The role of the Glucocorticoid Receptor in the Regulation of Diel Rhythmicity.

Virtually all organisms have adapted to the earth's day-night cycles by the evolution of endogenous rhythms that regulate most biological processes. Recent research has highlighted the role of glucocorticoids and the Glucocorticoid receptor (GR) in coordinating clock function across various levels of biological organisation. In the present study, we have explored the role of the GR in the rhythmicity of the biological clock, by comparing 5 day old wildtype zebrafish larvae (gr+) with mutant larvae with a non-functional GR (grs357). The mutants display a weaker rhythmicity in locomotor activity in wildtypes than in mutants, while the rhythmicity of the angular velocity was higher for wildtypes. The melatonin production of the mutants showed a weaker rhythmicity, but surprisingly, there were no differences in the rhythmicity of clock-related gene expression between genotypes that could explain a mechanism for GR functionality at the transcriptional level. Furthermore, our results show that grs357 larvae have a more erratic swimming path, and cover more distance during locomotor activity than wild type larvae, in line with previously described behaviour of this mutant. Therefore, these results suggest that GR affects the diel rhythmicity of zebrafish larvae at the behavioural and endocrine level, but that these effects are not mediated by changes in the expression of clock-related genes.

Profound effects of glucocorticoid resistance on anxiety-related behavior in zebrafish adults but not in larvae.

Previously, adult zebrafish with a mutation in the gene encoding the glucocorticoid receptor (Gr) were demonstrated to display anxiety- and depression-like behavior that could be reversed by treatment with antidepressant drugs, suggesting that this model system could be applied to study novel therapeutic strategies against depression. Subsequent studies with zebrafish larvae from this grs357 line and a different gr mutant have not confirmed these effects. To investigate this discrepancy, we have analyzed the anxiety-like behavior in 5 dpf grs357 larvae using a dark/tapping stimulus test and a light/dark preference test. In addition, grs357 adult fish were subjected to an open field test. The results showed that in larvae the mutation mainly affected general locomotor activity (decreased velocity in the dark/tapping stimulus test, increased velocity in the light/dark preference test). However, parameters considered specific readouts for anxiety-like behavior (response to dark/tapping stimulus, time spent in dark zone) were not altered by the mutation. In adults, the mutants displayed a profound increase in anxiety-like behavior (time spent in outer zone in open field test), besides changes in locomotor activity (decreased velocity, increased angular velocity and freezing time). We conclude that the neuronal circuitry involved in anxiety- and depression-like behavior is largely affected by deficient Gr signaling in adult fish but not in larvae, indicating that this circuitry only fully develops after the larval stages in zebrafish. This makes the zebrafish an interesting model to study the ontology of anxiety- and depression-related pathology which results from deficient glucocorticoid signaling.