Although the protective effects of social bonds on drug use/abuse have been well documented, we know little about the underlying neural mechanisms. Using the prairie vole (Microtus ochrogaster)—a socially monogamous rodent that forms long-term pair bonds after mating—we demonstrate that amphetamine (AMPH) conditioning induced a conditioned place preference (CPP) in sexually naïve (SN), but not pair-bonded (PB), males. Although AMPH treatment induced a similar magnitude of DA release in the nucleus accumbens (NAcc) of SN and PB males, it had differential effects on NAcc D1 receptor (D1R) binding. Specifically, AMPH treatment increased D1R binding in SN, but decreased D1R binding in PB males. NAcc D1R, but not D2R, antagonism blocked AMPH-induced CPP in SN males and NAcc D1R activation prior to AMPH conditioning enabled AMPH-induced CPP in PB males. Together, our data demonstrate that pair bonding experience decreases the rewarding properties of AMPH through a D1R mediated mechanism.
It is well recognized that drug use and abuse have profound consequences on a variety of social behaviors, including social bonding (Young et al., 2011a). Reciprocally, social factors, such as the presence or absence of strong social attachments during development or throughout adulthood, may impact drug use and the vulnerability to drug abuse. For example, strong adolescent-parent attachments have been associated with decreased odds of substance use problems (Ellickson et al., 1999; Bell et al., 2000). Additionally, in individuals who are already addicted, close relationships between spouses aid in recovery from drug addiction (Kosten et al., 1987). In contrast, weak social attachments may increase substance abuse vulnerability as insecure adult attachment styles are positively associated with alcohol and illicit substance abuse (Brennan and Shaver, 1995; Vungkhanching et al., 2004; Caspers et al., 2005).
The neural mechanisms underlying the interaction between social bonding and drug use/abuse are still largely unknown, however, the mesolimbic dopamine (DA) system—particularly DA neurotransmission within the nucleus accumbens (NAcc)—may be involved (Young et al., 2011a). Studies in the prairie vole (Microtus ochrogaster)—a socially monogamous rodent that forms enduring bonds between adult mates (i.e., pair bonds) (Insel and Hulihan, 1995; Mattson et al., 2001)—have shown that NAcc DA mediates both the formation and maintenance of pair bonds (Gingrich et al., 2000; Aragona et al., 2003; Aragona et al., 2006). Additionally, NAcc DA neurotransmission is activated by all known drugs of abuse (Di Chiara and Imperato, 1988; Bergman et al., 1990; Koob and Nestler, 1997; Nestler, 2005) and repeated psychostimulant drug exposure alters DA release and receptor sensitivity as well as the morphology of NAcc neurons (Henry et al., 1989; Robinson and Kolb, 1999). These changes are thought to underlie drug-induced modifications in behaviors (Robinson and Becker, 1986), including social behaviors (Fiorino and Phillips, 1999).
As both pair bonding behavior and its regulation by DA neurotransmission within the NAcc have been well characterized in the prairie vole (Gingrich et al., 2000; Aragona et al., 2003; Aragona et al., 2006), recent efforts have been made to establish this species as an animal model in which to examine the behavioral interaction between social bonding and drug use/abuse, as well as its underlying neural mechanisms. AMPH has been shown to have rewarding properties in prairie voles, as AMPH conditioning induces a conditioned place preference (CPP) in both sexes (Aragona et al., 2007; Liu et al., 2010; Young et al., 2011b), and this process is mediated by DA neurotransmission in the NAcc (Curtis and Wang, 2007; Liu et al., 2010). Most interestingly, repeated AMPH exposure inhibits the formation of mating-induced partner preferences in male prairie voles and this AMPH-induced impairment of pair bonding is regulated—at least in part—by NAcc DA D1-type receptor (D1R) activation (Liu et al., 2010). In the present study, we investigated the effects of pair bonding experience on AMPH-induced CPP. We hypothesized that pair bonding experience would decrease the rewarding effects of AMPH and that NAcc DA may be involved in this behavioral phenomenon.
MATERIALS AND METHODS
Subjects were male prairie voles (M. ochrogaster) from a laboratory breeding colony. Subjects were weaned at 21 days of age and housed in same-sex sibling pairs in plastic cages (12 × 28 × 16 cm). Water and food were provided ad libitum. All cages were maintained under a 14:10 light-dark cycle and the temperature was kept at 20°C. Subjects around 75 days of age were either continuously housed with their same-sex sibling (and thus kept sexually naïve (SN)) or paired with an unrelated intact female for two weeks to become pair bonded (PB). Both SN and PB subjects were tested at about 90 days of age.
