Evidence map›Paper›PMID 28424208›Full record

ArticleAmerican journal of physiology. Renal physiology2017

Architecture of the rat nephron-arterial network: analysis with micro-computed tomography.

Donald J Marsh, Dmitry D Postnov, Douglas J Rowland, Anthony S Wexler, Olga V Sosnovtseva, Niels-Henrik Holstein-Rathlou

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

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  13. Rho kinase inhibitors reduce voltage-dependent CaAmerican journal of physiology. Renal physiology · 2019
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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

6 authors at 3 institutions in 2 countries.

Donald J MarshDepartment of Molecular Pharmacology, Physiology, and Biotechnology, Brown University, Providence, Rhode Island; donald_marsh@brown.edu.ORCID http://orcid.org/0000-0002-9848-7691
Dmitry D PostnovDepartment of Biomedical Sciences, Panum Institute, University of Copenhagen, Copenhagen, Denmark.
Douglas J RowlandDepartment of Biomedical Engineering and Center for Molecular and Genomic Imaging, University of California, Davis, Davis, California; and.
Anthony S WexlerDepartment of Mechanical and Aerospace Engineering, University of California, Davis, Davis, California.
Olga V SosnovtsevaDepartment of Biomedical Sciences, Panum Institute, University of Copenhagen, Copenhagen, Denmark.
Niels-Henrik Holstein-RathlouDepartment of Biomedical Sciences, Panum Institute, University of Copenhagen, Copenhagen, Denmark.
University of Copenhagen · DKUniversity of California, Davis · USBrown University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Among solid organs, the kidney's vascular network stands out, because each nephron has two distinct capillary structures in series and because tubuloglomerular feedback, one of the mechanisms responsible for blood flow autoregulation, is specific to renal tubules. Tubuloglomerular feedback and the myogenic mechanism, acting jointly, autoregulate single-nephron blood flow. Each generates a self-sustained periodic oscillation and an oscillating electrical signal that propagates upstream along arterioles. Similar electrical signals from other nephrons interact, allowing nephron synchronization. Experimental measurements show synchronization over fields of a few nephrons; simulations based on a simplified network structure that could obscure complex interactions predict more widespread synchronization. To permit more realistic simulations, we made a cast of blood vessels in a rat kidney, performed micro-computed tomography at 2.5-μm resolution, and recorded three-dimensional coordinates of arteries, afferent arterioles, and glomeruli. Nonterminal branches of arcuate arteries form treelike structures requiring two to six bifurcations to reach terminal branches at the tree tops. Terminal arterial structures were either paired branches at the tops of the arterial trees, from which 52.6% of all afferent arterioles originated, or unpaired arteries not at the tree tops, yielding the other 22.9%; the other 24.5% originated directly from nonterminal arteries. Afferent arterioles near the corticomedullary boundary were longer than those farther away, suggesting that juxtamedullary nephrons have longer afferent arterioles. The distance separating origins of pairs of afferent arterioles varied randomly. The results suggest an irregular-network tree structure with vascular nodes, where arteriolar activity and local blood pressure interact.

Indexed as

X-Ray MicrotomographyAnimalsArteriolesComputed Tomography AngiographyMaleModels, AnatomicModels, CardiovascularNephronsRats, Sprague-DawleyRenal ArteryReplica Techniquesafferent arteriole distributionnephron dynamicsnetwork dynamicsrenal blood flow regulationrenal vascular network

Identifiers

PMID28424208
PMCPMC5582900
OpenAlexW2606354061

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.