Adolescence is a vulnerable period of development when limbic connection of the prefrontal cortex (PFC) involved in emotional processing may be rendered dysfunctional by chronic exposure to delta-9-tetrahydrocannabinol (∆9-THC), the major psychoactive compound in marijuana. Cannabinoid-1 receptors (CB1Rs) largely mediate the central neural effects of ∆9-THC and endocannabinoids that regulate NMDA receptor-dependent synaptic plasticity of glutamatergic synapses in the prelimbic prefrontal cortex (PL-PFC). Thus, chronic occupancy of CB1Rs by ∆9-THC during adolescence may competitively decrease the functional expression and activity of NMDA receptors in the mature PL-PFC. We used a multidisciplinary approach to test this hypothesis in adult C57BL/6J male mice that received vehicle or ∆9-THC in escalating doses (2.5–10 mg/kg/ip) through adolescence (postnatal day 29–43). In comparison with vehicle, the mice receiving ∆9-THC showed a hyperpolarized resting membrane potential, decreased spontaneous firing rate, increased current-induced firing threshold, and decreased depolarizing response to NMDA in deep-layer PL-PFC neurons analyzed by current-clamp recordings. Electron microscopic immunolabeling in the PL-PFC of adult mice that had received Δ9-THC only during adolescence showed a significant (1) decrease in the extrasynaptic plasmalemmal density of obligatory GluN1-NMDA subunits in dendrites of all sizes and (2) a shift from cytoplasmic to plasmalemmal distribution of GluN1 in large dendrites receiving mainly inhibitory-type synapses from CB1R-labeled terminals. From these results and concomitant behavioral studies, we conclude that social dysfunctions resulting from excessive intake of ∆9-THC in the increasingly available marijuana products used by male teens may largely reflect circuit defects in PL-PFC networks communicating through endocannabinoid-regulated NMDA receptors.
The psychoactive compound in marijuana, delta-9-tetrahydrocannabinol (∆9-THC), binds cannabinoid-1 receptors (CB1Rs) that are primary mediators of activity-dependent retrograde endocannabinoid signaling that decreases transmitter release . CB1Rs are highly expressed in presynaptic terminals located in layers 2/3 and 5 of the prefrontal cortex (PFC), where they regulate the synaptic strength and synaptic plasticity of glutamatergic inputs to pyramidal cells [2, 3]. Chronic exposure to ∆9-THC during adolescence produces long-term behavioral dysfunctions that have some similarity to certain symptoms of psychiatric and neurodevelopmental disorders [4, 5], in which there is decreased functionality of NMDA receptors in the PFC .
NMDA receptors are ion channels whose functions are dependent on expression of GluN1 subunits . At birth, GluN1 is expressed at low levels and rapidly increases throughout the early postnatal period to the third postnatal week coinciding with preadolescence [8, 9]. GluN1 deletion in the prelimbic prefrontal cortex (PL-PFC) produces changes in social interactions and anxiety-like behaviors that have also been observed following chronic perinatal and adolescent administration of ∆9-THC [10, 11]. The prominent role of CB1Rs in actomyosin-dependent cytoskeletal remodeling  further suggests that the neurons most affected by adolescent administration of ∆9-THC may have altered somatodendritic morphology and inputs from terminals containing CB1Rs. Thus, the behavioral abnormalities produced by chronic exposure to increasingly large quantities of ∆9-THC during adolescence may be concurrent with altered NMDA activity and GluN1 expression in PL-PFC neurons having distinct cytoarchitecture and afferent inputs. We examined this unexplored possibility using behavioral testing, current-clamp recording, and electron microscopic immunolabeling in the PL-PFC of adult C57/BL6 male mice that received chronic escalating doses of ∆9-THC only through adolescence. This model has important implications for understanding the cellular mechanisms underlying behavioral effects produced by the heavy consumption of ∆9-THC by teenage males.