AMPH conditioning and CPP testing
These procedures were performed as previously described (Liu et al., 2010; Young et al., 2011b). Briefly, the testing apparatus for CPP consisted of two cages (12 × 28 × 16 cm); one black with a metal top and one white with a mesh top, joined by a hollow tube (7.5 × 16 cm). Although prairie voles generally tend to prefer the white over the dark cage (Aragona et al., 2007), there are a great deal of individual differences in this preference. Therefore, on day 1, we tested all subjects for their initial cage preferences during a 30 min pre-test. During this test, all subjects were allowed free access to both cages and we quantified the amount of time each individual spent in each cage. On days 2–4, subjects received two 40 min conditioning sessions, 6 hrs apart from one another. In the morning session, subjects received 1.0 mg/kg AMPH (Sigma, St. Louis, MO, USA) dissolved in 0.9% saline (SN-AMPH and PB-AMPH groups) or saline alone (SN-saline and PB-saline groups) and were placed into the cage in which they spent less time during the pre-test (conditioned cage). In the afternoon session, all subjects received an injection of saline and were placed into the other cage. On day 5, subjects were tested again for cage preferences in a 30 min post-test. Immediately after the post-test, subjects were rapidly decapitated and their brains were frozen on dry-ice. Brain sections were subsequently processed for D1R and DA D2-type receptor (D2R) autoradiographic binding.
Brain microdialysis and HPLC-ECD analysis
Microdialysis probes were constructed as previously described (Curtis and Wang, 2007) and were implanted into the left NAcc (stereotaxic coordinates from bregma: anterior 2.1 mm, lateral 0.6 mm, ventral 6.3 mm) under sodium pentabarbitol anesthesia (1mg/10kg body weight). Animals were allowed to recover overnight and were then tested the following morning. Probes were perfused continuously at 2.3 µl/min with a solution isotonic for sodium, potassium, calcium and magnesium (144 mM NaCl, 2.8 mM KCl, 1.2 mM CaCl2 and 0.9 mM MgCl2 (Sved and Curtis, 1993)).
Following overnight recovery, four 20 min baseline samples were collected into vials containing 5µl of 0.1N perchloric acid. Thereafter, subjects received an intraperitoneal (ip) injection of AMPH (1.0mg/kg) and dialysate samples were continuously collected at 20 min intervals for 3 hrs. Dialysate samples were immediately frozen at −80°C until analyzed. The amounts of DA and DOPAC in each sample were determined using high performance liquid chromatography with electrochemical detection (HPLC-ECD) as described previously (Curtis and Wang, 2007). At the end of the sampling period, subjects were sacrificed to assess probe placement.
DA receptor autoradiography
Coronal brain sections (20 µm) at 120-µm intervals were processed for DA receptor autoradiographic binding using an established method (Aragona et al., 2006). Briefly, sections were rinsed in 50 mM Tris-HCl (pH 7.4) and incubated in 50 mM Tris-HCl ion buffer containing 120 mM NaCl, 5 mM KCl, 2 mM CaCl2 and 1 mM MgCl2 with either [125I]SCH23982 (D1R ligand) or [125I]2’-iodospiperone (D2R ligand) (PerkinElmer). Thereafter, sections were fixed in 0.1% paraformaldehyde and rinsed thoroughly in Tris-HCl ion buffer. Slides were dipped in distilled water, blown dry and exposed to BioMax MR film (Kodak) to generate autoradiograms. The optical densities of D1R and D2R binding in the NAcc and CP were quantified in 3 anatomically matched brain sections per animal from autoradiograms using a computerized image program (NIH IMAGE 1.64).
Stereotaxic cannulation and microinjection
Subjects were anesthetized with sodium pentobarbital and 26-gauge bilateral stainless steel cannulae (Plastics One Inc., Roanoke, VA) were stereotaxically implanted and aimed at the NAcc, as described previously (Aragona et al., 2003). Subjects were allowed to recover for 3–7 days. On each of the 3 days of conditioning, 30 min prior to AMPH injections, subjects received microinjections of either artificial cerebrospinal fluid (CSF; 200nl/side) or CSF containing the D1R agonist, SKF 38393, the D1R antagonist, SCH 23390, or the D2R antagonist, eticlopride (Sigma, St. Louis, OH). After CPP testing, all subjects were rapidly decapitated and their brains were extracted to verify injection sites histologically. Subjects with misplaced cannulae were excluded from data analysis.
