Evidence map›Paper›PMID 24187534›Full record

ArticleFrontiers in systems neuroscience2013

Apis mellifera octopamine receptor 1 (AmOA1) expression in antennal lobe networks of the honey bee (Apis mellifera) and fruit fly (Drosophila melanogaster).

Irina T Sinakevitch, Adrian N Smith, Fernando Locatelli, Ramon Huerta, Maxim Bazhenov, Brian H Smith

Open access · goldAbstract read
In one paragraph

Article in Frontiers in systems neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.7field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Tyramine and itseLife · 2023
    Article
  4. Article
  5. Article
  6. Review
  7. Olfactory coding in honeybees.Cell and tissue research · 2021
    Review
  8. Article
  9. Article
  10. Morphofunctional experience-dependent plasticity in the honeybee brain.Learning & memory (Cold Spring Harbor, N.Y.) · 2017
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Learning modifies odor mixture processing to improve detection of relevant components.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2015
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 2 countries.

Irina T SinakevitchSchool of Life Sciences, Arizona State University Tempe, AZ, USA.
Adrian N Smith
Fernando Locatelli
Ramon Huerta
Maxim Bazhenov
Brian H Smith
Arizona State University · USConsejo Nacional de Investigaciones Científicas y Técnicas · ARUniversity of California, Riverside · USUniversity of California San Diego · US

Funding

CRCNS: Dyanamic and Distributed Memory in OlfactionR01DC011422 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HUERTA, RAMON · 2010 to 2014
$1.7M
CRCNS: Multiple roles of inhibition in the olfactory systemR01DC012943 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI BAZHENOV, MAKSIM V · 2012 to 2016
$1.3M
NIDCD NIH HHS R01 DC011422NIDCD NIH HHS R01 DC012943
6 · The paper itself

Abstract

Octopamine (OA) underlies reinforcement during appetitive conditioning in the honey bee and fruit fly, acting via different subtypes of receptors. Recently, antibodies raised against a peptide sequence of one honey bee OA receptor, AmOA1, were used to study the distribution of these receptors in the honey bee brain (Sinakevitch et al., 2011). These antibodies also recognize an isoform of the AmOA1 ortholog in the fruit fly (OAMB, mushroom body OA receptor). Here we describe in detail the distribution of AmOA1 receptors in different types of neurons in the honey bee and fruit fly antennal lobes. We integrate this information into a detailed anatomical analysis of olfactory receptor neurons (ORNs), uni- and multi-glomerular projection neurons (uPNs, and mPNs) and local interneurons (LNs) in glomeruli of the antennal lobe. These neurons were revealed by dye injection into the antennal nerve, antennal lobe, medial and lateral antenno-protocerbral tracts (m-APT and l-APT), and lateral protocerebral lobe (LPL) by use of labeled cell lines in the fruit fly or by staining with anti-GABA. We found that ORN receptor terminals and uPNs largely do not show immunostaining for AmOA1. About seventeen GABAergic mPNs leave the antennal lobe through the ml-APT and branch into the LPL. Many, but not all, mPNs show staining for AmOA1. AmOA1 receptors are also in glomeruli on GABAergic processes associated with LNs. The data suggest that in both species one important action of OA in the antennal lobe involves modulation of different types of inhibitory neurons via AmOA1 receptors. We integrated this new information into a model of circuitry within glomeruli of the antennal lobes of these species.

Indexed as

biogenic amine receptorsG-protein receptorslearning and plasticityoctopamineolfactory pathways

Identifiers

PMID24187534
PMCPMC3807565
OpenAlexW2107565452

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.