Evidence map›Paper›PMID 37092612›Full record

ArticleActa bio-medica : Atenei Parmensis2023

Crocin lessens desipramine-induced phospholipidosis biomarker levels via targeting oxidative stress- related PI3K/Akt/mTOR signaling pathways in the rat liver.

Amal Ahmed El-Sheikh, Heba A Mahmoud, Eman Ali El-Kordy, Amal M Abdelsattar, Fatma H Rizk, Radwa Mahmoud El-Sharaby, Shimaa S Mashal, Amira A El Saadany, Rania H Shalaby, Amira M Elshamy and 3 more

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In one paragraph

Article in Acta bio-medica : Atenei Parmensis, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 24% 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

1 citing paper in PubMed, 3 citations in OpenAlex.

  1. Article
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

13 authors at 5 institutions in 6 countries.

Amal Ahmed El-Sheikh. amal.sheikh@iau.edu.sa.
Heba A Mahmoud. heba.mahmoud1@med.tanta.edu.eg.
Eman Ali El-Kordy. ea.elkordy@imamu.edu.sa.
Amal M Abdelsattar. amal_hamada@med.tanta.edu.eg.
Fatma H Rizk. Fatma_rizk@med.tanta.edu.eg.
Radwa Mahmoud El-Sharaby. radwa_elsharaby@med.tanta.edu.eg.
Shimaa S Mashal. Shaimaa_mashal@med.tanta.edu.eg.
Amira A El Saadany. amira_elsadani@med.tanta.edu.eg.
Rania H Shalaby. rania_shalabi@med.tanta.edu.eg.
Amira M Elshamy. amira_elshamy@med.tanta.edu.eg.
Omnia Safwat El-Deeb. omnia_eldeeb@med.tanta.edu.eg.
Rowida Raafat Ibrahimmedical biochemistry. rowaida.yousef@med.tanta.edu.eg.
Hoda A Ibrahim. Hoda_Ibrahim@Med.Tanta.Edu.Eg.
Tanta University · EGSheikh Bahaei University · IRTanta University Hospital · EGImam Sadiq University · IRInstitute for Soil Sciences · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aim Crocin is a pharmacologically active chemical found in the spice saffron from Crocus sativus L. It possesses antioxidant and anti-radical properties that can minimize the hepatic phospholipidosis triggered using the tricyclic antidepressant desipramine. The aim of this study was to examine the effect of crocin on desipramine-induced hepatic phospholipidosis targeting the oxidative stress-related PI3K/Akt/mTOR signaling pathways.

methodsForty adult male rats were divided into 4 groups (n =10): control group, a group receiving intraperitoneal (IP) crocin (50 mg/kg/day), a group receiving IP desipramine (10 mg/kg/day), and a group receiving both IP crocin and desipramine.

resultsAfter 3 weeks of treatment, the combined treatment group showed diminished desipramine-induced hepatic phospholipidosis, along with significant reductions in total oxidant status (TOS) , the levels of inflammatory markers including interleukin 6 (IL6) and tumor necrosis factor α (TNF-α) and apoptotic markers including caspase3 and Bcl2 (B-cell lymphoma 2) while other markers including total antioxidant capacity (TAC), superoxide dismutase (SOD), phosphoinositide 3-kinases (PI3K), and mammalian target of rapamycin (mTOR) were increased. The gene expression of lysosomal enzymes including ELOVL6, SCD1 and HMGR was notably downregulated, while AP1S1 was upregulated in the combined treatment group compared to the desipramine group. No ultrastructural signs of hepatic phospholipidosis, in the form of multilamellar bodies, were apparent in the combined treatment group.

conclusionsThese data collectively suggest that crocin has a protective effect against desipramine-induced phospholipidosis. (www.actabiomedica.it).

Indexed as

AntioxidantsPhosphatidylinositol 3-KinasesAnimalsCarotenoidsDesipramineLiverMaleOxidative StressProto-Oncogene Proteins c-aktRatsSignal TransductionTOR Serine-Threonine KinasesAntioxidantsCarotenoidscrocinDesipraminemTOR protein, ratPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktTOR Serine-Threonine Kinases

Identifiers

PMID37092612
PMCPMC10210559
OpenAlexW4366822180

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.