The Endocannabinoid System as it Relates to Autism

Joe Stone; Christian Bogner, M.D.

The importance of the discovery and continued elucidation of the crucial role that
the endocannabinoid system (ECS) plays in human health and disease cannot be
understated. Cannabinoid receptors are the most highly expressed of any GPCR. Theyre
the only ones to play a direct role in virtually every aspect of the human body (CNS and
immune systems, throughout the periphery, presynaptic, and postsynaptic). (Alger 2013)
The growing body of data in regards to this aspect of physiology continues to lead to
the further elucidation of the physiological basis in a growing number of diseases
(including psychiatric) (Pacher 2006). One reason that this is important is because one
such pathogenesis is for that of autism (ASD). There are a number of direct correlations
between ASD and the ECS. Some will be outlined in this paper.
NL3 Mutations Inhibit Tonic Endocannabinoid Secretions
Rare mutations in neuroligins and nerexins predispose to autism (Fldy 2013).
Neuroligin-3 is the only known protein required for tonic secretion of endocannabinoids
that include AEA and 2-AG (Fldy 2013). Neuroligin-3 mutations have been shown to
inhibit tonic endocannabinoid secretion (Fldy 2013). These alterations in
endocannabinoid signaling may contribute to autism pathophysiology (Fldy 2013,
Krueger 2013, Onaivi 2011, Siniscalco 2013). These finding have in part prompted
researchers to apply to conduct research with nonhuman primates in order to further
elucidate this link (Malcher-Lopes 2013).
Endocannabinoid system deficiencies are suggested to be involved in the
pathophysiology of a growing number of diseases (Marco 2012, Russo 2003). Pacher
and Pertwee both cover the endocannabinoid system in detail (Pacher 2006, Pertwee
2010). The number of functions that endocannabinoid signaling regulate in the human
body is extensive and beyond the scope of this paper (Pertwee 2010). For sake of brevity
only a few potentially relevant aspects will be listed:

Endocannabinoids are key modulators of synaptic function (Castillo 2012).

Tonic secretions of endocannabinoids regulate GI functions (including

metabolism) (Di Marzo 2011, Li 2011).

Endocannabinoids (and exogenous cannabinoids) suppress proliferation and

cytokine release (Cencioni 2010).

Endocannabinoids regulate stress responses, in part via the modulation of the

5-HT system (Haj-Dahmane 2011).

CB2 is expressed in Purkinje cells (Gong 2006). In the cerebellar cortex,

CB1Rs regulate several forms of synaptic plasticity at synapses onto Purkinje
cells, including presynaptically expressed short-term plasticity and, somewhat
paradoxically, a postsynaptic form of long-term depression (LTD) (Carey
2011).

CB1 variations modulate the striatal function that underlies the perception of
signals of social reward, such as happy faces. This suggests that CB1 is a key
element in the molecular architecture of perception of certain basic emotions.
This may have implications for understanding neurodevelopmental conditions
marked by atypical eye contact and facial emotion processing, such as ASC
(Chakrabarti 2011).

Additional targets of endocannabinoids (and exogenous cannabinoids),

PPAR, PPAR, and GPR55 expression levels have shown reductions in a
valproic acid model of autism in rats (Kerr 2013).

Endocannabinoids and CB1 agonists increase cerebrocortical blood flow

(Iring 2013).

The expression patterns in malformations of cortical development highlight

the role of cannabinoid receptors as mediators of the endocannabinoid
signaling and as potential pharmacological targets to modulate neuronal and
glial cell function in epileptogenic developmental pathologies (Zurolo 2010).

The endocannabinoid signalosome is a molecular substrate for fragile X

syndrome, which might be targeted for therapy (Jung 2012).

Exogenous cannabinoids from cannabis display similar pharmacological

characteristics to that of endogenous cannabinoids (Pertwee 2010). The potential
therapeutic value of systemic administration of phytocannabinoids has been suggested in
the treatment of a number of diseases with suspected underlying endocannabinoid
deficiencies (Russo 2003). Documentation of their safety and clinical efficacy in a
variety of treatments continues to grow (Hazekamp 2013). Some similar characteristics
include:

Neurogenesis (Galve-Roperh 2007, Jiang 2005, Avraham 2014, Campos 2013)

Neuroprotection (Hampson 2003, Lara-Celador 2013, Sanchez 2012)
Antioxidants (Borges 2013, Pertwee 2010, Hampson 1998, Hampson 2003)
Neuromodulation (Davis 2007, Lara-Celador 2013, Pertwee 2010, Youssef 2012)
Anti-inflammatory (Pertwee 2010, Izzo 2009, Nagarkatti 2009, Klein 2005)

Based on their relative safety, the similar pharmacological characteristics to

endocannabinoids that are inhibited in ASD, and the significant role those endogenous
cannabinoids play in human health, its possible that cannabinoids from cannabis could
prove therapeutic value in treatments.

