Delta-opioid and 5-HT3 receptor antagonist effects on ethanol reward and discrimination in C57BL/6 mice.

The effects of the receptor antagonists MDL 72222 (MDL, 5-HT3) and naltrindole (delta-opioid) on ethanol reward and its discrimination were examined in ethanol-preferring C57BL/6 (C57) mice. MDL attenuated lever responding for 12% ethanol delivered on a fixed-ratio 8 reinforcement schedule at a dose that did not influence responding for water reward, thus confirming a previous report that ICS 205-930 reduced ethanol reward for Long-Evans rats. Our study in combination with the reduced ethanol consumption reported for C57 mice injected with odansetron indicates that 5-HT3 receptor systems are involved in mediating behavior directed toward obtaining ethanol as well as its consumption.

Naltrexone effects on ethanol reward and discrimination in C57BL/6 mice.

The effects of the opioid antagonist, naltrexone, on operant responding for oral ethanol reward delivered on a fixed-ratio schedule, and on the discriminative stimulus properties of intraperitoneally injected ethanol, was examined in two separate experiments. The ages, food/water motivational conditions, and naltrexone doses for the two experiments were similar to allow a direct comparison of naltrexone effects on the two measures. Male food-deprived C57BL/6 mice responded for ethanol during either preprandial (low thirst, high hunger motivation) or postprandial (high thirst, low hunger motivation tests).

Cocaine discrimination: relationship to local anesthetics and monoamine uptake inhibitors in C57BL/6 mice.

Although the discriminative properties of cocaine have been examined extensively in rats, and to a lesser extent in other species, there are currently no reports on cocaine discrimination by mice. In one of our experiments, C57BL/6 (C57) mice acquired cocaine discrimination (10 mg/kg training dose) and exhibited dose responsive generalization to lower doses of the drug, which was similar to previous reports using rats. In addition, mazindol, a general monoamine uptake inhibitor similar to cocaine, and nomifensine, which is relatively specific for the dopamine transporter, substituted completely for cocaine, as described for rats.

Long-term intracranial cannula stabilization in mice with light cured resin composites.

A simple and rapid method is described for the introduction and stabilization of chronic indwelling cannulae in mice. Materials and adhesive bonding techniques commonly used in restorative dentistry were used to stabilize the cannulae. The effectiveness of this method was evaluated by shear strength testing across time and histological evaluation of coronal brain sections.

Prenatal cocaine exposure increases the reinforcing strength of oral ethanol in C57 mice.

Pregnant C57BL/6J mice received daily injections of 10 mg/kg cocaine or saline during gestation days 12-18. Although a previous report indicated that this dose of cocaine did not alter maternal weight gain, birth weight, growth, or adult weight, the present study indicates that it did increase the reinforcing efficacy of ethanol in fully mature male and female offspring. Food-deprived subjects responded on fixed ratio-8 (FR-8) and progressive ratio-2 (PR-2) schedules of reinforcement for 10-, 5-, or 3-s access to various ethanol concentrations.