Evidence map›Paper›PMID 36678503›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

Possible Implication of Nrf2, PPAR-γ and MAPKs Signaling in the Protective Role of Mangiferin against Renal Ischemia/Reperfusion in Rats.

Abdallah M Gendy, Amira A El-Gazar, Ghada M Ragab, Asmaa K Al-Mokaddem, Alaadin E El-Haddad, Heba Mohammed Refat M Selim, Einas Mohamed Yousef, Najat O Hamed, Sherihan Salaheldin Abdelhamid Ibrahim

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
5.2field-weighted citation impact, top 5% 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, 18 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 6 institutions in 2 countries.

Abdallah M GendyPharmacology and Toxicology Department, Faculty of Pharmacy, October 6 University, Giza 12585, Egypt.ORCID 0000-0001-5032-3594
Amira A El-GazarPharmacology and Toxicology Department, Faculty of Pharmacy, October 6 University, Giza 12585, Egypt.ORCID 0000-0002-8372-4682
Ghada M RagabPharmacology and Toxicology Department, Faculty of Pharmacy, Misr University for Science and Technology, Giza 12585, Egypt.
Asmaa K Al-MokaddemPathology Department, Faculty of Veterinary Medicine, Cairo University, Giza 12211, Egypt.
Alaadin E El-HaddadPharmacognosy Department, Faculty of Pharmacy, October 6 University, Giza 12585, Egypt.ORCID 0000-0002-3924-9263
Heba Mohammed Refat M SelimPharmaceutical Sciences Department, Faculty of Pharmacy, Al-Maarefa University, Diriyah, Riyadh 13713, Saudi Arabia.
Einas Mohamed YousefHistology and Cell biology Department, Faculty of Medicine, Menoufia University, Menoufia 11411, Egypt.ORCID 0000-0002-8935-0183
Najat O HamedPharmaceutical Sciences Department, Faculty of Pharmacy, Al-Maarefa University, Diriyah, Riyadh 13713, Saudi Arabia.
Sherihan Salaheldin Abdelhamid IbrahimPharmacology and Therapeutics Department, Faculty of Pharmacy, Pharos University in Alexandria, Alexandria 21523, Egypt.ORCID 0000-0003-3467-5172
October 6 University · EGAlfaisal University · SACairo University · EGMenoufia University · EGMisr University for Science and Technology · EGPharos University in Alexandria · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mangiferin (Mang) is a known glucosylxanthone that has proven its shielding effect against ischemia/reperfusion (Is/R). However, its full underlying mechanistic perspective against renal Is/R induced lesions is not fully revealed. Consequently, the purpose of this study is to track further non-investigated modulatory signals of Mang against the renal Is/R model involving nuclear factor erythroid 2-related factor (Nrf)2/heme oxygenase (HO)-1, peroxisome proliferator-activated receptor (PPAR)-γ/nuclear factor (NF)-κB, p38 mitogen-activated protein kinase (MAPK), and c-Jun N-terminal kinase (JNK) signaling. To ratify our aim, Mang was administrated (20 mg/kg, i.p for seven days) before the induction of bilateral Is/R. Mechanistic maneuver revealed that Mang balanced oxidative state via increasing the expression of the antioxidant Nrf2/HO-1 cue with subsequent enhancement of GSH besides MDA lessening. Additionally, Mang enhanced PPAR-γ mRNA expression and declined

Indexed as

mangiferinMAPK/JNKNrf2/HO-1PPAR-γ/NF-κBrenal ischemia

Identifiers

PMID36678503
PMCPMC9863472
OpenAlexW4313468508

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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.