Evidence map›Paper›PMID 22527118›Full record

ArticleBrain structure & function2013

Serotonergic innervation and serotonin receptor expression of NPY-producing neurons in the rat lateral and basolateral amygdaloid nuclei.

M Bonn, A Schmitt, K-P Lesch, E J Van Bockstaele, E Asan

Open access · hybridAbstract read
In one paragraph

Article in Brain structure & function, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

35 citing papers in PubMed, 62 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Lateralization of the 5-HTAmino acids · 2024
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. 5-HTScientific reports · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Control of Amygdala Circuits by 5-HT Neurons via 5-HT and Glutamate Cotransmission.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    Article
  19. Article
  20. Review
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

5 authors at 2 institutions in 2 countries.

M BonnInstitute of Anatomy and Cell Biology, University of Wuerzburg, Koellikerstr. 6, 97070, Würzburg, Germany.
A Schmitt
K-P Lesch
E J Van Bockstaele
E Asan
University of Würzburg · DEThomas Jefferson University · US

Funding

OPIOID MODULATION OF THE COERULEO-CORTICAL PATHWAYR01DA009082 · NIDA · THOMAS JEFFERSON UNIVERSITY · PI VAN BOCKSTAELE, ELISABETH J · 2001 to 2017
$6.0M
OPIOID MODULATION OF THE COERULEO-CORTICAL PATHWAYR29DA009082 · NIDA · WEILL MEDICAL COLLEGE OF CORNELL UNIV · PI VAN BOCKSTAELE, ELISABETH J · 1994 to 1998
–
NIDA NIH HHS DA 09082NIDA NIH HHS R01 DA009082
6 · The paper itself

Abstract

Pharmacobehavioral studies in experimental animals, and imaging studies in humans, indicate that serotonergic transmission in the amygdala plays a key role in emotional processing, especially for anxiety-related stimuli. The lateral and basolateral amygdaloid nuclei receive a dense serotonergic innervation in all species studied to date. We investigated interrelations between serotonergic afferents and neuropeptide Y (NPY)-producing neurons, which are a subpopulation of inhibitory interneurons in the rat lateral and basolateral nuclei with particularly strong anxiolytic properties. Dual light microscopic immunolabeling showed numerous appositions of serotonergic afferents on NPY-immunoreactive somata. Using electron microscopy, direct membrane appositions and synaptic contacts between serotonin-containing axon terminals and NPY-immunoreactive cellular profiles were unequivocally established. Double in situ hybridization documented that more than 50 %, and about 30-40 % of NPY mRNA-producing neurons, co-expressed inhibitory 5-HT1A and excitatory 5-HT2C mRNA receptor subtype mRNA, respectively, in both nuclei with no gender differences. Triple in situ hybridization showed that individual NPY mRNA-producing interneurons co-express both 5-HT1A and 5-HT2C mRNAs. Co-expression of NPY and 5-HT3 mRNA was not observed. The results demonstrate that serotonergic afferents provide substantial innervation of NPY-producing neurons in the rat lateral and basolateral amygdaloid nuclei. Studies of serotonin receptor subtype co-expression indicate a differential impact of the serotonergic innervation on this small, but important, population of anxiolytic interneurons, and provide the basis for future studies of the circuitry underlying serotonergic modulation of emotional stimulus processing in the amygdala.

Indexed as

AmygdalaAnimalsBehavior, AnimalFemaleImmunohistochemistryIn Situ HybridizationInterneuronsMaleMicroscopy, ElectronNeuropeptide YRatsRats, WistarReceptor, Serotonin, 5-HT1AReceptor, Serotonin, 5-HT2CReceptors, SerotoninReceptors, Serotonin, 5-HT3Neuropeptide YReceptor, Serotonin, 5-HT1AReceptor, Serotonin, 5-HT2CReceptors, SerotoninReceptors, Serotonin, 5-HT3RNA, MessengerSerotoninSerotonin Plasma Membrane Transport ProteinsSlc6a4 protein, rat

Identifiers

PMID22527118
PMCPMC3580143
OpenAlexW2001273526

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.