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5. Neurogenesis domains in the adult zebrafish brain. Proliferation domains are schematically indicated as gray zones or dots on a representation of the adult brain at a midsagital level (anterior left). All these domains contain label-retaining progenitors and are neurogenic, except for proliferating cells in the OB (empty dots) and MO (empty zone). Cb: cerebellum; CCe: corpus cerebelli; Di: diencephalon; DIL: diffuse nucleus of the nferior lobe of the hypothalamus; Dm: medial domain of the dorsal telencephalon; Dp: posterior domain of the dorsal telencephalon; Ha: habenula; Hc: caudal zone of periventricular hypothalamus; Hd: dorsal zone of periventricular hypothalamus; IPZ: isthmic proliferation zone; LH: lateral hypothalamic nucleus; Mes: mesencephalon; MO: medulla oblongata; PO: pre-optic area; PT: posterior thalamus; OB: olfactory bulb; Tel: telencephalon; TL: torus longitudinalis; TP: posterior tuberculum; TPZ: tectal proliferation zone; V: ventral domain of the telencephalon; Va: valvula cerebelli; VT: ventral thalamus

5. Neurogenesis domains in the adult zebrafish brain. Proliferation domains are schematically indicated as gray zones or dots on a representation of the adult brain at a midsagital level (anterior left). All these domains contain label-retaining progenitors and are neurogenic, except for proliferating cells in the OB (empty dots) and MO (empty zone). Cb: cerebellum; CCe: corpus cerebelli; Di: diencephalon; DIL: diffuse nucleus of the nferior lobe of the hypothalamus; Dm: medial domain of the dorsal telencephalon; Dp: posterior domain of the dorsal telencephalon; Ha: habenula; Hc: caudal zone of periventricular hypothalamus; Hd: dorsal zone of periventricular hypothalamus; IPZ: isthmic proliferation zone; LH: lateral hypothalamic nucleus; Mes: mesencephalon; MO: medulla oblongata; PO: pre-optic area; PT: posterior thalamus; OB: olfactory bulb; Tel: telencephalon; TL: torus longitudinalis; TP: posterior tuberculum; TPZ: tectal proliferation zone; V: ventral domain of the telencephalon; Va: valvula cerebelli; VT: ventral thalamus

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... This organism is unique, in that it has a very mammalian kind of brain and structure of arrangements, as well as the function, a model for research. Nevertheless, both the way of functioning and the building blocks and method of constructing those structures like the hippocampus, diencephalon, tectum, tegmentum, and cerebellum are shared by the zebrafish and the mammals [1]. The research points out the fact that zebrafish development and neurodisorders have a common element, and this idea should be emphasized [2]. ...
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Zebrafish are emerging as a novel model for studying learning and memory. However, the number of behavioural paradigms which minimize handling stress and are suited to their social nature is limited. We developed an automated learning paradigm to condition groups of adult and juvenile zebrafish in their home tanks. Fish consistently learned to associate an auditory stimulus with the presentation of food and showed robust conditioned responses as early as the 5th trial. Memory of the association persisted for at least 2 days after training, when fish were tested either as groups or as individuals. This retention in juveniles was associated with increased immunoreactivity to phosphorylated ERK, a marker of neural activity, in the dorsolateral telencephalon. This simple paradigm permits scalable conditioning of zebrafish with minimal intervention, reducing variability and labour-intensiveness. In addition, these results support the use of phosphorylated ERK to examine the neural correlates of learning and memory.
... The fish telencephalon contains limbic-like areas and is the equivalent of the mammalian limbic system (Chandroo et al., 2004;Northcutt, 2006;Jesuthasan, 2012). The optic tectum is a midbrain structure that plays a fundamental role in the control of fine motor programmes and sensory-motor coupling and participates in the triggering of avoidance and escape behaviours (Bally-Cuif & Vernier, 2010;Broglio et al., 2011). Finally, neuroendocrine stress responses are important mechanisms for survival during exposure to life-threatening stimuli. ...
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Juvenile Senegalese sole Solea senegalensis were subjected for short periods to two different types of handling-related stress: air exposure stress and net handling stress. The S. senegalensis were sacrificed 2 and 24 h after the stress events and the levels of serotonin (5-HT), noradrenaline (NA), dopamine (DA) and their respective major metabolites, 5-hydroxyindoleacetic acid (5-HIAA), 3-methoxy-4-hydroxyphenylglycol (MHPG) and 3,4-dihydroxyphenylacetic acid (DOPAC), were measured in three brain regions (telencephalon, hypothalamus and optic tectum) and compared with those in control, non-stressed S. senegalensis. Neither type of stress caused any significant alteration of serotoninergic activity (5-HIAA:5-HT ratio) or NA levels. Dopaminergic activity (DOPAC:DA ratio) was lower in stressed fish in all of the brain regions studied. For both air exposure stress and net handling stress, DA levels were significantly higher (P < 0·05) than in the control S. senegalensis. In addition, the higher DA levels after net handling stress were always significantly higher (P < 0·05) than those observed after acute air exposure stress, except in the telencephalon after 24 h. The significantly lower DOPAC:DA ratio (P < 0·05) in all of the brain regions studied was only observed in response to net handling stress.