Increased Expression of CB2 Receptors Associated with ASD

The second direct link, of possibly equal or greater relevance for treatment, is the
upregulation of CB2 receptors in the brains of those with ASD (Siniscalco 2013). This is
believed to be part of an endogenous neuroprotective role of the endocannabinoid system:

CB2 receptors have been identified in the healthy brain, mainly in glial
elements and, to a lesser extent, in certain subpopulations of neurons, and that
they are dramatically up-regulated in response to damaging stimuli, which
supports the idea that the cannabinoid system behaves as an endogenous
neuroprotective system. This CB2 receptor up-regulation has been found in
many neurodegenerative disorders including HD and PD, which supports the
beneficial effects found for CB2 receptor agonists in both disorders. In
conclusion, the evidence reported so far supports that those cannabinoids
having antioxidant properties and/or capability to activate CB2 receptors may
represent promising therapeutic agents (Fernndez 2011).

CB2 expression is increased by inflammatory stimuli suggests that they may

be involved in the pathogenesis and/or in the endogenous response to injury
receptors may be part of the general neuroprotective action of the ECS by
decreasing glial reactivity. Neuropathological findings in human brains
suggest that the upregulation of CB2 receptors is a common pattern of
response against different types of chronic injury of the human CNS. In
addition, their selective presence in microglial cells is highly suggestive of an
important role in disease-associated neuroinflammatory processes. The antiinflammatory effects triggered by the activation of the CB2 receptor make it an
attractive target for the development of novel anti-inflammatory therapies
(Benito 2008).

Given that CB2 is upregulated, and that its believed to play a neuroprotective role in
the human brain, CB2 activation is believed to be a potential target for treatment of ASD
(Siniscalco 2013). Endocannabinoids (AEA, 2-AG) and the most prominent
cannabinoids in cannabis (including THC) are CB2 agonists (Izzo 2009).
Elevated Cytokine Levels Associated with ASD
Elevated cytokine levels are associated with ASD (Napolioni 2013). Whether this is a
direct result of inhibited tonic secretion of endocannabinoids remains uncertain.
However, endocannabinoids (AEA, 2-AG) have been shown to play key roles inhibiting
cytokines via CB2 activation (Cencioni 2010, Panikashvili 2006). Both THC and CBD
have been shown to decrease cytokine production via CB1/CB2 dependent and
independent mechanisms (Juknat 2012, Kozela 2010). The majority of cannabinoids are
PPAR gamma agonists (Izzo 2009), which have been shown to inhibit cytokine
production (Jiang 1998).

Clinically Diagnosing ASD

A team of researchers recently discovered and patented a process that claims that its
possible to clinically diagnose ASD, and susceptibility to it, via observation of the degree
of modulation that acetaminophen has on endocannabinoid levels (Schultz 2012).
Botanical Extracts > Dronabinol
Of equal relevance to this issue is the substantial data, including clinical studies,
suggesting that the combined administration of CBD along with THC (and possibly other
cannabinoids/terpenes present in cannabis) exhibit additive and synergistic effects
resulting in greater clinical efficacies when compared to either cannabinoid alone
(McPartland 2001, Izzo 2009, Russo 2011). The second most prominent cannabinoid in
cannabis is CBD (Gertch 2010). CBD has been shown to inhibit intoxication, sedation,
and tachycardia associated with THC (Russo 2006). Its been shown to increase the
clinical efficacy of THC, while adding therapeutic value in its own right (Russo 2006).

