Multiple neuropeptides in the Drosophila antennal lobe suggest complex modulatory circuits
Abstract
The fruitfly, Drosophila, is dependent on its olfactory sense in food search and reproduction. Processing of odorant information takes place in the antennal lobes, the primary olfactory center in the insect brain. Besides classical neurotransmitters, earlier studies have indicated the presence of a few neuropeptides in the olfactory system. In the present study we made an extensive analysis of the expression of neuropeptides in the Drosophila antennal lobes by direct profiling using matrix‐assisted laser desorption/ionization‐time‐of‐flight (MALDI‐TOF) mass spectrometry and immunocytochemistry. Neuropeptides from seven different precursor genes were unambiguously identified and their localization in neurons was subsequently revealed by immunocytochemistry. These were short neuropeptide F, tachykinin related peptide, allatostatin A, myoinhibitory peptide, SIFamide, IPNamide, and myosuppressin. The neuropeptides were expressed in subsets of olfactory sensory cells and different populations of local interneurons and extrinsic (centrifugal) neurons. In some neuron types neuropeptides were colocalized with classical neurotransmitters. Our findings suggest a huge complexity in peptidergic signaling in different circuits of the antennal lobe. J. Comp. Neurol. 518:3359–3380, 2010. © 2010 Wiley‐Liss, Inc.
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The "ALl1 dorsal" and "ALv2" hemilineages that produce antennal lobe local neurons seem to break Dale's law and Lacin's law, with similar morphology types predicted to express different transmitters.
“They seem to break Dale’s law104,106 and Lacin’s law (Figure 7C), with similar morphology types predicted to express different transmitters (Figures S5F and S5G).”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
The fan-shaped body is known to express leucokinin, allatostatin A, short neuropeptide F, Drosophila neuropeptide F, tachykinin, proctolin, dFMRFa, SIFamide and myoinhibitory peptide in a highly specific and layer-wise manner.
“The fan-shaped body is known to express leucokinin, allatostatin A, short neuropeptide F, Drosophila neuropeptide F, tachykinin, proctolin, dFMRFa, SIFamide and myoinhibitory peptide in a highly specific and layer-wise manner.106,175,177,184”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
Transmitter usage in antennal lobe local neurons breaks Dale's law, Lacin's law, and the expectation of uniform transmitter expression within a type.
“transmitter usage in these local neurons seems to break Dale’s law,104,106 Lacin’s law (Figure 7C) and the expectation of uniform transmitter expression within a type (Figures S5F and S5G)”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
Some cholinergic local neurons have been mispredicted dopaminergic because at least approximately 3 cholinergic neurons co-express allatostatin A and approximately 10-15 co-express myoinhibitory peptide.
“We suspect that some cholinergic local neurons have been mispredicted dopaminergic because at least ∼ 3 cholinergic neurons co-express allatostatin A and ∼ 10-15 co-express myoinhibitory peptide.106”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
Tachykinin co-expresses in approximately 40 GABAergic 'ALl1 dorsal' neurons per hemisphere.