Materials and methods
Animals and drug treatment
All experimental procedures were carried out in accordance with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals and were approved by the Institutional Animal Care and Use Committees (IACUC) at Weill-Cornell Medical College. C57BL/6J male mice were obtained commercially from Jackson Laboratory (Bar Harbor, ME) immediately after weaning at postnatal day (PD) 21 and reared in groups of 4–5 mice/cage until reaching adulthood at PD70 . All animals were kept in a temperature- and humidity-controlled environment, and maintained with HEPA-filtered air on a 12-h light/dark cycle (lights on from 7 a.m. to 7 p.m.). Food and water were available ad libitum.
An alcohol solution of ∆9-THC was obtained from the Drug Supply Program of the National Institute on Drug Abuse (Rockville, MD, USA). Nitrogen gas was used to evaporate the alcohol from this solution [13, 14]. The ∆9-THC residue was solubilized by briefly heating at <100 °C in 0.9% NaCl (saline) solutions containing Tween-80 . The vehicle (saline and Tween-80) was used to prepare 2.5, 5.0, and 10.0 mg/kg doses of ∆9-THC, each of which was administered by once-daily intraperitoneal injections for 5 consecutive days from postnatal day (PD) 28 to 43, a period which corresponded to the later stage of adolescence in rodents . The mice were assigned randomly to ∆9-THC- and vehicle treatment groups. After completion of the last injection on PD 43, the mice were returned to their home cages without further injections while conducting behavioral tests in the 27-day interim from PD 43 to young adulthood at PD70.
Whole-cell current-clamp recordings
Whole-cell current-clamp recording was used to determine whether adolescent administration of ∆9-THC has a long-term effect on the electrophysiological activities in layer V of the PL-PFC [2, 16]. For this, slice preparations of frontal cortical tissue from vehicle- (n = 6) and Δ9-THC-pretreated (n = 6) mice were obtained and stored in ice-cold sucrose-artificial cerebrospinal fluid (s-aCSF), and perfused with the Mg2+-free extracellular perfusion . After the whole-cell configuration was formed, the access and membrane resistances were continuously monitored through the recording. Only those cells, in which access resistance was stable (change <10%), were included in the data analysis. Stable baseline recordings of the resting membrane potentials (RMP) were achieved before local application of the buffer control, NMDA, or MK-801 buffers. Major classes of pyramidal cells and interneurons were defined by their spontaneous firing patterns without or with an injected current [17, 18]. Data are expressed as means ± SEM in recorded cells from at least four mice per treatment group. The two-tailed unpaired t-test was used to compare the difference between the vehicle and drug-induced effect on the RMP and spontaneous firing rate. Statistically, P < 0.05 and P < 0.01 were considered significant and very significant, respectively. RMP and spontaneous firing were recorded using Window pClamp Clampex 10.3 and analyzed offline using Clampfit 10.3 (Molecular Devices).
Electron microscopic immunolabeling
Vehicle- and ∆9-THC-pretreated adult mice were deeply anesthetized by intraperitoneal injection of sodium pentobarbital (150 mg/kg), and subjected to sequential vascular perfusion with 3.75% acrolein and 2% paraformaldehyde in 0.1 M phosphate buffer (PB; pH 7.4) saline. Coronal sections through the PL-PFC at 1.5–2.5 mm anterior to Bregma  were collected from the aldehyde fixed brains of mice in each treatment group (n = 10/group). These were processed using previously described methods for dual immunoperoxidase and immunogold-silver labeling [20, 21]. For this, these sections were incubated for 24 h at room temperature in a solution containing mouse monoclonal GluN1 antibody (Pharmingen, San Diego, CA, USA) and guinea pig polyclonal CB1R affinity-purified antisera at the respective dilutions of 1:50 and 1:3200 in Tris-buffered saline (TS; pH 7.6) and 0.1% bovine serum albumin (BSA; Sigma-Aldrich, St. Louis, MO).
