- Open Access
Effects of a selectively bred novelty-seeking phenotype on the motivation to take cocaine in male and female rats
© Cummings et al; licensee BioMed Central Ltd. 2011
Received: 13 October 2010
Accepted: 11 March 2011
Published: 11 March 2011
Gender and enhanced novelty reactivity can predispose certain individuals to drug abuse. Previous research in male and female rats selectively bred for high or low locomotor reactivity to novelty found that bred High Responders (bHRs) acquire cocaine self-administration more rapidly than bred Low Responders (bLRs) and that bHR females in particular self-administered more cocaine than the other groups. The experiments presented here aimed to determine whether an individual's sex and behavioral phenotype interact to affect motivation to take cocaine.
We examined motivation for taking cocaine in two experiments using a range of doses on a progressive ratio (PR) schedule of responding in bHR or bLR males and females. Additionally, we included a measure of continuing to respond in the absence of reinforcement, a feature of addiction that has been recently incorporated into tests of animal models on the basis of the criteria for substance use disorder in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition. Statistical analyses were performed using PASW Statistics 18.0 software. Data were analyzed using repeated-measures analysis of variance followed by a Bonferroni correction post hoc test when applicable.
We found sex differences as well as effects of novelty reactivity on the motivation to self-administer cocaine. Specifically, females demonstrated higher breaking points on the PR schedule compared with males, regardless of phenotype, and bHR males and females exhibited higher motivation than bLR animals at a number of the doses studied.
An individual's sex continues to be a predisposing factor with respect to drug abuse liability and can be compounded by additional individual differences such as reactivity to novelty.
Drug abuse vulnerability can vary with an individual's sex, hormone status and personality traits (that is, novelty reactivity), among other factors. In humans, personality traits such as novelty-seeking, reactivity to novelty, sensation-seeking and impulsivity contribute to an enhanced likelihood of substance abuse [1–4]. People who exhibit a heightened response to novelty use more drugs compared with those with an attenuated novelty reactivity response. Thus, novelty responsivity is considered to be a predictor of drug abuse liability.
Analogously to humans, individual behavioral traits in rats influence psychostimulant self-administration [5–8]. Indeed, animals that exhibit high novelty-induced locomotor behavior (High Responders (HRs)) have increased sensitivity to the reinforcing effects of drugs compared with Low Responders (LRs) . Numerous studies have used the HR-LR model to demonstrate the relationship between novelty-induced locomotor activity, drug taking and other risk-taking behaviors [7, 9].
A line of rats has been selectively bred on the basis of their locomotor behavior in a novel, mildly stressful environment, thus producing bred High Responder (bHR) and bred Low Responder (bLR) rats . This selectively bred line of animals shares many characteristics with outbred animals that are commercially purchased and subsequently screened and classified to be HRs or LRs [7, 11]. The bHR rats exhibit enhanced acquisition of cocaine self-administration relative to bLR rats  as well as increased impulsivity (for example, reduced behavioral inhibition or increased responding on a task requiring inhibition compared with bLR rats) . The bHR rats also exhibit an enhanced corticosterone response to stress and higher levels of glucocorticoid receptor mRNA expression in the hippocampus relative to bLR rats . The experiments using the bHR and bLR rat lines demonstrate that the phenotypes are strongly genetically driven and highly predictable from one generation to the next . The phenotypic differences in reactivity to novelty have become more pronounced and less variable with subsequent generations of breeding, such that phenotypic classification of animals can be predicted with >95% certainty. Selective breeding has also amplified many of the differences seen in outbred animals and has revealed additional components of the phenotype that appear to be significant with respect to drug abuse liability .
An additional factor that puts individuals at increased risk for drug abuse is whether the individual is female or male. Women begin using cocaine at earlier ages, progress through the stages of addiction more quickly, enter rehabilitation facilities after a shorter period of use and have shorter periods of abstinence compared with men . Women also report a stronger dependence on cocaine and greater cue-induced craving compared with men . Hormones have been indicated in some of the effects, as women also report greater pleasure from smoked cocaine when their estradiol levels are elevated during their menstrual cycle [16, 17].
The preclinical literature supports the idea that there is a biological basis for, and a hormonal modulation of, effects of sex and hormones on drug abuse liability. Female rats demonstrate greater behavioral sensitization to cocaine after repeated cocaine treatment compared with males [18, 19] and acquire cocaine self-administration more readily than males [20–24]. Estradiol enhances the reinforcing effects of cocaine, as female rats work harder to obtain cocaine during estrus when estradiol is high or when ovariectomized (OVX) rats are given estradiol [22, 25, 26], and they prefer higher doses of cocaine when in estrus compared with the other phases of the cycle . Females also work harder on a progressive ratio (PR) schedule when in estrus or after estradiol treatment of OVX rats [25, 28].