Data quantification and statistical analysis
CPP was determined by a paired-samples t test comparing the time that subjects spent in the conditioned cage between pre- and post-tests. Cage entries between pre- and post-tests were also analyzed by a t test to assess whether AMPH or a D1R agonist or D1R or D2R antagonist affected locomotor activity. Absolute amounts of baseline DA and DOPAC in dialysates were compared between groups using a t test. For assessment of AMPH effects across time, the amounts of DA and DOPAC in each baseline and post-AMPH sample were expressed as a percentage of the mean baseline amount. These values then were analyzed by repeated measures ANOVA followed by a Student-Neuman-Keuls (SNK) posthoc test. Finally, group differences in the densities of D1R and D2R binding in the NAcc and CP were analyzed by a two-way ANOVA followed by a SNK posthoc test.
Experiment 1 was designed to reveal the effects of pair bonding experience on AMPH-induced CPP. SN and PB males were pre-tested in the CPP apparatus. They were then divided into 4 groups that received injections of saline (n=5 for SN and n=9 for PB males) or AMPH (1.0mg/kg; n=8 for SN and n=8 for PB males) during morning conditioning sessions over the next three days (Liu et al., 2010). Thereafter, all subjects received a CPP post-test.
Experiment 2 compared AMPH-induced DA release in the NAcc between SN (n=6) and PB (n=5) males. Subjects were implanted with a microdialysis probe aimed at the NAcc. After overnight recovery with continuous perfusion of an isotonic solution through the probes, four 20 min baseline dialysate samples were collected. Thereafter, subjects received an ip injection of AMPH (1.0mg/kg) and dialysate samples were continuously collected every 20 mins for 3 hrs. These samples were subsequently analyzed for DA and 3,4-Dihydroxyphenylacetic acid (DOPAC) concentrations using HPLC-ECD analysis (Curtis and Wang, 2007).
Experiment 3 examined the effect of interactions between pair bonding and AMPH treatment on DA receptor binding in the NAcc. Brain sections from the subjects tested in Experiment 1 were processed for D1R and D2R binding using receptor autoradiography.
Experiment 4 tested the role of NAcc DA receptors in AMPH-induced CPP. SN males were implanted with guide cannulae bilaterally aimed at the NAcc. After a 3 d recovery, subjects received a CPP pre-test and were then randomly assigned into one of 5 experimental groups that received intra-NAcc injections of CSF (n=8) or CSF containing a low (4ng/side; n=8) or high (100ng/side; n=6) dose of a D1R antagonist, SCH 23390, or a low (4ng/side; n=8) or high (100ng/side; n=7) dose of a D2R antagonist, eticlopride. Thirty-mins later, subjects received an injection of AMPH (1.0mg/kg; ip). This procedure was repeated for 3 consecutive days during AMPH conditioning. Thereafter, subjects received a CPP post-test.
Experiment 5 examined the role of NAcc D1Rs in mediating AMPH-induced CPP in PB males. PB subjects were divided into three groups that received intra-NAcc injections of CSF (n=10) or CSF containing a D1R agonist, SKF 38393 (0.4ng/side; n=12), or a D1R antagonist, SCH 23390 (4ng/side, n=10), prior to AMPH conditioning. Brain cannulation, AMPH injections, and CPP tests were the same as described in Experiment 4.
Pair bonding experience decreases the rewarding properties of AMPH
In our previous study, AMPH treatment impaired mating-induced partner preferences in male prairie voles, indicating an inhibitory effect of AMPH exposure on pair bonding behavior (Liu et al., 2010). In the present study, we tested the reciprocal relationship: the effects of pair bonding experience on AMPH reward. Three days of conditioning with 1.0 mg/kg AMPH induced a CPP in SN males (t = 2.45, p < 0.05) but not in males that had been paired with a female for 2 weeks (i.e., PB males) (Figure 1a). Saline injections had no effect in either group. Importantly, no differences were found in the frequencies of animal’s cage crossing between pre- and post-tests, suggesting that impaired CPP in PB males was not due to altered locomotor activity during the behavioral test (Figure 1b).
