It has been documented widely that the endocannabinoid (eCB) signaling plays a fundamental role in many human health and disease processes of the central nervous system. This has opened an avenue for researchers to exploit the potential of eCB-oriented treatments for the management of neurodegenerative, psychiatric and neuroinflammatory disorders. Here, we will give you a summary of studies showing how cannabidiol (CBD), a cannabinoid derived from the cannabis plant, interacts with the body to counteract autism through the eCB system.
Autism spectrum disorder (ASD) is a complicated behavioral condition that manifests during early childhood and lasts a lifetime for the majority of cases since it has no known cure. In the last three decades, scientists have been busy studying the main components of the recently discovered endocannabinoid (eCB) system. This is a rather intricate collection of lipid signals called endocannabinoids, their target receptors, metabolic enzymes and purported transporters.
What is Autism? A Brief Overview
Autism belongs to a wider group of ailments known as pervasive neurodevelopmental disorders that are caused by a combination of both genetic and environmental factors. Autism was first described and named 60 years ago. According to the Center for Disease Control and Prevention (CDC), approximately 1 in every 68 children suffers from some form of autism in the U.S alone. This represents a tenfold increase in the diagnosis of the condition over just four decades, and these numbers seem to be rising. Furthermore, boys are 4-5 times more likely to develop the condition compared to girls.
The disease is characterized by conspicuous cognitive and emotional isolation and detachment. Autistic children display; an inability to form human relationships, abnormal or absent speech, repetitive and stereotypic verbal and non-verbal behaviors, as well as a limited range of interests and activities.
Up until now, no behavioral, genetic, electrophysiological or brain imaging test can specifically validate a clinical diagnosis of autism. Furthermore, this disorder has no defined mechanisms of pathogenesis, which makes it very difficult to provide curative therapy. Nonetheless, the aforementioned procedures are often utilized to test for any syndromic forms of the illness.
The available treatments for autism can be grouped into: nutritional, behavioral and medical approaches. There is no defined standard approach for treating autism.
Autism is a devastating and so far, an incurable disease. The available pharmaceutical products have such limited efficacy and come with some serious side-effects. As a result, physicians and patients alike have been actively seeking out alternative therapies.
One of the best candidates so far is cannabidiol (CBD), a non-psychotropic compound derived from the Cannabis plant that has proven to contain a wide range of therapeutic effects. Here are some of the tests scientists have done with regards to the use of CBD for autism therapy.
A Summary of Studies testing CBD for Autism Treatments
As mentioned, physicians try to control autism using various approaches such as behavior modification therapies and special diets alongside antipsychotic medication. However, there is no one true cure for autism, this situation that has pushed patients to look for other alternatives. In the same breath, researchers have been busy trying to look for new approaches to treat this serious condition. As it stands, cannabidiol (CBD), a compound derived from Cannabis, has shown great potential in tackling the symptoms associated with autism by influencing the endocannabinoid system in various ways.
This can be demonstrated by one study which investigated the involvement of the endocannabinoid system in peripheral blood mononuclear cells (PBMCs) from children with autism in comparison to age-matched, normal, healthy developing controls. It is known that autistic children manifest immune system dysregulation and show an altered immune response of PBMCs.
The results showed that mRNA level for cannabinoid receptor type 2 (CB2) was significantly higher in the autistic children compared to the healthy subjects. CB1 and fatty acid amide hydrolase mRNA levels remained unchanged. Lastly, the CB-2 protein levels were also significantly higher in autistic children. This data signifies that the CB2 receptor, which is heavily influenced by cannabidiol, is a potential therapeutic target for the development of novel agents for managing autism.
By conducting studies in rodents, scientists have found that neuroligin-3, a protein that is mutated in some patients with autism, plays a role in relaying endocannabinoid signals that moderate communication between neurons. Neuroligins are postsynaptic cell-adhesion molecules that interact with presynaptic neurexins. Rare mutations in neuroligins and neurexins increase the occurrence of autism. These mutations include neuroligin-3 amino acid substitution (R451C) and a neuroligin-3 deletion.
In one study, researchers introduced different autism-associated mutations in neuroligin-3 proteins into mice models. The results demonstrated that signaling was blocked and the overall excitability of the brain was changed.
These findings uncovered an unexpected link between neuroligin-3 protein and the endocannabinoid signaling system that had not been previously thought to be particularly important in the pathogenesis of autism. More importantly, the results indicate that targeting components of the endocannabinoid signaling system may present new potential treatment strategies for autism.
Another study sought to find out the involvement of the endocannabinoid system in the pathogenesis of fragile X syndrome (FXS) using Fmr1 knockout mice as subjects. FXS is the most common monogenic cause of inherited intellectual disability and autism. This condition is caused by the silencing of the FMR1 gene, which leads to the loss of fragile X mental retardation protein (FMRP).
First, the authors appreciated that the endocannabinoid system (ECS) is a key modulator of synaptic plasticity, nociception, seizure susceptibility cognitive performance, and anxiety, all of which are affected in FXS. The cannabinoid receptors CB1 (CB1R) and CB2 (CB2R) are activated by phospholipid-derived endocannabinoids such as 2-Ag, but can also be affected by phyto-cannabinoids derived from plants, such as CBD.