Recent data from our laboratory demonstrated that bHR male and female rats acquire cocaine self-administration behavior significantly faster than bLR male and female rats and also that bHR female rats ingest greater amounts of cocaine compared with bHR males as well as bLR males and females . On the basis of these findings, we wanted to know whether increased motivation for the drug was the cause of bHR females' greater drug intake. Therefore, the current study sought to determine the impact of sex and the bHR and bLR behavioral phenotypes on the motivation to self-administer cocaine using a PR schedule with a range of doses of cocaine, with the inclusion of a test to examine the animals' responses to cocaine availability in the absence of reinforcement.
Materials and methods
Adult bHR and bLR male and female Sprague-Dawley rats (~100 days old) were acquired from the Akil Laboratory (University of Michigan, Ann Arbor, MI, USA) in-house breeding colony, where lines are maintained. Animals from the 18th and 19th generations were used for Experiment 1, and animals from the 21st, 23rd and 24th generations were used for Experiment 2. A description of the breeding strategy and initial behavioral characterization of the bHR and bLR lines was published previously . Male and female rats were housed in a 14-hour light:10-hour dark cycle (lights on at 7:00 AM). Food and water were available ad libitum, and all experiments were conducted in accordance with the National Institutes of Health guidelines on laboratory animal use and care using a protocol approved by the University of Michigan Committee on Use and Care of Animals.
Approximately 5 days following transfer from the breeding colony room, rats underwent implantation of indwelling intravenous jugular catheters connected to a back port. Jugular catheter construction and implantation were performed using previously described procedures . In short, catheters were constructed by gluing Silastic tubing (0.51 mm inner diameter × 0.94 mm outer diameter, Dow Corning, Midland, MI, USA) to an external guide cannula (22-G guide cannula; Plastics One, Roanoke, VA, USA) using cranioplastic cement. A polypropylene mesh was secured to the bottom of the cannula using the same cement. Rats received an injection of buprenorphine (0.02 mg/kg subcutaneous injection) 30 minutes before they were anesthetized with isoflurane (5% isoflurane in oxygen). The free end of the Silastic tubing of the catheter apparatus was inserted into the right jugular vein of the animal and secured using 4-0 silk sutures around the tubing and the venous tissue. The catheter port exited dorsally from the animal. After successful implantation, the animal's catheter was flushed with 0.2 mL each of heparin (30 U/mL in 0.9% sterile saline) and gentamicin (3 mg/kg) to prevent clotting and infection, respectively. A dummy stylet was then inserted into the port opening. Two days after surgery the catheters were flushed with 0.2 mL of heparin (30 U/mL in 0.9% sterile saline) and gentamicin (3 mg/kg) and with gentamicin every day after that. Prior to the beginning of each cocaine self-administration session, the catheters were flushed with 0.1 mL of sterile saline and, following the rats' cocaine self-administration, the catheters were flushed with gentamicin (3 mg/kg). Female estrous cycle was monitored via daily vaginal lavage and microscopic examination of vaginal cells collected immediately following the cocaine self-administration session. Catheter patency was checked weekly using a solution of Pentothal (thiopental sodium, 15 mg/mL concentration; range, 0.08 to 0.20 mL) in sterile water.
Cocaine self-administration apparatus
Cocaine self-administration was performed in standard operant chambers (Med Associates, Inc., Georgia, VT, USA), during which time animals could poke their noses ("nose poke") into the active hole for cocaine or into an inactive hole, which resulted in no consequences. Rats were connected to the infusion syringe via a swivel mounted to a counterbalanced arm, which allowed animals to move freely in the testing environment.
Experiment 1: cocaine self-administration protocol
Fixed ratio training (week 1)
One week following catheter implantation animals were allowed to nose poke to self-administer cocaine using a fixed-ratio 1 (FR1) schedule of reinforcement (that is, one nose poke in the active hole resulted in receipt of one intravenous infusion of cocaine) for 3 hours daily for 5 days at a cocaine dose of 0.5 mg/kg/infusion with a maximum of 15 infusions possible per day. At the start of the test a house light was turned on, indicating drug availability. During FR1 testing, each active hole nose poke resulted in a 50-μL infusion of cocaine HCl delivered over 2.8 seconds accompanied by a stimulus light in the active hole. Each infusion during this portion of the test was followed by a 5-second timeout period, during which time nose pokes were recorded but had no consequences. The dose (0.5 mg/kg/infusion) was chosen because it is one that has been shown to result in fairly rapid acquisition of the drug-taking behavior . Twelve animals began the experiment in each treatment group. Animals that reached the criteria of 15 infusions on the FR1 schedule were moved to the FR2 schedule (two active hole nose pokes resulted in one infusion). Only animals that achieved 15 infusions on the FR2 schedule continued to the PR schedule. The total number of animals to complete the study comprised 11 bHR females, 9 bLR females, 8 bHR males and 5 bLR males. Animals that failed to acquire self-administration behavior (that is, those that did not receive 15 infusions on the FR1 and FR2 schedules, comprising two bLR females, one bHR male and five bLR males) or animals that lost patency during the experiment (one bHR female, one bLR female, three bHR males and two bLR males) were removed from the study. The low number of bLR males acquiring drug-taking behavior is in agreement with our previously published data .
