Lasting impacts of prenatal cannabis exposure and the role of endogenous cannabinoids in the developing brain

Human studies

Despite the fact that marijuana is the most widely used illicit drug by pregnant women, there are few studies on the prevalence of prenatal drug exposure. Most information is derived from two longitudinal cohort studies, the Ottawa Prenatal Prospective Study (OPPS) and the Maternal Health Practices and Child Development Study (MHPCD). OPPS, initiated in 1978, focused on assessing prenatal exposure effects of tobacco and marijuana in a low-risk, mainly Caucasian, predominantly middle-class Canadian cohort [46]. Initiated in 1982, the MHPCD focused mainly on prenatal alcohol and marijuana exposure in a group of women from Pittsburgh, Pennsylvania. These women were generally of low socioeconomic status and comprised of approximately half Caucasian and half African–American ethnicity [47]. In both the OPPS and MHPCD studies, cannabis use during pregnancy was not associated with increased miscarriage rates, premature deliveries or any other complications (Table 1). Physically, marijuana exposure was not correlated with any changes in head circumference at the mid-gestational stage (17–22 weeks), although a significant reduction in foot length and bodyweight at this gestational period was reported [48]. These changes in bodyweight and foot length were not present at birth [35], although head circumference was reportedly larger in the exposed cohort at 8 months [49]. These anthropometric measurements were used as an indication of normal fetal development, which correlates with brain development [50].

The OPPS study found that prenatal marijuana exposure was highly correlated with an increase in exaggerated startles and tremors as well as with a significant reduction in habituation to light at the neonatal stage [46,51]. Altered sleep patterns were found in the MHPCD study, and the authors also reported a non-significant trend towards increased irritability [49]. A study on neonates from adolescent mothers found in cannabis-exposed infants transiently increased irritability, excitability and arousal 24–72 h after birth [52]. However, these symptoms were not reported within the MHPCD cohort [53] or in an ethnographic field study based in Jamaica [54]. The MHPCD cohort also demonstrated that a higher amount of cannabis use per day (defined as more than one joint per day) during the third trimester of pregnancy was associated with decreased mental scores of the Bayley Scales of Infant Development at 9 months of age, a difference that disappeared by 18 months [26]. No cognitive deficit was observed during early childhood in the OPPS study, particularly between the ages of 1 and 3 years, suggesting that CNS abnormalities might be absent or subclinical in toddlers [55,56].

For 3–4 year old children, prenatal marijuana exposure negatively affected the verbal and memory domains in both the OPPS and MHPCD studied groups. Cognitive development assessed by the Stanford-Binet Intelligence Scale demonstrated a negative association of short-term memory and verbal reasoning with first and/or second trimester marijuana usage [57]. Similarly, memory and verbal domains, measured by the McCarthy Scales of Children's Abilities, decreased with daily marijuana usage [56]. However, composite intelligence scores in both studies were not impacted at this age by maternal marijuana use.

When children reach school age at around 5–6 years old, reports on the consequences of prenatal marijuana exposure begin to diverge. Exposed children from the OPPS cohort appear to have no memory deficits [58], while those from the MHPCD cohort report short-term memory deficits that correlate strongly with heavy second trimester exposure [59]. Cannabis-exposed children in the OPPS cohort scored significantly lower in tests for sustained attention, while those from the MHPCD group actually displayed increased attention (measured by fewer errors of omission in a continuous performance task) from second trimester exposure [60]. Both groups reported an increase in impulsive and hyperactive behaviors. Follow-up studies found that problems of depression, hyperactivity, inattention and impulsivity persist into the 9–12 year age range [47,61–64], raising speculation of deficits in higher cognitive processes such as executive function [65].

Upon closer inspection, the impact of prenatal marijuana exposure is a little more difficult to discern. For example, one report from the MHPCD cohort found that heavy first- and third-trimester exposure (rated as >0.89 joints/day) was associated with increased hyperactivity and impulsivity [62], while another found that heavy second trimester exposure was significantly associated with increased impulsivity [47]. First- and third-trimester exposure also predicted increased levels of depressive symptoms, assessed by the Children's Depression Inventory [61,64], whereas second-trimester usage was associated with some depressive, but fewer internalizing, symptoms compared with the extent observed in first- and third-trimester exposure groups [62]. Verbal IQ, reading comprehension, overall IQ, presence of psychotic symptoms and sleep patterns do not seem to be impacted [63,66–68]. A recent study has assessed volumetric changes using functional MRI (fMRI) in the brains of children exposed to a number of drugs, including marijuana, during pregnancy. This study found evidence of reduced cortical gray matter and parenchymal volume in children (aged 10- to 14-years old) with intra-uterine marijuana exposure [69].

