Evidence map›Paper›PMID 27421686›Full record

ArticleCNS neuroscience & therapeutics2017

Melatonin Stimulates the SIRT1/Nrf2 Signaling Pathway Counteracting Lipopolysaccharide (LPS)-Induced Oxidative Stress to Rescue Postnatal Rat Brain.

Shahid Ali Shah, Mehtab Khan, Myeung-Hoon Jo, Min Gi Jo, Faiz Ul Amin, Myeong Ok Kim

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 138 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
138citing papers in PubMed, 2 pooled it
8.2field-weighted citation impact, top 2% 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

138 citing papers in PubMed, 2 syntheses or guidelines pooled it, 239 citations in OpenAlex.

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  14. Macroalgae Polysaccharides Enhance Brain Health by Mitigating Scopolamine-induced Oxidative Stress and Inflammation Via Nrf-2/TLR4/NF-kB Pathways.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2025
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78 more citing papers are in PubMed but not listed here.

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.

Shahid Ali ShahDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Mehtab KhanDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Myeung-Hoon JoDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Min Gi JoDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Faiz Ul AminDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Myeong Ok KimDepartment of Biology and Applied Life Science, College of Natural Sciences, Gyeongsang National University, Jinju, Republic of Korea.
Gyeongsang National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsLipopolysaccharide (LPS) induces oxidative stress and neuroinflammation both in vivo and in vitro. Here, we provided the first detailed description of the mechanism of melatonin neuroprotection against LPS-induced oxidative stress, acute neuroinflammation, and neurodegeneration in the hippocampal dentate gyrus (DG) region of the postnatal day 7 (PND7) rat brain.

methodsThe neuroprotective effects of melatonin against LPS-induced neurotoxicity were analyzed using multiple research techniques, including Western blotting, immunofluorescence, and enzyme-linked immunosorbent assays (ELISAs) in PND7 rat brain homogenates and BV2 cell lysates in vitro. We also used EX527 to inhibit silent information regulator transcript-1 (SIRT1).

resultsA single intraperitoneal (i.p) injection of LPS to PND7 rats significantly induced glial cell activation, acute neuroinflammation, reactive oxygen species (ROS) production and apoptotic neurodegeneration in hippocampal DG region after 4 h. However, the coadministration of melatonin significantly inhibited both LPS-induced acute neuroinflammation and apoptotic neurodegeneration and improved synaptic dysfunction in the hippocampal DG region of PND7 rats. Most importantly, melatonin stimulated the SIRT1/Nrf2 (nuclear factor-erythroid 2-related factor 2) signaling pathway to reduce LPS-induced ROS generation. The beneficial effects of melatonin were further confirmed in LPS-stimulated BV2 microglia cell lines in vitro using EX527 as an inhibitor of SIRT1. LPS-induced oxidative stress, Nrf2 inhibition, and neuroinflammation are SIRT1-dependent in BV2 microglia cell lines.

conclusionThese results demonstrated that melatonin treatment rescued the hippocampal DG region of PND7 rat brains against LPS-induced oxidative stress damage, acute neuroinflammation, and apoptotic neurodegeneration via SIRT1/Nrf2 signaling pathway activation.

Indexed as

AnimalsAnimals, NewbornAntioxidantsCarbazolesDeoxyguanine NucleotidesFluoresceinsGlial Fibrillary Acidic ProteinHippocampusLipopolysaccharidesMaleMelatoninMiceNeurogliaNF-E2-Related Factor 2Oxidative StressRats6-chloro-2,3,4,9-tetrahydro-1H-carbazole-1-carboxamide8-oxodeoxyguanosine triphosphateAntioxidantsCarbazolesDeoxyguanine NucleotidesFluoresceinsfluoro jadeGlial Fibrillary Acidic ProteinLipopolysaccharidesMelatoninNfe2l2 protein, ratNF-E2-Related Factor 2Sirt1 protein, ratSirtuin 1LipopolysaccharideMelatoninNeuroinflammationNuclear factor-erythroid 2-related factor 2Reactive oxygen speciesSilent information regulator transcript-1

Identifiers

PMID27421686
PMCPMC6492734
OpenAlexW2475113336

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.