Opiate abuse and addiction have become a worldwide epidemic with great societal and financial burdens, highlighting a critical need to understand the neurobiology of opiate addiction. Although several studies have focused on drug-dependent changes in neurons, the role of glia in opiate addiction remains largely unstudied. RNA sequencing pathway analysis from the prefrontal cortex (PFC) of male rats revealed changes in several genes associated with oligodendrocyte differentiation and maturation following heroin self-administration. Among these genes changed was Sox10, which is regulated, in part, by the chromatin remodeler BRG1/SMARCA4. To directly test the functional role of Sox10 in mediating heroin-induced behavioral plasticity, we selectively overexpressed Sox10 and BRG1 in the PFC. Overexpression of either Sox10 or BRG1 decreased the motivation to obtain heroin infusions in a progressive ratio test without altering the acquisition or maintenance of heroin self-administration. These data demonstrate a critical, and perhaps compensatory, role of Sox10 and BRG1 in oligodendrocytes in regulating the motivation for heroin.
Drug addiction is a large societal and financial burden on the United States, with more than $190 billion dollars spent annually on costs associated with addiction. Opiate addiction, including heroin use and abuse, has risen by more than 50% in the past decade (Dart et al, 2015), leading to a nationwide opiate epidemic. This is in part due to one of the hallmark characteristics of drug addiction, namely persistent and compulsive drug seeking that leads to relapse. Although studies have progressed our knowledge of how drug use can transition from acute to persistent drug taking, the underlying neuroadaptations that control the motivation to seek the drug remain understudied. A better understanding of the neurobiology underlying these behaviors is critically needed to aid the development of pharmacotherapies.
The uncontrollable drive to seek drugs and the diminished motivation to seek nondrug rewards are trademarks of substance abuse (Goldstein and Volkow, 2002; Goldstein and Volkow, 2011; Kalivas et al, 2005). These behaviors have been attributed to persistent alterations in the prefrontal cortex (PFC), a region directly connected to other key regions of the mesolimbic dopamine reward system (Koob and Volkow, 2010). The PFC is heavily involved in cognition, working memory, and executive function (Kennerley and Walton, 2011), all of which are critical components of drug addiction (Goldstein and Volkow, 2011). Previous studies have demonstrated critical roles for the PFC in drug craving (Capriles et al, 2003; Koya et al, 2006; McFarland et al, 2004; Schmidt et al, 2005), along with encoding reward-related memories (Kalivas et al, 2005), including those specifically related to heroin (Schmidt et al, 2005).
The studies that have begun to dissect the role of the PFC in opiate addiction have primarily focused on neurons, leaving the role of non-neuronal cells (eg, glia) in regulating drug-related behaviors largely understudied (for review, see Cadet and Bisagno, 2014 and Miguel-Hidalgo, 2009). Oligodendrocyte precursor cells (OPCs) are glial stem/progenitor cells within the central nervous system (CNS) that, in response to the expression of various transcription factors, can proliferate and differentiate into oligodendrocytes. These oligodendrocytes support neuronal survival and are essential for efficient action potential propagation (Emery et al, 2009; Fields, 2005; Tognatta and Miller, 2016). Disruptions of OPC and oligodendrocyte gene expression have been implicated in psychiatric diseases such as major depression (Aston et al, 2005; Birey et al, 2015; Liu et al, 2012; Makinodan et al, 2012) and schizophrenia (Iwamoto et al, 2005). Although several studies have documented the involvement of oligodendrocytes in addiction, the focus has been on psychostimulants and ethanol (Arezoomandan et al, 2016; Mandyam et al, 2007; Navarro and Mandyam, 2015; Vargas et al, 2014; George et al, 2008). A more mechanistic and causal role for glia has yet to be explored in the context of heroin exposure.
The aim of this study was to investigate the role of OPC and oligodendrocyte gene expression in the PFC on the motivation to take opiates and drug-taking behaviors. Sox10 is a member of the Sry-related high-mobility group box (Sox) E family of transcription factors and is a lineage marker of oligodendroglia (for review, see Weider and Wegner, 2017) that is functionally important for regulating oligodendrocyte differentiation and myelin induction (Wang et al, 2014). The expression of Sox10 is regulated by the chromatin remodeler BRG1, which has an important role in drug-induced plasticity (Wang et al, 2016). Here we demonstrate that heroin self-administration induces Sox10 expression via BRG1 in the PFC and that its overexpression reduces the motivation to seek heroin.
