This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.Aggression is a ubiquitous component of social behavior across the animal kingdom. The signals exchanged in aggressive interactions are a great functional importance due to their role in determining social status and in mediating access to resources. Size relationships exert a strong influence on aggressive contests. Many aggressive signals may function to advertise size, and the assessment of rival size appears to play an important role in governing the course and the outcome of aggressive contests. The neural, sensory, genetic and cognitive mechanisms that permit such assessments to be performed remain largely unexplored. These mechanisms are important to elucidate in order to understand the evolution and function of aggressive signals. Stalk-eyed flies exhibit morphological specializations, combat rituals, and visual capabilities that indicate an unusually promising system for the study of visually mediated mechanisms of rival size assessment. The goal of the current proposal is to establish stalk-eyed flies as a model system for the study of rival size assessment by (a) testing whether rival size is assessed in contests, (b) examining at what stage or stages in the agonistic sequence this assessment is made, and (c) comparing the importance of eye stalks versus the offensive weapon in rival assessment.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR015567-08
Application #
7627582
Study Section
Special Emphasis Panel (ZRR1-RI-8 (02))
Project Start
2007-06-01
Project End
2008-05-31
Budget Start
2007-06-01
Budget End
2008-05-31
Support Year
8
Fiscal Year
2007
Total Cost
$16,118
Indirect Cost
Name
University of South Dakota
Department
Neurosciences
Type
Schools of Medicine
DUNS #
929930808
City
Vermillion
State
SD
Country
United States
Zip Code
57069
Robertson, James M; Achua, Justin K; Smith, Justin P et al. (2017) Anxious behavior induces elevated hippocampal Cb2 receptor gene expression. Neuroscience 352:273-284
Burrell, Brian D (2017) Comparative biology of pain: What invertebrates can tell us about how nociception works. J Neurophysiol 117:1461-1473
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Smith, Justin P; Prince, Melissa A; Achua, Justin K et al. (2016) Intensity of anxiety is modified via complex integrative stress circuitries. Psychoneuroendocrinology 63:351-61
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Hahn, Elizabeth; Burrell, Brian (2015) Pentylenetetrazol-induced seizure-like behavior and neural hyperactivity in the medicinal leech. Invert Neurosci 15:177
Novick, Andrew M; Forster, Gina L; Hassell, James E et al. (2015) Increased dopamine transporter function as a mechanism for dopamine hypoactivity in the adult infralimbic medial prefrontal cortex following adolescent social stress. Neuropharmacology 97:194-200
Ranek, Mark J; Kost Jr, Curtis K; Hu, Chengjun et al. (2014) Muscarinic 2 receptors modulate cardiac proteasome function in a protein kinase G-dependent manner. J Mol Cell Cardiol 69:43-51
Watt, Michael J; Roberts, Christina L; Scholl, Jamie L et al. (2014) Decreased prefrontal cortex dopamine activity following adolescent social defeat in male rats: role of dopamine D2 receptors. Psychopharmacology (Berl) 231:1627-36

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