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First published online November 19, 2004
Journal of Experimental Biology 207, 4479-4488 (2004)
Published by The Company of Biologists 2004
doi: 10.1242/jeb.01316
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Bacterial lipopolysaccharide (LPS) modulates corticotropin-releasing hormone (CRH) content and release in the brain of juvenile and adult tilapia (Oreochromis mossambicus; Teleostei)

P. P. L. M. Pepels*, S. E. Wendelaar Bonga and P. H. M. Balm

Department of Animal Physiology, Faculty of Sciences, Radboud University Nijmegen, Toernooiveld 1, 6525 ED Nijmegen, The Netherlands



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Fig. 1. Depicts the major CRH-ir cells groups and CRH-ir pathways in a sagittal section of the brain of tilapia (original data in Pepels et al., 2002aGo, 2004Go). Each circle represents approximately 25 CRH-ir cells. The hypophysiotropic CRH-ir neurons located in the nucleus preopticus (npo), nucleus recessus lateralis (nrl) and nucleus lateralis tuberis (nlt) project into the pituitary (pit). The largest CRH-ir cell group is found in the lateral part of the ventral telencephalon (Vl) and projects mainly into the anterior subdivision of the lateral part of the dorsal telencephalon (Dla). CRH-ir terminals have also been found locally in Vl. Many blood capillaries are found in close proximity of the CRH-ir cells in Vl and a collecting vein is located in the sulcus of Vl (Pepels et al., 2004Go). In the vagal lobe (LX) CRH-ir terminals are present.

 


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Fig. 2. Effects of injection with saline or E. coli LPS on brain and pituitary tissue CRH levels in tilapia (N=6 in all cases). Open bars indicate pre-confinement values and solid bars indicate values of fish sampled following 24 h confinement. The asterisks (*) indicate confinement effects within a saline- or LPS-treatment group (see Presentation of data and statistics for details). Upper left panel: sagittal overview of the brain of tilapia showing the dissected parts (telencephalon, diencephalon, rhombencephalon and pituitary). The grey areas indicate brain parts that were discarded: tectum and midbrain, and the rostral part of the spinal cord.

 


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Fig. 3. (A) Basal and stimulated in vitro CRH release by telencephalic tissues. Tissues were stimulated for 30 min with 5x10–6 mol l–1 norepinephrine (NE) or 5x10–6 mol l–1 serotonin (5-HT). (B) Maximally stimulated in vitro CRH release by telencephalic tissue stimulated (grey bars) with 5x10–6 mol l–1 norepinephrine (NE) or 56 mmol l–1 K+. Before stimulation, tissues were superfused with control medium or with medium containing LPS (50 µg LPS ml–1).

 

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© The Company of Biologists Ltd 2004