Materials and methods
Male Sprague–Dawley rats weighing 250–300 g (Envigo Laboratories, Indianapolis, IN) at the beginning of the experiments were housed at 22–25 °C under a 12 : 12 reverse light–dark cycle with lights on at 1800 h and ad libitum access to food and water. Testing took place 7 d/week in the dark portion of the light–dark cycle. All experiments were conducted in accordance with the Institutional Animal Care and Use Committee of The State University of New York at Buffalo.
Solutions of heroin hydrochloride (0.07 mg/ml; generously gifted from the NIDA drug supply program) in 0.9% sterile saline were prepared weekly. The pump durations for infusions were adjusted according to body weight on a daily basis, to ensure the delivery of the correct dose of drug for each animal.
Self-Administration Test Chambers
The experimental chambers have been described elsewhere (Gancarz et al, 2015; Sun et al, 2016; Wang et al, 2016). Briefly, 24 standard Med Associates Inc. (St. Albans, VT) chambers containing two nose-poke holes each with infrared monitoring were used. Two stimulus lights were mounted above each nose-poke hole, with a house light in the center back wall of the test chamber. All chambers are housed in sound-attenuating boxes and controlled through a Med Associates interface.
Jugular Catheterization and Patency
The animals were implanted with chronic indwelling jugular catheters, as previously described (Gancarz et al, 2015; Wang et al, 2016). To preserve patency, the catheters were flushed daily with 0.2 ml of heparinized saline (50 IU/ml) containing enrofloxacin (4 mg/ml). Catheter patency was tested once per week throughout the duration of the experiments by observing behavioral responses (loss of righting reflex and muscle tone) to an injection of ketamine hydrochloride (5 mg/ml in 0.5 ml, i.v.). Only data from rats with patent catheters were included in analyses.
The rats were trained to self-administer heroin (0.02 mg/kg/inf) or saline for 3 h each day for a total of 10 d beginning 1 week after jugular catheter surgery. Responses in the active nose-poke holes resulted in an infusion of drug, followed by a 20 s time-out period using a fixed ratio (FR) 1 schedule of reinforcement; this was increased daily from the first day to the third to an FR3 schedule, which was maintained for the remainder of the experiment. Responses in the inactive hole had no programed consequences. Following each self-administration session, the catheters were flushed and the rats were returned to the colony room. Twenty-four hours after the last self-administration session, the rats were rapidly decapitated and their brains were collected and sectioned into 1 mm-thick sections. From the prefrontal cortical regions (according to Paxinos and Watson, 2005), 2 mm-diameter biopsy punches were taken, ensuring that cortical tissue devoid of callosal fibers was reliably obtained.
Viral Overexpression of Sox10 and BRG1 in the PFC
Lentiviral vectors encoding either Sox10-HA or mCherry (lenti-Sox10 or lenti-mCherry, respectively) under the control of an EF1α promoter were prepared as previously described (Wang et al, 2014). In addition, we also utilized a lentiviral vector encoding BRG1-Flag under the control of the Sox10:MCS5 promoter (Wang et al, 2014; VectorBuilder) for glial lineage expression (lenti-BRG1); all virus titers were >1.0 × 107. The rats were assigned to receive prelimbic PFC injections of lenti-mCherry, lenti-Sox10, or lenti-BRG1; the injectors were set at a 10° angle with coordinates of AP, +3.2; ML, +1.2; and DV, −3.2 mm (Paxinos and Watson, 2005). The viruses were manually infused over 10 min (0.2 μl/min, total infusion volume of 2 μl), and the needles were left in place for 10 min to allow for diffusion. Lenti-mCherry was injected to serve as the control for behavioral and cellular changes that are normally induced by heroin self-administration. The animals were allowed 1 week to recover before jugular catheter implantation, which was conducted as previously described.
Heroin Self-Administration and Progressive Ratio After Sox10/BRG1 Overexpression
The animals were trained to self-administer heroin as described above, with the exception that the FR schedule was gradually increased from FR1 to FR10 over 13 days of training. After training, the animals were allowed to self-administer heroin on a progressive ratio (PR) schedule of reinforcement for 6 h. The session ended if no infusions were delivered within 1 h of the last infusion. The schedule of delivery increased after each infusion, using the progression 1, 2, 3, 4, 6, 8, 12, 24, 32, 48, etc. (Gancarz et al, 2012). After testing, the catheters were flushed with heparin-saline and the animals were returned to the colony room.