AMPH treatment induces DA release in the NAcc in both SN and PB males
There were no significant differences between SN and PB males in the absolute amounts of DA or DOPAC in microdialysis baseline samples (Figure 2, insets). AMPH administration produced significant increases in extracellular DA (F(12, 108) = 8.42, p < 0.001). However, the magnitude and duration of these increases did not differ between SN and PB males—DA levels were significantly higher than baseline in both groups for each of the first two sampling periods (40 min total) and then slowly returned to baseline (Figure 2, top panel). AMPH administration significantly decreased extracellular DOPAC in the NAcc in both SN and PB males (F(12, 108) = 13.54, p < 0.001) and, again, these effects were similar in both groups. Neither SN nor PB males regained baseline levels prior to the end of sampling (Figure 2, lower panel).
AMPH treatment differentially alters D1R binding in the NAcc of SN and PB males
Previous studies have demonstrated that AMPH treatment enhances NAcc D1R gene and protein expression (Liu et al., 2010). Additionally, pair bonding experience elevates D1R binding (Aragona et al., 2006) in the NAcc of male prairie voles. Therefore, we hypothesized that alterations in DA receptor binding in the NAcc may underlie the behavioral interaction between pair bonding and AMPH reward. We processed brain sections from subjects used in the CPP tests for DA receptor autoradiographic binding. Two-way ANOVA analysis indicated a significant interaction between social experience (SN or PB) and injection type (saline or AMPH) on D1R binding in the NAcc (F(1, 29) = 17.63, p < 0.01). The posthoc test revealed that the densities of D1R binding in the NAcc of SN-AMPH and PB-saline groups were comparable and significantly higher than those of SN-saline and PB-AMPH groups (Figure 3a). Neither AMPH treatment nor pair bonding experience altered the density of D2R binding in the NAcc (Figure 3b). In addition, no group differences were found in either D1R or D2R binding in the caudate putamen (data are not shown).
NAcc D1R activation mediates AMPH reward in SN males
In male prairie voles, subcutaneous injections of a D1R, but not D2R, antagonist before AMPH conditioning sessions eliminated AMPH-induced CPP (Liu et al., 2010). Given the established role of NAcc DA in AMPH reward in other rodent species (Yokel and Wise, 1975; Kehoe et al., 1996), we hypothesized that access to D1Rs in the NAcc during conditioning is essential for AMPH-induced CPP in SN male prairie voles. We found that SN males that received cerebrospinal fluid (CSF) injections into the NAcc displayed AMPH-induced CPP (t = 2.90, p < 0.01) (Figure 4). However, intra-NAcc administration of a D1R antagonist, SCH 23390, at either a low (4 ng/side) or high (100 ng/side) dose prior to conditioning sessions, eliminated AMPH-induced CPP (Figure 4). In contrast, intra-NAcc administration of a D2R antagonist, eticlopride, at either a low (4 ng/side; t = 3.25, p < 0.01) or high (100 ng/side; t = 2.30, p < 0.05) dose, did not block AMPH-induced CPP (Figure 4). No differences were found in the frequencies of cage crosses between the pre-and post-tests in any group, indicating no effect of treatment on locomotor activity (data are not shown).
Activation of D1Rs in the NAcc enables AMPH-induced CPP in PB males
Previous studies have shown that NAcc D1R activation is essential for AMPH-induced CPP and selective aggression, and impairs partner preference formation in male prairie voles (Aragona et al., 2006; Liu et al., 2010). Given the role of D1Rs in those behaviors and the finding that NAcc D1R binding is lower in PB-AMPH males than in PB-saline and SN-AMPH males (Figure 3a), we hypothesized that decreased D1R activity in the NAcc may be responsible for the lack of AMPH-induced CPP in PB males. To test this hypothesis, we injected CSF or CSF containing a D1R agonist or antagonist site-specifically into the NAcc prior to each of the three conditioning sessions and then tested for the presence of AMPH-induced CPP. As expected, PB males that received CSF injections did not show AMPH-induced CPP (Figure 5). However, PB males that received intra-NAcc injections of the D1R agonist (t = 4.69, p < 0.001), but not antagonist, displayed AMPH-induced CPP (Figure 5). There were no differences in the frequencies of cage crosses between the pre-and post-test for any group (data are not shown).
