Evidence map›Paper›PMID 27341008›Full record

ArticleJournal of visualized experiments : JoVE2016

Receptor Autoradiography Protocol for the Localized Visualization of Angiotensin II Receptors.

Andrea Linares, Leena E Couling, Eduardo J Carrera, Robert C Speth

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.4field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Imaging Diagnostics and Pathology in SARS-CoV-2-Related Diseases.International journal of molecular sciences · 2020
    Review
  6. Synthesis of the Novel ATACS omega · 2020
    Article
  7. The Role of Nuclear Medicine for COVID-19: Time to Act Now.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2020
    Article
  8. Mapping COVID-19 functional sequelae: the perspective of nuclear medicine.American journal of nuclear medicine and molecular imaging · 2020
    Review
  9. Article
  10. 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

4 authors at 2 institutions in 1 country.

Andrea LinaresFarquhar College of Arts and Sciences, Nova Southeastern University.
Leena E CoulingDepartment of Pharmaceutical Sciences, College of Pharmacy, Nova Southeastern University.
Eduardo J CarreraSchool of Medicine, University of Colorado.
Robert C SpethDepartment of Pharmaceutical Sciences, College of Pharmacy, Nova Southeastern University; rs1251@nova.edu.
Nova Southeastern University · USUniversity of Colorado Denver · US

Funding

Development of a radioligand for assay of angiotensin-converting enzyme-2(ACE-2)R15HL113905 · NHLBI · NOVA SOUTHEASTERN UNIVERSITY · PI SPETH, ROBERT CHARLES · 2013 to 2013
$436k
NHLBI NIH HHS R15 HL113905
6 · The paper itself

Abstract

This protocol describes receptor binding patterns for Angiotensin II (Ang II) in the rat brain using a radioligand specific for Ang II receptors to perform receptor autoradiographic mapping. Tissue specimens are harvested and stored at -80 °C. A cryostat is used to coronally section the tissue (brain) and thaw-mount the sections onto charged slides. The slide-mounted tissue sections are incubated in (125)I-SI-Ang II to radiolabel Ang II receptors. Adjacent slides are separated into two sets: 'non-specific binding' (NSP) in the presence of a receptor saturating concentration of non-radiolabeled Ang II, or an AT1 Ang II receptor subtype (AT1R) selective Ang II receptor antagonist, and 'total binding' with no AT1R antagonist. A saturating concentration of AT2 Ang II receptor subtype (AT2R) antagonist (PD123319, 10 µM) is also present in the incubation buffer to limit (125)I-SI-Ang II binding to the AT1R subtype. During a 30 min pre-incubation at ~22 °C, NSP slides are exposed to 10 µM PD123319 and losartan, while 'total binding' slides are exposed to 10 µM PD123319. Slides are then incubated with (125)I-SI-Ang II in the presence of PD123319 for 'total binding', and PD123319 and losartan for NSP in assay buffer, followed by several 'washes' in buffer, and water to remove salt and non-specifically bound radioligand. The slides are dried using blow-dryers, then exposed to autoradiography film using a specialized film and cassette. The film is developed and the images are scanned into a computer for visual and quantitative densitometry using a proprietary imaging system and a spreadsheet. An additional set of slides are thionin-stained for histological comparisons. The advantage of using receptor autoradiography is the ability to visualize Ang II receptors in situ, within a section of a tissue specimen, and anatomically identify the region of the tissue by comparing it to an adjacent histological reference section.

Indexed as

Angiotensin IIAngiotensin Receptor AntagonistsAnimalsAutoradiographyLosartanPyridinesRatsReceptors, AngiotensinAngiotensin IIAngiotensin Receptor AntagonistsLosartanPyridinesReceptors, Angiotensin

Identifiers

PMID27341008
PMCPMC4927780
OpenAlexW2409491282

What OpenQuestion holds

Textmetadata
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.