Cue-Induced Reinstatement After Sox10 Overexpression
A separate group of animals were trained to self-administer heroin, as described above. Extinction tests were initiated 24 h after the last training session, as previously described (Wang et al, 2016). Briefly, the rats were placed in dark experimental chambers and their responses were recorded but resulted in no programmed consequence. Extinction sessions continued until responding fell to fewer than 20 responses per session. Twenty-four hours after the last extinction session, the animals were placed back in the chambers for a 1 h cue-induced reinstatement test, during which the active responses produced cues previously paired with drug delivery.
RNA libraries were prepared using the Illumina TruSeq RNA library preparation kit and sequenced on the Illumina HiSeq 2500 system. A 50-cycle single-end flow cell was used. Alignments were performed against the RN5 (rat) genome built using the Tophat (version 2.0.13) alignment algorithm and the UCSC refGene annotation set. Differential expression analysis was performed using Cuffdiff under default parameters.
PFC tissue punches were homogenized in 25 mM Tris (pH 8.0) buffer with 0.25 M sucrose. Samples of extracted protein (30 μg) were loaded on 4–15% gradient Tris- SDS polyacrylamide gels for separation via electrophoresis and were then transferred to a nitrocellulose membrane and blocked in 5% nonfat milk or bovine serum albumin (BSA). All membranes were incubated overnight at 4 °C. The primary antibodies were diluted in blocking buffer (Rockland Immunochemicals, Inc., Limerick, PA), including rabbit anti-Sox10 (1 : 100; Santa Cruz Biotechnology, Dallas, TX), rabbit anti-BRG1 (1 : 2000; Abcam, Cambridge, MA), and mouse anti-β-actin (1 : 10 000; Cell Signaling Technologies, Inc., Danvers, MA). The membranes were incubated for 1 h at room temperature with IRDye secondary antibodies (1 : 5000; LI-COR, Inc., Lincoln, NE). The membranes were imaged using an Odyssey infrared imaging system (LI-COR, Inc.) and quantified by densitometry using ImageJ (National Institutes of Health, Bethesda, MD) with normalization to the β-actin loading control.
Twenty-four hours after the last self-administration session, rats were deeply anesthetized using Fatal Plus (Vortech Pharmaceuticals; 1 ml/kg, i.p.) and then transcardially perfused first with a solution containing 1 U/ml heparin in sterile phosphate-buffered saline (PBS) followed by 4% formaldehyde. Whole brains were stored in a 15% sucrose solution for 24 h and then transferred to a 30% sucrose solution for 48 h; after sucrose cryoprotection, the brains were stored at −20 °C until dissection. Coronal sections encompassing the PFC (+3.7 to +2.5 from bregma based on Paxinos and Watson, 2005) were sliced on a cryostat at a thickness of 30 μm, and every third section was collected; tissue sections containing the PFC were stored in sterile PBS containing 0.01% sodium azide at 4 °C until further use. The sections were first incubated in a blocking solution containing 50% normal donkey serum (Jackson ImmunoResearch), 5% BSA fraction V (Gibco), and 0.5% Triton X-100 for 1 h at room temperature and then incubated overnight at 4 °C in primary antibody (1 : 500 anti-rabbit oligodendrocyte transcription factor-2 (Olig 2; no. 9610) or 1 : 400 anti-rabbit HA (no. 05-904), EMD Millipore) diluted in a solution containing 25% normal donkey serum, 2.5% BSA fraction V, and 0.5% Triton X-100. After washing in PBS with Tween 20, the sections were incubated in blocking buffer for 1 h at room temperature and then 1 h at room temperature in secondary antibody (goat anti-rabbit IgG 488 (no. A 11034) or goat anti-mouse IgGγ3 594 (no. A 21155), Invitrogen) in a solution containing 25% normal donkey serum, 2.5% BSA fraction V, and 0.5% Triton X-100. Sections were mounted with Vectashield (H-1200; Vector Labs, Burlingame, CA) and were imaged with a × 20 objective on an LSM 510 Meta confocal microscope; images were taken and scored by an investigator blinded to the experimental conditions.
