabinoid receptors. Previous studies had concluded that cannabinoid receptor agonists were the key agents of neuroprotection; however, cannabidiol is not an agonist, so its neuroprotective potential must therefore be realised elsewhere.

CBD was also shown to reduce hydroperoxide (a type of ROS) toxicity in neuron cell cultures—further proving its effectiveness as an antioxidant. CBD’s ability to reduce toxicity was tested against two other known antioxidants, a-tocopherol and ascorbate, and was proven to be superior to both in terms of neuroprotective capacity. Although these tests were performed in vitro, preliminary in vivo studies into cerebral ischemia in rats suggest that it is effective across the board.

Perinatal hypoxic-ischemic event

It has been shown that CBD protects the neurons of the hippocampus from destruction following brain injury (Wellcome Images)
It has been shown that CBD protects the neurons of the hippocampus from destruction following brain injury (Wellcome Images)

A significant cause of brain injury in the neonatal period is perinatal hypoxic-ischemic event—when the flow of oxygen and blood to the infant brain is interrupted due to asphyxia, often during childbirth. This devastating condition leads to the death of 15-20% of children diagnosed, and to severe neurological impairment—including epilepsy, cerebral palsy, motor dysfunction and hyperactivity—in a further 25%. The developing brain is far more susceptible to hypoxic-ischemic events than the adult brain, as it contains a high concentration of blood vessels and higher water content, and the potential for damage-inducing events such as haemorrhage is greater.

Immediately following hypoxic-ischemic brain injury, a set of specific cellular mechanisms including increased production of glutamate is set in motion, triggering cell damage and finally leading to excitotoxicity (a type of cell death caused by excessive glutamatergic signalling). The precise nature of this process is not yet fully understood, due to the complexity of the molecular mechanisms that underlie the condition, and as such, there is a paucity of effective treatment options to mitigate the extent of neuronal damage. Now, however, rapid advances in our understanding of the field have led to a new class of neuroprotective therapies to be assessed and implemented if proven to be effective.

Using cannabinoid therapies on children

Among them, the endocannabinoid system is under investigation in order to ascertain its specific role in providing neuroprotection to the developing brain. While use of cannabinoid therapies on children remains controversial, there have been sufficient successes with using cannabinoids in various paediatric conditions (including epilepsy and cancer) without detrimental side-effects that the controversy is now rapidly being replaced with consensus among the scientific community that such therapies can be useful.

As well as modulating neural responses, cannabinoids have been shown to modulate vasodilation due to endothelial cell function and endothelin activity, regulate calcium homeostasis, and possess significant anti-excitotoxic and anti-inflammatory effects. There are also indications that certain anti-inflammatory treatments may actually improve recovery by promoting neurogenesis (growth of new neurons). Utilising the potential of the endocannabinoid system is therefore an important neuroprotective strategy for neonatal hypoxic-ischemic brain, and one that appears to have very little risk of detrimental side-effects.

Furthermore, the antioxidant and modulatory properties of cannabinoids, particularly their ability to inhibit glutamate release and other damaging compounds such as nitric oxide, make these compounds particularly attractive as a defence against hypoxic-ischemic progressive brain damage as it is known that glutamatergic excitotoxicity, nitric oxide toxicity and oxidative stress are all crucial factors in perinatal hypoxic-ischemic brain injury.

Effectiveness of synthetic cannabinoids

It is thought that cannabinoids provide a protective effect due to their role in glutamatergic signalling at the synapses (Ethan Hein)
It is thought that cannabinoids provide a protective effect due to their role in glutamatergic signalling at the synapses (Ethan Hein)

As well as endocannabinoids and phytocannabinoids, attention is now being paid to the potential of various synthetic cannabinoids. For example, in a study published in 1999 by the Journal of Neuroscience the synthetic cannabinoid agonist R(+)-WIN 55212-2 was found to decrease neuron loss in the hippocampus in vivo following global cerebral ischemia in rats, and reduce infarct volume following focal cerebral ischemia induced by occlusion of the middle cerebral artery.

The less active enantiomer (the “mirror image” molecule), S(-)-WIN 55212-3, was found to be ineffective, and the protective effect of R(+)-WIN 55212-2 was found to be blocked by the action of a specific CB1 receptor antagonist rather lengthily known as N-(piperidin-1-yl)-5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4-methyl-1H-pyrazole-3-carboxamide-hydrochloride.

Interestingly, the results varied between in vivo and in vitro models. In vitro, R(+)-WIN 55212-2 still exhibited a protective effect on the neurons, but the effect was not blocked by antagonists. Much further research is needed to ascertain the precise interactions at work here, but it is clear that there are potential applications for this and other synthetic cannabinoids as treatment for cerebral ischemia, including stroke.

