Oral intake of sweetened or sweetened alcoholic beverages and open-field behavior.

The relationship between the intake of sweetened alcoholic beverages and individual differences in an open field was assessed using an oral self-administration procedure in male Wistar rats (n = 41). After four sessions in the open field, rats were gradually reduced to 80% of their ad lib body weights over a 10-day period. Rats were then allowed to drink an alcohol-containing solution (10% v/v ethanol, 3% w/v glucose) (experimental group: n = 20) or a solution of glucose (3% w/v glucose) (control group: n = 21) for 1 h/day during 9 consecutive days. Experimental rats were divided into two groups on the basis of the mean daily ethanol dose ingested (g/kg/h) in the nine sessions. The high ethanol-consuming (HEI rats), when compared with the low ethanol-consuming rats (LEI rats), only showed a tendency (p = 0.062) towards fewer global number of rearings in the open field. No relationship between open-field defecation and ethanol intake was observed. With regard to the control rats, the higher consuming also showed lower number of rearings in the open field, similarly to the experimental rats. When we divided all experimental or control rats into two subgroups on the basis of the mean daily tap-water ingested during 23 h/day, no differences in the number of rearings were found. The results suggest that rearing in a novel environment could be a predictor of susceptibility to reinforcement by sweetened or palatable beverages.

Effects of ketamine, a noncompetitive NMDA antagonist, on the acquisition of the lever-press response in rats.

We analyzed the effects of ketamine, a noncompetitive NMDA antagonist, on the acquisition of the lever-press response in the Skinner box and on motor performance both in the open field and in the inclined screen. Ninety-six adult male Wistar rats were assigned at random to eight different groups (n = 12). The first four groups received an acute intraperitoneal (IP) injection of: (a) physiological saline, (b) 4 mg/kg ketamine, (c) 8 mg/kg ketamine, or (d) 12 mg/kg ketamine, and the subjects were tested in a free lever-press response shaping in the Skinner box. The second four groups received the same substances and doses as the first four, but the subjects were tested for locomotor activity in an open field and tested immediately afterwards for motor performance in an 80 degrees inclined screen. Results showed that ketamine impaired the acquisition of the lever-press response in a dose-dependent manner, with no effects on ambulation in the open field nor on length of stay in the inclined screen. These results suggest that ketamine effects on the acquisition of the lever-press response cannot be attributed to a motor impairment, indicating a possible specific effect of ketamine on the associative learning acquisition.

Effects of ethanol, caffeine, and clorazepate on hypertonic NaCl solution intake in rats.

Previous reports indicate that several anxiolytics enhance the intake of hypertonic saline in rehydrating rats. This experiment was conducted to determine the effects of repeated (5 sessions) injection (i.p.) of ethanol (0.4 or 0.8 g/kg), caffeine (20 or 40 mg/kg) or clorazepate (3 mg/kg) on the ingestion of hypertonic saline (1.8%) in water-deprived rats. Saline intake increased with the acute administration of both clorazepate and ethanol (two doses), but it decreased with caffeine (two doses). It seems that the increase or decrease of hypertonic saline ingestion following acute drug administration continues to correlate well with anxiolytic or anxiogenic actions. However, following repeated administration of caffeine and ethanol, the effects on saline intake were not maintained in a reliable manner.

The effects of caffeine in the social interaction test and on exploration in rats: comparison with ethanol and clorazepate.

The effects of caffeine (20mg/kg) in the holeboard and social interaction tests were compared with those of ethanol (0.4g and dipotassium clorazepate (3mg/kg), following acute administration in one group of rats or after five daily injections in another group. The rats were put in pairs into an unfamiliar arena with high levels of illumination (n = 80), or tested individually in the holeboard (n = 80). Acute caffeine produced no effect on the time spent in social interaction, although it enhanced the number of social contacts, and both genital and total sniffing. Following five injections, caffeine also increased the time spent in social interaction. Acute clorazepate enhanced this time but this effect showed partial tolerance after five injections. Clorazepate also enhanced the number and duration of social contacts, increasing social grooming and genital sniffing, regardless of the duration of the treatment. Ethanol increased the time spent in social interaction following five injections, and increased social grooming. In the holeboard, stimulant effects were observed for caffeine and clorazepate, showing partial tolerance and without any effect on head dipping. In the social interaction test, only a stimulant effect for caffeine was obtained. The results of this study suggest that, under some circumstances, caffeine may enhance social interaction, in a manner similar to standard anxiolytics. Such an effect is potentiated by repeated administration.

Effects of oral ethanol self-administration on the inhibition of the lever-press response in rats.

The effects of ethanol on the inhibition of a learned response were examined in adult, male Wistar rats from two treatment groups: oral self-administration of alcoholic solution (10% ethanol and 10% glucose in distilled water) and oral self-administration of sweet solution (10% glucose in distilled water). Subjects were food deprived and alcoholic or control solutions were available 1 h per day during 15 days. After this period, rats were tested in a two-bottle paradigm during 1 h per day and placed in the operant chambers immediately afterward. This phase went on for 19 days. Subjects were trained to lever press for food and were tested in a continuous reinforcement schedule, operant extinction, successive discrimination, and two-stimuli tests. Alcohol impaired the ability to inhibit previously reinforced responses but only in situations indicated by exteroceptive stimuli. Ethanol intake did not impair the lever-press behavior neither in the acquisition of the response nor in the continuous reinforcement schedule. These data suggest that the sedative effects of alcohol at this dose were not apparent in reinforcement situations, in contrast with extinction situations.