Evidence map›Paper›PMID 37786577›Full record

ArticlePeerJ2023

Antioxidant and anti-inflammatory effects of allicin in the kidney of an experimental model of metabolic syndrome.

Abraham Said Arellano Buendia, Juan Gabriel Juárez Rojas, Fernando García-Arroyo, Omar Emiliano Aparicio Trejo, Fausto Sánchez-Muñoz, Raúl Argüello-García, Laura Gabriela Sánchez-Lozada, Rafael Bojalil, Horacio Osorio-Alonso

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
4.4field-weighted citation impact, top 6% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  9. Targeting Autophagy: A Promising Therapeutic Strategy for Diabetes Mellitus and Diabetic Nephropathy.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
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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 3 institutions in 1 country.

Abraham Said Arellano BuendiaDoctorado en Ciencias Biológicas y de la Salud, Universidad Autónoma Metropolitana, Mexico, Xochimilco, Mexico.
Juan Gabriel Juárez RojasEndocrinología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.
Fernando García-ArroyoFisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.
Omar Emiliano Aparicio TrejoFisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.
Fausto Sánchez-MuñozInmunología, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.ORCID 0000-0001-6556-1632
Raúl Argüello-GarcíaGenética y Biología Molecular, Centro de Investigación y de Estudios Avanzados del IPN, México, Gustavo A. Madero, México.
Laura Gabriela Sánchez-LozadaFisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.
Rafael BojalilAtención a la Salud, Universidad Autónoma Metropolitana, Mexico, Xochimilco, México.ORCID 0000-0002-5806-3675
Horacio Osorio-AlonsoFisiopatología Cardio-Renal, Instituto Nacional de Cardiología Ignacio Chávez, Mexico, Tlalpan, México.ORCID 0000-0002-9238-4202
Instituto Nacional de Cardiología · MXUniversidad Autónoma Metropolitana · MXInstituto Politécnico Nacional · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Recent studies have suggested that metabolic syndrome (MS) encompasses a group of risk factors for developing chronic kidney disease (CKD). This work aimed to evaluate the antioxidant and anti-inflammatory effects of allicin in the kidney from an experimental model of MS. Methods: Male Wistar rats (220-250 g) were used, and three experimental groups ( Results: Before the treatment with allicin, the MS group showed more significant body weight gain, increased SBP, and FBG, glucose intolerance, and dyslipidemia. In addition, increased markers of kidney damage in urine and blood. Moreover, the MS increased oxidative stress and inflammation in the kidney compared to group C. The allicin treatment prevented further weight gain, reduced SBP, FBG, glucose intolerance, and dyslipidemia. Also, markers of kidney damage in urine and blood were decreased. Further, the oxidative stress and inflammation were decreased in the renal cortex of the MS+A compared to the MS group. Conclusion: Allicin exerts its beneficial effects on the metabolic syndrome by considerably reducing systemic and renal inflammation as well as the oxidative stress. These effects were mediated through the Nrf2 pathway. The results suggest allicin may be a therapeutic alternative for treating kidney injury induced by the metabolic syndrome risk factors.

Indexed as

Glucose IntoleranceMetabolic SyndromeRenal Insufficiency, ChronicAnimalsAnti-Inflammatory AgentsAntioxidantsBody WeightDisulfidesInflammationKidneyMaleModels, TheoreticalRatsRats, WistarSulfinic AcidsallicinAnti-Inflammatory AgentsAntioxidantsDisulfidesSulfinic AcidsAllicinChronic kidney diseaseHypertensionInflammationMetabolic syndromeOxidative stress

Identifiers

PMID37786577
PMCPMC10541809
OpenAlexW4387105003

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.