Chromatin Immunoprecipitation-Quantitative PCR
Chromatin Immunoprecipitation (ChIP) was performed for BRG1 as previously described (Gancarz et al, 2015; Wang et al, 2016) with minor modifications. Briefly, two PFC punches from two rats taken 24 h after the last self-administration session were pooled for each sample (n=1). These punches were immediately fixed in 1% formaldehyde for 12 min and then quenched in 2 M glycine for 5 min. Chromatin was sheared using a Biorupter 300 (Diagenode Diagnostics, Seraing, Belgium) at 4 °C at a high sonication intensity for 30 s on and 30 s off for 10 min followed by a 10 min rest, which was repeated a total of three times. Chromatin fragment sizes of 250–1000 bp were verified using agarose gel electrophoresis. Magnetic sheep anti-rabbit beads (Invitrogen of Thermo Fisher Scientific, Waltham, MA) were incubated with anti-BRG1 antibody rotating overnight at 4 °C. After washing, 70 μl of the magnetic bead/antibody slurry was incubated with the sheared chromatin for 16 h at 4 °C; 5% of the sheared chromatin was saved as an input control. Samples were washed with LiCl and Tris-EDTA buffer. Reverse cross-linking took place overnight at 65 °C and proteins and RNA were removed using proteinase K (Invitrogen) and RNase (Roche, Basel, Switzerland), respectively. DNA was purified using a DNA purification kit (Qiagen, Hilden, Germany). Immunoglobulin G was used to control for nonspecific binding. Quantitative PCR (qPCR) was performed to identify the binding of BRG1 to proximal promoter regions of the Sox10 gene and to NFκB (forward, 5′-GAGCAGAGAGGACCTTCCCT-3′; reverse, 5′-CCGTCCGCCCGTCGCCCGTC-3′) and Smad3 (forward, 5′-GCTGTAAGACCACCACTCCT-3′; reverse, 5′-TGTCTCTCGTCTCTCCTGG-3′). Amplification reactions were run in triplicates with iQ SYBR green (Bio-Rad Laboratories, Inc., Hercules, CA), and each sample was normalized to an immunoglobulin G control. Fold changes were calculated relative to the saline control.
All statistical analyses were performed using Prism (GraphPad Software, Inc., La Jolla, CA). Differences in self-administration were analyzed by two-way repeated measures analyses of variance (ANOVAs). Differences in behavioral responding during the PR test were analyzed using a one-way ANOVA. The ANOVA was followed-up with an appropriate post-hoc test corrected for multiple comparisons when interactions were indicated. Differences in western blot and qPCR results and cell counts were analyzed using Student’s t-tests. The criterion for statistical significance was a P-value of <0.05. All data are presented as means±SEMs.
Upregulation of Myelin-Associated Genes Following Heroin Self-Administration
Rats were trained (3 h/d for 10 d) to nose poke for an intravenous infusion of saline or heroin (Figure 1a; two-way repeated-measures ANOVA, drug effect: F1,140=215.8, P<0.001; session effect: F9,140=4.988, P<0.001; interaction effect: F9,140=2.115, P=0.0320). To analyze gene expression following heroin self-administration, RNA-sequencing (RNA-seq) was performed on PFC tissue punches taken 24 h after the last heroin exposure. A pathway analysis of RNA-seq results revealed an upregulation of glial cell differentiation and myelination pathways following heroin self-administration (Figure 1b; Supplementary Table S1) (Stolt et al, 2002), including a significant regulation of the key transcription factor Sox10 (saline vs. heroin, log fold change (logFC)=−0.826, P<0.01, n=3/group). In addition, a number of genes upregulated following heroin self-administration, such as those encoding myelin basic protein (MBP) and myelin proteolipid protein, are under the control of Sox10 (Lee et al, 2008; Srinivasan et al, 2012), suggesting a key regulatory role for Sox10 in opiate-induced changes in glial pathways.