Progressive ratio testing (weeks 2 to 4)
Animals had 2 days off and then began daily cocaine self-administration sessions on a PR schedule for 5 days/week for 3 weeks using cocaine doses of 0.3 mg/kg/infusion, 0.4 mg/kg/infusion and 0.5 mg/kg/infusion, respectively. While the dose range was narrow, significantly different effects have been found with respect to drug taking [24, 26]. Each dose was given for 1 week, and doses were counterbalanced among animals and across groups using a Latin square design. We utilized a 6-hour PR schedule of reinforcement that escalated through an exponential series, namely, 1, 3, 6, 9, 12, 17, 24, 32, 42, 56, 73, 95, 124, 161, 208 required nose pokes per infusion and so on, adapted from Richardson and Roberts . A higher breaking point (BP) is an indication that the animal is more motivated to get the cocaine, as they are willing to work harder to obtain an infusion of the drug. The number of infusions, nose pokes in the active hole, nose pokes in the inactive hole and last completed ratio within 1 hour of the last infusion (BP) were recorded. The session terminated after 6 hours or if 1 hour elapsed without an infusion.
Experiment 2: cocaine self-administration protocol
Fixed ratio training (week 1 and days 1 and 2 of week 2)
One week following catheter implantation animals were allowed to nose poke to self-administer cocaine using the FR1 and FR2 schedules for 3 hours daily for 7 days (5 days on, 2 days off, 2 days on) at a cocaine dose of 0.4 mg/kg/infusion with the maximum number of infusions possible being 15. Animals that reached the criteria of 15 infusions on the FR1 schedule were moved to the FR2 schedule. Animals remained on the FR2 schedule until PR training and were moved to the next phase of the experiment only if they achieved 15 infusions on the FR2 schedule. After excluding animals that did not acquire the behavior (one bHR male and two bLR males) or those that had catheters that were not patent (one bHR female, two bLR females, two bHR males and two bLR males), the final group numbers were 11 bHR females, 10 bLR females, 9 bHR males and 8 bLR males.
Progressive ratio training (days 3 to 5 of week 2)
Animals were then given 3 days of experience on the PR schedule at a cocaine dose of 0.4 mg/kg/infusion. We used the same PR schedule used in Experiment 1. The number of infusions, nose pokes in the active hole, nose pokes in the inactive hole and last completed ratio within 1 hour (BP) were noted.
Progressive ratio testing (weeks 3 to 5)
Animals had 2 days off and then began daily cocaine self-administration sessions on a PR schedule of 5 days/week for 3 weeks using cocaine doses of 0.25 mg/kg/infusion, 0.5 mg/kg/infusion and 0.75 mg/kg/infusion, respectively. Each dose was given for 1 week, and doses were counterbalanced as described above using the same procedures described for Experiment 1.
Fixed ratio 5 (week 6)
For 4 days animals were put on an FR5 schedule for two 40-minute periods per day (separated by a 15-minute drug nonavailability period) during which they could self-administer cocaine (0.4 mg/kg/infusion) on a FR5 schedule (each infusion was followed by a 40-second timeout) with a maximum of 50 infusions/period (11 bHR females, 8 bLR females, 9 bHR males and 5 bLR males; numbers were reduced compared to week 2 because of loss of patency). Drug availability was signaled by illumination of the house light, which was turned off when the drug was unavailable. The second FR5 drug availability session was used to prevent extinction of the drug-taking behavior. The number of infusions and the number of active and inactive pokes (during drug-available and nonavailable sessions) were recorded, as well as the number of inefficient pokes (pokes during the 40-second timeout), which did not count toward receiving an infusion.
Statistical analyses were performed using PASW Statistics 18.0 software (SPSS, Inc., Somers, NY, USA). FR1, FR2 and PR data were analyzed using repeated-measures analysis of variance (ANOVA) with dose and day as within-subject variables and phenotype (bLR or bHR) and sex (male or female) as between-subject variables, followed by a Bonferroni correction post hoc test when applicable. Data obtained with the FR5 reinforcement paradigm were analyzed separately for the drug availability and nonavailability periods using repeated-measures ANOVA with day as the within-subject variable and phenotype and sex as between-subject variables, followed by a Bonferroni correction post hoc test when applicable. For the drug-available sessions, the number of nose pokes in the active and inactive holes, number of infusions and number of ineffective nose pokes in the active hole were analyzed. For the 15-minute no-drug session, the number of nose pokes in the previously active and inactive holes was analyzed. The percentage changes in poking rates (nose pokes per minute) between the first drug session and the following no-drug period were calculated. Sphericity assumed modeling with Greenhouse-Geisser and Huynh-Feldt adjustments was applied .
