Evidence map›Paper›PMID 27216079›Full record

ArticleJournal of the renin-angiotensin-aldosterone system : JRAAS

Feasibility of fluorescence energy transfer system for imaging the renoprotective effects of aliskiren in diabetic mice.

Kengo Kidokoro, Minoru Satoh, Seiji Itano, Atsunori Kuwabara, Tamaki Sasaki, Naoki Kashihara

Open access · hybridAbstract read
In one paragraph

Article in Journal of the renin-angiotensin-aldosterone system : JRAAS. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 38% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Review
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 1 institution in 1 country.

Kengo KidokoroDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan.
Minoru SatohDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan msatoh@med.kawasaki-m.ac.jp.
Seiji ItanoDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan.
Atsunori KuwabaraDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan.
Tamaki SasakiDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan.
Naoki KashiharaDepartment of Nephrology and Hypertension, Kawasaki Medical School, Japan.
Kawasaki Medical School · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWe investigated the feasibility of using a fluorescence resonance energy transfer system to image enzymatic activity in order to evaluate the effects of aliskiren (a direct renin inhibitor) on diabetic nephropathy. MATERIALS AND

methodsFirst, we induced diabetes in C57BL/6J mice using streptozotocin, then treated them with either aliskiren (25 mg/kg/day) or the angiotensin type 1 receptor blocker valsartan (15 mg/kg/day) for four weeks. Finally, we utilized renin fluorescence resonance energy transfer substrate to assess renin activity.

resultsRenin activity was much higher in the kidneys of diabetic mice compared to those of the non-diabetic control mice. While aliskiren inhibited this activity, valsartan did not. We noted that production of reactive oxygen species intensified and the bioavailability of nitric oxide diminished in the glomeruli of diabetic mice. Aliskiren and valsartan significantly ameliorated these effects. They suppressed glomerular production of reactive oxygen species and urinary albumin excretion. In fact, urinary albumin excretion in diabetic mice treated with aliskiren or valsartan was lower than that in untreated diabetic mice. Furthermore, aliskiren and valsartan significantly reduced glomerular permeability by maintaining the glomerular endothelial surface layer.

conclusionFluorescence resonance energy transfer could provide a new tool for evaluating tissue and plasma enzymatic activity.

Indexed as

Fluorescence Resonance Energy TransferImaging, Three-DimensionalAlbuminuriaAmidesAnimalsDiabetes Mellitus, ExperimentalFeasibility StudiesFumaratesKidneyKidney GlomerulusMacromolecular SubstancesMaleMice, Inbred C57BLNitric OxidePermeabilityProtective AgentsaliskirenAmidesFumaratesMacromolecular SubstancesNitric OxideProtective AgentsReninSuperoxidesalbuminuriadiabetic nephropathyfluorescence resonance energy transferin vivo imagingRenin

Identifiers

PMID27216079
PMCPMC5841571
OpenAlexW2400388282

What OpenQuestion holds

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LicenceCC BY-NC
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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.