“Tachykinin is also known to co-express in ∼ 40 GABAergic ‘ALl1 dorsal’ neurons per hemisphere106”
From Neurotransmitter classification from electron microscopy images at synaptic sites in Drosophila melanogaster (2024) · cites this paper as [106]
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Davie, K., Janssens, J., Koldere, D., De Waegeneer, M., Pech, U., Kreft, Ł., Aibar, S., Makhzami, S., Christiaens, V., Bravo González-Blas, C., et al. (2018) · Cell · doi:10.1016/j.cell.2018.05.057 · Cited by 840 · see citing works
Presynaptic facilitation by neuropeptide signaling mediates odor-driven food search
Root, C. M., Ko, K. I., Jafari, A., & Wang, J. W. (2011) · Cell · doi:10.1016/j.cell.2011.02.008 · Cited by 526 · see citing works
Early Olfactory Processing in <i>Drosophila</i>: Mechanisms and Principles
Wilson, R. I. (2013) · Annual Review of Neuroscience · doi:10.1146/annurev-neuro-062111-150533 · Cited by 394 · see citing works
Recent advances in neuropeptide signaling in Drosophila, from genes to physiology and behavior
Nässel, D. R., & Zandawala, M. (2019) · Progress in Neurobiology · doi:10.1016/j.pneurobio.2019.02.003 · Cited by 367 · see citing works
Self-citationNässel, D. R., & Wegener, C. (2011) · Peptides · doi:10.1016/j.peptides.2011.03.013 · Cited by 316 · see citing works
Self-citationEckstein, N., Bates, A. S., Champion, A., Du, M., Yin, Y., Schlegel, P., Lu, A. K.-Y., Rymer, T., Finley-May, S., Paterson, T., et al. (2024) · Cell · doi:10.1016/j.cell.2024.03.016 · Cited by 233 · see citing works
Elucidating the Neuronal Architecture of Olfactory Glomeruli in the Drosophila Antennal Lobe
Grabe, V., Baschwitz, A., Dweck, H. K. M., Lavista-Llanos, S., Hansson, B. S., & Sachse, S. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.08.063 · Cited by 186 · see citing works
Metabolism and growth adaptation to environmental conditions in Drosophila
Koyama, T., Texada, M. J., Halberg, K. A., & Rewitz, K. (2020) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03547-2 · Cited by 152 · see citing works
Olfactory coding in the insect brain: data and conjectures
Galizia, C. G. (2014) · European Journal of Neuroscience · doi:10.1111/ejn.12558 · Cited by 151 · see citing works
Tachykinins: Neuropeptides That Are Ancient, Diverse, Widespread and Functionally Pleiotropic
Nässel, D. R., Zandawala, M., Kawada, T., & Satake, H. (2019) · Frontiers in Neuroscience · doi:10.3389/fnins.2019.01262 · Cited by 153 · see citing works
Self-citationNässel, D. R. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00083 · Cited by 119 · see citing works
Self-citationMyoinhibitory peptide regulates feeding in the marine annelid Platynereis
Williams, E. A., Conzelmann, M., & Jékely, G. (2015) · Frontiers in Zoology · doi:10.1186/s12983-014-0093-6 · Cited by 120 · see citing works
Cannell, E., Dornan, A. J., Halberg, K. A., Terhzaz, S., Dow, J. A. T., & Davies, S. A. (2016) · Peptides · doi:10.1016/j.peptides.2016.02.004 · Cited by 119 · see citing works
Synaptic organization of the Drosophila antennal lobe and its regulation by the Teneurins
Mosca, T. J., & Luo, L. (2014) · eLife · doi:10.7554/elife.03726 · Cited by 113 · see citing works
Kahsai, L., & Winther, Å. M. E. (2011) · Journal of Comparative Neurology · doi:10.1002/cne.22520 · Cited by 115 · see citing works
Neuropeptides Modulate Female Chemosensory Processing upon Mating in Drosophila
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Neuropeptide modulation of microcircuits
Nusbaum, M. P., & Blitz, D. M. (2012) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2012.01.003 · Cited by 107 · see citing works
The CCHamide 1 receptor modulates sensory perception and olfactory behavior in starved Drosophila
Farhan, A., Gulati, J., Große‐Wilde, E., Vogel, H., Hansson, B. S., & Knaden, M. (2013) · Scientific Reports · doi:10.1038/srep02765 · Cited by 92 · see citing works
Regulation of insect behavior via the insulin-signaling pathway
