Evidence map›Paper›PMID 27484743›Full record

ArticleThe Journal of pharmacy and pharmacology2016

S-Nitrosoglutathione ameliorates acute renal dysfunction in a rat model of lipopolysaccharide-induced sepsis.

Devadoss J Samuvel, Anandakumar Shunmugavel, Avtar K Singh, Inderjit Singh, Mushfiquddin Khan

Open access · greenAbstract read
In one paragraph

Article in The Journal of pharmacy and pharmacology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 22 citations in OpenAlex.

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  9. HPharmacological research · 2020
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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

5 authors at 1 institution in 1 country.

Devadoss J SamuvelDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Anandakumar ShunmugavelDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Avtar K SinghDepartment of Pathology and Laboratory Medicine, Medical University of South Carolina, Charleston, SC, USA.
Inderjit SinghDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC, USA.
Mushfiquddin KhanDepartment of Pediatrics, Medical University of South Carolina, Charleston, SC, USA. khanm@musc.edu.
Medical University of South Carolina · US

Funding

EXTRAMURAL RESEARCH FACILITIES CONSTRUCTIONC06RR018823 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND, JOHN R · 2003 to 2003
$2.9M
MUSC FACIL EXPANSION &RENOV: SLE C06RR015455 · NCRR · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI RAYMOND, JOHN R · 2002 to 2002
$2.0M
Nitrosylation Mechanisms for Protection Against Neurovascular Inflammatory InjuryR01NS072511 · NINDS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI SINGH, AVTAR K · 2011 to 2015
$1.6M
NCRR NIH HHS C06 RR015455NCRR NIH HHS C06 RR018823NINDS NIH HHS R01 NS072511
6 · The paper itself

Abstract

objectiveSepsis induces an inflammatory response that results in acute renal failure (ARF). The current study is to evaluate the role of S-Nitrosoglutathione (GSNO) in renoprotection from lipopolysaccharide (LPS)-induced sepsis.

methodsRats were divided to three groups. First group received LPS (5 mg/kg body weight), second group was treated with LPS + GSNO (50 μg/kg body weight), and third group was administered with vehicle (saline). They were sacrificed on day 1 and 3 post-LPS injection. Serum levels of nitric oxide (NO), creatinine and blood urea nitrogen (BUN) were analysed. Tissue morphology, T lymphocyte infiltrations, and the expression of inflammatory (TNF-α, iNOS) and anti-inflammatory (IL-10) mediators as well as glutathione (GSH) levels were determined. KEY FINDING: Lipopolysaccharide significantly decreased body weight and increased cellular T lymphocyte infiltration, caspase-3 and iNOS and decreased PPAR-γ in renal tissue. NO, creatinine and BUN were significantly elevated after LPS challenge, and they significantly decreased after GSNO treatment. TNF-α level was found significantly increased in LPS-treated serum and kidney. GSNO treatment of LPS-challenged rats decreased caspase-3, iNOS, TNF-α, T lymphocyte infiltration and remarkably increased levels of IL-10, PPAR-γ and GSH.

conclusionGSNO can be used as a renoprotective agent for the treatment of sepsis-induced acute kidney injury.

Indexed as

Acute Kidney InjuryAnimalsAnti-Inflammatory AgentsBlood Urea NitrogenCaspase 3CreatinineFemaleGlutathioneInterleukin-10KidneyLipopolysaccharidesNitric OxideNitric Oxide Synthase Type IIRatsRats, Sprague-DawleySepsisAnti-Inflammatory AgentsCaspase 3CreatinineGlutathioneInterleukin-10LipopolysaccharidesNitric OxideNitric Oxide Synthase Type IIS-NitrosoglutathioneTumor Necrosis Factor-alphaacute kidney injurylipopolysacchariderenoprotectionsepsisS-Nitrosoglutathione

Identifiers

PMID27484743
PMCPMC5028274
OpenAlexW2502504825

What OpenQuestion holds

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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.