Cannabinoids demonstrably possess neuroprotective properties

Cannabinoids can mitigate the damage caused by perinatal hypoxic-ischemic event, a significant cause of developmental disorders in children (Godverbs)
Cannabinoids can mitigate the damage caused by perinatal hypoxic-ischemic event, a significant cause of developmental disorders in children (Godverbs)

There is abundant evidence indicating the effectiveness of phytocannabinoids, particularly CBD, in the management and mitigation of traumatic brain injury and ischemic stroke. Furthermore, our understanding of the role that the endogenous cannabinoids anandamide and 2-AG play in the modulation of inflammation and cerebral blood flow is growing, and our ability to synthesise targeted synthetic cannabinoids that can precisely mimic the actions of these endocannabinoids is improving with it.

Of course, there is a vast amount of information still to uncover, but the pace at which research is advancing is beginning to pick up. At this rate, it is likely that targeted neuroprotective therapies to mitigate the damage caused by traumatic brain injury and ischemic stroke will be in widespread use within a few years.

Comment Section

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To whom it may concern
My name is Warren Elliott 57 I,m the single pension and Disable,My friend wrote this because I can,t or spell very much so I dictated what I say I,ve right side Hemiplegia which is my right side is much weaker than the other side threw a car accident 35 years age which left me Brain damage,got arthritis threw out my body, scoliosis in my back, had 22 operation,s ana more to came going to have an operation on my back soon. I can only use one arm to do things which gives me pain all the time.I take pain killers (OxyContin and Endone) I don,t like taking them there very addictive. I smoke which helps much more, when I can get it, afford it. it would be much appreciated if you could help me get Medical Marijuana or Cannabis I,m finding it very expensive MEDICAL trail
Sent from my iPad Australia New South Wales.



Hi Warren,

Unfortunately we are not in a position to assist anybody in obtaining medical cannabis. However, I can perhaps suggest that you may find some support or further information from the community at Nimbin, NSW.

I wish you all the best!




jim skeptical

where's the sources? where's the link to studies etc? would appreciate a little update with citing specifc sources.



Hi Jim,

While I have sourced most of the points made in this article, there are a few that I may have missed. I will endeavour to correct this, but if there is a specific point that you wish to view the source for please let me know and I will start there.



mary rich

Yes I have stenosis facit 4and5Disic in spine scoliosis slipped Disc I would love to see something that would help


rita douglas

what a wondrful article. i really didn't know why i had a bad picture of cannabis and those who use it. We all have that idea that smoking it is irresponsable and reckless, just because we are maybe programmed to think so. the media, the school.. brainwashed us.
i really thank you for this exquisite article that changed this gray opinion of mine. and i will use this sacred plant whenever i feel i need it. fear from cannabis was just inplanted and not scientifically proven.



Hi Rita, I'm thrilled to hear it. As a full-time cannabis writer, hearing that people have been convinced to change their views after reading my work is the best part of the job as it means my efforts are not going to waste.



Hi and thank you for your time. I have been involved in the medical cannabis industry since 2008 in Michigan. We are a legal state which leads me to my question. My girlfriend has suffered a blow to the head this summer. She has had head aches, dizziness, and many of the symptoms that accompany the injury. She went to a follow up today because her symptoms are getting worse. The doctors say she may have a blood clot on her brain. I am looking for information that could help. How can we treat the injury topically or ingest it? Any certain strains indica or sativa? Any info about this would help us and many others who the information could benefit. Thank you again for your time.



Hi. My brother suffered a hypoxic brain injury last December and is left severely brain damaged. He is 34. And is looking to go home to be cared for by his wife. Hopefully by Xmas. Do you think that cannabis oil or cbd would be beneficial to him as we are hoping to get his meds reduced. But that is very stressful to him. So we are trying to research how this could be beneficial to him. And I'm trying to find sources of information on it please email me a reply of help or links to who can help with advice on this. In the uk


Scarlet Palmer

Hi Rhian,

Thank you for commenting, we are sorry to hear about your brother's condition. As Sensi Seeds is not a medicinal practitioner, I'm afraid we cannot offer any advice on this kind of question other than to consult your GP. We do have this article which is aimed specifically at healthcare professionals who may be unaware of the many properties of cannabis, so when seeing your doctor this might be useful. Also, since you are in the UK I strongly recommend you get in touch with the United Patients Alliance (you can find them on Facebook), a group of people who are campaigning for the acceptance and legalisation of medicinal cannabis, since they also act as a support group and there may be members who are in a similar situation.

With best wishes,



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