Erion, R., & Sehgal, A. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00353 · Cited by 91 · see citing works
Endocrine cybernetics: neuropeptides as molecular switches in behavioural decisions
Nässel, D. R., & Zandawala, M. (2022) · Open Biology · doi:10.1098/rsob.220174 · Cited by 83 · see citing works
Self-citationFeeding regulates sex pheromone attraction and courtship in Drosophila females
Lebreton, S., Trona, F., Borrero‐Echeverry, F., Bilz, F., Grabe, V., Becher, P. G., Carlsson, M. A., Nässel, D. R., Hansson, B. S., Sachse, S., et al. (2015) · Scientific Reports · doi:10.1038/srep13132 · Cited by 83 · see citing works
Self-citationChrist, P., Reifenrath, A., Kahnt, J., Hauser, F., Hill, S. R., Schachtner, J., & Ignell, R. (2017) · PLoS ONE · doi:10.1371/journal.pone.0188243 · Cited by 75 · see citing works
Self-citationFood odors trigger an endocrine response that affects food ingestion and metabolism
Lushchak, O. V., Carlsson, M. A., & Nässel, D. R. (2015) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-1884-4 · Cited by 67 · see citing works
Self-citationMusashe, D. T., Purice, M. D., Speese, S. D., Doherty, J., & Logan, M. A. (2016) · Cell Reports · doi:10.1016/j.celrep.2016.07.022 · Cited by 56 · see citing works
Sayın, S., Boehm, A. C., Kobler, J. M., Backer, J. D., & Kadow, I. C. G. (2018) · Frontiers in Cellular Neuroscience · doi:10.3389/fncel.2018.00011 · Cited by 60 · see citing works
Intrinsic and Extrinsic Neuromodulation of Olfactory Processing
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Neuropeptides in the antennal lobe of the yellow fever mosquito, Aedes aegypti
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Self-citationDrosophila olfaction: past, present and future
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Neuropeptides in insect mushroom bodies
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Self-citationNeurogenetics of Female Reproductive Behaviors in Drosophila melanogaster
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Lange, A. B., Alim, U., Vandersmissen, H. P., Mizoguchi, A., Broeck, J. V., & Orchard, I. (2012) · Frontiers in Neuroscience · doi:10.3389/fnins.2012.00098 · Cited by 50 · see citing works
Nagata, S., Matsumoto, S., Nakane, T., Ohara, A., Morooka, N., Konuma, T., Nagai‐Okatani, C., & Nagasawa, H. (2012) · Frontiers in Endocrinology · doi:10.3389/fendo.2012.00003 · Cited by 48 · see citing works
Neuropeptides in modulation of Drosophila behavior: how to get a grip on their pleiotropic actions
Nässel, D. R., Pauls, D., & Huetteroth, W. (2019) · Current Opinion in Insect Science · doi:10.1016/j.cois.2019.03.002 · Cited by 48 · see citing works
Self-citationModulation of neural circuits: how stimulus context shapes innate behavior in Drosophila
Su, C.-Y., & Wang, J. W. (2014) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2014.04.008 · Cited by 47 · see citing works
Sizemore, T. R., & Dacks, A. M. (2016) · Scientific Reports · doi:10.1038/srep37119 · Cited by 48 · see citing works
Olfactory Habituation in Drosophila—Odor Encoding and its Plasticity in the Antennal Lobe
Isabell, T., Lee, J. A., & Ramaswami, M. (2014) · Progress in brain research · doi:10.1016/b978-0-444-63350-7.00001-2 · Cited by 46 · see citing works
Spit, J., Badisco, L., Verlinden, H., Wielendaele, P. V., Zels, S., Dillen, S., & Broeck, J. V. (2012) · Canadian Journal of Zoology · doi:10.1139/z2012-014 · Cited by 42 · see citing works
Serotonergic modulation across sensory modalities
Sizemore, T. R., Hurley, L. M., & Dacks, A. M. (2020) · Journal of Neurophysiology · doi:10.1152/jn.00034.2020 · Cited by 40 · see citing works
Coates, K. E., Majot, A. T., Zhang, X., Michael, C. T., Spitzer, S. L., Gaudry, Q., & Dacks, A. M. (2017) · Journal of Neuroscience · doi:10.1523/jneurosci.0192-17.2017 · Cited by 39 · see citing works
Carlsson, M. A., Enell, L. E., & Nässel, D. R. (2013) · Cell and Tissue Research · doi:10.1007/s00441-013-1660-4 · Cited by 40 · see citing works
