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BEHAVIORAL PHARMACOLOGY

Maternal Separation and Handling Affects Cocaine Self-Administration in Both the Treated Pups as Adults and the Dams

Division of Neuroscience, Yerkes National Primate Research Center, Emory University, Atlanta, Georgia (M.C.M., J.H., M.J.K.); Departments of Psychology and Public Health, University of California, Berkeley, California (D.F.); and Department of Biochemistry and Molecular Biology, Indiana University School of Medicine, Indianapolis, Indiana (S.P.S., W.I.D.)

Received January 10, 2006; accepted March 2, 2006.

	Abstract

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Repeated maternal separation of pups from dams is often used as an early life stressor that causes profound neurochemical and behavioral changes in the pups that persist into adulthood. The effects of maternal separation on both the dams and the treated pups as adults on cocaine self-administration were examined using four separation conditions: 15- or 180-min separation (MS15 and MS180), brief handling without separation (MS0), and a nonhandled group (NH). The separations and handling occurred daily on postnatal days 2 to 15. The acquisition of cocaine self-administration (0.0625–1.0 mg/kg/infusion) was evaluated in the treated pups as adults. The MS180 group acquired cocaine self-administration at the lowest dose tested (0.0625 mg/kg/infusion), whereas the MS15s did not respond for cocaine at rates greater than that seen with saline administration. The NH group received the greatest number of infusions and intake at the highest doses. After self-administration, no differences were observed between groups in activity of two liver carboxylesterases involved in the inactivation of cocaine, ES10 and ES4. Maternal separation affected cocaine self-administration in the dams as well. Although there was an overall significant affect of treatment on cocaine self-administration, the length of separation (15 or 180 min) did not affect cocaine self-administration on the dams. The MS0 dams averaged a greater number of infusions per session than NH group during the 1st week of acquisition. These data suggest that in addition to the profound changes that occur in pups as result of maternal separation, the dams are also susceptible to alterations in behaviors.

Animal models of early life stress, such as maternal separation and neonatal isolation, have been developed in an attempt to elucidate the neurochemical and behavioral alterations resulting from exposure to the early life stressor. In animal models, perinatal stress affects behavioral response to various drugs of abuse. Neonatal isolation and prolonged maternal separation alter the self-administration of cocaine in rats (Matthews et al., 1999; Flagel et al., 2003; Kosten et al., 2004; Zhang et al., 2005). Early life stress also alters conditioned place preference for amphetamine (Campbell and Spear, 1999), cocaine-induced locomotor activity (Brake et al., 2004), behavioral sensitization to cocaine (Li et al., 2003), ethanol preference and consumption (Ploj et al., 2003; Jaworski et al., 2005), and responses to morphine (Kalinichev et al., 2003). In addition, several neurochemical alterations in the dopamine mesolimbic system and the serotonergic system have been reported that may underlie some of the observed behavioral changes (Hall et al., 1999; Meaney et al., 2002; Brake et al., 2004; Vicentic et al., 2006). Most of the above studies use two or three groups of experimental animals that sometimes include separated, handled, and nonhandled animals with varying definitions of those groups. Also in experiments using neonatal isolation, the pups are separated individually from the dam, whereas in maternal separation, the litter as a whole is separated from the dam.

In our experimental approach, we use four groups of litters with variations in the time of separation and variations in handling, which provides additional data for interpretation (Jaworski et al., 2005). The various litters of pups were picked up and put back down with no separation into different cages (MS0), separated from their mother for 15 min/day (MS15), separated from their mother for 180 min/day (MS180), or were handled only once for a bedding change [nonhandled (NH)], which is required by the Emory Institutional Animal Care and Use Committee.

In addition to studying the effects of maternal separation on cocaine self-administration in the treated pups as adults, we also looked at potential pharmacokinetic differences. The rapid hydrolysis of cocaine to two major inactive metabolites, benzoylecgonine and ecgonine methyl ester, is an important step in the inactivation of cocaine (Bosron et al., 1997). Serum cholinesterase catalyzes the hydrolysis of cocaine to ecgonine methyl ester, whereas human carboxysylesterase-1 hydrolyzes the methyl ester group of cocaine to form benzoylecgonine (Bosron et al., 1997). In this study, we measure two major class 1 isoenzymes, ES10 and ES4, that play a crucial role in rat liver carboxylesterase activity (Sanghani et al., 2002).