Total number of infusions during acquisition
Phenotype significantly affected the total number of infusions during the acquisition phase (F 1,29 = 25.481, P < 0.001). Post hoc analysis showed that bHR males and females had a greater number of infusions during the FR1 and FR2 schedules than their bLR counterparts (F 1,29 = 11.730, P = 0.001, and F1,29 = 11.730, P = 0.002, respectively; data not shown). Greater cocaine intake prior to the PR schedule did not enhance the BP; in fact, the only correlation identified was for bHR females, in which greater cocaine intake during acquisition was negatively correlated with the BP at the 0.5 mg/kg/infusion dose (r = -0.719, P = 0.013).
Impact of bHR-bLR phenotype and sex on breaking point
Total number of infusions during acquisition of cocaine self-administration
Phenotype significantly affected cocaine intake during acquisition (F 1,37 = 6.304, P = 0.017), with bHR males administering a greater number of infusions during FR1 and FR2 than their bLR counterparts (F 1,37 = 5.385, P = 0.026). The effect was not significant in females (data not shown). BP was not correlated with the number of infusions during FR1 and FR2 for any of the groups at any of the cocaine doses (data not shown).
Impact of bHR-bLR phenotype and sex on breaking point using an expanded dose range
Impact of bHR-bLR phenotype and sex differences on responding on an FR5 schedule of reinforcement and during periods with no reinforcement
Percentage change in active hole nose pokes
Change in the number of active nose pokes per minute between the first drug-available and no-drug sessions expressed as percentage changes from the drug-available sessiona
We did not identify any significant effects of estrous cycle on any behaviors measured for either phenotype (data not shown). In Experiments 1 and 2, 15 of 20 and 14 of 19 of the females, respectively, exhibited regular estrous cycles for the duration of the study.
In the present experiments, we investigated sex differences and the effect of selective breeding for novelty reactivity on the motivation to self-administer cocaine and for responding in the absence of reinforcement. We report that bHR males and females exhibited higher motivation to self-administer cocaine compared with bLR rats. There is also an underlying sex difference in the motivation to self-administer cocaine regardless of phenotype, with females showing greater motivation than males. Motivation for cocaine increased with dose, so that all animals except bLR males demonstrated significantly greater BPs at the highest dose tested (0.75 mg/kg/infusion) compared with lower doses. Thus, motivation contributes to the increased cocaine-taking seen in bHR females and is likely affected by both sex and phenotype.
Impact of the bHR-bLR phenotype on motivation for cocaine
Prior research conducted at our laboratory demonstrated that bHR males and females acquire cocaine self-administration behavior significantly faster than bLR males and females, and bHR female rats self-administer greater amounts of cocaine than bHR males and bLR males and females . The current study aimed to determine whether the higher drug intake previously seen in bHR females is due to higher motivation for the drug. We found that, in general, bHR rats exhibited higher BPs than bLR rats, indicating an increased motivation to take cocaine in the bHR versus bLR animals.
The mesolimbic dopamine system, specifically dopaminergic projections from the ventral tegmental area (VTA) to the nucleus accumbens (NAc), has been studied extensively for its role in mediating the rewarding effects of drugs of abuse and may be responsible for mediating the differences in motivation seen in the bHR and bLR animals. Indeed, bHR and bLR animals exhibit differences in their dopaminergic system, with bHR animals exhibiting differences in dopamine (DA) receptors and sensitivity . Studies conducted with outbred HR and LR animals have shown similar findings, with HR animals exhibiting increased responsivity to DA [32–34], higher basal DA levels in the NAc  and more persistent elevation in DA cell firing in the VTA compared with LR animals , a neuroadaptation that appears to be critical for the development of addictive behaviors [36, 37]. These differences in the dopaminergic reward system may play a role in the enhanced motivation for cocaine that we see in bHR animals.
Normally, within the dose range used in this study, the amount of cocaine administered increases with dose . Interestingly, bLR males did not exhibit amplified motivation to take cocaine at the highest dose, in contrast to significant increases in motivation demonstrated by the other groups, including bLR females. It appears that while the bLR phenotype is "protective" to a certain degree by reducing the motivation for cocaine, this protection is limited in females, and ultimately sex overrides behavioral phenotype in this situation, resulting in increased response for cocaine at a high dose (0.75 mg/kg/infusion).
The level of motivation to self-administer cocaine can be influenced by prior cocaine intake during self-administration training (for review, see ). For example, a level of 20 mg/kg/day during initial exposure results in an escalation of subsequent BPs, whereas an intake of 60 or even 100 mg/kg/day results in stable responding on a PR schedule . In the experiments presented here, the 5- and 7-day FR "training" period that preceded PR testing resulted in bHR rats' receiving more cocaine than bLR rats, which could have affected the animals' motivation for cocaine and subsequent BPs. However, the intake differences in the current study were significantly less than those reported by Morgan et al. , where they resulted in significant differences in BP, with intake differences remaining within 3 mg/kg/day.
