Distinct neural circuits reflect sex, sexual maturity, and reproductive status in response to stress in Drosophila melanogaster

Neuroscience

Volumn 156, Issue 4, 2008, Pages 841-856

  Neckameyer, W S ^a   Matsuo, H ^b  

^a SAINT LOUIS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b SAINT LOUIS UNIVERSITY   (United States)

Author keywords

central complex; heart rate; mushroom bodies; oxidative stress

Indexed keywords

ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; DROSOPHILA MELANOGASTER; ENVIRONMENTAL STRESS; HEART FUNCTION; HEART RATE; LOCOMOTION; NERVE CELL; NERVE CELL PLASTICITY; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; REPRODUCTION; SEXUAL BEHAVIOR; SEXUAL MATURITY; STRESS;

ANIMALS; BEHAVIOR, ANIMAL; BRAIN; DROSOPHILA MELANOGASTER; DROSOPHILA PROTEINS; FEMALE; HEART RATE; LOCOMOTION; MALE; MUSHROOM BODIES; MUTATION; NEURAL PATHWAYS; OXIDATIVE STRESS; REPRODUCTION; SEXUAL BEHAVIOR, ANIMAL; STARVATION;

EID: 53949088233     PISSN: 03064522     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuroscience.2008.08.020     Document Type: Article

References (48)