CBD is demonstrated to antagonize some undesirable effects of THC

including intoxication, sedation and tachycardia, while contributing analgesic,
anti-emetic, and anti-carcinogenic properties in its own right. In modern
clinical trials, this has permitted the administration of higher doses of THC,
providing evidence for clinical efficacy and safety for cannabis based extracts
in treatment of spasticity, central pain and lower urinary tract symptoms in
multiple sclerosis, as well as sleep disturbances, peripheral neuropathic pain,
brachial plexus avulsion symptoms, rheumatoid arthritis and intractable
cancer pain. Prospects for future application of whole cannabis extracts in
neuroprotection, drug dependency, and neoplastic disorders are further
examined. The hypothesis that the combination of THC and CBD increases
clinical efficacy while reducing adverse events is supported (Russo 2006).

Several studies suggest that CBD is non-toxic in non-transformed cells and

does not induce changes on food intake, does not induce catalepsy, does not
affect physiological parameters (heart rate, blood pressure and body
temperature), does not affect gastrointestinal transit and does not alter
psychomotor or psychological functions. Also, chronic use and high doses up
to 1,500 mg/day of CBD are reportedly well tolerated in humans (Machado
2011).

An argument could be made that botanical extracts with CBD present offer safer
options for patients, with greater clinical efficacy, when compared to THC (Dronabinol)
alone (Russo 2006). CBD offers more than simply increasing the safety and efficacy of
THC (Izzo 2009).

CBD has been shown to have an inhibitory effect on the inactivation of

endocannabinoids (i.e. inhibition of FAAH enzyme), thereby enhancing the action

of these endogenous molecules on cannabinoid receptors, which is also noted in

certain pathological conditions. CBD acts not only through the endocannabinoid
system, but also causes direct or indirect activation of metabotropic receptors for
serotonin or adenosine, and can target nuclear receptors of the PPAR family and
also ion channels (Campos 2012).
Here are some of the demonstrated pharmacological characteristics of CBD that may
be relevant:

CB1/CB2 agonist blocker (can inhibit overstimulation of CB1 by THC)

FAAH inhibition increases endocannabinoid levels (including AEA, 2-AG)
AEA reuptake inhibitor
5-HT1a agonist
Suppressor of tryptophan degradation
PPAR alpha and gamma agonist
Positive allosteric modulator at glycine receptors
TRPV1 and TRPV2 agonist
Adenosine uptake competitive inhibitor
Antagonist at abnormal-CBD receptor
Regulator of intracellular Ca 2+
T-type Ca 2+ channel inhibitor
(Izzo 2009)

If we accept that tonic secretions of AEA and 2-AG are inhibited via NL3 mutations
in ASD (both of which being CB1 and CB2 agonists), then it might be possible to
suppose the potential benefits of low doses of THC in treatments as well. This seems
especially true when the striking pharmacological similarities between THC and AEA are
reviewed (Pertwee 2010). The majority of the research conducted thus far with ASD and
cannabinoids has been with THC alone. Dronobinal has indicated potential in a single
adolescent case study of autism (Kurz 2010). This might suggest that THC along with
CBD might offer increased clinical efficacy (Russo 2006).
Treating Symptoms Associated with ASD
A considerably greater body of data can be gathered in regards to aspects of the
involvement (and targeting for treatment) of the endocannabinoid system in a number of
the symptoms, and diseases, associated with ASD (in comparison to the pathophysiology
of ASD itself):

G.I. Disorders (Camilleri 2013, Di Sabatino 2011, Wright 2008,)

Repetitive Behaviors (Casarotto 2010, Deiana 2012, Gomes 2011, Kinsey 2011)
Seizures (Jones 2012, Porter 2013, van Rijn 2011)
Sleep Dysfunction (Murillo-Rodriguez 2011, Ware 2010)
Self Injurious Behavior and Tantrums (Mller-Vahl 2004, Onaivi 2011, Passie
2012)
Tuberous Sclerosis (Krueger 2013, Shu, Hai-Feng 2013, Zurolo 2010)

Cerebral Ischemia (Schmidt 2012, Choi 2013, Murikinati 2010, Garcia-Bonilla

2014)
Depression/Anxiety (Hill 2009, Almeida 2013, Campos 2013, Schier 2012)
Cachexia (Engeli 2012, Gamage 2012, Marco 2012)

Conclusion
Given the known role of the endocannabinoid system in ASD it seems entirely
possible, if not likely, that cannabinoid rich botanical extracts from cannabis can be
utilized as useful agents targeting the pathophysiology of ASD, as well as the many
debilitating symptoms and conditions associated with it. We believe that families and
physicians should have the legal right to explore these options on an individual basis
without fear of prosecution.

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