This study established that genetic and pharmacological blockade of CB1 receptors in male Fmr1 knockout (Fmr1(-/y)) mice through pharmacological and genetic approaches normalized cognitive impairment, nociceptive desensitization, susceptibility to audiogenic seizures, overactivated mTOR signaling and altered spine morphology. On the other hand, pharmacological blockade of CB2 receptors normalized anxiolytic-like behavior. The researchers were able to reverse some of these traits by pharmacological inhibition of mammalian target of rapamycin (mTOR) or metabotropic glutamate receptor 5 (mGluR5). In a nutshell, the scientists were able to prove that blockade of the endocannabinoid system is a potential therapeutic approach to control specific alterations in FXS and hence help in the management of autism.
How CBD for autism works: Available evidence
Inflammation in the brain during early-life has been shown to exert profound consequences on brain development and behavior. These include altered emotional behavior, stress responsivity and neurochemical receptor expression and function. As such, some researchers sought out to examine the impact of inflammation, induced by the bacterial compound lipopolysaccharide (LPS) on postnatal day (P) 14, on social behavior during adolescence. They also investigated the involvement of the endocannabinoid system in sociability after early-life LPS using Sprague Dawley rats as subjects.
The results indicated that P14 LPS decreases adolescent social behavior in males and females at P40. This behavioral change is characterized by decreased CB1 binding, increased anandamide levels and increased FAAH activity. They also noted that oral administration of the FAAH inhibitor PF-04457845 (1mg/kg) normalizes LPS-induced changes in social behavior, while not affecting social behavior in the control group. Furthermore, infusion of 10ng PF-04457845 into the basolateral amygdala regulated social behavior in LPS injected females.
The data from this study suggest that alterations in eCB signaling after postnatal inflammation contribute to deficiencies in social behavior during adolescence. Moreover, they established that inhibition of the fatty acid amide hydrolase (FAAH) enzyme, which metabolizes the endocannabinoid anandamide, could be a novel target for disorders involving social deficits such autism or other social anxiety disorders. Cannabidiol, a natural phyto-cannabinoid has been shown to influence the eCB system towards the same effects, and this study sheds some light on its possible mechanisms of action.
The parents of autistic children know the true burden that comes with this illness, and it’s heavy. A child’s inability to communicate their feelings, impulsiveness as well as destructive and self-destructive behavior can take a toll on any parent or caregiver, leading to both physical and emotional exhaustion. As a result, if a more effective therapeutic alternative can be found, it would come as great news to millions of patients suffering from this condition. As shown from the evidence above, cannabidiol for autism treatment is a viable potential agent that should be investigated more thoroughly to establish its efficacy.
- How do I find the right dosage of CBD for Autistic-Related symptoms?
- What is CBD and how does it work?
- What is the endocannabinoid system and why it matters to your health?
FDA Disclosure: CBD products are not approved by the FDA for the diagnosis, cure, mitigation, treatment, or prevention of any disease. While we publish and refer to currently available research on cannabidiol, terpenoids and other properties of hemp-derived cannabis oils, it is important to note: None of the products or information available on this website are intended to be a treatment protocol for any disease state. The information presented is for educational purposes only and is not intended to be an enticement to purchase, and should not be construed as medical advice or instruction. Links to third party websites do not constitute an endorsement of these organizations by Green Flower Botanicals, LLC and none should be inferred. The FDA would want us to remind you: You should always seek the advice of a physician before adding any supplements to your diet.
In this video presented at Autism One, Dr Tracy Fritz M.D. discusses the implications of using Cannabidiol (CBD) to treat ASD. Length 36:48
Current Research on Cannabis to treat Autism ASD:
The current research abstracts and case studies as published at the US National Library of Medicine National Institutes of Health
- Endocannabinoid Signaling in Autism
- Mutations found in individuals with autism interfere with endocannabinoid signaling in the brain
- Cannabinoid receptor type 2, but not type 1, is up-regulated in peripheral blood mononuclear cells of children affected by autistic disorders
- A novel approach to the symptomatic treatment of autism
- Consequences of cannabinoid and monoaminergic system disruption in a mouse model of autism spectrum disorders
- Targeting the endocannabinoid system in the treatment of fragile X syndrome
- Deficient adolescent social behavior following early-life inflammation is ameliorated by augmentation of anandamide signaling
Research on Cannabidiol (CBD) as Treatment For:
- General Research Acne ADD - ADHD Addiction AIDS ALS Alzheimers Anorexia Antibiotic Resistance Anxiety Arthritis Asthma Atherosclerosis Autism ASD Bipolar Disorder Cancer Chronic Pain Depression Diabetes Digestive Issues Endocrine Disorders Epilepsy - Seizures Fibromyalgia Glaucoma Heart Disease Huntington's Disease Inflammation Irritable Bowel Syndrome Liver Disease Metabolic Syndrome Migraines Mood Disorders Motion Sickness Multiple Sclerosis (MS) Nausea Neurodegeneration Obesity OCD Osteoporosis Parkinson's Disease PTSD Rheumatism Schizophrenia Sickle Cell Anemia Skin Conditions Sleep Disorders Stress Stroke