Executive functions comprise capacities such as cognitive flexibility, sustained and focused attention, and working memory; these can not be assessed with global, standardized tests of cognition [70]. Data from both OPPS and MHPCD cohorts demonstrated deficits in executive functions, which seemed to persist into late adolescence and young adulthood in children of cannabis users [47,63]. The two tests that were found to be negatively affected in marijuana-exposed children both involve the visual analysis and impulse control aspects of executive functions [63]. In the OPPS cohort, 13–16 year olds that were heavily exposed (rated as >0.86 joints/day) displayed deficits in visual memory, visual analysis [27] and the ability to maintain attention (referred to as stability) [71]. fMRI studies with Go/No–Go paradigms conducted to assess response inhibition with 18–22 year-old subjects from the OPPS group found that prenatal exposure was associated with alterations of neural activity in various brain areas during certain tasks [72]. fMRI analysis of visuospatial working memory tasks with the same group also revealed significant changes in levels of activity in the cannabis-exposed group [73]. Peculiarly, prenatal exposure had both positive and negative associations with fMRI response; whereas mostly left brain regions experienced an increase in activity, right brain regions experienced the opposite during tasks. Whether these differences in regional activation/deactivation are a result of various compensatory mechanisms, or if these changes reflect a behavioral alteration that can only be observed with different or more sensitive testing requires further investigation.

Data addressing whether prenatal marijuana exposure can clearly alter the structural and molecular composition of the fetal brain are scarce. Hurd et al. developed a post-mortem human fetal brain collection of midgestational subjects with maternal cannabis use that has begun to provide the first insights into the molecular and biochemical alterations associated with prenatal cannabis exposure on human neuro-development [48]. In the mid gestation human fetus, prenatal cannabis exposure was associated with decreased pro-enkephalin mRNA levels in the striatum, increased μ-opioid receptor expression in the amygdala and reduced κ-opioid receptor mRNA levels in the mediodorsal thalamus [74]. These data suggest that striatal enkephalin/D2 receptor and the opioid system in the limbic-related structures are vulnerable to prenatal cannabis exposure.

In summary, cannabis consumption during pregnancy has profound but variable effects on offspring in several areas of cognitive development [28]. Most of the information on the long-term consequences of prenatal exposure to cannabis comes from longitudinal studies of the OPPS and MHPCD cohorts. By comparing data from the cohorts, a pattern emerges where maternal cannabis use is associated with impaired high-order cognitive function in the offspring, including attention deficits and impaired visuoperceptual integration. It is possible that genetic and environmental interactions may affect the extent of long-term neurobehavioral deficits resulting from prenatal exposure. Recent advances in methodology in prenatal substance use research employ novel approaches to disentangle the exposure to substance effects from correlated risk factors [75]. For example, in the prospective Generation R Study, where 7452 mothers were enrolled during pregnancy and information on substance use and ultrasound measures of fetal growth in early, mid- and late pregnancy were collected, information on paternal cannabis use was also included [41]. Thus, maternal cannabis use during pregnancy was associated with growth restriction in mid and late pregnancy, and also with lower birthweight, while no such association was found for paternal cannabis use in the same period, demonstrating a direct biological effect of maternal intrauterine exposure to cannabis on fetal growth [41]. Refined study designs and novel approaches will assist in confirming and extending the findings of associations between prenatal cannabis exposure and offspring outcomes [75].

Animal studies

Epidemiological studies on long-term neurobehavioral effects of drugs of abuse are subject to a number of confounding factors such as dosage, poly-substance abuse, length and frequency of drug usage, pregnancy stage and environmental factors such as maternal nutrition and socioeconomic problems, commonly associated with drug abuse. Animal models provide tighter experimental control over these factors and a wealth of data have been generated on the behavioral and molecular changes associated with prenatal exposure to cannabis preparations or synthetic compounds (termed ‘cannabinoids’ for the following discussion). Overall, pre- and early post-natal exposure to cannabinoids lead to changes in social interactions, novelty responses and memory in the adult offspring [29–32]. In addition, drug addictive behaviors are modified in cannabinoid-exposed offspring, as indicated by sensitized responses to the reinforcing effects of heroin and morphine in conditioned place preference tests [76,77]. While the exact molecular pathways underlying these behavioral changes are not clear, numerous studies demonstrated that prenatal cannabinoid exposure may lead to alterations in GABAergic, glutamatergic, dopaminergic, serotoninergic and opioidergic systems in offspring [28,32,78]. In addition, perinatal cannabinoid exposure disrupts neurodevelopment through modifications of gene expression [79] involved in neuronal specification and synapse physiology [80].

