These findings indicate that transient early alterations to dopaminergic neurotransmission can trigger long-term impairments in behavioural plasticity. The habenula (Hb) is a part of the epithalamus that projects to brain stem nuclei including the raphe nucleus and ventral tegmentum. The subdivisions of the habenula are similar in zebrafish and other species: the dorsal and ventral Hb (dHb and vHb) of fish correspond to the mammalian medial Hb and lateral Hb respectively

[28]. Inhibition of the lateral subnucleus of the dHb by expression of the tetanus selleck inhibitor toxin light chain (TeTxLC) does not induce changes in locomotion but increases freezing indicating that the Hb is important for the response to fear [29]. Larval zebrafish learn to avoid a light when paired with a mild shock but are unable to learn when submitted to an inescapable shock. Photobleaching Hb afferents or expressing TeTxLC in the dHb can block this avoidance response, suggesting that abnormalities in Hb function may contribute to anxiety disorders [7]. Zebrafish exposed to alarm substance (AS) also show a fear response that includes erratic movements and freezing. Intercranial administration of the neuropeptide Kisspeptin decreases the behavioural response

to AS. Furthermore, inactivation of Kiss-Receptor1-expressing neurons using Kiss1 peptide conjugated to saporin, a ribosome inactivating protein, both reduces Kiss1 immunoreactivity and c-fos mRNA in the habenula and decreases the AS-evoked fear response reinforcing the role of Kisspeptin in this AZD8055 purchase behaviour [30]. Although these studies have already demonstrated a role for the Hb in fear, a complete description of the genes and signalling pathways that underlie this behaviour now needs to be produced. Zebrafish display learning and memory capabilities

and both short and long-term memory formation have been evaluated in this species 31 and 32]. Tenoxicam There is evidence that glutamatergic and cholinergic signalling are implicated in the acquisition and consolidation phases of memory processing [31]. Classical and operant learning behaviours can be observed from 3 weeks post-fertilisation reaching maximal performance at week 6 [33]. In addition, associative conditioning learning has been shown to be protein synthesis-dependent and NMDA receptor-dependent using a paradigm developed for larval zebrafish [34•]. Recent work using a genetically encoded calcium-sensitive protein, inverse pericam, has identified an area of the dorsal telencephalon that is activated during long-term memory retrieval [8••]. This functional map changes when the behavioural task is altered, suggesting that memory traces are dynamically modified during the learning process [8••]. In larvae, calcium indicators have been used to image neuronal activity during behaviour.