Although the effects of maternal separation on the pups as adults have been studied, there is little known about the effects of maternal separation on the dams. Human mothers who had been separated from their children were more likely to have a substance abuse disorder (Zlotnick et al., 2003). Therefore, there is a definite need to understand the effects of separation on the vulnerability to drug abuse in mothers.

Our hypothesis is that separation of pups from dams (MS) and variations in handling during the perinatal period will produce changes in cocaine self-administration behavior in pups as adults and in the dams as well. Understanding the mechanisms of these changes could lead to new strategies for developing treatments of addictive disorders resulting from MS/handling in the perinatal period.

	Materials and Methods

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Animals. Thirty-three timed-pregnant Long Evans rats (Charles River Laboratories, Wilmington, MA) were received at the animal facility on gestation days 12 to 13. The dams were singly housed in static cages (27 x 48 x 20 cm) in a temperature- and humidity-controlled animal care facility and maintained on a 12-h light/dark schedule (lights on at 7:00 AM) with food and water available ad libitum. The pups were group-housed by sex in static cages after weaning until 3 months of age at which time they were individually housed. Water was available ad libitum throughout the experiment. Food was available ad libitum from weaning until venous catheter implantation at 3 months of age. The treated adults were food-restricted after surgery through the conclusion of the food training sessions, at which time free access to food was restored. All procedures were approved by the Emory Animal Care and Use Committee and in accordance with the Principles of Laboratory Animal Care (National Institutes of Health publication 85-23).

Separation and Handling Procedures. As the pups were born, the litter was randomly assigned to one of four groups (Jaworski et al., 2005). The experimental groups are as follows: NH, pups and dams were handled only on PN11 for a cage change and not separated; MS0, the dam was picked up and moved to the opposite end of the cage followed by the individual handling of each pup by picking the pup up and moving it to the opposite end of the cage with no separation into different cages; MS15, the pups in this group were exposed to 15 min of maternal separation from PN2–15; and MS180, the pups were exposed to 180 min of maternal separation from PN2–15. The MS0, MS15, and MS180 groups provide time course data on the effects of maternal separation and handling. The MS0 and NH groups provide data to control for handling during the separation procedure. Another group that is often used in maternal separation as a control group is the animal facility-reared group. In this group, the pups are subjected only to routine handling by the animal facility staff. The data obtained from an animal facility-reared group are often difficult to compare between laboratories due to the variations in care at the animal facility of each institution and are therefore not used in the current study. It has been suggested that separation and handling during the 2nd, not the 1st, week is critical in lasting behavioral effects (Flagel et al., 2003). To ensure that the separation occurred during a critical point in the pups' lives, the pups were separated daily during the first 2 weeks of life. Eight litters were assigned to each treatment group, with the extra litter assigned to the MS15 group. One litter assigned to the MS180 group died during separation on PN2, and the dam was sacrificed.

The manipulation of the pups in the MS15 and MS180 was initiated at 10:00 AM by removal of the dams from the maternity cage and placing them in individual cages until the end of the manipulation. After removal of the dams, the litters were removed from the nest, weighed, and placed in a cage assigned to that litter for the remainder of the experiment. The cage contained 3 cm of bedding material (Bed O' Cobs; The Andersons, Maumee, OH) and was placed on a heating pad set to maintain 37°C. At the conclusion of the separation period, the pups were returned to their maternity cage, and the dam was returned. The bedding material in the maternity cages was changed on PN11 for all the groups as required by Emory University's Institutional Animal Care and Use Committee. The pups were weaned on PN21 and group-housed by sex and by litter. A one-way analysis of variance (ANOVA) determined that the average litter size (NH, 11.88 ± 0.67, MS0, 11.88 ± 0.55; MS15, 12.22 ± 0.32; and MS180, 11.43 ± 0.72) or the sex ratio (NH, 1.39 ± 0.36; MS0, 1.05 ± 0.16; MS15, 1.28 ± 0.19; and MS180, 1.43 ± 0.72) did not significantly vary by group [litter size, F(3,32) = 0.3296, p = 0.80; sex ratio, F(3,32) = 0.6845, p = 57]. The average pup weight showed a trend for greater average weight in the MS180 group (46.94 ± 2.33) compared with the other groups (NH, 41.30 ± 0.99; MS0, 42.93 ± 1.13; and MS15, 41.40 ± 1.40) but did not reach significance [F(3,32) = 2.870, p = 0.054].