Overview of the endocannabinoid system

Endocannabinoids are amides, esters and ethers of long-chain polyunsaturated fatty acids. There are two major families of eCBs, acyl amides and acyl esters. Anandamide (arachidonoyl ethanolamide [AEA]) and 2-arachidonoyl glycerol (2-AG), respectively, are the prototypical members of each family. The enzymes that synthesize AEA are still uncertain, with at least four routes of AEA biosynthesis proposed to occur in brain homogenates [83]. These enzymes include N-acyl-phosphatidyl-ethanolamine-specific phospholipase D, α,β-hydrolase domain-containing 4, glycerophosphodiesterase-1 and phosphatases such as PTPN22 [5,84,85]. These biosynthetic pathways demonstrate substantial overlap and may be able to substitute for one another. AEA is hydrolyzed to arachidonic acid and ethanolamine by fatty acid amide hydrolase (FAAH) [15,86]. 2-AG is synthesized by sn-1-selective diacylglycerol lipases α and β (DAGLα and DAGLβ) [87]. Recent data from genetic ablation of these two isoforms suggest DAGLα is the major CNS form in adult mice and is important for postsynaptic release of 2-AG to transiently suppress GABA-mediated transmission at inhibitory synapses in the hippocampus [88]. Interestingly, DAGLα mRNA level is found to be decreased in the hippocampus of epileptic human patients, while DAGLβ isoform levels were unchanged, suggesting that under pathophysiological conditions, DAGLα is the affected isoform [89]. However, it remains to be determined which DAGL isoform is responsible for 2-AG production in humans. 2-AG is hydrolyzed to arachidonic acid and glycerol by monoglyceride lipase (MAGL) [90] and α/β-hydrolase domain-containing serine hydrolases (ABHD6/12) [91].

The eCBs elicit diverse central and peripheral effects by activating the cannabinoid receptors: CB₁R and CB₂R[92,93], G-protein coupled receptor 55 (GPR55) [94–97], the transient receptor potential of vanilloid type-1 (TRPV1) channel, the peroxisome proliferators-activated receptor (PPAR)α [4] and at least two, as yet molecularly uncharacterized, receptors [98]. The signal transduction mechanisms include Gi-mediated inhibition of adenylyl cyclase and modulation of ion channels. Cannabinoid signaling often inhibits voltage-dependent Ca²⁺ channels (N and P/Q type) or activates inwardly rectifying K⁺ channels [99]. In addition, cannabinoids stimulate various signaling pathways involved in the regulation of cell fate, such as the MAP kinase family (ERK, JNK and p38), protein kinase B and the sphingolipid pathway [100,101].

Ontogeny of the endocannabinoid system

Owing to their lipophilic nature, endocannabinoids are highly unstable and difficult to quantify, hence the paucity of data on endocannabinoid levels during development. The only available data comes from older studies employing mass spectrometry, where levels of AEA and 2-AG have been shown to vary substantially in rodent brains throughout prenatal development [78,102]. AEA is present at low concentrations in the brain at midgestation and gradually increases through the perinatal period until adult levels are reached [102], whereas fetal 2-AG levels gradually increase through the prenatal period, with a surge occurring at birth [102,103]. Notably, 2-AG concentrations (2–8 nmol/g tissue) are approximately 1000 fold higher than those of AEA (3–6 pmol/g tissue) throughout brain development [102]. However, additional studies are required to substantiate these findings.

The ontogeny of the metabolizing enzymes and receptors of the endocannabinoid system has not been extensively characterized. Nevertheless, current data suggest that the endocannabinoid system exists from the earliest stage of pregnancy, in the preimplantation embryo and uterus [104], placenta [105] and in the developing fetal brain [78], presenting multiple points of vulnerability to exogenous cannabis or cannabimimetic drug exposure throughout gestation. In the mouse, stimulation of CB₁R arrests the development of two-cell embryos into blastocytsts in culture [104]. AEA is present in the pregnant uterus at relatively high levels (5–10 nmol/g tissue) that fluctuate with changes in the pregnancy status, with higher levels associated with a nonreceptive uterine environment [104]. Indeed, low levels of the AEA-degrading enzyme FAAH and high levels of CB₁R expression in human placenta are associated with spontaneous miscarriage [106]. Studies characterizing the endocannabinoid system in early human pregnancy (weeks 7–12 gestation) demon strated that CB₂R and FAAH are expressed in relatively constant levels in trophoblasts in early gestation, but their cellular distribution changed from syncytio trophoblast to the mesenchymal core of the villus [105].

