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Comparison of octopamine-like immunoreactivity in the brains of the fruit fly and blow fly.

A serum raised against conjugated octopamine reveals structurally comparable systems of perikarya and arborizations in protocerebral neuropils of two species of Diptera, Drosophila melanogaster and Phaenicia sericata; the latter is used extensively for electrophysiological studies of the optic lobes and their central projections. Clusters of cell bodies in the brain as well as midline perikarya provide octopamine-like immunoreactive processes to the optic lobes, circumscribed regions of the protocerebrum and the central complex, particularly the protocerebral bridge, fan-shaped body, and ellipsoid body. Ventral unpaired median somata provide immunoreactive processes within the subesophageal ganglion and tritocerebrum. Ascending neurites from these cells also supply the antennal lobe glomeruli, regions of the lateral protocerebrum, the mushroom body calyces, and the lobula complex. The mushroom body's gamma lobes contain immunoreactive processes that originate from processes that arborize in the protocerebrum. The present observations are discussed with respect to similarities and differences between two species of Diptera, one of which has neurons large enough for intracellular penetrations. The results are also discussed with respect to recent studies on octopamine-immunoreactive organization in honey bees and cockroaches and the suggested roles of octopamine in sensory processing, learning, and memory.

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How flies fly.

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Animals↗

Evidence for a fruit fly hemangioblast and similarities between lymph-gland hematopoiesis in fruit fly and mammal aorta-gonadal-mesonephros mesoderm.

The Drosophila melanogaster lymph gland is a hematopoietic organ and, together with prospective vascular cells (cardioblasts) and excretory cells (pericardial nephrocytes), arises from the cardiogenic mesoderm. Clonal analysis provided evidence for a hemangioblast that can give rise to two daughter cells: one that differentiates into heart or aorta and another that differentiates into blood. In addition, the GATA factor gene pannier (pnr) and the homeobox gene tinman (tin), which are controlled by the convergence of Decapentaplegic (Dpp), fibroblast growth factor (FGF), Wingless (Wg) and Notch signaling, are required for the development of all cardiogenic mesoderm, including the lymph gland. Here we show that an essential genetic switch that differentiates between the blood or nephrocyte and vascular lineages involves the Notch pathway. Further specification occurs through specific expression of the GATA factor Serpent (Srp) in the lymph-gland primordium. Our findings suggest that there is a close parallel between the molecular mechanisms functioning in the D. melanogaster cardiogenic mesoderm and those functioning in the mammalian aorta-gonadal-mesonephros mesoderm.

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Peripheral plasma progesterone concentrations in pregnant and non-pregnant greyheaded flying-foxes (Pteropus poliocephalus) and little red flying-foxes (P. scapulatus).

Blood was collected from breeding-season and pregnant P. poliocephalus females shot in the wild and from captive pregnant and ovariectomized P. poliocephalus and P. scapulatus females. Peripheral plasma progesterone concentrations measured by radioimmunoassay were similar to those obtained by gas chromatography-mass spectroscopy: in intact non-pregnant P. poliocephalus females without corpora lutea (CLs) values ranged from 2 to 30 ng mL-1; after ovariectomy, they ranged from 1 to 85 ng mL-1. A significant source of progesterone in these bats may be the adrenal. In P. poliocephalus, peripheral plasma progesterone concentrations showed relatively little change over the breeding season or in early pregnancy when a CL formed, but increased from mid pregnancy to reach 200-800 ng mL-1 in late pregnancy. A mid-pregnancy ovary with CL contained 2.80 ng progesterone whereas the contralateral ovary contained 0.13 ng. Overall, CL size decreased during pregnancy and was negatively correlated with plasma progesterone concentrations. In late pregnancy, the main source of progesterone appears to be the placenta; plasma concentrations increase with placental growth and are significantly correlated with placental weight, and placentas contain 4-8 micrograms progesterone g-1. There was no evidence that progesterone concentrations fall before parturition. Limited observations indicated that peripheral progesterone concentrations follow similar patterns in P. scapulatus.

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