Regulation of Sox10 in the PFC Following Heroin Self-Administration
To examine whether the enrichment of Sox10 mRNA was leading to an increase in protein, we examined Sox10 protein via western blot analysis 24 h after the last heroin exposure (Figure 2a; two-way repeated-measures ANOVA, drug effect: F1,214=296.1, P<0.0001; session effect: F9,214=4.313, P<0.001; interaction effect: F9,214=3.17, P=0.0013). Sox10 protein expression was increased in the PFC compared with that from saline controls (Figure 2b; Student’s t-test, t9=1.834, P=0.049; n=5–6/group), with no changes in the nucleus accumbens (NAc; Supplementary Fig. S1; Student’s t-test, t9=0.639, P>0.05; n=5–6/group). BRG1, a chromatin remodeler of the SWI/SNF complex, has been reported as a critical epigenetic mediator in the expression of Sox10 and in OPC differentiation and has been implicated in the epigenetic and transcriptional adaptions that occur after exposure to drugs of abuse (Bischof et al, 2015; He et al, 2016; Wang et al, 2016; Yu et al, 2013). Following heroin self-administration, BRG1 protein expression in the PFC was increased compared with that from control saline animals (Figure 2c; Student’s t-test, t9=2.989, P=0.015; n=5–6/group). To directly evaluate the transcriptional regulation of Sox10 mediated by BRG1 after heroin exposure, we performed a quantitative ChIP assay. Previous studies have demonstrated that BRG1 and NFκB form a transcriptional complex to regulate glial cell differentiation (Limpert et al, 2013); we sought to investigate if BRG1 was binding at NFκB sites to regulate Sox10 expression after exposure to heroin. We found there was an increase in BRG1 binding at NFκB binding elements on the Sox10 promoter compared with that from saline controls (Figure 2d; Student’s t-test, t11=2.509, P=0.014; n=5–8/group). In addition, given the known role of the BRG1-Smad3 complex in regulating responses to drugs of abuse (Wang et al, 2016), we next examined BRG1 binding at Smad3 DNA-binding sites and found that this interaction was indeed increased following heroin self-administration (Figure 2e; Student’s t-test, t11=1.832, P=0.047; n=5–8/group) compared with that from saline controls.
Overexpression of Sox10 in the PFC Decreases the Rewarding Effects of Heroin
To examine the cellular consequences of manipulating Sox10 directly and via BRG1, we stereotaxically microinjected lentiviruses harboring transcripts for mCherry, Sox10, or Sox10-specific BRG1 (Figure 3a) into the prelimbic region of the PFC (Figure 3b). As expected, the Sox10-specific BRG1 lentivirus increased the expression of BRG1 protein (Figure 3c; Student’s t-test, t10=1.846, P=0.047; n=5–7/group) as well as Sox10 (Figure 3d; Student’s t-test, t10=2.23, P=0.049; n=5–7/group) compared with that from lenti-mCherry controls. Furthermore, compared with that from lenti-mCherry controls, intra-PFC injections of lenti-Sox10 increased the density of cells positive for Olig2, a transcription factor marker for the oligodendrocyte lineage (Weider et al, 2015) (Figure 3e; Student’s t-test, t6=1.955, P=0.049; n=5–6/group). Behaviorally, the overexpression Sox10 or BRG1 (via lenti-Sox10 or lenti-BRG1, respectively) did not result in any differences in the acquisition of heroin taking as measured by the number of infusions per test session across days of training (Figure 4a; two-way repeated-measures ANOVA, all P-values <0.05, n=7–8/group). We next sought to determine whether the viral-mediated changes in BRG1 and Sox10 expression could alter the motivation to take heroin. To this end, animals were tested in a PR paradigm, which is thought be a model of motivation for obtaining a reinforcer (Pelloux et al, 2007). There was a main effect of viral manipulation on the number of active responses during the PR paradigm (Figure 4b; F2,17=16.19, P=0.0001, n=7–8/group). A post-hoc analysis determined that the overexpression of Sox10 or BRG1 in the prelimbic PFC resulted in fewer responses in the active hole (P<0.01 for both lenti-Sox10 and lenti-BRG1). Furthermore, this reduction in active responding resulted in significantly fewer infusions of heroin (Figure 4c; main effect of virus: F2,17=11.89, P=0.0006, n=7–8/group), which was different in the lenti-Sox10 (P<0.05) and lenti-BRG1 (P<0.01) animals compared with that in lenti-mCherry controls, and a lower breakpoint (Supplementary Fig. S2; main effect of virus: F2,17=12.47, P=0.0005), which also differed in lenti-Sox10 and lenti-BRG1 animals compared with that from the lenti-mCherry controls (both P<0.01). Importantly, there were no differences in inactive responses (all P>0.05). In a separate group of animals, we found no changes in the responding of lenti-Sox10 animals during a cue-induced reinstatement test compared to that from lenti-mCherry controls (Supplementary Fig. S3; Student’s t-test, t13=1.846, P=0.730; n=7–8/group).
