2003
DOI: 10.1002/cne.10965
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Distribution of tyrosine hydroxylase, dopamine, and serotonin in the central nervous system of amphioxus (Branchiostoma lanceolatum): Implications for the evolution of catecholamine systems in vertebrates

Abstract: To investigate the evolutionary transition that has shaped the catecholaminergic systems of vertebrates, the organization of catecholamine-synthesizing neurons and the nature of the catecholamines were examined in the central nervous system of adult amphioxus (Branchiostoma lanceolatum), a cephalochordate. We isolated a gene transcript encoding tyrosine hydroxylase (TH), the limiting enzyme of catecholamine biosynthesis, and studied its distribution together with that of dopamine and serotonin. Dopamine and TH… Show more

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Cited by 61 publications
(83 citation statements)
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“…In situ hybridization was carried out on 20-mm cryosections from gelatine/sucrose-embedded embryos, as described previously 54 .…”
Section: Methodsmentioning
confidence: 99%
“…In situ hybridization was carried out on 20-mm cryosections from gelatine/sucrose-embedded embryos, as described previously 54 .…”
Section: Methodsmentioning
confidence: 99%
“…Determination of Monoamine Neurotransmitters by High Performance Liquid Chromatography (HPLC)-HPLC separation of monoamine neurotransmitters was performed as described elsewhere (8). Cultured CD36-negative and CD36-positive gustatory cells were incubated with LA, as mentioned in the legends, and at the end of incubation supernatant was removed and supplemented with equal volume of solution A (0.2 M perchloric acid, 2.7 mM EDTA, 5.26 mM sodium metabisulfite), then 100 pg of an internal standard (3,4-dihydroxybenzylamine hydrobromide) was added to each sample.…”
Section: Detection Of Mrna Of Enzymes Involved In the Synthesis Of Nementioning
confidence: 99%
“…Alternatively, 150 m vibratome sections were used for confocal analysis. In situ hybridization was performed as described previously (Moret et al, 2004). For immunostaining, cryosections, vibratome sections, embryos or explants were incubated overnight with the following antibodies diluted in 2% bovine serum albumin blocking solution: mouse anti-Myc (1/100; 9E10; Sigma, USA), goat anti-neuropilin 1 (1/50; R&D Systems, Minneapolis, USA), mouse anti-neurofilament 160 kDa (NF160kD; 1/100; RMO-270; Zymed, San Francisco, USA).…”
Section: Histological Analysesmentioning
confidence: 99%