Venous Catheterization and Drug Delivery. The dams were implanted with indwelling jugular catheters 5 to 8 days after weaning of the pups. The treated pups were implanted with a jugular catheter around 3 months of age. Under anesthesia induced by a combination of ketamine (70 mg/kg i.p.) and medetomidine (0.5 mg/kg i.p.), the catheter (0.3048-mm i.d. x 0.635-mm o.d., silicone tubing) was inserted into the right posterior facial vein and pushed down into the jugular until it terminated outside the right atrium. The catheter was anchored to the surrounding tissue and continued s.c. to the back where it exited at the base of the skull. The catheter was connected to a 22-gauge guide cannula (Plastics One Inc., Roanoke, VA), which was mounted to the top of the skull using stainless steel screws and cranioplastic cement (Plastics One Inc.) for attachment to a leash. After the surgery, the rats were given atipamezole (0.2 mg/kg s.c.) to reverse the sedative effects of medetomidine.

The leash was attached to the guide cannula assembly and to a fluid swivel suspended above the operant chamber. The swivel and leash assembly were counterbalanced to allow relatively unrestricted movement in the operant chamber. Tubing ran from the swivel to a 20-ml syringe in a motor-driven pump (Razel, St. Albans, VT) located outside the sound-attenuating chamber. Before the start of the behavioral session, blood was obtained from the catheter to ensure patency. If blood was not obtained, the rat was injected via the catheter with methohexital sodium (1.5 mg i.v.) at the conclusion of the experiment. An immediate light anesthesia indicated the catheter was patent. After the session, the rats were disconnected from the leash assembly and flushed with streptokinase (0.67 mg/ml) and ticarcillin/clavulanic acid mixture (67 mg/ml) in a volume of 0.1 ml.

Apparatuses. Module test cages (12-inch width x 10-inch depth x 12-inch height) contained within sound-attenuating enclosures (Coulbourn Instruments, Allentown, PA) were used for the self-administration experiments. Each chamber was equipped with two response levers located 6 cm above the floor and 13 cm apart. A stimulus light was located 8 cm above each of the response levers. The house light was mounted 19 cm above the chamber floor on the wall opposite the response levers. Sucrose pellets (45 mg; Research Diets, New Brunswick, NJ) were dispensed into a trough located between the two response levers. The chambers were connected to a PC-compatible computer via Lab Linc V interface (Coulbourn Instruments). The experiments were programmed and the data collected using Graphic State 3 software (Coulbourn Instruments).

Locomotor activity was measured in a 40 x 40 x 30-cm Plexiglas cage (Omnitech Electronics, Columbus, OH) equipped with 16 photobeams front to back and 16 photobeams side to side spaced 2.4 cm apart. The activity cages were located in stainless steel sound-attenuating chambers equipped with an exhaust fan and a 10-W light. The experimental data were collected and analyzed on a PC-compatible computer using Digipro software (Omnitech Electronics).

Acquisition of Cocaine Self-Administration: Dams. The dams were given between 5 and 7 days to recover from surgery before the start of the 2-week self-administration sessions. The sessions were conducted between 8:00 AM and 6:00 PM, 7 days a week for 2 h a day. At the start of the session, the lever light above the active drug lever was illuminated, signaling that drug was available for self-administration. Responding on the active lever (fixed-ratio 1) resulted in the darkening of the lever light and the illumination of the house light for the duration of the infusion (0.2 ml over 6 s). There was a 20-s time-out after the infusions during which all lights were darkened and responses on either lever were recorded but had no programmed consequences. At the end of the time-out, the lever light was once again illuminated, and drug was available for self-administration. Responses on the inactive lever were recorded but had no programmed consequences at any time during the self-administration session.

Food Training: Treated Pups at Adulthood. The treated pups at adulthood were given 7 to 12 days to recover from surgery before the start of food training. During the recovery time, the MS adults were slowly food-restricted to 85% of their free-feeding weight. All behavioral test sessions were conducted between 8:00 AM and 8:00 PM, Monday through Friday. The rats were divided into four groups with an equal number of rats from each treatment condition (i.e., NH, MS0, MS15, and MS180). Each group of rats was run at the same time each day. The food sessions lasted for 1 h or until 100 food pellets were earned. At the start of the session, the lever light above the active food lever was illuminated. Responses on the lever (FR1) resulted in the presentation of a food pellet and darkening of the lever light. After a 10-s time-out, during which lever responses were recorded but had no consequences, the lever light above the active was once again illuminated. All responses on the inactive lever were recorded. The food sessions were conducted daily for 2 weeks, at which time self-administration sessions began.