1. Acevedo S., Froudarakis E., Kanellopoulos A., and Skoulakis W. Protection from premature habituation requires functional mushroom bodies in Drosophila. Learn Mem 14 (2007) 376-384
2. Autor A. Biochemical mechanisms of paraquat toxicity (1977), Academic Press, New York
3. Chaudhuri A., Bowling K., Funderburk C., Lawal H., Inamdar A., Wang Z., and O'Donnell J. Interaction of genetic and environmental factors in a Drosophila parkinsonism model. J Neurosci 27 (2007) 2457-2467
4. de Belle S., and Heisenberg M. Expression of Drosophila mushroom body mutations in alternative genetic backgrounds: A case study of the mushroom body miniature (mbm) gene. Proc Natl Acad Sci U S A 93 (1996) 9875-9880
5. de Velasco B., Erclik T., Shy D., Sclafani J., Lipshitz H., McInnes R., and Hartenstein V. Specification and development of the pars intercerebralis and pars lateralis, neuroendocrine command centers in the Drosophila brain. Dev Biol 302 (2007) 309-323
6. Dias-Santagata D., Fulga T., Duttaroy A., and Feany M. Oxidative stress mediates tau-induced neurodegeneration in Drosophila. J Clin Invest 117 (2007) 236-245
7. Drugan R., Basile A., Ha J., and Ferland R. The protective effects of stress control may be mediated by increased brain levels of benzodiazepine receptor agonists. Brain Res 661 (1994) 127-136
8. Dulcis D., and Levine R. Innervation of the heart of the adult fruit fly, Drosophila melanogaster. J Comp Neurol 465 (2003) 560-578
9. Fleshner M., and Laudenslager M. Psychoneuroimmunology: then and now. Behav Cogn Neurosci Rev 3 (2004) 114-130
10. Gailey D., Jackson F., and Siegel R. Male courtship in Drosophila: the conditioned response to immature males and its genetic control. Genetics 102 (1982) 771-778
11. Goldenschwege T., Kristiansen L., Uthaman S., Hortsch M., and Murphy K. A conserved role for Drosophila Neuroglian and human L1-CAM in central synapse formation. Curr Biol 16 (2006) 12-23
12. Gotz K. Visual guidance in Drosophila. Basic Life Sci 16 (1980) 391-407
13. Gronli J., Murison R., Fiske E., Bjorvatn B., Sorenson E., Portas C., and Ursin R. Effects of chronic mild stress on sexual behavior, locomotor activity and consumption of sucrose and saccharine solutions. Physiol Behav 84 (2005) 571-577
14. Hanesch U., Fischbach K., and Heisenberg M. Neuronal architecture of the central complex in Drosophila melanogaster. Cell Tissue Res 257 (1989) 343-366
15. Harshman L., Moore K., Sty M., and Magwire M. Stress resistance and longevity in selected lines of Drosophila melanogaster. Neurobiol Aging 20 (1999) 521-529
16. Heisenberg M. What do the mushroom bodies do for the insect brain?. An introduction. Learn Mem 5 (1998) 1-10
17. Helfrich-Forster C., Wulf J., and de Belle J. Mushroom body influence on locomotor activity and circadian rhythms in Drosophila melanogaster. J Neurogenetics 16 (2002) 73-109
18. Homberg U., Christiansen T., and Hildebrand J. Structure and function of the deutocerebrum in insects. Annu Rev Entomol 34 (1989) 477-501
19. Manning-Boig A., McCormack A., Li J., Uversky V., Fink A., and Di Monte D. The herbicide paraquat causes up-regulation and aggregation of alpha-synuclein in mice: paraquat and alpha-synuclein. J Biol Chem 277 (2002) 36588-36595
20. Martijena I., Rodriguez Manzanares P., Lacerra C., and Molina V. GABAergic modulation of the stress response in frontal cortex and amygdala. Synapse 45 (2002) 86-94
21. Martin J., Ernst R., and Heisenberg M. Mushroom bodies suppress locomotor activity in Drosophila melanogaster. Learn Mem 5 (1998) 179-191
22. Martin J., Ernst R., and Heisenberg M. Temporal pattern of locomotor activity in Drosophila melanogaster. J Comp Physiol A 184 (1999) 73-84
23. Martin J., Raabe T., and Heisenberg M. Central complex substructures are required for the maintenance of locomotor activity in Drosophila melanogaster. J Comp Physiol A 185 (1999) 277-288
24. Meincke U., Light G., Geyer M., Braff D., and Gouzoulis-Mayfrank E. Sensitization and habituation of the acoustic startle reflex in patients with schizophrenia. Psychiatry Res 126 (2004) 51-61
25. Metz G. Stress as a modulator of motor system function and pathology. Rev Neurosci 18 (2007) 209-222
26. Moghaddam B., and Jackson M. Effect of stress on prefrontal cortex function. Neurotox Res 6 (2004) 73-78
27. Neckameyer W. Dopamine modulates female sexual receptivity in Drosophila melanogaster. J Neurogenet 12 (1998) 101-114
28. Neckameyer W., and Weinstein J. Stress affects dopaminergic signaling pathways in Drosophila melanogaster. Stress 8 (2005) 117-132
29. Nichols R. FMRFamide-related peptides and serotonin regulate Drosophila melanogaster heart rate: mechanisms and structure requirements. Peptides 27 (2006) 1130-1137
30. Osborne K., de Belle J., and Sokolowski M. Foraging behavior in Drosophila larvae: mushroom body ablation. Chem Senses 26 (2001) 223-230
31. Paternostro G., Vignola C., Bartsch D., Omens J., McCulloch A., and Reed J. Age-associated cardiac dysfunction in Drosophila melanogaster. Circ Res 88 (2001) 1053-1058
32. Pesah Y., Pham T., Heather Burgess H., Middlebrooks B., Verstreken P., Zhou Y., Harding M., Bellen H., and Mardon G. Drosophila parkin mutants have decreased cell mass and cell size and increased sensitivity to oxygen radical stress. Development 131 (2004) 2183-2194
33. Phillips J., Campbell S., Michaud D., Charbonneau M., and Hillaker A. Null mutation of copper/zinc superoxide dismutase in Drosophila confers hypersensitivity to paraquat and reduced longevity. Proc Natl Acad Sci U S A 86 (1989) 2761-2765
34. Popov A., Peresleni A., Savvateeva-Popova E., Wolf R., and Heisenberg M. Role of mushroom bodies and the central complex of Drosophila melanogaster in the organisation of courtship behavior and communicative vocalization. J Evolutionary Biochem Physiol 40 (2004) 521-530
35. Rein K., Zockler M., Mader M., Grubel C., and Heisenberg M. The Drosophila standard brain. Curr Biol 12 (2002) 227-231
36. Raabe T., Clemens-Ricjter S., Twardzik T., Ebert A., Gramlich G., and Heisenberg M. Identification of mushroom body miniature, a zinc finger protein implicated in brain development of Drosophila. Proc Natl Acad Sci U S A 101 (2004) 14276-14281
37. Reveillaud I., Niedzwiecki A., Bensch K., and Fleming J. Expression of bovine superoxide dismutase in Drosophila melanogaster augments resistance to oxidative stress. Mol Cell Biol 11 (1991) 632-640
38. Reveillaud I., Kongpachith A., Park R., and Fleming J. Stress resistance of Drosophila transgenic for bovine CuZn superoxide dismutase. Free Radic Res Commun 17 (1992) 73-85
39. Rion S., and Rawecki J. Evolutionary biology of starvation resistance: what we have learned from Drosophila. J Evol Biol 20 (2007) 1655-1664
40. Rush B., Sandver S., Bruer J., Roche R., Wells M., and Giebultowicz J. Mating increases starvation resistance and decreases oxidative stress resistance in Drosophila melanogaster females. Aging Cell 6 (2007) 723-726
41. Strausfeld N. Atlas of an insect brain (1976), Springer, Berlin
42. Strauss R. The central complex and the genetic dissection of locomotor behavior. Curr Opinion Neurobiol 12 (2002) 633-638
43. Strauss R., and Heisenberg M. A higher control center of locomotor behavior in the Drosophila brain. J Neurosci 13 (1993) 1852-1861
44. Tavares R., Pelosi G., and Correa F. The paraventricular nucleus of the hypothalamus is involved in cardiovascular responses to acute restraint stress in rats. Stress (2008). http://www.ncbi.nlm.nih.gov/pubmed Epub ahead of print. http://www.ncbi.nlm.nih.gov/pubmed/
45. Varnum C., Strauss R., de Belle J., and Sokolowski M. Larval behavior of Drosophila central complex mutants: interactions between no bridge, foraging and chaser. J Neurogenetics 11 (1996) 99-115
46. Veelaert D., Schoofs L., and De Loof A. Peptidergic control of the corpus cardiacum-corpora allata complex of locusts. Int Rev Cyt 182 (1998) 249-302
47. Wessells R., and Bodmer R. Screening assays for heart function mutants in Drosophila. Biotechniques 37 (2004) 58-60
48. Willner P. Animal models as simulations of depression. Trends Pharmacol Sci 12 (1991) 131-136