Studies in both humans and animal models have demonstrated a strong relationship between drug use/abuse and social behavior (Young et al., 2011a). Due to its well known role in the generation of motivated behaviors, the mesolimbic DA system is in a key position to mediate the interaction between drugs of abuse and social behavior. We have recently demonstrated that repeated exposure to AMPH impairs pair bond formation in male prairie voles and that NAcc DA mediates this effect (Liu et al., 2010). In the present study, we demonstrate that pair bonding experience impairs AMPH-induced CPP and that this effect is also mediated by NAcc DA. Taken together, these studies demonstrate a reciprocal interaction between pair bonding and AMPH reward and suggest a role for NAcc DA in regulating such interactions.
In the current study, we used a previously established CPP paradigm (Liu et al., 2010; Young et al., 2011b) to investigate the effects of pair bonding experience on the rewarding properties of AMPH. We use the ambiguous term ‘rewarding properties’ to describe the impact of AMPH on place conditioning because it allows us to simultaneously address the individual components of reward—including hedonics, associative learning, and incentive motivation (Berridge and Robinson, 2003)—that have been implicated in processes underlying place conditioning (Hnasko et al., 2005; White et al., 2005; Cunningham and Patel, 2007), without distinguishing between them. Our results demonstrate that AMPH conditioning induced a CPP in SN, but not PB, male voles, and as such, offer the first empirical evidence that pair bonding experience decreases the rewarding properties of AMPH. Although this is the only study to investigate the effects of pair bonding experience on the rewarding properties of drugs of abuse, previous studies have demonstrated that other social experiences/factors may also influence drug reward. For example, rats reared with multiple social cohorts self-administered less AMPH (Bardo et al., 2001) and cocaine (Schenk et al., 1987) over repeated sessions than rats reared alone. Similarly, rats reared in an enriched environment that contained novel objects and social cohorts self-administered less AMPH, extinguished self-administration behavior sooner, and required higher doses of AMPH to reinstate drug-seeking than did rats housed alone (Bardo et al., 2001; Green et al., 2002; Stairs et al., 2006; c.f., Schenk et al., 1988; Bardo et al., 1995). Furthermore, female rats trained to lever-press for cocaine showed markedly fewer responses after becoming pregnant and following parturition (Hecht et al., 1999), suggesting that the reproductive process and neurobiological changes involved with maternal experience may decrease the reinforcing properties of cocaine. This notion is further supported by the finding that virgin rats preferred an environment associated with cocaine and readily expressed a cocaine-induced CPP (Seip et al., 2008), whereas lactating dams strongly preferred an environment associated with pups over one associated with cocaine (Mattson et al., 2001). Together, these studies imply that social factors may reduce the rewarding properties of psychostimulants. Our results extend these findings and demonstrate that pair bonding experience impairs AMPH reward in prairie voles.
The rewarding properties of psychostimulant drugs of abuse, such as AMPH, are dependent upon drug-induced increases in NAcc DA release and the subsequent activation of DA receptors (Yokel and Wise, 1975; Di Chiara and Imperato, 1988; Bergman et al., 1990; Kehoe et al., 1996). Therefore, alterations in either of these factors may underlie the effects of pair bonding experience on AMPH reward. Levels of released DA have been closely correlated with the positive subjective effects of drugs of abuse (Volkow et al., 1999; Drevets et al., 2001; Leyton, 2010) and psychostimulant-induced NAcc DA release has been altered by social experience in some cases (e.g., isolation early in life: (Kehoe et al., 1996; Kosten et al., 2005)), but not others (e.g., enriched social housing: (Bardo et al., 1995)). In the present study, AMPH treatment increased the level of extracellular DA in the NAcc, which is consistent with previous reports (Di Chiara and Imperato, 1988; Curtis and Wang, 2007; McKittrick and Abercrombie, 2007). Furthermore, AMPH induced an immediate and prolonged decrease in the level of extracellular DOPAC in both groups. This finding is consistent with those of previous studies and the known role of AMPH in the inhibition of monoamine oxidase—an enzyme involved in the degradation of DA (Green and el Hait, 1978; Jones et al., 1998; Curtis and Wang, 2007). In both cases, the magnitude and temporal pattern of extracellular changes in the NAcc were comparable between SN and PB males, suggesting that it is unlikely that the effects of pair bonding on AMPH reward are related to the release or metabolism of NAcc DA.
