Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
44
pubmed:dateCreated
2010-11-4
pubmed:abstractText
Neuropeptides are found in both mammals and invertebrates and can modulate neural function through activation of G-protein-coupled receptors (GPCRS). The precise mechanisms by which many of these GPCRs modulate specific signaling cascades to regulate neural function are not well defined. We used Drosophila melanogaster as a model to examine both the cellular and behavioral effects of DPKQDFMRFamide, the most abundant peptide encoded by the dFMRF gene. We show that DPKQDFMRFamide enhanced synaptic transmission through activation of two G-protein-coupled receptors, Fmrf Receptor (FR) and Dromyosupressin Receptor-2 (DmsR-2). The peptide increased both the presynaptic Ca(2+) response and the quantal content of released transmitter. Peptide-induced modulation of synaptic function could be abrogated by depleting intracellular Ca(2+) stores or by interfering with Ca(2+) release from the endoplasmic reticulum through disruption of either the ryanodine receptor or the inositol 1,4,5-trisphosphate receptor. The peptide also altered behavior. Exogenous DPKQDFMRFamide enhanced fictive locomotion; this required both the FR and DmsR-2. Likewise, both receptors were required for an escape response to intense light exposure. Thus, coincident detection of a peptide by two GPCRs modulates synaptic function through effects of Ca(2+)-induced Ca(2+) release, and we hypothesize that these mechanisms are involved in behavioral responses to environmental stress.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DMSR-2 protein, Drosophila, http://linkedlifedata.com/resource/pubmed/chemical/Drosophila Proteins, http://linkedlifedata.com/resource/pubmed/chemical/FMRFamide, http://linkedlifedata.com/resource/pubmed/chemical/FMRFamide receptor, http://linkedlifedata.com/resource/pubmed/chemical/Insect Hormones, http://linkedlifedata.com/resource/pubmed/chemical/Neuropeptides, http://linkedlifedata.com/resource/pubmed/chemical/Neurotransmitter Agents, http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, G-Protein-Coupled, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Invertebrate Peptide, http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Peptide, http://linkedlifedata.com/resource/pubmed/chemical/aspartyl-prolyl-lysyl-glutaminyl-asp..., http://linkedlifedata.com/resource/pubmed/chemical/neomyosuppressin
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
1529-2401
pubmed:author
pubmed:issnType
Electronic
pubmed:day
3
pubmed:volume
30
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
14724-34
pubmed:meshHeading
pubmed-meshheading:21048131-Animals, pubmed-meshheading:21048131-Behavior, Animal, pubmed-meshheading:21048131-Calcium Signaling, pubmed-meshheading:21048131-Drosophila Proteins, pubmed-meshheading:21048131-Drosophila melanogaster, pubmed-meshheading:21048131-Escape Reaction, pubmed-meshheading:21048131-FMRFamide, pubmed-meshheading:21048131-Female, pubmed-meshheading:21048131-Insect Hormones, pubmed-meshheading:21048131-Male, pubmed-meshheading:21048131-Motor Activity, pubmed-meshheading:21048131-Neuropeptides, pubmed-meshheading:21048131-Neurotransmitter Agents, pubmed-meshheading:21048131-Protein Precursors, pubmed-meshheading:21048131-Receptors, G-Protein-Coupled, pubmed-meshheading:21048131-Receptors, Invertebrate Peptide, pubmed-meshheading:21048131-Receptors, Peptide, pubmed-meshheading:21048131-Stress, Physiological, pubmed-meshheading:21048131-Synaptic Transmission
pubmed:year
2010
pubmed:articleTitle
Peptide-induced modulation of synaptic transmission and escape response in Drosophila requires two G-protein-coupled receptors.
pubmed:affiliation
Program in Developmental and Stem Cell Biology, Hospital for Sick Children, Toronto, Ontario, Canada. mklose@exchange.ubc.ca
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't