Evidence map›Paper›PMID 37440558›Full record

ArticlePloS one2023

Emodin alleviates chronic constriction injury-induced neuropathic pain and inflammation via modulating PPAR-gamma pathway.

Ismail Badshah, Neelum Gul Qazi, Fawad Ali, Amber Mahmood Minhas, Arooj Mohsin Alvi, Mahmoud Kandeel, Muhammad Imran, Syed Shams Ul Hassan, Simona Bungau

Expression of concernOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It carries an expression of concern. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

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  8. Pharmacological investigations of newly synthesized oxazolones and imidazolones as COX-2 inhibitors.Saudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 4 countries.

Ismail BadshahRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Neelum Gul QaziRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Fawad AliDepartment of Pharmacy, Kohat University of Science and Technology, Kohat, Pakistan.
Amber Mahmood MinhasRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.
Arooj Mohsin AlviRiphah Institute of Pharmaceutical Sciences, Riphah International University, Islamabad, Pakistan.ORCID 0000-0003-4719-6832
Mahmoud KandeelDepartment of Biomedical sciences, College of Veterinary Medicine, King Faisal University, Al-hofuf, Al-Ahsa, Saudia Arabia.
Muhammad ImranDepartment of Biomedical Science, Pak-Austria Fachhochule: Institute of Applied Science and Technology, Mang Haripur, KPK, Pakistan.
Syed Shams Ul HassanShanghai Key Laboratory for Molecular Engineering of Chiral Drugs, School of Pharmacy, Shanghai Jiao Tong University, Shanghai, China.ORCID 0000-0001-5188-6540
Simona BungauDepartment of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.
Riphah International University · PKKing Faisal University · SAKohat University of Science and Technology · PKShanghai Jiao Tong University · CNUniversity of Oradea · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neuropathic pain has been characterized as chronic pain resulting from pathological damage to the sensorimotor system. Because of its complex nature, it remains refractory to most of the therapeutic interventions, and surgical intervention and physiotherapy alongside steroidal treatments remain the only treatment protocols with limited success, hence solidifying the need to find efficacious therapeutic alternatives. Emodin was used as a post-treatment for its potential to be neuroprotective in the treatment of chronic constriction injury-induced NP. The first day following surgery, Emodin treatment began, and it lasted until the 21st day. On days 3, 7, 14 and 21, all behavioral investigations were conducted. The sciatic nerve and spinal cord were extracted for further molecular examination. Emodin elevated response latency, was able to delay the onset of mechanical hyperalgesia in rats on days 7, 14, and 21 and reduced the CCI-induced paw deformation. Emodin treatment significantly reduced lipid peroxidation and NO levels while restoring the GST, GSH and catalase. It significantly improved the disorientation of the sciatic nerve and spinal cord confirmed by H & E staining and reduced inflammatory markers as observed by the quantification of COX-2, TNF-α, p-NFκb and up-regulated PPAR-γ levels by ELISA and PCR. According to the findings, Emodin has antinociceptive and anti-hyperalgesic properties, which reduced pain perception and inflammation. We also suggested the involvement of PPAR-γ pathway in the therapeutic potential of emodin in chronic nerve injury.

Indexed as

EmodinNeuralgiaAnimalsConstrictionHyperalgesiaInflammationPeroxisome Proliferator-Activated ReceptorsRatsSciatic NerveSpinal CordEmodinPeroxisome Proliferator-Activated Receptors

Identifiers

PMID37440558
PMCPMC10343023
OpenAlexW4384155755

What OpenQuestion holds

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LicenceCC BY
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.