Drug-induced neuronal cellular plasticity within the mesolimbic dopamine circuit is a well-established pathogenesis of the addicted phenotype (for review, see Lüscher, 2013 and Russo et al, 2010). Here we document a role for the less-studied glial cells in regulating addiction-like behavior after exposure to heroin.
After heroin self-administration, there is an upregulation in transcripts from cellular pathways associated with glial cell differentiation and myelination in the PFC. Oligodendrocytes provide the myelin sheaths in the CNS that reduce the ATP energy requirement for restoring ion gradients in axonal fibers, while enhancing the speed of propagating signals (Nave, 2010). Some studies have begun to dissect the role of glial cells in addiction (for review see Miguel-Hidalgo, 2009), documenting a decrease in myelination within discrete regions of the mesolimbic dopamine system with exposure to cocaine and alcohol (Albertson et al, 2004; Kovalevich et al, 2012; Lewohl et al, 2000). In addition, Mandyam et al (2007) found that both short- and long-access methamphetamine self-administration reduced the number of OPCs in the medial PFC positive for the neural/glial antigen 2 marker, which would suggest there are fewer cells available to differentiate into mature myelinating oligodendrocytes.
Initial in vitro studies on the effects of opiates on oligodendroglial cells found that not only do oligodendroglial cells express the opioid receptors, but opiates have differential effects on cellular processes, including mitogenesis, DNA synthesis, and chromatin remodeling (Hauser et al, 1993; Knapp et al, 1998; Oguri et al, 1976). In vivo studies have shown an increase in MBP expression and other markers of mature oligodendrocytes in the NAc of pups from buprenorphine-treated mothers (Eschenroeder et al, 2012; Sanchez et al, 2008). Similarly, Vassoler et al (2017) identified a dysregulation of MBP in this region in the first- and second-generation offspring from a mother exposed to morphine during adolescence. To our knowledge, our study is the first to investigate the effects of opiates on adult OPCs in the PFC, and the adaptations we observed represent an understudied form of adult CNS plasticity that mediates behavioral outcomes such as drug taking.
Whereas psychostimulants such as methamphetamine are known to decrease myelin gene expression in the PFC (Mandyam et al, 2007), we found that the exposure to opiates increases the expression of oligodendrocyte lineage genes. It is interesting that both drug classes produce addiction-like behaviors in rodents, but the underlying neurobiological mechanisms mediating these behaviors appear to differ (Badiani et al, 2011).
Heroin self-administration leads to an increase in the expression of the SWI/SNF chromatin remodeler BRG1, which was previously shown to have an important role in regulating the expression of Sox10 (Stolt et al, 2002) and myelin-associated genes (Bischof et al, 2015; Limpert et al, 2013; Marathe et al, 2013). Consistent with this, we demonstrate that BRG1 binding at the promoter of Sox10 is increased at both the NFκB and Smad3 DNA-binding sites, suggesting that these transcriptional complexes may be critical for regulating the cellular plasticity induced by drugs of abuse (Gancarz et al, 2015, Wang et al, 2016). The BRG1-mediated increase in Sox10 expression in the PFC may represent a neuroprotective mechanism to compensate for heroin-induced changes in white matter (Li et al, 2013), as we do not see this increase in other areas of the mesolimbic dopamine system with low amounts of white matter, such as the NAc. Sox10 overexpression might potentiate the survival and integration of new oligodendrocytes, surpassing that induced by heroin, resulting in a greater abundance of Olig2+ cells in animals injected with lenti-Sox10 than in lenti-mCherry controls.