Self-citationBrain organization in Collembola (springtails)
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Self-citationKidd, S., Struhl, G., & Lieber, T. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005244 · Cited by 42 · see citing works
Levy, C., Brooks, J. M., Chen, J., Su, J., & Fox, M. A. (2014) · The Journal of Comparative Neurology · doi:10.1002/cne.23701 · Cited by 38 · see citing works
Organization of the Olfactory System of Nymphalidae Butterflies
Carlsson, M. A., Schäpers, A., Nässel, D. R., & Janz, N. (2013) · Chemical Senses · doi:10.1093/chemse/bjt008 · Cited by 37 · see citing works
Self-citationThe Wiring Logic of an Identified Serotonergic Neuron That Spans Sensory Networks
Coates, K. E., Calle-Schuler, S. A., Helmick, L. M., Knotts, V. L., Martik, B. N., Salman, F., Warner, L. T., Valla, S. V., Bock, D. D., & Dacks, A. M. (2020) · Journal of Neuroscience · doi:10.1523/jneurosci.0552-20.2020 · Cited by 36 · see citing works
Peptidomics and processing of regulatory peptides in the fruit fly Drosophila
Pauls, D., Chen, J., Reiher, W., Vanselow, J. T., Schlösser, A., Kahnt, J., & Wegener, C. (2014) · EuPA Open Proteomics · doi:10.1016/j.euprot.2014.02.007 · Cited by 32 · see citing works
Jung, J. W., Kim, J., Pfeiffer, R., Ahn, Y., Page, T. L., & Kwon, H. W. (2013) · PLoS ONE · doi:10.1371/journal.pone.0081361 · Cited by 35 · see citing works
Lu, H., & Pietrantonio, P. V. (2011) · BMC Neuroscience · doi:10.1186/1471-2202-12-57 · Cited by 35 · see citing works
Fine structure of synaptic sites and circuits in mushroom bodies of insect brains
Schürmann, F. (2016) · Arthropod Structure & Development · doi:10.1016/j.asd.2016.08.005 · Cited by 35 · see citing works
Structure and function of neuropeptide F in insects
Cui, H., & Zhao, Z. (2020) · Journal of Integrative Agriculture · doi:10.1016/s2095-3119(19)62804-2 · Cited by 34 · see citing works
Nässel, D. R. (2012) · Canadian Journal of Zoology · doi:10.1139/z2012-009 · Cited by 33 · see citing works
Self-citationWilson, R. I. (2011) · Current Opinion in Neurobiology · doi:10.1016/j.conb.2011.03.002 · Cited by 32 · see citing works
Presynaptic modulation of early olfactory processing in Drosophila
Wang, J. W. (2011) · Developmental Neurobiology · doi:10.1002/dneu.20936 · Cited by 33 · see citing works
Neuroblast lineage-specific origin of the neurons of the Drosophila larval olfactory system
Das, A., Gupta, T., Davla, S., Prieto-Godino, L. L., Diegelmann, S., Reddy, O. V., Raghavan, K. V., Reichert, H., Lovick, J. K., & Hartenstein, V. (2012) · Developmental Biology · doi:10.1016/j.ydbio.2012.11.003 · Cited by 30 · see citing works
Neuropeptidomics of the Carpenter Ant Camponotus floridanus
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Neuropeptidome of Tribolium castaneum antennal lobes and mushroom bodies
Binzer, M., Heuer, C. M., Kollmann, M., Kahnt, J., Hauser, F., Grimmelikhuijzen, C. J. P., & Schachtner, J. (2013) · The Journal of Comparative Neurology · doi:10.1002/cne.23399 · Cited by 31 · see citing works
Self-citationHigh-resolution AP-SMALDI mass spectrometry imaging of Drosophila melanogaster
Khalil, S. M., Pretzel, J., Becker, K., & Spengler, B. (2017) · International Journal of Mass Spectrometry · doi:10.1016/j.ijms.2017.04.001 · Cited by 31 · see citing works
Lehmann, P., Nylin, S., Gotthard, K., & Carlsson, M. A. (2017) · Proceedings of the Royal Society B Biological Sciences · doi:10.1098/rspb.2017.0897 · Cited by 30 · see citing works
Self-citationNutrient Sensing via Gut in Drosophila melanogaster
Chopra, G., Kaushik, S., & Kain, P. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052694 · Cited by 30 · see citing works
Schulze, J., Neupert, S., Schmidt, L., Predel, R., Lamkemeyer, T., Homberg, U., & Stengl, M. (2011) · The Journal of Comparative Neurology · doi:10.1002/cne.22785 · Cited by 30 · see citing works