The GluN1 antibody was directed against a fusion protein corresponding to amino acids 660–811 of GluN1. Western blot analysis of the GluR1 antibody in hippocampal homogenates and rat synaptic membranes shows one major band at 116 kD comparable with that seen in HEK293 cells transfected with cDNA encoding GluN1, which is absent in western blots of non-transfected cells . This antibody has been extensively used for light and electron microscopy in rodent  and shown to be specific in mouse forebrain by absence of immunolabeling after spatial–temporal GluN1 gene deletion . The CB1R was identified by an affinity-purified polyclonal antibody raised in guinea pig against a glutathione S-transferase fusion protein containing the C terminus [residues 401–473 of rat CB1R]. This antibody has been shown to have no immunoreactivity in CB1R knockout mice .
Following the incubation with primary antiserum, the tissue was incubated for 30 min in a TS and 0.1% BSA solution containing 1:200 dilution of donkey anti-guinea pig biotinylated IgG (Jackson Immunoresearch, West Grove, PA) then washed in TS and given a 30-min incubation in Vector ABC Elite kit (Vector Labs, Burlingame, CA). The peroxidase reaction product was visualized by reaction in 3, 3′-diaminobenzadine (DAB, Sigma-Aldrich, St. Louis, MO) with 0.1% hydrogen peroxide. Subsequently the tissue-sections were (1) washed in TS, (2) incubated overnight in a 1:50 dilution of Ultrasmall gold conjugated to goat anti-mouse IgG. (Electron Microscopy Sciences, Hatfield, PA), and (3) silver-intensified in Amersham Silver intense kit (GE Biosciences, Piscataway, NJ). Reversal of markers and immunolabeling with omission of one or both primary and secondary antisera were used as controls for spurious labeling. The immunolabeled sections were rinsed in 0.2 M citrate buffer and 0.1 M PB prior to postfixation in 2% osmium tetroxide and embedding in Epoxy resin using conventional electron microscopic methods .
The electron microscopic analysis was conducted in ultrathin sections collected from the PL-PFC in two plastic-embedded vibratome sections from ten adult mice that received vehicle (n = 5) or ∆9-THC (n = 5) during adolescence. The density of immunolabeled and unlabeled neuronal profiles was tabulated in a total surface area of 21,170 µm2 collected equally from ∼70 images from each of the ten mice. MCID Analysis software, Version 7.0 (Focus Ltd, Cambridge, UK) was used to determine the mean diameter of GluN1-labeled dendritic profiles. The immunolabeled dendritic profiles were statistically separated into small, medium, and large categories using cluster analysis. Differences in GluN1 density between drug treatment groups and dendritic size were analyzed with a two factor (drug × size) ANOVA using JMP Statistical Discovery from SAS (Cary, NC). Chi-square analysis was used to determine the statistical significance of between group differences in dendritic spine density in the PL-PFC. Differences were considered significant at p < 0.05.
Microscopic illustrations were prepared by importing digital images into Adobe Photoshop (CS4) and Powerpoint (Microsoft Office, 2016) to enhance contrast, prepare composite plates, and add lettering. Labeled neuronal and glial profiles were defined using the nomenclature of Peters et al. .
The following behavioral tests were conducted during the light phase of the light/dark cycle in a subgroup of young adult (PD70) mice that received vehicle (n = 4) or ∆9-THC (n = 3) from PD 28 to 43. The apparatus used for each behavioral task was cleaned thoroughly with 70% EtOH between mice in order to remove olfactory cue biases. To avoid potential confounding effects of behavior testing, these tests were done in a group of mice separate from those used for current-clamp recording or electron microscopic immunolabeling.
Locomotor activity was analyzed for 30 min in standard mouse open-field chambers (Med Associates, St. Albans, VT) using infrared beam breaks to measure both horizontal movement and rearing . The distance traveled (cm), average speed (cm/s), stereotypic counts, and ambulatory time in the center vs. periphery were video recorded. Unpaired t-tests (SPSS IBM Corp, version 20) were conducted for between group comparisons of each of these parameters with a p < 0.05 considered as statistical significant.
