Abstract
The biogenic amines octopamine (OA) and tyramine (TA) modulate insect motor behavior in an antagonistic manner. OA generally enhances locomotor behaviors such as Drosophila larval crawling and flight, whereas TA decreases locomotor activity. However, the mechanisms and cellular targets of TA modulation of locomotor activity are incompletely understood. This study combines immunocytochemistry, genetics and flight behavioral assays in the Drosophila model system to test the role of a candidate enzyme for TA catabolism, named Nazgul (Naz), in flight motor behavioral control. We hypothesize that the dehydrogenase/reductase Naz represents a critical step in TA catabolism. Immunocytochemistry reveals that Naz is localized to a subset of Repo positive glial cells with cell bodies along the motor neuropil borders and numerous positive Naz arborizations extending into the synaptic flight motor neuropil. RNAi knock down of Naz in Repo positive glial cells reduces Naz protein level below detection level by Western blotting. The resulting consequence is a reduction in flight durations, thus mimicking known motor behavioral phenotypes as resulting from increased TA levels. In accord with the interpretation that reduced TA degradation by Naz results in increased TA levels in the flight motor neuropil, the motor behavioral phenotype can be rescued by blocking TA receptors. Our findings indicate that TA modulates flight motor behavior by acting on central circuitry and that TA is normally taken up from the central motor neuropil by Repo-positive glial cells, desaminated and further degraded by Naz.
Highlights
Neuromodulatory substances shape central pattern generator (CPG) network and motoneuronal (MN) activity into many different forms, lending flexibility of the motor output to different behavioral requirements or to different internal states (Harris-Warrick and Marder, 1991)
The nuclei of glial cells in the central nervous system (CNS) were co-labeled with the glial cell marker Reversed polarity (Figure 1A, green), Repo, which is required for glial cell differentiation (Halter et al, 1995)
Naz localized to a subset of glial cells that align the flight motor neuropil borders and project extensions into the central neuropil regions
Summary
Neuromodulatory substances shape central pattern generator (CPG) network and motoneuronal (MN) activity into many different forms, lending flexibility of the motor output to different behavioral requirements or to different internal states (Harris-Warrick and Marder, 1991). Several different modulators affect motor output, and vice versa, the same modulator may act on multiple different levels (Marder et al, 2005). Analogous to noradrenaline (NA) in vertebrates, in insects ‘‘fight or flight’’ reactions are often attributed to the biogenic amine octopamine (OA; Stevenson and Rillich, 2012). Both Drosophila larval crawling (Fox et al, 2006) and adult flight motor behaviors (Brembs et al, 2007) are facilitated by OA. In invertebrates the biogenic amine tyramine (TA) regulates motor behaviors in an antagonistic manner to OA (Pflüger and Duch, 2011)
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