Cocaine Self-Administration: Treated Pups at Adulthood. In the self-administration sessions, the lever formerly associated with food-reinforced responding (the food active lever) was assigned as the inactive lever, and the lever previously assigned as the inactive lever during food training became the active drug lever. The lever light above the active drug lever was illuminated at the start of the session, indicating that drug was available for self-administration. The conditions during self-administration for the treated pups at adulthood were identical to those used for the dams. In brief, responses on the active lever (FR1) resulted in the illumination of the house light for the duration of infusion (0.2 ml over 6 s) followed by a 20-s time-out. The rats were allowed to self-administer saline during the 1st week to establish a baseline of responding. During the following weeks, cocaine was made available for self-administration starting at 0.0625 through 1.0 mg/kg/infusion. Each week, a single dose was available for self-administration, with the dose doubling each successive week.

Food Test Session: Treated Pups at Adulthood. One week after the conclusion of self-administration the MS, handled and nonhandled rats were retested on the food program used during food training. In brief, the rats were able to respond on a continuous schedule of food reinforcement until 100 food pellets were earned or 1 h had elapsed. In this experiment, the lever assigned as the active lever during cocaine self-administration was reassigned as the inactive lever.

Cocaine-Induced Locomotor Activity: Treated Pups at Adulthood. Two weeks after the conclusions of self-administration, cocaine-induced locomotor activity was measured. On the 1st day of testing, the rats were given 2 h to habituate to the activity chamber, during which time the total distance was measured. On each of the next 3 days, the rats received saline or 5 or 15 mg/kg cocaine i.p. after a 30-min habituation period in the activity chamber. Each rat received both doses of cocaine and saline, each on separate occasions in a counterbalanced order. The total distance traveled was measured for 2 h after the injection, after which the animals were returned to their home cages for 22 h.

Carboxylesterase Assays. One week after self-administration, the treated pups as adults were decapitated, and the livers were removed, placed on dry ice, and stored at –80°C. Frozen rat liver was powdered in liquid N₂. Approximately 100 mg weight was homogenized in 50 mM sodium phosphate buffer, pH 7.4, with 1 mM EDTA, 1 mM benzamidine, and 0.05% Triton X-100. The suspension was sonicated briefly and centrifuged. Six individual liver specimens each from the four treatment groups were analyzed. Carboxylesterase activity in rat liver supernatants was assayed by UV spectroscopy with 4-methylumbelliferyl acetate as substrate, and total protein was assayed by the Bio-Rad (Hercules, CA) Bradford protein assay with bovine serum albumin as standard.

Forty micrograms of total protein was analyzed for the expression of individual carboxylesterase isoenzyme by nondenaturing polyacrylamide gel electrophoresis. Gels were stained for activity with 4-methylumbelliferyl acetate as substrate with fluorescence detection followed by total protein staining with Coomassie Blue dye (Sanghani et al., 2002). The activity staining pattern resembled that seen by Sanghani et al. (2002) in rat liver extracts. The fluorescence band densities of the two major rat liver carboxylesterases, ES10 and ES4, and the control carboxylesterase loaded on each gel was determined. The ratio of ES10 and ES4 to that of the control was determined and compared across all groups.

Drugs. Ketamine (Fort Dodge Animal Health, Fort Dodge, IA) and medetomidine (Pfizer Animal Health, Exton, PA) were given i.p. before surgery. After surgery, atipamezole (Pfizer Animal Health) was used to reverse the sedative effects of medetomidine. Cocaine was a gift from the National Institute on Drug Abuse (NIDA; National Institutes of Health, Bethesda, MD) and was dissolved in bacteriostatic, heparinized 0.9% saline. The catheters were maintained by daily infusions of a ticarcillin/clavulanic acid (GlaxoSmithKline, Research Triangle Park, NC) and streptokinase (American Diagnostica Inc., Stamford, CT) cocktail. Catheter patency was checked by infusion with methohexital sodium (Monarch Pharmaceuticals, Bristol, TN).

Statistical Analysis. All statistical analyses were performed using either SPSS 13.0 for Windows (SPSS Inc., Chicago, IL) or GraphPad Prism version 4.0 for Windows (GraphPad Software Inc., San Diego, CA). Comparisons were made by either one- or two-way with repeated-measures ANOVA as stated in the results section. Post hoc comparisons were made using Tukey's multiple comparison test. Statistical significance is stated as p < 0.05.

