1996
DOI: 10.1016/s0024-3205(96)00562-0
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Reproduction and development in are dependent upon catecholamines

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Cited by 38 publications
(40 citation statements)
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References 15 publications
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“…dVMAT mutants show an eggretention phenotype similar to mutants with reduced octopamineric signaling. However, they also show reduced ovary size supporting previous pharmacologic data that suggest a role for dopamine and/or serotonin in ovarian development (Monastirioti et al 1996;Neckameyer 1996;Pendleton et al 1996;Willard et al 2006).…”
Section: Discussionsupporting
confidence: 82%
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“…dVMAT mutants show an eggretention phenotype similar to mutants with reduced octopamineric signaling. However, they also show reduced ovary size supporting previous pharmacologic data that suggest a role for dopamine and/or serotonin in ovarian development (Monastirioti et al 1996;Neckameyer 1996;Pendleton et al 1996;Willard et al 2006).…”
Section: Discussionsupporting
confidence: 82%
“…In addition, unlike mutants that reduce octopaminergic signaling (Monastirioti 1999;Lee et al 2003;Cole et al 2005), they show an additional defect in oocyte development that is most easily observed in virgin females. This difference is consistent with previous pharmacologic data suggesting that dopaminergic and possibly serotonergic inputs regulate oocyte development (Neckameyer 1996;Pendleton et al 1996;Willard et al 2006) (see discussion).…”
Section: P1supporting
confidence: 92%
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“…This result also suggests that the vesicular release of DA and 5-HT may be dispensable for larval development and adult survival under standard culture conditions, an observation that is surprising given the fundamental role of DA in many physiological processes and the lethal effects of genetic (pale) (Kobayashi et al 1995) or pharmacologic inhibition of tyrosine hydroxylase activity (Neckameyer 1996;Pendleton et al 1996). Similarly, it has been proposed that 5-HT has a critical role in fly development (Colas et al 1999;Sykes and Condron 2005;Willard et al 2006;Schaerlinger et al 2007).…”
Section: Discussionmentioning
confidence: 95%
“…The tyrosine hydroxylase (TH) gene is the rate-limiting step in the dopamine biosynthesis pathway and is responsible for the hydroxylation of tyrosine into 3,4-dihydroxy-L-phenylalanine, which is then converted into dopamine by dopa decarboxylase (49). Pharmacological inhibition of TH, catecholamine uptake, and α-adrenoreceptor antagonists at 1 mM concentration results in failure of viable progeny whereas lower concentration (0.1 mM) significantly delayed the development, indicating the essential function of catecholamines in Drosophila development and viability (50). Drosophila tyrosine hydroxylase is encoded by the pale locus (51), and mutations in the pale gene result in decreased dopamine pools in adult heads, even in the heterozygous state (22).…”
Section: Discussionmentioning
confidence: 99%