Evidence map›Paper›PMID 32341638›Full record

ArticleDrug design, development and therapy2020

Salidroside Alleviates Cartilage Degeneration Through NF-κB Pathway in Osteoarthritis Rats.

Hui Gao, Lu Peng, Chao Li, Qinlong Ji, Ping Li

Open access · goldAbstract read
In one paragraph

Article in Drug design, development and therapy, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

12 citing papers in PubMed, 28 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

5 authors at 1 institution in 1 country.

Hui Gao *Department of Orthopaedics, Tinglin Hospital, Shanghai 201505, People's Republic of China.
Lu Peng *Department of Orthopaedics, Hospital of Traditional Chinese Medicine, E'dong Healthcare Group, Huangshi 435000, People's Republic of China.
Chao LiDepartment of Orthopaedics, Tinglin Hospital, Shanghai 201505, People's Republic of China.
Qinlong JiDepartment of Orthopaedics, Tinglin Hospital, Shanghai 201505, People's Republic of China.
Ping LiDepartment of Rehabilitation, Hanchuan People's Hospital, Hanchuan, 431600, People's Republic of China.
Anyang Hospital of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOsteoarthritis (OA) is the most common disease, which seriously affects the daily life of the elderly. Currently, no traditional or drug therapy has been shown to explicitly block the progression of OA. Salidroside (Sal) is a bioactive component of

methodsWe established an anterior cruciate ligament transection (ACLT)-induced OA Rat model. The rats were divided into five groups (n = 10): Control group; ACLT group; ACLT + Sal (12.5 mg/kg) group; ACLT + Sal (25 mg/kg) group; ACLT + Sal (50 mg/kg) group.

resultsThe study showed that Sal could significantly promote the proliferation of chondrocytes in OA rats induced by ACLT and restore the histological alteration of cartilage. Besides, Sal upregulated the levels of Collagen II and Aggrecan, and downregulated the level of MMP-13. Furthermore, Sal could reduce the number of CD4+IL-17 DISCUSSION: Collectively, our study investigates the role and mechanism of Sal in OA, which lays a foundation for the application of Sal in OA.

Indexed as

AnimalsCartilage, ArticularCell ProliferationChondrocytesDisease Models, AnimalDose-Response Relationship, DrugFemaleGlucosidesInjections, IntraperitonealNF-kappa BOsteoarthritisPhenolsRatsRats, Sprague-DawleyStructure-Activity RelationshipGlucosidesNF-kappa BPhenolsrhodiolosidecartilage degenerationcollagen fibrosisimmune responsesinflammationNF-κBosteoarthritissalidroside

Identifiers

PMID32341638
PMCPMC7166061
OpenAlexW3016245625

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.