Impact of sex on motivation for cocaine
Females, in addition to acquiring cocaine self-administration faster , also have higher motivation than males to take cocaine. Thus, females may be more sensitive than males to the reinforcing effects of cocaine. These data confirm results in other reports that females are willing to work harder than males for the same dose of cocaine [22, 25, 40].
While females generally exhibit higher motivation for cocaine than males, all differences in motivation to self-administer cocaine were obscured at the highest dose (0.75 mg/kg/infusion). This finding is similar to what we have seen before, in that drug-taking differences are often exhibited only at lower cocaine doses . Motivation to self-administer cocaine often increases with escalating doses; thus, drug-taking differences are often obscured when high cocaine doses are administered, as all animals tend to exhibit elevated motivation for the drug at higher doses. It is often only at the lowest doses that subtle but significant differences emerge [23, 26].
It is interesting to note, however, that while the bLR females demonstrated a significant increase in motivation to self-administer cocaine at the highest dose, the bLR males did not. It is possible that the bLR females are more responsive than bLR males to the effects of cocaine. The effect of sex on motivation for cocaine may override the bLR phenotype at higher doses for the females, resulting in increased motivation for cocaine compared with bLR males.
Neurobiological differences between LR and HR and between bHR and bLR rats have been described for male rats; however, several of the brain regions where differences have been found are known to be sensitive to estradiol in females. For example, bHR males have a greater proportion of dopamine D2 (high) receptors in the striatum , and our laboratory has shown that dopamine release in the striatum is augmented by estradiol in females . In addition, corticotropin-releasing hormone (CRH) mRNA levels in the hypothalamic paraventricular nucleus (PVN) are lower in LR rats . Estrogen receptors affect activation of CRH neurons in the PVN , and estradiol in the PVN also modulates the responsivity of the stress axis . It is possible, therefore, that estradiol in the bLR females augments the rewarding effect of cocaine, but only at higher doses.
On the other hand, it is also possible that the brains of the bLR males are simply less responsive to the effects of the cocaine. Indeed, Flagel et al.  found differences in dopaminergic circuitry in bLR males compared with bHR males, and we have seen that bLR males do not exhibit as robust a behavioral response to cocaine sensitization as do bHR males .
Gonadal hormones have been shown to play a significant role in the sex differences that exist with regard to drug-taking behavior [21, 22, 25]. We did not, however, find an effect of estrous cycle on the motivation to take cocaine in the experiments presented here, even though the majority of females continued to exhibit regular estrous cycles for the duration of the experiment. We previously reported a similar lack of effect of the estrous cycle on the acquisition of cocaine-taking behavior , which is likely due to the large number of females that exhibited aberrant cycles or stopped cycling altogether as a result of cocaine exposure. Lynch et al.  also reported irregular estrous cycles during cocaine self-administration in female rats. It is important to note that the previous studies reporting the effects of endogenous estrous cycles on BPs differed from ours in a number of ways . For example, the animals in previous studies were reinforced with a much higher cocaine dose during self-administration training and PR testing (0.6 mg/infusion) than the dose that we used. The animals in the other studies also self-administered cocaine for a shorter period and were housed in self-administration boxes for the duration of the study. These are important methodological differences that could potentially affect the results.
Additionally, our finding of a lack of effect of the estrous cycle may be due, at least in part, to the variation in circulating hormone levels between females at the time of testing. We have previously seen clear effects of estradiol on cocaine self-administration when administered to OVX females [23, 26]. In these prior studies, however, the time of behavioral testing was tightly regulated with regard to the exogenously administered hormone. Variation between females in circulating hormone levels at the time of testing, independent of lavage readings, could add to the variation seen in motivation, which could obscure differences that would otherwise be identified during post hoc analysis.
Thus, the sex differences in cocaine self-administration may be exacerbated by, but do not appear to require, high levels of circulating gonadal hormones. Indeed, we have shown previously that OVX females that were not given estradiol replacement exhibited higher levels of self-administration than males, confirming that circulating hormones are not necessary to maintain a female's increased drug abuse liability .
Impact of phenotype and sex on continuing to response without reinforcement
In recent years, researchers have been attempting to more closely model human addiction by adding tests based on the criteria in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition , for substance dependence, such as persisting to respond to a drug in the absence of reinforcement or in the presence of a punishment [6, 46]. Animals that are unable to refrain from responding when the drug is not received are said to demonstrate increased drug-seeking, a marker of addiction.
