Evidence map›Paper›PMID 26909502›Full record

ArticleMetabolic brain disease2016

Salidroside suppresses inflammation in a D-galactose-induced rat model of Alzheimer's disease via SIRT1/NF-κB pathway.

Jin Gao, Rui Zhou, Xintong You, Fen Luo, He He, Xiayun Chang, Lingpeng Zhu, Xuansheng Ding, Tianhua Yan

Abstract read
PubMed Publisher
In one paragraph

Article in Metabolic brain disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
7.8field-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

58 citing papers in PubMed, 123 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Jin GaoDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
Rui ZhouDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
Xintong YouDepartment of Polymer Materials and Engineering, Nanjing Forestry University, Nanjing, 210037, China.
Fen LuoDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
He HeDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
Xiayun ChangDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
Lingpeng ZhuDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China.
Xuansheng DingDepartment of Clinical Pharmacy, China Pharmaceutical University, Nanjing, 210009, China. dxs0162@sina.com.
Tianhua YanDepartment of Physiology and Pharmacology, China Pharmaceutical University, Nanjing, 210009, China. yantianhuabest@126.com.
China Pharmaceutical University · CNNanjing Forestry University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Age-related inflammation is the predominant factor for neurodegenerative diseases like Alzheimer's disease (AD). In the present study, we examined memory performance and neuroinflammation in D-galactose (D-gal)-induced sub-acute aging model of rats. Our results demonstrated that chronic administration of D-gal (120 mg/kg) produced cognitive impairment as determined by Morris water maze (MWM) test and step-down passive avoidance test. D-gal also activated nuclear factor kappa B (NF-κB) p65/RelA by down-regulating the expression level of sirtuins 1 (SIRT1) in the hippocampus. Treatment with Salidroside (Sal, 20, 40 mg/kg) for 28 days ameliorated D-gal-induced memory deficits and inflammatory mediators including tumor necrosis factor-α (TNF-α) and interleukin-1β (IL-1β). Moreover, D-gal-induced activation of NF-κB signaling pathway in the brain was also inhibited by Sal via up-regulating SIRT1. These results suggest that D-gal-triggered memory impairment and inflammatory response may be associated with SIRT1/NF-κB signaling pathway, whereas treatment with Sal could positively affect these changes in hippocampus.

Indexed as

Alzheimer DiseaseAnimalsAvoidance LearningBrainCognitionDisease Models, AnimalGalactoseGlucosidesInflammationMaleMemoryNF-kappa BPhenolsRatsRats, Sprague-DawleySignal TransductionGalactoseGlucosidesNF-kappa BPhenolsrhodiolosideSirtuin 1AgingCognitive impairmentNeuroinflammationSalSIRT1/NF-κB pathway

Identifiers

PMID26909502
OpenAlexW2287368380

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.