The observed increases in Sox10 expression and the number of oligodendroglial lineage cells represent cellular plasticity within the PFC induced by heroin. This plasticity is observed as a change in the behavioral responses that characterizes the self-administration model of addiction. Surprisingly, overexpression of Sox10 did not exacerbate drug taking but rather attenuated the motivation to obtain the drug. This suggests that glial plasticity may occur as an attempt to compensate for heroin-induced changes. The medial portion of the PFC is known to have a direct role in modulating inhibitory control, which is disrupted in drug addiction and many other psychiatric disorders (Volkow et al, 2003). The prelimbic area has a critical role in encoding the value of rewards (Baldo, 2016) and is heavily involved in action-outcome associations (Gourley et al, 2010), such as during the PR test in which the value of the reward (drug) diminishes as the effort to obtain it increases. We found that an increase in Sox10 either by viral overexpression directly or via lenti-BRG1 reduced the numbers of active responses and infusions earned, as well as the breakpoint, which indicates a reduction in motivation. These overexpression effects were specific for motivation, as we did not see any changes in a cue-induced reinstatement paradigm, an animal model of drug craving. Previous studies have shown discrepancies in responding between PR and FR schedules (O'Connor et al, 2010; Ramirez-Nino et al, 2013), and this may be due in part to the brain regions regulating the behaviors involved. For example, we saw an increase in Sox10 expression in the PFC, which is heavily involved in regulating motivated behaviors (PR schedule of reinforcement, Koob and Volkow, 2010), whereas there was no change in the NAc, a region heavily implicated in regulating responses to drug-associated cues (FR schedule of reinforcement, Wang et al, 2016). Although previous studies have implicated the PFC in other aspects of addicted-like behaviors (ie, relapse and reinstatement; McFarland et al, 2004), the data presented here shows a specificity for Sox10 in regulating motivated behaviors in the PFC, highlight a possible divergence of OPC-mediate anatomical pathways regulating opiate-induced behaviors (Gourley and Taylor, 2016). These findings are of great importance, as addiction is epitomized by long-lasting maladaptive neuroadaptations that drive the motivation to seek more drug (Mandyam and Koob, 2012), and thus shed further insight into OPC mediated mechanism driving these behaviors.
Importantly, previous data form our lab demonstrated that BRG1 is regulated in the NAc after exposure to drugs of abuse (Wang et al, 2016). The regulation of Sox10 through BRG1 in combination with viral vector in which BRG1 expression is under control of the Sox10-enhancer promoter further supports a critical role for BRG1 in OPCs dependent plasticity following heroin. Although we cannot exclude the possibility that the effects on BRG1 after heroin exposure are from cell types other than OPCs, our work here demonstrates a critical role of BRG1 in oligodendroglial lineage cells in the PFC. The studies presented here, along with our previous work (Wang et al, 2016), highlight a cell type and brain regions specific role for BRG1 in mediated drug-induced behavioral and cellular plasticity.
How the increases in Sox10 expression and the number of oligodendroglial lineage cells translate to the observed behavioral plasticity requires further investigation. Birey et al (2015) demonstrated that ablation of OPCs in the PFC induced a neuropsychiatric (depression-like) phenotype, suggesting their importance in maintaining proper neural function. Therefore, following heroin self-administration, it is possible that Sox10 is stabilizing the OPC pool in the PFC, which may be secreting neurotrophic factors known to influence the activity and survival of surrounding neuronal cells (Du and Dreyfus, 2002), possibly including GABAergic interneurons. In addition, it is possible that oligodendrocytes are providing metabolic support to inhibitory axons (Lee et al, 2012), thus modifying their connectivity to other limbic structures. These cells may also be incorporated in ongoing adult myelination in the PFC (Norton and Poduslo, 1973), which is important for neuronal function as demonstrated by Xiao et al (2016), who demonstrated oligodendrocytes facilitate, and are key in the learning of new behaviors. The emergence of a compensatory mechanism may represent a fine-tuning of the system, a process that can be seen with exposure to other drugs of abuse, such as cocaine, which leads to neuroadaptations that unmask changes in both behavioral responses and cellular plasticity (LaPlant et al, 2010; Renthal et al, 2007).
The findings reported here reveal a novel mechanism of adult cellular plasticity within the CNS after chronic heroin exposure. Taken together, this and other studies deepen our understanding of potential areas of study towards a future therapeutic intervention for addiction.
Funding and disclosure
This work was supported by the National Institutes of Health (no. NIDA R01DA037257 to DMD, NIDA R01DA037257-S1 to JAM, NMSS RG 5505-A-2 to FJS, NCATS UL1TR001412 to JJP, and NIGMS R25GM09545902). The heroin used in these studies was generously gifted by the NIDA Drug Supply Program. The authors declare no conflict of interest.
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We thank Neneyo Mate-Kole for his assistance in cell counting and Moriah M. Cobb for her assistance in carrying out western blot experiments.
Supplementary Information accompanies the paper on the Neuropsychopharmacology website
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Martin, J., Caccamise, A., Werner, C. et al. A Novel Role for Oligodendrocyte Precursor Cells (OPCs) and Sox10 in Mediating Cellular and Behavioral Responses to Heroin. Neuropsychopharmacol. 43, 1385–1394 (2018). https://doi.org/10.1038/npp.2017.303
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