Thus, in Experiment 2, we added a test to examine the continuation of responding in the absence of reinforcement. During the first two 15-minute drug-free sessions, bLR females responded significantly more often than the bLR males; there were no differences between the bHR groups. To compare rates of responding during the drug-free and drug-available sessions, we calculated the number of pokes per minute during the 15-minute drug-free session and expressed that number as a percentage change from the poking rate during the drug-available session. In this part of the experiment, it was clear that the bLR females exhibited a significant increase in rates of responding during the non-reinforced (that is, drug-free) period compared with the period when the drug was available. According to these data, the bLR females demonstrated increased drug-seeking in the absence of reinforcement. However, analysis of the poking rate on subsequent days demonstrated that the bLR females were the only group that changed its rate of poking during the drug-free period in successive sessions and actually decreased its rates of responding during periods of no reinforcement on subsequent days. This change in poking rate was specific for the drug-free period, since poking rate during the drug-available session did not change. Interestingly, the other groups continued to respond at about the same rate as during the preceding drug-available period, showing no sign of learning that nose poking was not being reinforced during the drug-free session.
Summary and conclusion
The experiments presented here are the first to evaluate how the selectively bred, novelty-seeking phenotype as well as the sex of an individual affect motivation to self-administer cocaine. An individual's sex continues to increase drug abuse liability. We found underlying sex differences in motivation to take cocaine, with females having higher BPs than males, regardless of phenotype, demonstrating that these factors are dissociable. Additionally, reactivity to novelty affected motivation to take cocaine, as bHR animals had higher BPs than bLR animals at most of the doses tested. At the highest dose (0.75 mg/kg/infusion), all phenotype and sex differences disappeared, as all groups (except for bLR males) demonstrated significantly higher BPs than they did at the lower doses.
This study was funded by grants from the National Institutes of Drug Abuse to JBB (R01 DA12677) and HA (PPG 5P01DA021633-02) and the Office of Naval Research grant N00014-02-1-0879 to HA. Support for JAC was provided by the Reproductive Sciences Training Grant (T32 HD07048). We thank Brandon Luma and Melissa Luma for their technical assistance with these experiments and Shelly Flagel for her helpful review of the manuscript.
- Dawe S, Loxton NJ: The role of impulsivity in the development of substance use and eating disorders. Neurosci Biobehav Rev 2004, 28: 343–351. 10.1016/j.neubiorev.2004.03.007PubMedView ArticleGoogle Scholar
- Cloninger CR: A systematic method for clinical description and classification of personality variants: a proposal. Arch Gen Psychiatry 1987, 44: 573–588.PubMedView ArticleGoogle Scholar
- Perry JL, Carrol ME: The role of impulsive behavior in drug abuse. Psychopharmacology 2008, 200: 1–26. 10.1007/s00213-008-1173-0PubMedView ArticleGoogle Scholar
- Zuckerman M, Neeb M: Sensation seeking and psychopathology. Psychiatry Res 1979, 1: 255–264. 10.1016/0165-1781(79)90007-6PubMedView ArticleGoogle Scholar
- Davis BA, Clinton SM, Akil H, Becker JB: The effects of novelty-seeking phenotypes and sex differences on acquisition of cocaine self-administration in selectively bred High-Responder and Low-Responder rats. Pharmacol Biochem Behav 2008, 90: 331–338. 10.1016/j.pbb.2008.03.008PubMed CentralPubMedView ArticleGoogle Scholar
- Belin D, Mar AC, Dalley JW, Robbins TW, Everitt BJ: High impulsivity predicts the switch to compulsive cocaine-taking. Science 2008, 320: 1352–1355. 10.1126/science.1158136PubMed CentralPubMedView ArticleGoogle Scholar
- Piazza PV, Deminière JM, Le Moal M, Simon H: Factors that predict individual vulnerability to amphetamine self-administration. Science 1989, 245: 1511–1513. 10.1126/science.2781295PubMedView ArticleGoogle Scholar
- Piazza PV, Maccari S, Deminière JM, Le Moal M, Mormede P, Simon H: Corticosterone levels determine individual vulnerability to amphetamine self-administration. Proc Natl Acad Sci USA 1991, 88: 2088–2092. 10.1073/pnas.88.6.2088PubMed CentralPubMedView ArticleGoogle Scholar
