Eliana Ruetti

Administration of corticosterone after the first downshift trial enhances consummatory successive negative contrast

Rats given access to a 32% sucrose solution and then downshifted to a 4% solution exhibit less contact with the sipper tube than unshifted controls always given access to 4% solution. This phenomenon, called consummatory successive negative contrast, was facilitated in Experiment 1 by a post-trial injection of corticosterone (3 mg/kg) administered immediately after the first downshift trial. Experiment 2 demonstrated that this facilitatory effect of post-trial corticosterone does not occur when administered 3 hr after the first downshift trial. These results support the hypothesis that corticosterone strengthens an aversive emotional component elicited by the surprising downshift in reward magnitude during the initial downshift trial.

Posttrial corticosterone administration enhances the effects of incentive downshift: exploring the boundaries of this effect.

Posttrial administration of corticosterone was previously shown to enhance consummatory successive negative contrast (cSNC) in rats. The present series of experiments provides additional information that helps determine the boundaries of this effect. Posttrial corticosterone administration (1) enhances cSNC when rats experience a large downshift (32% to 4% sucrose), but not after a small downshift (8% to 4% sucrose; Experiment 1); (2) has no effect in an anticipatory negative contrast situation in which 4% sucrose precedes 32% sucrose in daily trials (Experiment 2); (3) does not support the development of a conditioned taste aversion to 4% sucrose, in the absence of an incentive downshift (Experiment 3); and (4) facilitates the extinction of consummatory behavior (Experiment 4). These results suggest that corticosterone facilitates the encoding of an egocentric aversive memory of the incentive downshift experience.

Effects of testosterone administration and gonadectomy on incentive downshift and open field activity in rats.

Previous research showed that the effects of incentive downshift in male rats are attenuated by a pretrial opportunity to ejaculate. Because ejaculation raises testosterone (T) levels and has anxiolytic-like effects in male rats, the present experiments were designed to assess the role of T and gonadectomy (GDX) on two situations involving incentive downshift. In consummatory successive negative contrast, a downshift from 32% to 4% sucrose leads to consummatory suppression. T alleviates such suppression (Experiment 1), but GDX does not affect it (Experiment 3). In consummatory extinction, animals are downshifted from 32% sucrose to an empty sipper tube. T enhances consummatory extinction (Experiment 2), but GDX does not affect it (Experiment 4). In agreement with published results, T increases (Experiment 2) and GDX reduces (Experiment 4) activity in the central area of an open field, thus behaviorally validating these manipulations. The results are discussed in terms of the anxiolytic-like properties of androgen hormones.