Evidence map›Paper›PMID 35397662›Full record

ArticlePflugers Archiv : European journal of physiology2022

Single nephron glomerular filtration rate measured by linescan multiphoton microscopy compared to conventional micropuncture.

Vincenzo Costanzo, Luciano D'Apolito, Donato Sardella, Anna Iervolino, Gaetano La Manna, Giovambattista Capasso, Sebastian Frische, Francesco Trepiccione

Abstract read
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. SerpinA3K Deficiency Reduces Oxidative Stress in Acute Kidney Injury.International journal of molecular sciences · 2023
    Article
  4. Article
  5. Biomedical optics express · 2023
    Article
  6. Article
  7. Review
  8. 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

8 authors.

Vincenzo CostanzoDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.ORCID 0000-0002-1995-7991
Luciano D'ApolitoBiogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.ORCID 0000-0003-4109-3680
Donato SardellaDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-7648-1408
Anna IervolinoBiogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.ORCID 0000-0003-0450-9587
Gaetano La MannaDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, Bologna, Italy.ORCID 0000-0001-5473-8551
Giovambattista CapassoBiogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy.ORCID 0000-0003-3469-8614
Sebastian FrischeDepartment of Biomedicine, Aarhus University, Aarhus, Denmark.ORCID 0000-0002-0270-3602
Francesco TrepiccioneBiogem, Institute of Molecular Biology and Genetics, Ariano Irpino, Italy. francesco.trepiccione@unicampania.it.ORCID 0000-0002-0622-6612

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal micropuncture, which requires the direct access to the renal tubules, has for long time been the technique of choice to measure the single nephron glomerular filtration rate (SNGFR) in animal models. This approach is challenging by virtue of complex animal preparation and numerous technically difficult steps. The introduction of intravital multiphoton microscopy (MPM) offers another approach to the measure of the SNGFR by mean of the high laser-tissue penetration and the optical sectioning capacity. Previous MPM studies measuring SNGFR in vivo relied on fast full-frame acquisition during the filtration process obtainable with high performance resonant scanners. In this study, we describe an innovative linescan-based MPM method. The new method can discriminate SNGFR variations both in conditions of low and high glomerular filtration, and shows results comparable to conventional micropuncture both for rats and mice. Moreover, this novel approach has improved spatial and time resolution and is faster than previous methods, thus enabling the investigation of SNGFR from more tubules and improving options for data-analysis.

Indexed as

MicroscopyNephronsAnimalsGlomerular Filtration RateKidneyKidney TubulesMicePuncturesRatsIschemia/reperfusionKidney physiologyLinescanMicropunctureMultiphoton microscopySingle nephron glomerular filtration rate

Identifiers

PMID35397662
PMCPMC9192459

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Registered trials

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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.