- Piazza PV, Deminière JM, Maccari S, Le Moal M, Mormède P, Simon H: Individual vulnerability to drug self-administration: action of corticosterone on dopaminergic systems as a possible pathophysiological mechanism. In The Mesolimbic Dopamine System: From Motivation to Action. Edited by: Willner P, Scheel-Krüger J. New York: John Wiley & Sons Ltd; 1991:473–495.Google Scholar
- Stead JD, Clinton S, Neal C, Schneider J, Jama A, Miller S, Vazquez DM, Watson SJ, Akil H: Selective breeding for divergence in novelty-seeking traits: heritability and enrichment in spontaneous anxiety-related behaviors. Behav Genet 2006, 36: 697–712. 10.1007/s10519-006-9058-7PubMedView ArticleGoogle Scholar
- Kabbaj M, Devine DP, Savage VR, Akil H: Neurobiological correlates of individual differences in novelty-seeking behavior in the rat: differential expression of stress-related molecules. J Neurosci 2000, 20: 6983–6988.PubMedGoogle Scholar
- Flagel SB, Robinson TE, Clark JJ, Clinton SM, Watson SJ, Seeman P, Phillips PE, Akil H: An animal model of genetic vulnerability to behavioral disinhibition and responsiveness to reward-related cues: implications for addiction. Neuropsychopharmacology 2010, 35: 388–400. 10.1038/npp.2009.142PubMed CentralPubMedView ArticleGoogle Scholar
- Clinton S, Miller S, Watson SJ, Akil H: Prenatal stress does not alter innate novelty-seeking behavioral traits, but differentially affects individual differences in neuroendocrine stress responsivity. Psychoneuroendocrinology 2008, 33: 162–177. 10.1016/j.psyneuen.2007.10.012PubMed CentralPubMedView ArticleGoogle Scholar
- Lynch WJ, Roth ME, Carroll ME: Biological basis of sex differences in drug abuse: preclinical and clinical studies. Psychopharmacology (Berl) 2002, 164: 121–137. 10.1007/s00213-002-1183-2View ArticleGoogle Scholar
- Robbins SJ, Ehrman RN, Childress AR, O'Brien CP: Comparing levels of cocaine cue reactivity in male and female outpatients. Drug Alcohol Depend 1999, 53: 223–230. 10.1016/S0376-8716(98)00135-5PubMedView ArticleGoogle Scholar
- Sofuoglu M, Dudish-Poulsen S, Nelson D, Pentel PR, Hatsukami DK: Sex and menstrual cycle differences in the subjective effects from smoked cocaine in humans. Exp Clin Psychopharmacol 1999, 7: 274–283. 10.1037/1064-12184.108.40.2064PubMedView ArticleGoogle Scholar
- Evans SM, Haney M, Foltin RW: The effects of smoked cocaine during the follicular and luteal phases of the menstrual cycle in women. Psychopharmacology 2002, 159: 397–406. 10.1007/s00213-001-0944-7PubMedView ArticleGoogle Scholar
- Glick SD, Hinds PA: Sex differences in sensitization to cocaine-induced rotation. Eur J Pharmacol 1984, 99: 119–121. 10.1016/0014-2999(84)90442-4PubMedView ArticleGoogle Scholar
- Hu M, Becker JB: Effects of sex and estrogen on behavioral sensitization to cocaine in rats. J Neurosci 2003, 23: 693–699.PubMedView ArticleGoogle Scholar
- Lynch WJ, Carroll ME: Sex differences in the acquisition of intravenously self-administered cocaine and heroin in rats. Psychopharmacology 1999, 144: 77–82. 10.1007/s002130050979PubMedView ArticleGoogle Scholar
- Lynch WJ, Roth ME, Mickelberg JL, Carroll ME: Role of estrogen in the acquisition of intravenously self-administered cocaine in female rats. Pharmacol Biochem Behav 2001, 68: 641–646. 10.1016/S0091-3057(01)00455-5PubMedView ArticleGoogle Scholar
- Carroll ME, Morgan AD, Lynch WJ, Campbell UC, Dess NK: Intravenous cocaine and heroin self-administration in rats selectively bred for differential saccharin intake: phenotype and sex differences. Psychopharmacology (Berl) 2002, 161: 304–313. 10.1007/s00213-002-1030-5View ArticleGoogle Scholar
- Hu M, Crombag HS, Robinson TE, Becker JB: Biological basis of sex differences in the propensity to self-administer cocaine. Neuropsychopharmacology 2004, 29: 81–85. 10.1038/sj.npp.1300301PubMedView ArticleGoogle Scholar
- Hu M, Becker JB: Acquisition of cocaine self-administration in ovariectomized female rats: effect of estradiol dose or chronic estradiol administration. Drug Alcohol Depend 2008, 94: 56–62. 10.1016/j.drugalcdep.2007.10.005PubMed CentralPubMedView ArticleGoogle Scholar
- Roberts DCS, Bennett SAL, Vickers GJ: The estrous cycle affects cocaine self-administration on a progressive ratio schedule in rats. Psychopharmacology 1989, 98: 408–411. 10.1007/BF00451696PubMedView ArticleGoogle Scholar
- Becker JB, Hu M: Sex differences in drug abuse. Front Neuroendocrinol 2008, 29: 36–47. 10.1016/j.yfrne.2007.07.003PubMed CentralPubMedView ArticleGoogle Scholar