Singh, A. P., Das, R. N., Kidiyoor, G. R., Aggarwal, A., Diegelmann, S., Evers, J. F., Karandikar, H., Landgraf, M., Rodrigues, V., & VijayRaghavan, K. (2013) · PLoS Genetics · doi:10.1371/journal.pgen.1003452 · Cited by 30 · see citing works
Calcium Imaging of Neural Activity in the Olfactory System of Drosophila
Strutz, A., Völler, T., Riemensperger, T. D., Fiala, A., & Sachse, S. (2012) · Neuromethods · doi:10.1007/978-1-62703-014-4_3 · Cited by 28 · see citing works
Distributed control circuits across a brain-and-cord connectome
Bates, A. S., Phelps, J. S., Kim, M., Yang, H. H., Matsliah, A., Ajabi, Z., Perlman, E., Delgado, K. M., Osman, M. A. M., Salmon, C. K., et al. (2026) · Nature · doi:10.1038/s41586-026-10735-w · Cited by 62 · see citing works
Jung, J., Kim, D., Han, G.-Y., & Kwon, H. W. (2018) · International Journal of Molecular Sciences · doi:10.3390/ijms19102855 · Cited by 29 · see citing works
Kołodziejczyk, A. M., & Nässel, D. R. (2010) · Cell and Tissue Research · doi:10.1007/s00441-010-1100-7 · Cited by 27 · see citing works
Self-citationFuscà, D., Schachtner, J., & Kloppenburg, P. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23757 · Cited by 24 · see citing works
Self-citationShort Neuropeptide F and Its Receptor Regulate Feeding Behavior in Pea Aphid (Acyrthosiphon pisum)
Amir, M. B., Shi, Y., Cao, H., Ali, M. Y., Ahmed, M. A., Smagghe, G. J., & Liu, T. (2022) · Insects · doi:10.3390/insects13030282 · Cited by 25 · see citing works
Kidd, S., & Lieber, T. (2016) · PLoS ONE · doi:10.1371/journal.pone.0151279 · Cited by 25 · see citing works
Sex peptides and MIPs can activate the same G protein-coupled receptor
Vandersmissen, H. P., Nachman, R. J., & Broeck, J. V. (2013) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2013.02.014 · Cited by 24 · see citing works
Structural plasticity of olfactory neuropils in relation to insect diapause
Eriksson, M., Janz, N., Nylin, S., & Carlsson, M. A. (2020) · Ecology and Evolution · doi:10.1002/ece3.7046 · Cited by 23 · see citing works
Self-citationVariations on a Theme: Antennal Lobe Architecture across Coleoptera
Kollmann, M., Schmidt, R., Heuer, C. M., & Schachtner, J. (2016) · PLoS ONE · doi:10.1371/journal.pone.0166253 · Cited by 23 · see citing works
Self-citationFunctional characterization of mosquito short neuropeptide F receptors
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Self-citationOdor processing in the cockroach antennal lobe—the network components
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The ability of Drosophila hybrids to locate food declines with parental divergence
Turissini, D. A., Comeault, A. A., Geoffrey, L., Lee, Y. C. G., & Matute, D. R. (2017) · Evolution · doi:10.1111/evo.13180 · Cited by 20 · see citing works
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Sizemore, T. R., Jonaitis, J., & Dacks, A. M. (2023) · Nature Communications · doi:10.1038/s41467-023-41012-3 · Cited by 21 · see citing works
Schmitt, F., Vanselow, J. T., Schlösser, A., Wegener, C., & Rößler, W. (2016) · The Journal of Comparative Neurology · doi:10.1002/cne.24109 · Cited by 18 · see citing works
Fruit fly behavior in response to chemosensory signals
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Dacks, A. M., & Nighorn, A. J. (2010) · Chemical Senses · doi:10.1093/chemse/bjq121 · Cited by 17 · see citing works
The neuropeptide SIFamide in the brain of three cockroach species
Arendt, A., Neupert, S., Schendzielorz, J., Predel, R., & Stengl, M. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23910 · Cited by 16 · see citing works
Lebreton, S., Carlsson, M. A., & Witzgall, P. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.00685 · Cited by 15 · see citing works
Self-citationLiu, Y., Luo, J., & Nässel, D. R. (2016) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2016.00097 · Cited by 14 · see citing works
Self-citationNovel antennal lobe substructures revealed in the small hive beetle Aethina tumida
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Self-citationInsect brain plasticity: effects of olfactory input on neuropil size
