Evidence map›Paper›PMID 38892513›Full record

ArticleNutrients2024

Lycopene in Combination with Insulin Triggers Antioxidant Defenses and Increases the Expression of Components That Detoxify Advanced Glycation Products in Kidneys of Diabetic Rats.

Ingrid Delbone Figueiredo, Tayra Ferreira Oliveira Lima, Paulo Fernando Carlstrom, Renata Pires Assis, Iguatemy Lourenço Brunetti, Amanda Martins Baviera

Abstract read
In one paragraph

Article in Nutrients, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Review
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

6 authors.

Ingrid Delbone FigueiredoDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.
Tayra Ferreira Oliveira LimaDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.
Paulo Fernando CarlstromDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.ORCID 0000-0002-2218-3616
Renata Pires AssisDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.
Iguatemy Lourenço BrunettiDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.
Amanda Martins BavieraDepartment of Clinical Analysis, School of Pharmaceutical Sciences, São Paulo State University (Unesp), Araraquara 14800-903, SP, Brazil.ORCID 0000-0003-0987-5295

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBiochemical events provoked by oxidative stress and advanced glycation may be inhibited by combining natural bioactives with classic therapeutic agents, which arise as strategies to mitigate diabetic complications. The aim of this study was to investigate whether lycopene combined with a reduced insulin dose is able to control glycemia and to oppose glycoxidative stress in kidneys of diabetic rats.

methodsStreptozotocin-induced diabetic rats were treated with 45 mg/kg lycopene + 1 U/day insulin for 30 days. The study assessed glycemia, insulin sensitivity, lipid profile and paraoxonase 1 (PON-1) activity in plasma. Superoxide dismutase (SOD) and catalase (CAT) activities and the protein levels of advanced glycation end-product receptor 1 (AGE-R1) and glyoxalase-1 (GLO-1) in the kidneys were also investigated.

resultsAn effective glycemic control was achieved with lycopene plus insulin, which may be attributed to improvements in insulin sensitivity. The combined therapy decreased the dyslipidemia and increased the PON-1 activity. In the kidneys, lycopene plus insulin increased the activities of SOD and CAT and the levels of AGE-R1 and GLO-1, which may be contributing to the antialbuminuric effect.

conclusionsThese findings demonstrate that lycopene may aggregate favorable effects to insulin against diabetic complications resulting from glycoxidative stress.

Indexed as

AntioxidantsDiabetes Mellitus, ExperimentalGlycation End Products, AdvancedInsulinKidneyLycopeneOxidative StressRats, WistarAnimalsAryldialkylphosphataseBlood GlucoseCatalaseDiabetic NephropathiesDrug Therapy, CombinationHypoglycemic AgentsInsulin ResistanceAger protein, ratAntioxidantsAryldialkylphosphataseBlood GlucoseCatalaseGlycation End Products, AdvancedHypoglycemic AgentsInsulinLactoylglutathione LyaseLycopenePon1 protein, ratReceptor for Advanced Glycation End ProductsSuperoxide Dismutaseantidiabetic activitydiabetic complicationsglycoxidative stressglyoxalasenatural bioactivesparaoxonase

Identifiers

PMID38892513
PMCPMC11173891

What Socratic holds

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Registered trials

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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 Socratic graph.