Social/Novel Object Interaction Test The conventional three-chamber paradigm test for sociability and preference for social approach and novelty  was modified with the use of a rectangular corrugated plastic box (27 × 16.5 × 9.25 in.) without dividing plastic walls. A metal wire was affixed across the top of the apparatus to separate the box into two equally-sized chambers. Each subject was given 5 min to acclimatize to the open box before being briefly placed back inside their home cage while a conspecific stranger mouse and an inanimate, novel object were placed in identical wire pencil cages on opposite chambers, respectively designated as those containing social (SOC) and novel object (NOV).
Mice were placed in the center of the box and given 10 min to explore the two chambers. ANY-maze software was used for video recording and tracking of each test to quantify the time spent and number of entries of the mouse into the respective SOC and NOV contact zones, which were defined by the perimeter of a 2–2.5-in. circle around the pencil cages. Two-way ANOVAs were used to assess main effects and potential interaction effects between treatment condition and zone(s). In the case that variances between groups were found to be significantly different (p < 0.05), a Welch’s adjustment was made for the Levene’s test for equality of variances.
Y-maze Spontaneous Alternation Task was used to assess spatial working memory and learning as previously described [22, 28]. The task involves testing the ability of the subject to remember a previously visited arm and takes advantage of the natural explorative drive of rodents. A lower spontaneous alternation (SA) score indicates reduced cognitive function. In this test, mice were placed in the center of the maze and given 10 min to freely explore each arm. An arm entry was recorded when 85% of a mouse’s body entered the arm. The total number of arm entries and percentage of SAs were recorded using ANY-maze software (Stoelting, Wood Dale, IL). A SA occurred when a mouse entered into a different arm of the maze in each of three consecutive arm entries. The percentage of SA was calculated as the total number of alternations (i.e., number of entries into three different arms consecutively), divided by the total number of arm entries, multiplied by 100.
Whole-cell current-clamp recording
Recordings from neurons located in deep layers of the PL-PFC (Fig. 1a) of adult mice showed that receipt of adolescent ∆9-THC during adolescence reduced glutamate activity (Fig. 1b), and increased the threshold for spontaneous firing (Fig. 1c: ∆9-THC vs vehicle, P < 0.01, N = 6). Bath application of NMDA (30 µM) elicited depolarization in PL-PFC neurons from vehicle-injected mice, which was attenuated in recordings from mice receiving ∆9-THC (Fig. 1d: control buffer vs. NMDA, P < 0.05, N = 5–6; vehicle vs. ∆9-THC, P < 0.01, N = 4–5). Bath application of NMDA (30 µM) also produced an increased firing rate in PL-PFL neurons from vehicle-injected animals (Fig. 1e: control buffer vs. NMDA, P < 0.05, N = 7–20), which was largely absent following bath application of NMDA receptor antagonist MK-801 (10 µM) and in adult mice receiving ∆9-THC through adolescence (Fig. 1e: NMDA vs. MK-801, P > 0.05, N = 4–6).
GluN1-immunogold distribution in dendritic and axonal profiles
GluN1 immunogold was predominately seen in dendritic shafts and dendritic spines in the PL-PFC of adult mice receiving systemic injections of either ∆9-THC or vehicle during adolescence (Fig. 2). In dendritic shafts, the GluN1 labeling was most abundant in the cytoplasm and often localized to tubulovesicles and outer mitochondrial membranes (Fig. 2a, d). GluN1-immunogold particles were also seen on synaptic and extrasynaptic plasmalemmas of varying sized dendritic spines that received asymmetric excitatory-type synapses from GluN1-labeled and unlabeled terminals in the PL-PFC of both vehicle and ∆9-THC recipient mice (Fig. 2). Larger dendritic spines in each treatment group frequently displayed in-folded, discontinuous postsynaptic membrane specializations that were decorated with GluN1 immunogold (Fig. 3a–d).