In the developing mouse brain, CB₁R are expressed as early as day 11 postgestation (comparable with 5–6-week old human embryos), with gradually increasing levels of both mRNA and receptor density (revealed by radiolabeled agonist binding) throughout the prenatal period in the whole brain [78] . CB₁R are abundantly expressed in corticolimbic areas of the fetal rodent brain [78]. Pharmacological studies of the ability of the CB₁R agonist, WIN55212-2, to stimulate [³⁵S] GTPγS binding indicate that CB₁Rs are functionally active from early stages of development [107]. In human fetal brains, CB₁Rs were detected at week 14 of gestation, with preferential expression in the cerebral cortex, hippocampus, caudate nucleus, putamen and cerebellar cortex. By week 20, intense expression is evident in CA2–CA3 of hippocampus and in the basal nuclear group of the amygdala [107,108].

More recently, several specific antibodies against different endocannabinoid system components have become available, making it possible to examine the distribution of specific enzymes at the light- and electron-microscopic level. In particular, immunohistological studies using specific antibodies have mapped the temporal and spatial distribution of CB₁R, DAGLα/β and MAGL during neural development in mice [103,109,110]. Similar to ligand binding and mRNA expression studies, CB₁R immunoreactivity can be detected by embryonic day (E)12.5, and is localized to reelin-expressing Cajal-Retzius cells and newly differentiated postmitotic glutamatergic neurons of the mouse telencephalon [111], and to the subpial area of the ganglionic eminence and marginal zone of the neocortex [112]. From E13.5 to birth, abundant CB₁R immunoreactivity is detected in several long-range axonal tracts including corticofugal tracts such as corticothalamic (Figure 1) and corticospinal tracts [109,111]. On the subcellular level, CB₁R is localized to somato-dendritic endosomes at E12.5 and then to developing axons of glutamatergic neurons at E13.5 and after this time[111] . The ‘atypical’ pattern of CB₁R expression in long-range glutamatergic axons disappears after birth [110,111]. During late gestation (E17–18), CB₁R immunoreactivity becomes detectable in axons and axonal growth cones of cholecystokinin (CCK)-positive GABAergic interneurons [113,114]. The origin of these CB₁R containing interneurons has been traced to the caudal ganglionic eminence and pallial–subpallial boundary at E11–12. These cells undergo a complex long-distance migration, first radially to the marginal zone, then tangentially in the lateral-to-medial direction within the dorsal telencephalon, eventually reaching their final destination in the cortex, hippocampus and dentate gyrus where they migrate radially and differentiate into CB₁/CCK⁺ or CB₁/reelin/calretinin⁺ GABAergic interneurons [112].

The overall protein levels of CB₁Rs are relatively constant throughout forebrain development, while DAGLα protein levels peak at E14.5/E16.5 and then dramatically decrease in neonates, furthermore MAGL transiently decreases around E18.5 (Figure 2) [103]. Similar to CB₁R, the distribution of DAGLα/β and MAGL are localized to long-range glutamatergic axons in the prenatal period (Figure 1) [103,110]. Interestingly, after E16.5, MAGL expression undergoes a dramatic change from cortical plate and long-range axon tracts to a restricted expression in perisomatic segments and proximal dendrites both in the late-gestational brain and at birth [103]. This coincides with the surge in cortical and hippocampal 2-AG concentrations, suggesting that MAGL plays an essential role in determining 2-AG availability in the developing brain.

Together, these expression studies indicate that components of the endocannabinoid system are expressed early in life and are positioned to modulate neuronal generation, differentiation, migration and neural circuit wiring during development.

Cell proliferation, neurogenesis & oligodendrogliogenesis

During mammalian embryogenesis, the generation of the CNS relies on a finely regulated balance of neuroprogenitor proliferation, differentiation and survival that is controlled by a number of extracellular signaling cues [117]. In the adult brain, identification of neuroprogenitor cells in the subgranular zone supports the existence of hippocampal neurogenesis, which is implicated in several brain functions including learning and memory, depression and brain repair [118–120].