	Results

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Maternal Separation and Handling. Pregnant dams were placed into one of four groups according to separation and handling as described under Materials and Methods. After weaning on PN21, the litter size, average pup weight, and body of the weight of the dams were measured (Table 1). One-way ANOVAs were used to analyze the average litter size, dam body weights, and pup weights. The average litter size did not significantly vary by group [litter size, F(3,32) = 0.3296, p = 0.80]. Although there were no significant differences in dam body weight between the groups at weaning or during self-administration, the average pup weight showed a trend for greater average weight in the MS180 group (46.94 ± 2.33) compared with the other groups (NH, 41.30 ± 0.99; MS0, 42.93 ± 1.13; and MS15, 41.40 ± 1.40) but did not reach significance [F(3,32) = 2.870, p = 0.054]. The trend of MS180 group weighing more than the other groups continued into adulthood (see below). Thus, the treatments had only a very minor effect on body weight and no effect on litter size at weaning.

Maternally Separated and Nonhandled Adult Self-Administration. When the pups reached adulthood, they were prepared for the self-administration paradigm as described under Materials and Methods.

Food Training. The rats were trained to respond for food on a continuous schedule of reinforcement during daily session. All four groups acquired food maintained responding in the 2 weeks of training; however, there was a trend for a significant effect of treatment (data not shown, p = 0.064). The average number of days to earn 90 food pellets in a session (Table 1) did not differ between groups [one-way ANOVA, F(3,32) = 2.612, p > 0.07]. Although there was a trend for the impaired acquisition of food-reinforced responding in the MS15 group, neither measure reached significance, and all rats acquired food-reinforced responding in the 2-week span. In addition, the MS15 group had comparable levels of food-reinforced responding measured at the completion of the self-administration experiment (see below).

There were no significant differences in body weight on the start of food training [one-way ANOVA, F(3,33) = 2.708, p = 0.0628]; however, significant differences in weight were seen at the start of self-administration [one-way ANOVA, F(3,33) = 3.627, p < 0.05], with the MS180 group weighing more than the NH group (p < 0.05) (Table 1). The differences seen in body weight were no longer evident by the end of self-administration [one-way ANOVA, F(3,32) = 2.112, p = 0.1204]. Again, there were no marked differences among the groups.

Cocaine Self-Administration. The self-administration data are presented as the mean number of infusions per session for the five sessions conducted for each dose. Figure 1 shows the typical inverted "U" cocaine dose-response curves for the adults from the four groups. A two-way repeated-measures ANOVA revealed a significant effect of dose [F(5,29) = 7.851, p < 0.001)]. The effect of dose alone did not account for the differences in curves as indicated by a group x dose interaction [F(15,29) = 2.602. p = 0.002]. Although the MS180 group appeared to receive more infusions at the 0.0625 mg/kg/infusion dose than the other groups, this was only a trend and failed to reach significance (p = 0.078). Separation of the curves was most evident at the two highest doses tested, with the NH group taking significantly more infusions than the MS15 group at the 0.5 (p < 0.05) and 1.0 (p < 0.01) mg/kg/infusion doses. Thus, the animals did show some differences in their sensitivity to cocaine.

View larger version (33K): [in this window] [in a new window]   Fig. 1. Dose-response curve for cocaine self-administration in maternally separated (MS15 and MS180), handled (MS0), and NH adults. The data points represent the group mean ± S.E.M. of the average number of infusions per session at each of the doses tested. *, p < 0.05 versus MS15. **, p < 0.01 versus MS15.

View larger version (43K): [in this window] [in a new window]   Fig. 2. Acquisition of cocaine self-administration presented by group. The data are redrawn from Fig. 1 and presented as the group means ± S.E.M. of the average number of infusions per session at each of the doses tested. *, p < 0.05 versus saline. **, p < 0.01 versus saline. ***, p < 0.001 versus saline.

The average intake (milligrams) per session (Fig. 3) varied by dose [F(4,29) = 135.7, p < 0.001] and by group [F(3,29) = 4.123, p < 0.05]. There was also a significant dose x group interaction [F(12,29) = 3.562, p < 0.001]. At the lowest dose tested, there was a trend for the MS180 group to have a higher average daily intake than the MS15 group (p = 0.068). Differences between the MS180 and MS15 groups were evident at the 0.125 mg/kg/infusion dose, with the MS180 group having significantly higher intake (p < 0.05). Similar to what was seen with the average infusions per session, the NH group had significantly higher levels of cocaine intake at the 0.5 and 1.0 mg/kg/infusion doses compared with the MS15 group (p < 0.05 and p < 0.01, respectively). These findings again indicate that the animals differed in their responses to cocaine.

