Animals
Male Wistar rats weighing 250-300 g were housed in plastic cages maintained at 21° ± 2° C on a 12-hour circadian cycle. The animals had water and food access ad libitum before and during the behavioral tests. All experimental procedures were done in accordance with institutional guidelines for laboratory animal care and use, as directed by the Mashhad University of Medical Sciences ″Animal Studies Ethics Committee″ (No. 910593). Each rat was used only once. A total of 42 rats were randomly divided in 7 groups (n = 6 in each group).
Drugs
Morphine sulfate was obtained from Daru Pakhsh, Iran and dissolved in normal saline. Topiramate was provided from Soha, Iran and was dissolved in normal saline with minimal amount of DMSO as co-solvent. The ratio of DMSO to saline was 1 to 5. Memantine was obtained from Osveh, Iran and was dissolved in normal saline. All drugs were injected intraperitoneally (i.p.).
CPP test
The CPP test is a well-recognized and most popular method which is used for evaluation the rewarding effects of drugs (
31). In place-conditioning paradigm, animals prefer an environment, which associated with drug administration such as opioids. A typical CPP experiment includes two different sets of environmental signs pairing with the stimulus of interest (
32). This test consists of three phases including pre conditioning phase, conditioning phase and post-conditioning phase which were explained completely below. Additionally, the apparatus which is used for our research was described as follows.
Apparatus
Identical plexiglass boxes consisting two equal size compartments (30 cm length × 30 cm width × 35 cm height) and a grey central area (15 cm length × 30 cm width × 35 cm height) were used. The compartments were separated by guillotine doors. One compartment had black walls and smooth floor and the other was white with a harsh texture (
33).
Pre conditioning phase
During the preconditioning phase, the rats had free access to both compartments of the apparatus for 15 min each day for 2 days. On day 3, the time spent by the animals in each compartment was recorded for 15 min. The animals with strong unconditioned aversion or preference (less than 33% or more than 66% of the session time) for any of the compartments were excluded from the study.
Conditioning phase
The conditioning phase was carried out on days 4 to 7. On each day, all groups were received normal saline immediately before confinement to the vehicle-paired compartment for 1 h. After a 4-h interval, the animals received drug injections and were confined in the white section, which was drug-paired compartment for 1 h.
The confinement was done by closing the guillotine door that separated the two compartments (
33) . According to the treatment during this phase, the animals were divided into 7 groups (n = 6): 1) Saline + saline (SAL). 2) Saline + 10 mg/kg of morphine (MOR) (34). 3-5) 10 mg/kg of morphine + 10, 50 or 100 mg/kg of topiramate (MOR+TOP10, MOR+TOP50, and MOR+TOP100, respectively) (
30). 6) Saline + 100 mg/kg topiramate (TOP100). 7) 10 mg/kg of morphine + 7.5 mg/kg of memantine as positive control (
35). All injections were done via the intraperitoneal (i.p.) route.
Post-conditioning phase
After conditioning phase, on day 8, each animal was placed in the apparatus, the guillotine door which separated two compartments was removed and the time spent by the animals in each compartment was recorded for 15 min. The time spent in the central area was equally divided between both conditioning compartments (
33,
36). Three phases of CPP test have been shown in
Figure 1.
Open field test (OFT)
At the next step for evaluation locomotor activity, open field test was performed. The apparatus for this test, made of white wood, had a floor of 100 × 100 cm and 30 cm high which divided by lines into 25 squares of 20 × 20 cm. Each rat was placed in the middle of the apparatus, and its behavior was observed for 15 min. The parameters evaluated were the total number of squares crossed (
37).
Tissue sampling
After behavioral tests, the rats were sacrificed; the brain tissues (cerebral cortex and hippocampus) were dissected and snap-frozen in liquid nitrogen. The samples were stored at −80 °C until use.
Western blot analysis
The samples were homogenized in the buffer containing 50 mM Tris-HCl (pH 7.4), 2 mM EDTA, 2 mM EGTA, 10 mM NaF, 1 mM sodium orthovanadate (Na3VO4), 10 mM β glycerophosphate, 0.2% W/V sodium deoxycholate, 1 mM phenylmethylsulfonyl fluoride (PMSF), and complete protease inhibitor cocktail (Sigma P8340). The homogenized tissue suspension was centrifuged (4 °C, 10 min, 10000 rpm) and the supernatant was collected. The total proteins were separated in 12% SDS-PAGE gels and transferred to polyvinylidene fluoride (PVDF) membranes.
The blots were blocked with skim milk (5% in TBST) for CREB and ERK proteins. For p-CREB and p-ERK proteins, the blots were blocked with Bovine Serum Albumin (BSA 5% in TBST). Blocking for each protein was done at room temperature for 1.5 h except ERK which was incubated in 4 °C overnight. Rabbit monoclonal anti-serum against CREB (Cell Signaling, USA: #9197), mouse monoclonal anti-serum against p-CREB (Cell Signaling, USA: #9196), rabbit polyclonal anti-serum against P44/42 MAPK (ERK1/2) (Cell Signaling, USA: #9102), mouse monoclonal anti-serum against Phospho-p44/42 MAPK (ERK1/2) (Cell Signaling, USA: #9106), rabbit polyclonal anti-serum against β-actin (Cell Signaling, USA: #4967) or mouse monoclonal anti-serum against β-actin (Cell Signaling, USA: #3700) were used as primary antibodies (diluted 1:1000) and added to PVDF membranes. For CREB, p-CREB and ERK, PVDF membranes were incubated with primary antibodies for 2 h. For p-ERK, membranes were exposed to primary antibody solution for 16 h at 4 °C. Anti-mouse IgG labeled with horseradish peroxidase (Cell Signaling, USA: #7076) and anti-rabbit IgG labeled with horseradish peroxidase (Cell Signaling, USA: #7074) were used as secondary antibodies (1:3000). The membranes were further incubated with secondary antibodies for 2 h at room temperature. Immunoreactive proteins were visualized by a chemiluminescence reaction (Pierce ECL western blotting substrate) and Alliance Gel-doc (Alliance 4.7 Gel doc, UVtec UK). All bands were normalized against β-actin. Quantification of bands density was done by UV Tec software (UK).
Statistical analysis
Results are expressed as mean ± SEM for CPP test. Statistical analysis was performed with Two-way analysis of variance (ANOVA), followed by Bonferroni test. For locomotor activity test and western blot analysis One-way ANOVA followed by Tukey-Kramer test was used. Statistical significance was defined as p < 0.05.