- Lynch WJ, Arizzi MN, Carroll ME: Effects of sex and the estrous cycle on regulation of intravenously self-administered cocaine in rats. Psychopharmacology 2000, 152: 132–139. 10.1007/s002130000488PubMedView ArticleGoogle Scholar
- Becker JB, Berkley KJ, Geary N, Hampson E, Herman JP, Young EA: Sex Differences in the Brain: From Genes to Behavior. New York: Oxford University Press; 2008.Google Scholar
- Crombag HS, Badiani A, Maren S, Robinson TE: The role of contextual versus discrete drug-associated cues in promoting the induction of psychomotor sensitization to intravenous amphetamine. Behav Brain Res 2000, 116: 1–22. 10.1016/S0166-4328(00)00243-6PubMedView ArticleGoogle Scholar
- Richardson NR, Roberts DC: Progressive ratio schedules in drug self-administration studies in rats: a method to evaluate reinforcing efficacy. J Neurosci Methods 1996, 66: 1–11. 10.1016/0165-0270(95)00153-0PubMedView ArticleGoogle Scholar
- Quintana SM, Maxwell SE: A Monte-Carlo comparison of 7 epsilon-adjustment procedures in repeated-measures designs with small sample sizes. J Educ Stat 1994, 19: 57–71. 10.2307/1165177View ArticleGoogle Scholar
- Hooks MS, Colvin AC, Juncos JL, Justice JB Jr: Individual differences in basal and cocaine-stimulated extracellualr dopamine in the nucleus accumbens using quantitative microdialysis. Brain Res 1992, 587: 306–312. 10.1016/0006-8993(92)91012-4PubMedView ArticleGoogle Scholar
- Hooks MS, Juncos JL, Justice JB Jr, Meiergerd SM, Povlock SL, Schenk JO, Kalivas PW: Individual locomotor response to novelty predicts selective alterations in D1 and D2 receptors and mRNAs. J Neurosci 1994, 14: 6144–6152.PubMedGoogle Scholar
- Hooks MS, Kalivas PW: Involvement of dopamine and excitatory amino acid transmission in novelty-induced motor activity. J Pharmacol Exp Ther 1994, 269: 976–988.PubMedGoogle Scholar
- McCutcheon JE, White FJ, Marinelli M: Individual differences in dopamine cell neuroadaptations following cocaine self-administration. Biol Psychiatry 2009, 66: 801–803. 10.1016/j.biopsych.2009.04.018PubMed CentralPubMedView ArticleGoogle Scholar
- Wolf ME, White FJ, Hu XT: MK-801 prevents alterations in the mesoaccumbens dopamine system associated with behavioral sensitization to amphetamine. J Neurosci 1994, 14: 1735–1745.PubMedGoogle Scholar
- Vezina P: Sensitization of midbrain dopamine neuron reactivity and the self-administration of psychomotor stimulant drugs. Neurosci Biobehav Rev 2004, 27: 827–839. 10.1016/j.neubiorev.2003.11.001PubMedView ArticleGoogle Scholar
- Roberts DC, Morgan D, Liu Y: How to make a rat addicted to cocaine. Prog Neuropsychopharmacol Biol Psychiatry 2007, 31: 1614–1624. 10.1016/j.pnpbp.2007.08.028PubMed CentralPubMedView ArticleGoogle Scholar
- Morgan D, Liu Y, Roberts DC: Rapid and persistent sensitization to the reinforcing effects of cocaine. Neuropsychopharmacology 2006, 31: 121–128. 10.1038/sj.npp.1300953PubMedView ArticleGoogle Scholar
- Blount J, Lynch W: Sex differences in motivation for cocaine as a function of stage of addiction. Ethn Dis 2009, 19: S7-S8.Google Scholar
- Becker JB, Rudick CN: Rapid effects of estrogen or progesterone on the amphetamine-induced increase in striatal dopamine are enhanced by estrogen priming: A microdialysis study. Pharmacol Biochem Behav 1999, 64: 53–57. 10.1016/S0091-3057(99)00091-XPubMedView ArticleGoogle Scholar
- Thammacharoen S, Geary N, Lutz TA, Ogawa S, Asarian L: Divergent effects of estradiol and the estrogen receptor-α agonist PPT on eating and activation of PVN CRH neurons in ovariectomized rats and mice. Brain Res 2009, 1268: 88–96. 10.1016/j.brainres.2009.02.067PubMedView ArticleGoogle Scholar
- Figueiredo HF, Ulrich-Lai YM, Choi DC, Herman JP: Estrogen potentiates adrenocortical responses to stress in female rats. Am J Physiol Endocrinol Metab 2007, 292: E1173-E1182. 10.1152/ajpendo.00102.2006PubMedView ArticleGoogle Scholar
- García-Fuster MJ, Perez JA, Clinton SM, Watson SJ, Akil H: Impact of cocaine on adult hippocampal neurogenesis in an animal model of differential propensity to drug abuse. Eur J Neurosci 2010, 31: 79–89.PubMed CentralPubMedView ArticleGoogle Scholar
- American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders. 4th edition. Washington, DC: American Psychiatric Association; 1994.Google Scholar
- Deroche-Gamonet V, Belin D, Piazza PV: Evidence for addiction-like behavior in the rat. Science 2004, 305: 1014–1017. 10.1126/science.1099020PubMedView ArticleGoogle Scholar
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