Unlabeled (Fig. 2a, b), GluN1-labeled (Fig. 2c, d), and dual GluN1/CB1R-labeled axon terminals (Fig. 2e) formed asymmetric excitatory-type synapses mainly on dendritic spines. In these terminals, the immunogold particles were either distributed over synaptic vesicles or localized to presynaptic or extrasynaptic plasmalemmas (Fig. 2c, d). Axon terminals forming symmetric inhibitory-type synapses showed a similar subcellular distribution of GluN1, but more often contained only CB1R immunoreactivity and preferentially contacted unlabeled and GluN1-labeled dendritic profiles (Fig. 2f, g). Astrocyte-like glial processes  frequently occupied portions of dendritic and axonal plasmalemmas without recognizable synaptic input in the PL-PFC of adult mice in both treatment groups (Fig. 2c–e and h).
Impact of adolescent ∆9-THC on synaptic and extrasynaptic GluN1 distribution
Receipt of ∆9-THC during adolescence substantially increased the number of asymmetric axospinous synapses on dendritic spines, the majority of which contained GluN1 immunogold (Table 1). Most of the presynaptic axon terminals at axospinous synapses also contained GluN1 immunogold (Table 2). In contrast with dendritic spines, there was a slight reduction in GluN1-positive and increase in GluN1-negative dendritic shafts receiving excitatory-type synapses in PL-PFC of ∆9-THC recipient mice (Table 1).
Administration of ∆9-THC during adolescence resulted in a qualitative increase in plasmalemmal and a decrease in cytoplasmic GluN1-immunogold particles in large, but not smaller dendritic profiles that received symmetric synapses from CB1R-labeled terminals in adult PL-PFC (Fig. 3a–d). Statistical analysis confirmed a significant shift from cytoplasmic to plasmalemmal distribution of GluN1 in large dendrites that received synaptic input from axon terminals in the PL-PFC of ∆9-THC recipient mice (Fig. 3e, f).
GluN1-immunogold density on extrasynaptic plasmalemmas of all dendritic profiles was significantly reduced in the PL-PFC of adult mice that received ∆9-THC compared with vehicle during adolescence (Figs. 4 and 5a, b). The diagrams in Fig. 5c, d respectively show GluN1-immunogold distribution in PL-PFC dendritic profiles of varying sizes from vehicle- and ∆9-THC- pretreated mice. Both synaptic (left) and extrasynaptic (right) distributions are represented in the two halves of each bisected dendritic segment.
Behavioral changes in adult mice receiving ∆9-THC during adolescence
Locomotor activity of adult mice receiving ∆9-THC during adolescence did not significantly differ (t-test, p > 0.05) from the vehicle controls in the open field or in chambers used for social/novel object testing in which there were no treatment-specific differences in total distance traveled (t(5) = 0.99, p = 0.37) or average speed (t(5) = 0.99, p = 0.37) within the apparatus. There was also no significant interaction between drug treatment and compartment (ambulatory time: (F(1,10) = 3.77, p = 0.081); number of entries: (F(1,10) = 3.82, p = 0.079).
There was a statistically significant effect for ambulatory time: (F(1,10) = 12.07, p = 0.006) and number of entries: (F(1,10) = 11.03, p = 0.008) for the interaction between treatment and contact zone (Fig. 5e, f). There was also a significant main effect of contact zone on ambulatory time (F(1,10) = 9.73, p = 0.011) and number of entries (F(1,10) = 12.84, p = 0.005). On average, mice receiving ∆9-THC as adolescents spent significantly more time in the SOC contact zone (258.43 ± 1.77) compared with controls (182.83 ± 15.30). They also made significantly less entries into the NOV contact zone (41 ± 4.62) compared with vehicle-treated mice (55.5 ± 2.99) (Fig. 5f and track plots in Fig. 5g).
When assessed for spatial working memory in the Y-maze, adolescent vehicle and ∆9-THC-treated mice performed similarly. Treatment groups did not differ significantly in the average percentage of spontaneous alternations made when tested as adults (t(5) = 0.184, p = 0.86). Mice that received vehicle and ∆9-THC during adolescence also showed no significant differences in measures of locomotor activity, as reflected in ambulatory distance traveled (t(5) = 0.25, p = 0.82), stereotypic counts (t(5) = 0.07, p = 0.95), or ambulatory episodes average speed (t(5) = 0.36, p = 0.73).