View larger version (23K): [in this window] [in a new window]   Fig. 3. The effects of experimental treatment on the average cocaine intake (milligrams) per session of MS0, MS15, MS180, and NH adults at each of the doses tested. The data points represent the group means ± S.E.M. *, p < 0.05 versus MS15 at the same dose. **, p < 0.01 versus MS15 at the same dose.

Despite the low level of responding by the MS15 group, the rats were able to discriminate between the active and inactive levers, although there was a significant effect of dose [lever, F(1,14) = 3.095, p < 0.05; dose, F(5,14) = 3.578, p < 0.01] evident in Fig. 4. The MS180 was the only other group able to discriminate between levers [lever, F(1,14) = 7.213, p < 0.05; dose, F(5,14) = 3.025, p < 0.05]. Both the NH and MS0 groups showed an increase in inactive lever responding as the dose of cocaine self-administered increased. The increased intake in cocaine may have led to nonspecific locomotor effects (dose effect reported above), which could explain the increase in inactive lever responding.

View larger version (32K): [in this window] [in a new window]   Fig. 4. Lever discrimination during cocaine self-administration for each group. The data points represent the average number of active and inactive lever presses per session (means ± S.E.M.) at each of the doses tested.

View larger version (33K): [in this window] [in a new window]   Fig. 5. Lever responses and food pellets earned during the food reinforced test session conducted at the end of cocaine self-administration testing. The data are presented as the mean ± S.E.M.

View larger version (31K): [in this window] [in a new window]   Fig. 6. Cocaine-induced locomotor activity in MS0, MS15, MS180, and NH adult rats. The bars represent the mean total distance traveled ± S.E.M. *, p < 0.05 versus NH.

The finding that the MS180 had significantly less locomotor activity at the highest dose tested is interesting. There were no significant differences in locomotor activity between groups after 5 mg/kg cocaine, saline, or during habituation. The results are somewhat difficult to interpret due to the unique histories of cocaine self-administration. Future experiments examining cocaine-induced locomotor activity in cocaine-naive animals are warranted.

Carboxylesterase Assay. The ratio of the density of activity bands for the two major carboxylesterase isoenzymes, ES10 and ES4, as well as the specific activity are presented in Fig. 7. One-way ANOVAs showed no significant differences in ES10 [F(3,22) = 1.413; p = 0.2700], ES4 [F(3,22) = 0.4473; p = 0.7221], or specific activity [F(3,22) = 1.690, p = 0.2029]. These data suggest that the differences in cocaine self-administration are due to pharmacodynamic differences rather than any pharmacokinetic differences.

View larger version (22K): [in this window] [in a new window]   Fig. 7. Lack of differences in the ratio of the density of activity bands for the two major carboxylesterase isoenzymes, ES10 and ES4, as well as the specific activity (units per milligram) in the treated pups as adults after self-administration. The data are presented as the mean ± S.E.M.

Dam Self-Administration. The length of separation from the pups did not appear to affect the acquisition of cocaine self-administration in the dams. Table 2 shows the average number of infusions per session for the MS15 and MS180 groups, and there were no statistical differences between the two [two-way repeated measures (1,12) = 0.118, p = 0.74; session F(13,12) = 4.453, p < 0.001; interaction F(13,12) = 0.5479, p = 0.89]. Therefore, the data from the MS15 and MS180 groups were combined into a MS group for statistical analysis of the average number of infusions per session during the 14 days of testing and are shown in Fig. 8. The rate of acquisition was analyzed using a two-way ANOVA with repeated measures looking at the effects of session and group on the average number of infusions per session. The average number of infusions per session increased as sessions progressed [session, F(13,25) = 10.28, p < 0.001]. Maternal separation, handling, or nonhandling had a significant affect on cocaine self-administration [group, F(2,25) = 3.807, p = 0.036]. Differences between groups are also seen when comparing the groups during the 1st week of acquisition [one-way ANOVA, F(2,27) = 4.025, p < 0.05] (Fig. 9). The MS0 group had a greater number of average infusions compared with the NH group during the 1st week (p < 0.05). By the 2nd week of acquisition, there were no significant differences between groups [one-way ANOVA, F(2,27) = 2.941, p = 0.07]. All three groups averaged greater infusions per session during the 2nd week compared with the 1st (NH, p < 0.01; MS0, p < 0.05; and MS, p < 0.01). It appears that the length of maternal separation (the MS group) does not affect the acquisition of cocaine self-administration in the dams; however, the group of dams who were handled and were present while their pups were removed (MS0) showed greater levels of self-administration during both weeks compared with the NH dams. The differences between in the acquisition of cocaine self-administration in the dams do not mirror the differences seen in the maternally separated, handled, and nonhandled adults. These data indicate that maternal separation has unique effects on both the dams and the pups.

