Evidence map›Paper›PMID 29286398›Full record

ArticleJournal of visualized experiments : JoVE2017

Evaluation of Vascular Control Mechanisms Utilizing Video Microscopy of Isolated Resistance Arteries of Rats.

Kathleen M Lukaszewicz, Matthew J Durand, Jessica R C Priestley, James R Schmidt, L Adrienne Allen, Aron M Geurts, Julian H Lombard

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact, top 79% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 1 country.

Kathleen M LukaszewiczDepartment of Physical Therapy, Marquette University.
Matthew J DurandMedical College of Wisconsin.
Jessica R C PriestleyDepartment of Physiology, Medical College of Wisconsin.
James R SchmidtGraduate Programs of Nurse Anesthesia, Texas Wesleyan University.
L Adrienne AllenOffice of Research, Medical College of Wisconsin.
Aron M GeurtsDepartment of Physiology, Medical College of Wisconsin.
Julian H LombardDepartment of Physiology, Medical College of Wisconsin; jlombard@mcw.edu.
Medical College of Wisconsin · USMarquette University · USTexas Wesleyan University · US

Funding

Role of Nrf2 in Vascular Antioxidant DefenseR01HL128242 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI LOMBARD, JULIAN H · 2016 to 2019
$1.8M
Oxidant Stress in the Nrf2 Knockout RatR21OD018309 · OD · MEDICAL COLLEGE OF WISCONSIN · PI LOMBARD, JULIAN H · 2014 to 2015
$416k
High Salt Diet, Angiotensin II, and Microvessel DilationR56HL065289 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI LOMBARD, JULIAN H · 2014 to 2014
$383k
NHLBI NIH HHS R01 HL128242NHLBI NIH HHS R56 HL065289NIH HHS R21 OD018309
6 · The paper itself

Abstract

This protocol describes the use of in vitro television microscopy to evaluate vascular function in isolated cerebral resistance arteries (and other vessels), and describes techniques for evaluating tissue perfusion using Laser Doppler Flowmetry (LDF) and microvessel density utilizing fluorescently labeled Griffonia simplicifolia (GS1) lectin. Current methods for studying isolated resistance arteries at transmural pressures encountered in vivo and in the absence of parenchymal cell influences provide a critical link between in vivo studies and information gained from molecular reductionist approaches that provide limited insight into integrative responses at the whole animal level. LDF and techniques to selectively identify arterioles and capillaries with fluorescently-labeled GS1 lectin provide practical solutions to enable investigators to extend the knowledge gained from studies of isolated resistance arteries. This paper describes the application of these techniques to gain fundamental knowledge of vascular physiology and pathology in the rat as a general experimental model, and in a variety of specialized genetically engineered "designer" rat strains that can provide important insight into the influence of specific genes on important vascular phenotypes. Utilizing these valuable experimental approaches in rat strains developed by selective breeding strategies and new technologies for producing gene knockout models in the rat, will expand the rigor of scientific premises developed in knockout mouse models and extend that knowledge to a more relevant animal model, with a well understood physiological background and suitability for physiological studies because of its larger size.

Indexed as

AnimalsArteriesMaleMicroscopy, VideoModels, AnimalRatsVascular Resistance

Identifiers

PMID29286398
PMCPMC5755532
OpenAlexW2771945306

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.