Our results provides new evidence that the firing pattern of deep-layer PL-PFC neurons in vehicle-injected mice is similar to that previously described in adult rats  and markedly disrupted by chronic adolescent administration of ∆9-THC. The electrophysiological evidence for NMDA receptor hypofunction in these neurons is consistent with the observed decrease in extrasynaptic plasmalemmal density of GluN1 in dendritic profiles of all sizes in medial layers of the PL-PFC, which contain apical dendrites of many deep layer neurons. However, adolescent administration of ∆9-THC also produces a shift in GluN1 distribution from cytoplasmic to plasmalemmal sites in larger dendritic profiles that are major targets of inhibitory terminals that express CB1Rs . These results together with the observed changes in number of axospinous synapses in the PL-PFC of adult mice that received ∆9-THC during adolescence suggest a lasting impact of adolescent ∆9-THC on the emergence of corticolimbic networks controlling adult behaviors as discussed below.
Adult male mice receiving ∆9-THC during adolescence have a higher density of GluN1-labeled axospinous synapses in PL-PFC
We observed an increase in excitatory-type axospinous synapses in the PL-PFC of adult male mice receiving repeated injections of ∆9-THC in an escalating dose schedule similar to that described by Rubino et al. . In this earlier study, adolescent administration of ∆9-THC decreased CB1R and CB1/G-protein activity in hippocampus and amygdala, but not in the PFC of male rats. The downregulation of CB1R signaling in GABAergic terminals presynaptic to glutamatergic output neurons in amygdala and hippocampus, which project extensively to the PL-PFC  may serve to maintain less active dendritic spines normally eliminated during the protracted frontal cortical maturation . The selective formation of dendritic spines contacted by axon terminals expressing presynaptic NMDA receptors and/or elimination of spines contacted by axon terminals lacking these receptors provides an equally plausible explanation for the observed increase in number of dendritic spines in the PL-PFC (see refs. [32, 33] for review). The glial profiles contacting excitatory-type synapse expressing pre-and/or postsynaptic GluN1 may represent sites of relevance to glial control of NMDA receptor-mediated glutamatergic transmission .
The notable increase in axonal distribution of GluN1 following chronic ∆9-THC activation of CB1Rs may reflect diminish endocannabinoid signaling that is implicated in axonal outgrowth and GluN1 polarization in cortical pyramidal cells . The present detection of GluN1 in axon terminals in the PL-PFC of adult mice adds to the growing evidence that GluN1/GluN2B containing NMDA receptors are presynaptic autoreceptors and heteroreceptors in the mature as well as in the developing neocortex . Many of these terminals form asymmetric excitatory-type synapses with dendritic spines and rarely express detectable levels of CB1R immunoreactivity, which is most prevalent in inhibitory-type terminals, some of which also contain GluN1 immunogold. In dually labeled terminals, CB1R-mediated retrograde signaling may oppose the NMDA-evoked release of GABA .
Adolescent ∆9-THC increases plasmalemmal density and decreased cytoplasmic GluN1 immunogold in large dendrites recipient to CB1R terminals
Competitive disruption of CB1R-mediated endocannabinoid signaling may largely account for the observed increase in plasmalemmal and corresponding decrease in cytoplasmic GluN1 in PL-PFC dendrites of adults chronically exposed to ∆9-THC during adolescence. The large size of the affected dendrites is consistent with the known prevalence of CB1R terminals mainly on larger somatodendritic profiles of pyramidal neurons in the cerebral cortex .