Eriksson, M., Nylin, S., & Carlsson, M. A. (2019) · Royal Society Open Science · doi:10.1098/rsos.190875 · Cited by 14 · see citing works
Self-citationWhat Drosophila can tell us about state-dependent peptidergic signaling in insects
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Self-citationShort neuropeptide F in integrated insect physiology
Cholewiński, M., Chowański, S., Lubawy, J., Urbański, A., Walkowiak‐Nowicka, K., & Marciniak, P. (2024) · Journal of Zhejiang University SCIENCE B · doi:10.1631/jzus.b2300355 · Cited by 12 · see citing works
The degradome and the evolution of Drosophila sex peptide as a ligand for the MIP receptor
Isaac, R. E., Kim, Y., & Audsley, N. (2014) · Peptides · doi:10.1016/j.peptides.2013.12.016 · Cited by 12 · see citing works
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Self-citationArguello, J. R., Abuin, L., Armida, J., Mika, K., Chai, P. C., & Benton, R. (2021) · eLife · doi:10.7554/elife.63036 · Cited by 10 · see citing works
Kołodziejczyk, A. M., & Nässel, D. R. (2011) · Cell and Tissue Research · doi:10.1007/s00441-011-1198-2 · Cited by 12 · see citing works
Self-citationLismont, E., Mortelmans, N., Verlinden, H., & Broeck, J. V. (2017) · General and Comparative Endocrinology · doi:10.1016/j.ygcen.2017.10.014 · Cited by 12 · see citing works
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Self-citationSynaptic connectome of a neurosecretory network in the Drosophila brain
McKim, T. H., Gera, J., Gayban, A. J. B., Christie, K., Shin, J., Reinhard, N., Manoli, G., Hilpert, S., Callaerts, P., van Breugel, F., et al. (2026) · eLife · doi:10.1101/2024.08.28.609616 · Cited by 16 · see citing works
Functional characterization of the dual allatostatin-A receptors in mosquitoes
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The anatomical basis for modulatory convergence in the antennal lobe of Manduca sexta
Lizbinski, K. M., Metheny, J. D., Bradley, S. P., Kesari, A., & Dacks, A. M. (2015) · The Journal of Comparative Neurology · doi:10.1002/cne.23926 · Cited by 9 · see citing works
Odor response adaptation in Drosophila—a continuous individualization process
Jafari, S., & Alenius, M. (2021) · Cell and Tissue Research · doi:10.1007/s00441-020-03384-6 · Cited by 10 · see citing works
- Authors
- Carlsson, M. A., Diesner, M., Schachtner, J., & Nässel, D. R.
- Affiliations
- Stockholm University (SE)
- Philipps University of Marburg (DE)
- Corresponding author
- Carlsson, Mikael A.
- Nässel, Dick R.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 2010-06-23
- Volume
- 518
- Issue
- 16
- Pages
- 3359-3380
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W1979540477
- Cited by
- 146
- References
- 92
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 8 · 2023: 6 · 2022: 5 · 2021: 12 · 2020: 5 · 2019: 4 · 2018: 9 · 2017: 11 · 2016: 10 · 2015: 11 · 2014: 13 · 2013: 12 · 2012: 13
- FWCI
- 5.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- The Journal of Comparative Neurology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurobiology and Insect Physiology Research
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuropeptides and Animal Physiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Keywords
- neuropeptides, olfactory system, short neuropeptide F, tachykinin-related peptides, allatostatin A, myoinhibitory peptides, SIFamide, myosuppressin, olfactory sensory neurons, local interneurons, neurotransmitter co-localization, peptidergic signaling, olfactory processing
- MeSH terms
- Amino Acid Sequence, Animals, Brain, Drosophila melanogaster, Female, Hormone Antagonists, Interneurons, Male, Molecular Sequence Data, Neuropeptides, Olfactory Pathways, Smell, Signal Transduction, Olfactory Receptor Neurons, Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization, Drosophila Proteins
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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