Several lines of evidence support a role for eCBs in neural progenitor proliferation [24,121–123]. The expression of CB₁R, FAAH, DAGL and MAGL in VZ/SVZ neuroprogenitor cells has been reported [103,109,121,122,124] . CB₁R activation promotes progenitor cell proliferation, while genetic deletion of CB₁R decreases cortical progenitor proliferation in VZ/SVZ in the embryonic brain [121]. By contrast, deletion of FAAH increases neural progenitor proliferation in the embryonic brain [121] and inhibition of FAAH by the inhibitor URB597 increased VZ/SVZ progenitor proliferation in embryonic brain slices [109]. Thus, the reciprocal consequences of blockading CB₁R and increasing AEA suggest that local AEA levels acting through CB₁R, modulate neural progenitor proliferation in the embryonic brain.

The effect of CB₁R activation on neurogenesis has been examined in early postnatal and adult brains and in neurospheres, with conflicting results (reviewed in [24,125]). It should be noted that the net effect of cannabinoids on neurogenesis during postnatal development, in adults and in culture, is probably influenced by the status of nervous system maturation, where inherent characteristics of the neural progenitors may differ. Increased proliferation of neural progenitors is observed in the hippocampus of adult FAAH knockout mice [121], consistent with the observation of decreased neuroprogenitor proliferation in the hippocampus of both early postnatal and adult CB₁R knockout mice [122]. Furthermore, using a kainate-induced excitotoxicity model, excitotoxicity-induced hippocampal neural progenitor proliferation is abrogated in CB₁R knockout mice and in wildtype mice treated with the CB₁R antagonist, SR141716 [126]. HU210, a synthetic CB₁R agonist, increases adult hippocampal neurogenesis and exerts anxiolytic and antide-pressant effects in rats [127], while the synthetic CB₁R/CB₂R agonist, WIN55212-2, partially restores hippocampal neurogenesis in the aged rat brain [128]. By contrast, methanandamide, a non-hydrolyzable AEA analog, significantly decreases neurogenesis in the adult hippocampus of rats [129]. Moreover, AEA decreases the expression of a mature neuronal marker and inhibits neurite outgrowth of cortical neural progenitors in vitro, while the CB₁R antagonist SR141716 increases the rates of neuronal differentiation of neural progenitors [129]. The same group later reported that activation of CB₁R on neural progenitors promotes the differentiation of the latter into glia cells [122]. Together, these studies suggest an endogenous AEA tone that actively modulates neural progenitor differentiation through the CB₁R. Furthermore, a role for 2-AG in adult neurogenesis has been demonstrated [88,124]. A DAGL antagonist inhibits the proliferation of cultured neural stem cells, and the proliferation of progenitor cells in young adult mice, and adult neurogenesis in the SVZ and hippocampus, is impaired in both DAGLα and DAGLβ knockout mice [88,124]. Interestingly, a sex difference in cell proliferation in developing rat amygdala, mediated by 2-AG, has recently been reported [130]. Newborn females had higher rates of cell proliferation than males, which were abrogated by inhibition of MAGL in females [130]. The impact of prenatal THC exposure on neurogenesis remains to be examined.

Cannabinoid signaling has also been suggested to participate in postnatal myelination processes [131–133]. Postnatal myelination involves radial migration of astrocyte-like (type B) precursor cells from the SVZ to the overlying white matter, where these cells are differentiated into astrocytes and oligodendrocytes (reviewed in [134,135]). CB₁R is expressed in radial glia-like cells and B-like type cells, while CB₂R is expressed in a subpopulation of SVZ cells containing the polysialylated neural cell adhesion mole cule [122,132]. The 2-AG synthesizing enzymes, DAGLα and β, and degrading enzyme, MAGL, are also found in oligodendrocytes in various differentiation stages[136]. Agonist stimulation of CB₁R and CB₂R increases the expression of myelin basic protein in subcortical white matter [132]. Furthermore, cannabinoid signaling has been suggested to participate in adult oligodendrogenesis after toxic or autoimmune demyelinating lesions, when precursor cells are recruited from the SVZ towards the injured area and give rise to oligodendrocytes [14,131,133].

