Evidence map›Paper›PMID 31605364›Full record

ArticleEuropean journal of drug metabolism and pharmacokinetics2020

Evaluation of Neutrophil Gelatinase-Associated Lipocalin as a Predictor of Glomerular Filtration Rate and Amikacin Clearance During Early Rat Endotoxemia: Comparison with Traditional Endogenous and Exogenous Biomarkers.

Šárka Studená, Eva Doleželová, Jolana Cermanová, Alena Prašnická, Drahomíra Springer, Stanislav Mičuda, Jaroslav Chládek

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In one paragraph

Article in European journal of drug metabolism and pharmacokinetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Šárka StudenáDepartment of Pharmacology, Charles University, Faculty of Medicine Hradec Králové, Šimkova 870, 500 38, Hradec Králové, Czech Republic.
Eva DoleželováDepartment of Biological and Medical Sciences, Charles University, Faculty of Pharmacy, Akademika Heyrovského 1203, 500 05, Hradec Králové, Czech Republic.
Jolana CermanováDepartment of Pharmacology, Charles University, Faculty of Medicine Hradec Králové, Šimkova 870, 500 38, Hradec Králové, Czech Republic.
Alena PrašnickáDepartment of Pharmacology, Charles University, Faculty of Medicine Hradec Králové, Šimkova 870, 500 38, Hradec Králové, Czech Republic.
Drahomíra SpringerInstitute of Medical Biochemistry and Laboratory Diagnostics, 1st Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, U nemocnice 2, 128 08, Praha 2, Czech Republic.
Stanislav MičudaDepartment of Pharmacology, Charles University, Faculty of Medicine Hradec Králové, Šimkova 870, 500 38, Hradec Králové, Czech Republic.
Jaroslav ChládekDepartment of Pharmacology, Charles University, Faculty of Medicine Hradec Králové, Šimkova 870, 500 38, Hradec Králové, Czech Republic. chladekj@lfhk.cuni.cz.ORCID http://orcid.org/0000-0002-9052-6318
Charles University · CZ

Funding

Grantová Agentura České Republiky Progres Q40
6 · The paper itself

Abstract

BACKGROUND AND

objectivesRenal elimination of amikacin and other aminoglycosides is slowed down in sepsis-induced acute kidney injury increasing the risk of adverse effects. Since neutrophil gelatinase-associated lipocalin (NGAL) and aminoglycosides share the mechanisms for renal excretion, the predictive power of NGAL was examined towards the changes in amikacin pharmacokinetics during early endotoxemia in anesthetized Wistar rats.

methodsEndogenous biomarkers of inflammation and acute kidney injury were assessed including NGAL in saline-injected controls and two groups of rats challenged with an intravenous injection of bacterial lipopolysaccharide (5 mg/kg)-a fluid-resuscitated group (LPS) and a fluid-resuscitated group infused intravenously with 8 μg/kg/h terlipressin (LPS-T). Sinistrin and amikacin were infused to measure glomerular filtration rate (GFR) and amikacin clearance (CL

resultsWithin 3 h of injection, systemic and renal inflammatory responses were induced by lipopolysaccharide. Gene and protein expression of NGAL was increased in the kidneys and the concentrations of NGAL in the plasma (pNGAL) and urine rose 4- to 38-fold (P < 0.01). The decreases in CL

conclusionsDuring early endotoxemia in the rat, pNGAL has a moderate predictive ability towards CL

Indexed as

Rats, WistarAcute Kidney InjuryAmikacinAnimalsBiomarkersCytokinesEndotoxemiaGlomerular Filtration RateInflammationKidneyLipocalin-2LipopolysaccharidesMaleMetabolic Clearance RateModels, AnimalOligosaccharidesAmikacinBiomarkersCytokinesLipocalin-2LipopolysaccharidesOligosaccharidessinistrin

Identifiers

PMID31605364
OpenAlexW2980275042

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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.