1999
DOI: 10.1002/(sici)1097-0029(19990415)45:2<106::aid-jemt5>3.0.co;2-3
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Biogenic amine systems in the fruit flyDrosophila melanogaster

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Cited by 229 publications
(53 citation statements)
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“…4), but we were not able to detect dTdc2-GAL4 expression in any nonneural peripheral tissues. The dTdc2-GAL4 pattern of expression in the brain and nerve cord is strikingly similar to that seen with TBH immunoreactivity (25), although some of the TBH neurons reported to be located in the dorsal protocerebrum could not be detected. Furthermore, several clusters of cells not known to contain TBH in the central brain are detected with dTdc2-GAL4 (Fig.…”
Section: Ro54supporting
confidence: 73%
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“…4), but we were not able to detect dTdc2-GAL4 expression in any nonneural peripheral tissues. The dTdc2-GAL4 pattern of expression in the brain and nerve cord is strikingly similar to that seen with TBH immunoreactivity (25), although some of the TBH neurons reported to be located in the dorsal protocerebrum could not be detected. Furthermore, several clusters of cells not known to contain TBH in the central brain are detected with dTdc2-GAL4 (Fig.…”
Section: Ro54supporting
confidence: 73%
“…5), but was completely absent from the female reproductive tract (data not shown). Although the presence of tyramine and octopamine in the Drosophila CNS is well established (25), tyramine was only recently shown to modulate transepithelial chloride conductance in the Drosophila Malpighian tubule (7). Since we detect dTdc1 expression and tyramine, but not octopamine, in these nonneural tissues (data not shown), we predict that dTdc1 is responsible for this nonneural tyramine production.…”
Section: Ro54supporting
confidence: 61%
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“…1a,b). In invertebrates, OA is synthesized from the amino acid tyrosine via the action of tyrosine decarboxylase (TDC) and tyramine β-hydroxylase (Tβh) 40 . The Tdc2 gene encodes the neuronal TDC and the tdc2-gal4 driver can be used to manipulate OA/TA neurons 41 .…”
Section: Resultsmentioning
confidence: 99%
“…The dynamics of the 5-HT system in insects shares several features with vertebrates, including (a) 5-HT synthesis from tryptophan (3,7), (b) calcium-dependent release and activation of second messengers (15,29), and (c) recapture by nerve endings (2) for subsequent inactivation. In insects, however, the main catabolic process for inactivation of 5-HT is N-acetylation (44), although inactivation of 5-HT by oxidative deamination may also take place, since 5-hydroxyindoleacetic acid (5-HIAA) has been detected in the nervous system of some insect species (49)(50)(51)(52).…”
mentioning
confidence: 99%