Neuronal migration

Following mitosis, newborn pyramidal progenitor cells in the VZ/SVZ migrate radially into the cortical plate and populate distinct cortical layers [116]. Proper regulation of this migration is important for appropriate cortical patterning. Genetic deletion or blockade of CB₁R leads to delayed migration of cortical neurons. In cultured brain slices, elevating AEA levels through FAAH gene removal or pharmacological blockade enhances the migration of newly borne postmitotic neurons into the cortical plate [109]. In contrast to pyramidal neurons, cortical inhibitory interneurons migrate tangentially from the ganglionic eminences to the cortical plate. CB₁R signaling is also implicated in the regulation of the long-distance migration CCK-positive interneurons [112,113]. Stimulation with AEA and WIN55,212–2, in cooperation with brain-derived neurotrophic factor, a major prodifferentiating neurotrophin for this cell class, induces the long-distance migration of GABA-containing interneurons in the ganglionic eminence [137]. Prenatal THC has been demonstrated to increase the density of CCK-expressing interneurons in the rat hippocampus in vivo [137]. Thus, eCBs modulate both migration of cortical principal neurons and certain classes of interneurons. Increases in local AEA concentration probably affect the proper placement of pyramidal neurons and/or CCK⁺ basket cells. Furthermore, DAGLα and MAGL have been demonstrated to be expressed in mouse migratory neuroblasts that travel along the rostral migratory stream to populate the olfactory bulb, and DAGL inhibition results in decreased migration in scratch wound assays and in explant cultures, suggesting a role for 2-AG in regulating cell migration following adult neurogenesis [138].

Axon pathfinding & fasciculation

Once pyramidal neurons reach their final destination, they must project their axons to connect to their postsynaptic partners. Axon tracts navigate along stereotyped pathways, and fasciculate and defasciculate in distinctive domains along their path [139,140]. The formation of precise neural circuits requires orchestrated interactions between axon tracts, and between the navigating axonal growth cones and the environmental cues at distinctive locations. Genetic deletion of CB₁R or prenatal CB₁R pharmacological blockade in mice led to increases in the number of axons with aberrant trajectories in the corpus callosum and to abnormal fasciculation of long-range axons [109,110]. Similarly, knockdown of CB₁R in zebrafish leads to abnormal axonal fasciculation [141].

Thalamic axons projecting into the cortex provide the majority of cortical sensory input, while reciprocal innervations from the cortex to the thalamus send critical feed-back to modulate the thalamic responses required to perform the complex information gathering and integration that underlie sensory processing [142–144]. A ‘handshake hypothesis’, which proposes that thalamocortical axons and corticothalamic axons interact and serve as scaffolds to guide each other to their final destinations, has been postulated [145–147]. Recent data suggest that the endocannabinoid system may be modulating this handshake interaction [110]. When thalamic and cortical axons meet and intermingle in the basal telencephalon during development, CB₁R is localized to corticothalamic axons, while the 2-AG synthesizing enzymes, DAGLα/β and degrading enzyme MAGL, are present in both thalamocortical and corticothalamic axons (Figure 1) [103,110]. Thus, 2-AG could be produced in both axonal tracts to act in both an autocrine and paracrine fashion, while MAGL may serve to restrict 2-AG availability. Interestingly, genetic deletion of CB₁R in cortical neurons leads to aberrant fasciculation in both corticothalamic and thalamocortical axons despite normal target recognition [110], suggesting that 2-AG-mediated signaling at CB₁R may be modulating the fasciculation process during the handshake interaction between cortical and thalamic axons.

More recently, a role for CB₁R in axonal guidance has been demonstrated in the retinal system [148]. Eye-specific segregation of retinal projections in the dorsal lateral geniculate nucleus of thalamus is impaired in CB₁R knockout mice. Furthermore, CB₁R appears to act in concert with the adhesion molecule deleted in colorectal cancer (DCC; a receptor for axonal guidance molecule, netrin-1) to influence axonal growth cone behavior [148].

At the subcellular level, a recent morphometric study provided evidence for a microgradient of 2-AG in elongating axons [106]. While MAGL is coexpressed with both CB₁R and DAGLα in cultured cortical neurons, MAGL is differentially recruited to distinct subcellular domains, particularly in the consolidated axon shaft. In this paradigm, CB₁Rs are maintained in a state of inactivity by the absence of 2-AG (owing to presence of MAGL) while undergoing vesicular transport along the consolidated axon. The absence of MAGL at the growth cones lifts the restriction on CB₁R signaling and promotes cell-autonomous axonal growth. This scheme may serve to prevent ectopic branching and axon guidance errors, since in vitro study in pyramidal cells found that CB1R activation leads to increased neurite branching [112].

These findings firmly demonstrate multiple roles for the endocannabinoid system in brain development. A detailed knowledge of eCB signaling is important in understanding the long-term consequences of alterations in CB₁R activity during neurodevelopment, a potential etiology for the mental health disorders linked to prenatal or adolescent cannabis use, or following therapeutic manipulations of the endocannabinoid system.