Evidence map›Paper›PMID 27532263›Full record

ArticlePloS one2016

Polymyxin B Nephrotoxicity: From Organ to Cell Damage.

Maria de Fátima Fernandes Vattimo, Mirian Watanabe, Cassiane Dezoti da Fonseca, Luciana Barros de Moura Neiva, Edson Andrade Pessoa, Fernanda Teixeira Borges

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed, 1 pooled it
6.4field-weighted citation impact, top 4% 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

40 citing papers in PubMed, 1 synthesis or guideline pooled it, 67 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Polymyxin B-Associated Muscle Injury: A Case Report.Infection and drug resistance · 2026
    Article
  6. Molecular mechanisms attributed to colistin renal proximal tubular epithelial cytotoxicity.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2025
    Review
  7. Revolutionizing antibiotic therapy: Polymyxin B and FeJournal of pharmaceutical analysis · 2025
    Article
  8. Observational
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  10. Review
  11. Article
  12. Article
  13. Article
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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 2 institutions in 1 country.

Maria de Fátima Fernandes VattimoExperimental Laboratory of Animal Models (LEMA), School of Nursing of the University of Sao Paulo, Sao Paulo, Brazil.
Mirian WatanabeExperimental Laboratory of Animal Models (LEMA), School of Nursing of the University of Sao Paulo, Sao Paulo, Brazil.
Cassiane Dezoti da FonsecaExperimental Laboratory of Animal Models (LEMA), School of Nursing of the University of Sao Paulo, Sao Paulo, Brazil.
Luciana Barros de Moura NeivaExperimental Laboratory of Animal Models (LEMA), School of Nursing of the University of Sao Paulo, Sao Paulo, Brazil.
Edson Andrade PessoaNephrology Division, Federal University of Sao Paulo, Sao Paulo, Brazil.
Fernanda Teixeira BorgesNephrology Division, Federal University of Sao Paulo, Sao Paulo, Brazil.
Universidade de São Paulo · BRUniversidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Polymyxins have a long history of dose-limiting toxicity, but the underlying mechanism of polymyxin B-induced nephrotoxicity is unclear. This study investigated the link between the nephrotoxic effects of polymyxin B on renal metabolic functions and mitochondrial morphology in rats and on the structural integrity of LLC-PK1 cells. Fifteen Wistar rats were divided into two groups: Saline group, rats received 3 mL/kg of 0.9% NaCl intraperitoneally (i.p.) once a day for 5 days; Polymyxin B group, rats received 4 mg/kg/day of polymyxin B i.p. once a day for 5 days. Renal function, renal hemodynamics, oxidative stress, mitochondrial injury and histological characteristics were assessed. Cell membrane damage was evaluated via lactate dehydrogenase and nitric oxide levels, cell viability, and apoptosis in cells exposed to 12.5 μM, 75 μM and 375 μM polymyxin B. Polymyxin B was immunolocated using Lissamine rhodamine-polymyxin B in LLC-PK1 cells. Polymyxin B administration in rats reduced creatinine clearance and increased renal vascular resistance and oxidative damage. Mitochondrial damage was confirmed by electron microscopy and cytosolic localization of cytochrome c. Histological analysis revealed tubular dilatation and necrosis in the renal cortex. The reduction in cell viability and the increase in apoptosis, lactate dehydrogenase levels and nitric oxide levels confirmed the cytotoxicity of polymyxin B. The incubation of LLC-PK1 cells resulted in mitochondrial localization of polymyxin B. This study demonstrates that polymyxin B nephrotoxicity is characterized by mitochondrial dysfunction and free radical generation in both LLC-PK1 cells and rat kidneys. These data also provide support for clinical studies on the side effects of polymyxin B.

Indexed as

AnimalsAnti-Bacterial AgentsApoptosisCell SurvivalCytochromes cKidneyL-Lactate DehydrogenaseLLC-PK1 CellsMaleMicroscopy, Electron, TransmissionMitochondriaNecrosisNitric OxideOxidative StressPolymyxin BRatsAnti-Bacterial AgentsCytochromes cL-Lactate DehydrogenaseNitric OxidePolymyxin B

Identifiers

PMID27532263
PMCPMC4988638
OpenAlexW2513532815

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LicenceCC BY
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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.