Evidence map›Paper›PMID 29971248›Full record

ArticleeNeuro

Optogenetic Study of Anterior BNST and Basomedial Amygdala Projections to the Ventromedial Hypothalamus.

Ryo Yamamoto, Nowrin Ahmed, Tetsufumi Ito, Nur Zeynep Gungor, Denis Pare

Open access · goldAbstract read
In one paragraph

Article in eNeuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Total Number and Ratio of GABAergic Neuron Types in the Mouse Lateral and Basal Amygdala.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  15. Article
  16. Differential Encoding of Predator Fear in the Ventromedial Hypothalamus and Periaqueductal Grey.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    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

5 authors at 3 institutions in 4 countries.

Ryo YamamotoDepartment of Physiology, Kanazawa Medical University, Ishikawa 920-0293, Japan.
Nowrin AhmedCenter for Molecular and Behavioral Neuroscience, Rutgers University-Newark, 197 University Avenue, Newark, NJ.
Tetsufumi ItoDepartment of Anatomy, Kanazawa Medical University, Ishikawa 920-0293, Japan.ORCID 0000-0003-4516-9283
Nur Zeynep GungorRIKEN Center for Brain Science 2-1 Hirosawa, Wako-shi, Saitama 351-0198, Japan.
Denis PareCenter for Molecular and Behavioral Neuroscience, Rutgers University-Newark, 197 University Avenue, Newark, NJ.
Kanazawa Medical University · JPRutgers, The State University of New Jersey · USRIKEN Center for Brain Science · JP

Funding

Functional Organization of the Bed Nucleus of the Stria TerminalisR01MH098738 · NIMH · RUTGERS THE STATE UNIV OF NJ NEWARK · PI PARE, DENIS · 2012 to 2016
$1.9M
NIMH NIH HHS R01 MH098738
6 · The paper itself

Abstract

The basomedial amygdala (BM) influences the ventromedial nucleus of the hypothalamus (VMH) through direct glutamatergic projections as well as indirectly, through the anterior part of the bed nucleus of the stria terminalis (BNSTa). However, BM and BNSTa axons end in a segregated fashion in VMH. BM projects to the core of VMH, where VMH's projection cells are located, whereas BNSTa projects to the shell of VMH, where GABAergic cells that inhibit core neurons are concentrated. However, the consequences of this dual regulation of VMH by BM and BNSTa are unknown. To study this question, we recorded the responses of VMH's shell and core neurons to the optogenetic activation of BM or BNSTa inputs in transgenic mice that selectively express Cre-recombinase in glutamatergic or GABAergic neurons. Glutamatergic BM inputs fired most core neurons but elicited no response in GABAergic shell neurons. Following BM infusions of AAV-EF1α-DIO-hChR2-mCherry in Vgat-ires-Cre-Ai6 mice, no anterograde labeling was observed in the VMH, suggesting that GABAergic BM neurons do not project to the VMH. In contrast, BNSTa sent mostly GABAergic projections that inhibited both shell and core neurons. However, BNSTa-evoked IPSPs had a higher amplitude in shell neurons. Since we also found that activation of GABAergic shell neurons causes an inhibition of core neurons, these results suggest that depending on the firing rate of shell neurons, BNSTa inputs could elicit a net inhibition or disinhibition of core neurons. Thus, the dual regulation of VMH by BM and BNSTa imparts flexibility to this regulator of defensive and social behaviors.

Indexed as

Action PotentialsAnimalsCorticomedial Nuclear ComplexFemaleGABAergic NeuronsMaleMiceMice, TransgenicNeural PathwaysNeuronsOptogeneticsSeptal NucleiVentromedial Hypothalamic NucleusAmygdalaanxietyBNSTdefensive behaviorsfearventromedial hypothalamus

Identifiers

PMID29971248
PMCPMC6027956
OpenAlexW2808347623

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.