Evidence map›Paper›PMID 22922351›Full record

ArticleNeuroscience2012

Distribution of angiotensin type 1a receptor-containing cells in the brains of bacterial artificial chromosome transgenic mice.

A D Gonzalez, G Wang, E M Waters, K L Gonzales, R C Speth, T A Van Kempen, J Marques-Lopes, C N Young, S D Butler, R L Davisson and 4 more

Abstract read
In one paragraph

Article in Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

50 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Angiotensin ATiScience · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Molecular Ontology of the Nucleus of Solitary Tract.The Journal of comparative neurology · 2024
    Article
  7. Article
  8. Article
  9. The ATMolecules (Basel, Switzerland) · 2023
    Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Limbic Neuropeptidergic Modulators of Emotion and Their Therapeutic Potential for Anxiety and Post-Traumatic Stress Disorder.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Review
  15. β-Arrestin-Biased Agonist Targeting the Brain ATHypertension (Dallas, Tex. : 1979) · 2021
    Article
  16. Review
  17. GABA is a mediator of brain ATHypertension research : official journal of the Japanese Society of Hypertension · 2020
    Review
  18. Article
  19. Review
  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

14 authors at 3 institutions in 1 country.

A D GonzalezDivision of Neurobiology, Department of Neurology and Neuroscience, Weill Cornell Medical College, 407 East 61st Street, New York, NY 10065, USA.
G Wang
E M Waters
K L Gonzales
R C Speth
T A Van Kempen
J Marques-Lopes
C N Young
S D Butler
R L Davisson
C Iadecola
V M Pickel
J P Pierce
T A Milner
Cornell University · USNova Southeastern University · USRockefeller University · US

Funding

The Nonhuman Primate CoreP01AG016765 · NIA · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI BAXTER, MARK G, MORRISON, JOHN H · 1999 to 2016
$26.1M
Radiotelemetry CoreP01HL096571 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI DAVISSON, ROBIN L · 2009 to 2013
$8.8M
ULTRASTRUCTURAL INTERACTIONS OF OPIOIDS IN HIPPOCAMPUSR01DA008259 · NIDA · WEILL MEDICAL COLL OF CORNELL UNIV · PI MILNER, TERESA A · 1993 to 2019
$6.4M
PHARMACOLOGY AND NEUROSCIENCE OF DRUG ABUSET32DA007274 · NIDA · WEILL MEDICAL COLL OF CORNELL UNIV · PI SZETO, HAZEL H · 1991 to 2011
$4.8M
TARGETED ABLATION OF BRAIN ANGIOTENSINGERGIC SYSTEMSR01HL063887 · NHLBI · UNIVERSITY OF IOWA · PI DAVISSON, ROBIN L · 2000 to 2014
$4.4M
MENOPAUSAL CHANGES IN HYPOTHALAMUS AND HYPERTENSION SUSCEPTIBILITYR01HL098351 · NHLBI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MILNER, TERESA A · 2011 to 2014
$1.7M
BDNF-Estrogen Interactions with Perimenopausal Mood and CognitionR21AG039850 · NIA · ROCKEFELLER UNIVERSITY · PI MILNER, TERESA A, WATERS, ELIZABETH M · 2011 to 2012
$399k
NHLBI NIH HHS HL063887NHLBI NIH HHS HL096571NHLBI NIH HHS HL098351NHLBI NIH HHS P01 HL096571NHLBI NIH HHS R01 HL063887NHLBI NIH HHS R01 HL098351NIA NIH HHS AG016765NIA NIH HHS AG039850NIA NIH HHS P01 AG016765NIA NIH HHS R21 AG039850NIDA NIH HHS DA08259NIDA NIH HHS DA08259-S1NIDA NIH HHS R01 DA008259NIDA NIH HHS T32 DA007274
6 · The paper itself

Abstract

In the central nervous system, angiotensin II (AngII) binds to angiotensin type 1 receptors (AT(1)Rs) to affect autonomic and endocrine functions as well as learning and memory. However, understanding the function of cells containing AT(1)Rs has been restricted by limited availability of specific antisera, difficulties discriminating AT(1)R-immunoreactive cells in many brain regions and, the identification of AT(1)R-containing neurons for physiological and molecular studies. Here, we demonstrate that an Agtr1a bacterial artificial chromosome (BAC) transgenic mouse line that expresses type A AT(1)Rs (AT1aRs) identified by enhanced green fluorescent protein (EGFP) overcomes these shortcomings. Throughout the brain, AT1aR-EGFP was detected in the nuclei and cytoplasm of cells, most of which were neurons. EGFP often extended into dendritic processes and could be identified either natively or with immunolabeling of GFP. The distribution of AT1aR-EGFP cells in brain closely corresponded to that reported for AngII binding and AT1aR protein and mRNA. In particular, AT1aR-EGFP cells were in autonomic regions (e.g., hypothalamic paraventricular nucleus, central nucleus of the amygdala, parabrachial nucleus, nuclei of the solitary tract and rostral ventrolateral medulla) and in regions involved in electrolyte and fluid balance (i.e., subfornical organ) and learning and memory (i.e., cerebral cortex and hippocampus). Additionally, dual label electron microscopic studies in select brain areas demonstrate that cells containing AT1aR-EGFP colocalize with AT(1)R-immunoreactivity. Assessment of AngII-induced free radical production in isolated EGFP cells demonstrated feasibility of studies investigating AT1aR signaling ex vivo. These findings support the utility of Agtr1a BAC transgenic reporter mice for future studies understanding the role of AT(1)R-containing cells in brain function.

Indexed as

AnimalsArginine VasopressinAutonomic Nervous SystemBrainBrain ChemistryChromosomes, Artificial, BacterialGreen Fluorescent ProteinsHumansImage Processing, Computer-AssistedImmunoenzyme TechniquesImmunohistochemistryMiceMice, TransgenicMicroscopy, ElectronMicroscopy, ImmunoelectronReactive Oxygen SpeciesArginine VasopressinGreen Fluorescent ProteinsReactive Oxygen SpeciesReceptor, Angiotensin, Type 1RNA, MessengerTyrosine 3-Monooxygenase

Identifiers

PMID22922351
PMCPMC3505886
OpenAlexW1984163963

What OpenQuestion holds

Textmetadata
LicenceTDM
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.