Although pair bonding experience did not influence AMPH-induced DA release or metabolism, it did influence the effects of AMPH on NAcc DA receptor binding (i.e., DA receptor expression and/or affinity). For example, consistent with previous studies, AMPH treatment increased NAcc D1R expression in SN males (Liu et al., 2010) and pair bonding experience also elevated NAcc D1R binding (Aragona et al., 2006). However, the effect of AMPH on NAcc D1R binding was reversed in PB males as compared to SN males, as PB males showed a significant decrease in D1R binding following AMPH treatment. No group differences were found in NAcc D2R binding in either the current or previous studies (Aragona et al., 2006; Liu et al., 2010). Together these data demonstrate that pair bonding experience and AMPH exposure each leads to D1R-specific changes within the NAcc of SN males. Further, as AMPH oppositely affected NAcc D1R binding in SN and PB voles, our data indicate that social bonding may be an important mediating factor in the effects of AMPH on the mesolimbic DA system. Correspondingly, cocaine has been found to induce a robust positive blood-oxygen-level-dependent (BOLD) signal change throughout the mesolimbic DA system in virgin females, yet a largely negative BOLD response in lactating dams, as measured by functional magnetic resonance imaging (Ferris et al., 2005)—further indicating that social/sexual experience may play an important role in the neurobiological response to drugs of abuse. Alterations in receptor binding, such as those described above, may have profound effects on behavior because they modify the brain’s responsiveness to released neurotransmitters. In SN males, for example, AMPH-induced increases in D1R binding may play an important role during AMPH conditioning as intra-NAcc blockade of D1R, but not D2R, inhibited AMPH-induced CPP—a finding consistent with those in other species (Baker et al., 1998; Pitchers et al., 2010). Consequently, in PB males, decreased NAcc D1R binding may underlie the lack of an AMPH-induced CPP as NAcc D1R activation during AMPH conditioning enabled AMPH-induced CPP in PB males. Collectively, these data indicate that AMPH-induced decreases in NAcc D1R expression/affinity may underlie the effects of pair bonding experience on AMPH reward.
Two interesting parallels between our findings and those from other studies that have investigated the relationship between drugs of abuse and social behavior are worth mentioning. First, pair bonding and repeated AMPH exposure each independently resulted in similar changes in the mesolimbic DA system of male prairie voles (i.e. enhanced D1R binding (Aragona et al., 2006) and expression (Liu et al., 2010) in the NAcc). Similarly, sexual experience and repeated exposure to psychostimulants each increased the density of dendritic spines on medium spiny neurons within the NAcc shell in rats (Robinson and Kolb, 1999; Pitchers et al., 2010). Furthermore, pup suckling in lactating dams and cocaine administration in virgin females induced similar patterns of positive BOLD activation in the mesocorticolimbic system (Ferris et al., 2005). Together these data support the notion that drugs of abuse usurp neural mechanisms and circuits that mediate adaptive behaviors (Panksepp et al., 2002). Secondly, our data suggest that the differential neurobiological responses to AMPH in SN and PB males may underlie group differences in AMPH-induced behavior. Similarly, lactating rats showed a suppression of activity within the mesocorticolimbic DA system in response to cocaine (as opposed to the increase in activity noted in virgin females) (Ferris et al., 2005) and a reduction in cocaine self-administration (Hecht et al., 1999), further supporting the notion that physiological changes associated with social experience may attenuate the rewarding properties of drugs of abuse.
The presence of strong social bonds in adulthood may decrease the vulnerability to drug abuse (Kosten et al., 1987). However, the neural mechanisms underlying this behavioral phenomenon are relatively unknown—perhaps due to the lack of an appropriate animal model. In the present study, we established the prairie vole as an animal model to investigate the neural mechanisms underlying the protective effects of adult social bonding on the vulnerability to drug abuse. Our findings indicate that pair bonding experience decreases the rewarding properties of AMPH and that the mesolimbic DA system—particularly DA neurotransmission in the NAcc—mediates this effect. These findings, together with those from our previous studies (Liu et al., 2010), establish a foundation for future investigation of the neural mechanisms underlying the reciprocal relationship between drug use/abuse and social bonding, which may ultimately provide important insight into the prevention or treatment of drug abuse.
We thank Claudia Lieberwirth, Kelly Lei, Melissa Martin, and Adam Smith for their critical reading of this manuscript. Additionally, we thank Terry E. Robinson for reading an early draft of this manuscript and for providing his valuable suggestions. This work was supported by National Institutes of Health grants DAF31-25570 to KAY, HDR01-48462 to JTC, and DAR01-19627, DAK02-23048, and MHR01-58616 to ZXW.
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