The cytoplasmic and plasmalemmal distribution of GluN1 immunogold in dendrites of the PL-PFC confirms and extends earlier studies of GluN1 distribution in normal rodents [39, 40]. Within the cytoplasm, we often detected GluN1 immunogold along membranes of tubulovesicles and outer mitochondrial membranes, which play a key role in regulation of Ca2+ dynamics as well as in the intracellular trafficking, recycling, and degradation of GluN1 [40, 41]. The availability of a cytoplasmic pool of GluN1 subunits on these intracellular membranes may facilitate the regulation of NMDA receptor-mediated glutamatergic transmission in accordance with ongoing activity and stage of development [42, 43].
Repeated ∆9-THC administration during adolescence decreases extrasynaptic plasmalemmal density of GluN1 and NMDA current in PL-PFC neurons of adult mice
There was a significant reduction in GluN1 plasmalemmal and cytoplasmic density in large and the plasmalemma density in small and medium sized dendrites without synaptic contact in the PL-PFC of adult mice chronically exposed to ∆9-THC as adolescence. This suggests that as previously demonstrate for the developmentally regulated GluN2 subunits  GluN1 is internalized and internally sorted through degradative pathways. Our data further indicate that during the sensitive period of adolescent development chronic exposure to ∆9-THC may promote the activation of extrasynaptic NMDA receptors resulting from increased glutamate release. This possibility is supported by our results showing that many of the dendritic profiles without synaptic contacts are opposed to glial processes and/or neighboring excitatory-type axon terminals that are potential sources of glutamate and glycine, a co-agonist of extrasynaptic NMDA receptors , which inhibits surface trafficking of NMDA receptors .
Adolescent exposure to Δ9-THC during adolescence produces behavioral changes aligned with NMDA plasticity in PL-PFC neurons
Adult male mice chronically exposed to increasingly high doses of ∆9-THC during later stages of adolescence spent significantly more time and tended to have more entries into the contact zone around a conspecific stranger mouse. We also observed a significant decrease in NMDA current and plasmalemmal expression of GluN1 in PL-PFC neurons in separate subgroups of adult mice that received adolescent injections of ∆9-THC in a paradigm identical to the one used for testing social interactions. Together these results suggest that exposure to escalating doses of ∆9-THC during late adolescence increases preference for social novelty in adult mice through mechanisms involving downregulation of functional NMDA receptors in PL-PFC, which is similar to that produced by spatial–temporal GluN1 deletion in the medial PFC . However, additional behavioral testing is needed to exclude other possibilities such as decreased social anxiety that also may be influenced by decreased NMDA receptor signaling in output neurons within the PFC .
As opposed to the increase in social interactions in ∆9-THC-pretreated mice, these mice made significantly fewer entries into the contact zone around a novel object without any notable effect on the duration of time spent in this zone. This suggests that adolescent ∆9-THC may decrease exploratory behavior outside of social context, which provides sensory cues that promote lingering in the contact zone.
We observed no significant effect of adolescent administered ∆9-THC on measure of spatial working memory or spontaneous alternations in Y-maze testing of a subgroup of adult mice with identical drug treatment to those showing decreased NMDA GluN1 expression in PL-PFC neurons. The absence of effect on these tasks by a drug treatment that reduced glutamate activity in the PL-PFC is consistent with the know limited effect of cytotoxic PFC lesions on memory-related behaviors in adult mice . These findings contribute to the emerging evidence that the complex cognitive and social behaviors are differentially dependent on output from prefrontal cortical and hippocampal networks . However, there remains the possibility that subtle impairment of cognitive functions in mice receiving adolescent ∆9-THC may have been unrecognized because of the relatively small sample size in our study.
Funding and disclosure
This research was supported by NIDA funding DA042943 to VMP and DA043982 to KM. ∆9-THC was provided by the Drug Supply Program of the National Institute on Drug Abuse (Bethesda, MD, USA). The authors declare no competing interests.
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Pickel, V.M., Bourie, F., Chan, J. et al. Chronic adolescent exposure to ∆9-tetrahydrocannabinol decreases NMDA current and extrasynaptic plasmalemmal density of NMDA GluN1 subunits in the prelimbic cortex of adult male mice. Neuropsychopharmacol. 45, 374–383 (2020). https://doi.org/10.1038/s41386-019-0466-9
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