Evidence map›Paper›PMID 32715758›Full record

ArticleAmerican journal of physiology. Renal physiology2020

Systemic inhibition of miR-451 increases fibrotic signaling and diminishes autophagic response to exacerbate renal damage in Tallyho/Jng mice.

Maurice B Fluitt, Narayan Shivapurkar, Manju Kumari, Sarojini Singh, Lijun Li, Swasti Tiwari, Carolyn M Ecelbarger

Open access · bronzeAbstract read
In one paragraph

Article in American journal of physiology. Renal physiology, 2020. 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
1.0field-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

10 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Role of microRNAs in Obesity-Related Kidney Disease.International journal of molecular sciences · 2021
    Review
  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

7 authors at 2 institutions in 2 countries.

Maurice B FluittDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, District of Columbia.
Narayan ShivapurkarDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, District of Columbia.
Manju KumariDepartment of Molecular Medicine and Biotechnology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Sarojini SinghDepartment of Molecular Medicine and Biotechnology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Lijun LiDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, District of Columbia.
Swasti TiwariDepartment of Molecular Medicine and Biotechnology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.
Carolyn M EcelbargerDivision of Endocrinology and Metabolism, Department of Medicine, Georgetown University, Washington, District of Columbia.
Georgetown University · USSanjay Gandhi Post Graduate Institute of Medical Sciences · IN

Funding

Translational Biomedical Science Training GrantTL1TR001431 · NCATS · GEORGETOWN UNIVERSITY · PI LEE, DEXTER L, SANDBERG, KATHRYN L · 2015 to 2024
$4.8M
NCATS NIH HHS TL1 TR001431
6 · The paper itself

Abstract

miRNAs provide fine tuning of gene expression via inhibition of translation. miR-451 has a modulatory role in cell cycling via downregulation of mechanistic target of rapamycin. We aimed to test whether chronic systemic inhibition of miR-451 would enhance renal fibrosis (associated with deranged autophagy). Adult TallyHo/Jng mice (obese insulin resistant) were randomized to two treatment groups to receive either miR-451 inhibition [via a locked nucleic acid construct] or a similar scrambled locked nucleic acid control for 8 wk. All mice were fed a high-fat diet (60% kcal from fat) ad libitum and humanely euthanized after 12 wk. Kidneys and blood were collected for analysis. Renal expression of miR-451 was sixfold lower in inhibitor-treated mice compared with control mice. miR-451 inhibition increased kidney weight and collagen and glycogen deposition. Blood chemistry revealed significantly higher Na

Indexed as

AnimalsAutophagyDiet, High-FatFibrosisGene Expression RegulationInsulin ResistanceKidneyKidney DiseasesMaleMiceMice, Inbred StrainsMicroRNAsObesityPeptidesRandom AllocationSignal TransductionMicroRNAsMirn451 microRNA, mousePeptidesautophagydiabetesdiabetic nephropathymicroRNAs

Identifiers

PMID32715758
PMCPMC7509278
OpenAlexW3045782789

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.