Evidence map›Paper›PMID 36937479›Full record

ArticleJournal of medicine and life2023

Investigating the renoprotective effect of C21 in male mice with sepsis via modulation of p-AKT/PI3K expression.

Huda Jabber, Bassim Mohammed, Najah Rayish Hadi

Open access · diamondFull text read
In one paragraph

Article in Journal of medicine and life, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

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  6. Macrophage angiotensin ATAmerican journal of physiology. Renal physiology · 2023
    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

3 authors at 2 institutions in 1 country.

Huda JabberDepartment of Pharmacology and Therapeutics, College of Medicine, University of Al-Qadisiyah, Iraq.
Bassim MohammedDepartment of Pharmacology and Therapeutics, College of Medicine, University of Al-Qadisiyah, Iraq.
Najah Rayish HadiDepartment of Pharmacology and Therapeutics, Faculty of Medicine, University of Kufa, Kufa, Iraq.
University of Al-Qadisiyah · IQUniversity of Kufa · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate if C21 could prevent acute renal injury induced by sepsis by regulating the expression of p-AKT/PI3K. Five equal groups of 25 adult male Swiss-albino mice were randomly divided (n=5): sham (laparotomy without CLP), CLP, vehicle (equivalent amount of DMSO one hour before CLP), and C21 (0.03 mg/kg, one hour before CLP). ELISA was used to measure serum inflammatory mediators, and the expression of PI3K and P-AKT was determined using PCR and immunohistochemistry (IHC), respectively. TNF, TNF receptor, F8-isoprostane, urea, creatinine, and IL-6 blood levels were considerably lower in the CLP group (p<0.05) compared to the sham group, whereas the C21 treated group had significantly (p<0.05) greater levels of these inflammatory mediators. The IHC analysis revealed that P-AKT expression was significantly lower (p<0.05) in the CLP group compared to the sham group, while the C21 pretreatment group had significantly higher levels of P-AKT expression compared to the CLP group (p<0.05). The PI3K expression in the CLP group was significantly lower than in the sham group (p<0.05), according to PCR results, whereas the PI3K expression in the C21 pretreatment group was significantly greater than in the CLP group (p<0.05). This study showed that C21 might reduce levels of pro-inflammatory cytokines, including TNF-, IL-6, and TNF receptor, by modulating the PI3K/AKT signaling pathways, which can, in turn, reduce renal dysfunction during CLP-induced sepsis in male mice.

Indexed as

Phosphatidylinositol 3-KinasesSepsisAnimalsImidazolesInflammation MediatorsInterleukin-6MaleMiceProto-Oncogene Proteins c-aktSulfonamidesThiophenescompound 21ImidazolesInflammation MediatorsInterleukin-6Phosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSulfonamidesThiophenesACR – Urinary Albumin and CreatinineAcute kidney injuryAKT – Acute Kidney InjuryBUN – Blood Urea NitrogenC21CDC – Centers for Disease Control and PreventionCLP – Cecal Ligation ProcedureIHC – ImmunohistochemistrymiceP-AKT – Phosphorylated Protein kinase BP-AKT/PI3KPCR – Polymerase Chain ReactionPI3K – Phosphatidylinositol-3-kinaseRAS – Renin-Angiotensin SystemSCR – Serum CreatininesepsisUF – Urine FlowUNaV – Urinary Na Volume

Identifiers

PMID36937479
PMCPMC10015579
OpenAlexW4327898015

What OpenQuestion holds

Textfull text, public
LicenceCC BY
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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.