View larger version (26K): [in this window] [in a new window]   Fig. 8. Acquisition of cocaine self-administration by the dams. Data represent the mean number of infusions per session ± S.E.M. There was a significant overall effect of both SESSION (p < 0.001) and group (p < 0.05).

View larger version (34K): [in this window] [in a new window]   Fig. 9. Average number of cocaine infusions per session by the dams during the 1st and 2nd weeks of self-administration. Data are presented as the mean ± S.E.M. *, p < 0.05 versus NH during week 1. , p < 0.05 versus week 1 value of the same group. , p < 0.01 versus week 1 value of the same group.

	Discussion

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Animal models of early life stressors such as maternal separation have been used in an attempt to elucidate the neurochemical and behavioral effects of the stressor in later life. Previous work has shown an effect of maternal separation on cocaine-induced locomotor activity (Brake et al., 2004), cocaine self-administration (Matthews et al., 1999), responses to primary and conditioned incentives (Matthews and Robbins, 2003), cocaine sensitization in rats (Li et al., 2003), and pharmacologically altered lateral hypothalamic intracranial electric self-stimulation thresholds (Matthews and Robbins, 2003). Another animal model of early life stress, neonatal isolation, has been demonstrated to enhance the acquisition of cocaine self-administration in rats (Kosten et al., 2004) and to impair amphetamine-induced conditioned place preference (Campbell and Spear, 1999).

Our data significantly extend this body of literature by the use of additional separation groups allowing for time course data to be gathered (MS0, MS15, and MS180), the inclusion of an NH group, a complete dose-response curve for cocaine self-administration, and the interesting new findings concerning the dams. In the present experiments, maternal separation had a significant impact on cocaine self-administration of the treated pups as adults. The MS180 group appeared to have a leftward shift in the dose-response curve, with acquisition occurring at the 0.0625 mg/kg/infusion dose. Although the MS0 group did not fully acquire by the definition used, an inverted U dose-response curve was evident. The NH group acquired at the 0.125 mg/kg/infusion dose and continued a high level of responding through the highest dose tested. Interestingly, the MS15 had a relatively flat dose-response curve with responding at any dose no greater than what was seen with saline. The lack of responding for cocaine did not seem to be related to an inability to complete the operant task because the MS15 group had similar rates of responding to the other groups during both the initial food training and the food test session at the end of the experiment. The MS15 group was also able to discriminate between the active and inactive lever by preferentially responding on the active lever. The lack of cocaine-reinforced responding by the MS15 group suggests that the reinforcing effects of cocaine may possibly be blunted in this group.

Carboxylesterases are nonspecific ester hydrolases with broad substrate specificity. Human liver has two major carboxylesterase isoenzymes, CES1 and CES2. CES1 is a class I isoenzyme and is responsible for hydrolysis of methyl ester of cocaine resulting in formation of benzoylecgonine (Brzezinski et al., 1994). The human class II enzyme (CES2) is responsible for hydrolysis of the benzoyl ester of cocaine (Pindel et al., 1997) and formation of ecgonine methylester. In comparison, the rat liver has at least four class 1 isoforms and three class 2 isoforms (Sanghani et al., 2002). A cocaine pharmacokinetic study in rats shows that benzoylecgonine is a major metabolite (Mets et al., 1999). Two class I enzymes, ES10 and ES4, account for >90% of total rat liver esterase activity and are likely to be responsible for formation of benzoylecgonine. There were no differences in the levels of CES activity or isoenzyme pattern of CESs among the four treatment groups after cocaine self-administration testing. Therefore, the differences between the various groups in cocaine-reinforced responding are unlikely to be caused by differences in pharmacokinetics.

Potential mechanisms of these changes have been examined. Others (Plotsky and Meaney, 1993; Pryce and Feldon, 2003) have shown a correlation with stress responses and the different paradigms and proposed that the relative stress among the groups is the major factor in their changes. In this case, the neurochemical responses to glucocorticoids are proposed to somehow cause the changes (Huot et al., 2002; Vazquez et al., 2002; Ploj et al., 2003). MS15 rats had a lower HPA response to acute and chronic stress in adulthood compared with the MS180s or NHs (Meaney et al., 1991; Plotsky and Meaney, 1993; Meaney, 2001). Stress and the subsequent activation of the HPA axis facilitate the acquisition of cocaine self-administration (Tidey and Miczek, 1997; Mantsch et al., 1998); manipulations of the HPA axis resulting in a reduction of function through pharmacological or surgical means can attenuate the acquisition of cocaine self-administration in rats (Goeders and Guerin, 1996). In the current experiment, we show that the MS15 group did not acquire cocaine self-administration, and this could possibly be attributed to or contributed by a reduction of HPA axis reactivity.

Some studies have examined the cellular and molecular mechanisms that might underlie the changes in the effects of psychostimulants. Decreases in dopamine transporter, D3, and D1 receptors in maternally separated rats compared with controls have been demonstrated (Meaney et al., 2002; Brake et al., 2004). Enhancement of stress- and psychostimulant-induced dopamine release in the nucleus accumbens of rats that underwent prolonged maternal separation (Hall et al., 1999) or neonatal isolation (Kosten et al., 2005) has also been shown. The differences seen in the acquisition of cocaine self-administration may be a result of the altered dopaminergic system because dopamine is important in psychostimulant self-administration. The MS15 group may have a blunted accumbal dopamine response to cocaine, thereby reducing the rewarding properties of cocaine, whereas the MS180 group may have enhanced dopamine release facilitating the acquisition of cocaine self-administration (Hooks et al., 1991; Rouge-Pont et al., 1993).

In the current study, we demonstrate that maternal separation affects the acquisition of cocaine self-administration in the dams. The length of separation appeared not to affect the dams' behavior. However, the dams whose pups were not separated (MS0) averaged more infusions per session during the 1st week than the NH group, but this effect was not seen in the 2nd week. This may suggest that the effect of maternal separation on the dams will be lost over time. Future experiments will explore the duration of the effects of maternal separation on cocaine self-administration in the dams.

Although it has been shown repeatedly that maternal separation causes neurochemical and behavioral alterations in the pups that persist into adulthood, less is known about how the separation procedure affects the dams. Interestingly, although the dams in the MS15 and MS180 groups did not differ in the acquisition of cocaine self-administration, these conditions had an impact on the behavior of the pups. The differences seen in the acquisition of cocaine self-administration in the dams may be attributable to the stress experienced by the separation procedure. The key stressful event would be the removal of the dams from their home cage. Both the MS15 and MS180 dams experience the same procedure by first being removed and placed in a separate cage and later reunited with the pups. The NH dams never experience the separation or the handling. However, the MS0 dams were present while the pups were being handled, and the intrusion of the experimenter's hand is a potentially powerful stressor.

Some evidence suggests that the reactions of the dams to separation and handling are important and actually produce the changes in the pups (Denenberg, 1999; Kalinichev et al., 2000; Champagne et al., 2004). Huot et al. (2004), utilizing fostering of litters, suggested that effects of MS may result largely from alterations in the quality of maternal care rather than from direct effects of the separation per se on the pups. Kalinichev et al. (2000) reported anxiety-like behavior in dams in the MS paradigm. Weaver et al. (2004) found that pups of mothers exhibiting high rates of licking and grooming and arched-back nursing had differences in DNA methylation in a glucocorticoid gene promoter in the hippocampus. These differences occurred in the 1st week of life, were reversed by cross fostering, and persisted into adulthood.

MS produced interesting changes in self-administration behavior in both the dams and the pups as adults. In the male adults, MS facilitated the acquisition of cocaine self-administration in the MS180 group, whereas the MS15 group did not self-administer cocaine at rates that differed from saline administration. The length of separation did not have a significant effect on cocaine self-administration in the dams; however, enhanced acquisition was seen in the MS0 group. Further study is warranted to investigate the mechanisms by which MS produces changes in vulnerability to drug abuse in both the dams and offspring.

	Acknowledgements

 
We thank Liling Shen for technical support and NIDA for supplying cocaine.

	Footnotes

 
This work was supported by National Institutes of Health/NIDA Grants RR 00165, DA00418, and T32 DA15040.

doi:10.1124/jpet.106.101139.

ABBREVIATIONS: MS0, brief handling without maternal separation; MS15, 15-min maternal separation; MS180, 180-min maternal separation; NH, nonhandled; MS, maternal separation; PN, postnatal; ANOVA, analysis of variance; CES, carboxylesterase; HPA, hypothalamic-pituary-adrenal.

Address correspondence to: Dr. Mark Moffett, Division of Neuroscience, Yerkes National Primate Research Center, Emory University, 954 Gatewood Road NE, Atlanta, GA 30329. E-mail: mcmoffe{at}emory.edu

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