Evidence map›Paper›PMID 35628465›Full record

ArticleInternational journal of molecular sciences2022

Improvement of Glycaemia and Endothelial Function by a New Low-Dose Curcuminoid in an Animal Model of Type 2 Diabetes.

Sara Oliveira, Tamaeh Monteiro-Alfredo, Rita Henriques, Carlos Fontes Ribeiro, Raquel Seiça, Teresa Cruz, Célia Cabral, Rosa Fernandes, Fátima Piedade, Maria Paula Robalo and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. 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
0.8field-weighted citation impact, top 34% 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, 12 citations in OpenAlex.

  1. Article
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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

12 authors at 4 institutions in 2 countries.

Sara OliveiraCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0002-0423-7959
Tamaeh Monteiro-AlfredoCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.
Rita HenriquesFaculty of Pharmacy, University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0003-4650-1081
Carlos Fontes RibeiroClinical-Academic Center of Coimbra (CACC), University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0002-9707-4895
Raquel SeiçaInstitute of Physiology, Faculty of Medicine, University of Coimbra, 3000-548 Coimbra, Portugal.
Teresa CruzFaculty of Pharmacy, University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0001-9846-6754
Célia CabralCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0003-4562-6683
Rosa FernandesCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.
Fátima PiedadeCQE, Complexo I, Instituto Superior Técnico, University of Lisbon, 1049-001 Lisbon, Portugal.ORCID 0000-0002-5335-8810
Maria Paula RobaloCQE, Complexo I, Instituto Superior Técnico, University of Lisbon, 1049-001 Lisbon, Portugal.ORCID 0000-0002-8200-6910
Paulo MatafomeCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.ORCID 0000-0002-3422-290X
Sónia SilvaCoimbra Institute of Clinical and Biomedical Research (iCBR), Faculty of Medicine and Center for Innovative Biomedicine and Biotechnology (CIBB), University of Coimbra, 3000-548 Coimbra, Portugal.
University of Coimbra · PTIscte – Instituto Universitário de Lisboa · PTPolytechnic Institute of Coimbra · PTUniversidade Federal da Grande Dourados · BR

Funding

CENTRO-01-0145-FEDER 000012-HealthyAging2020Fundação para a Ciência e Tecnologia Strategic Projects UID/NEU/04539/2013; UID/QUI/00100/2019; UIDB/NEU/04539/2020
6 · The paper itself

Abstract

Curcumin has been suggested as a promising treatment for metabolic diseases, but the high doses required limit its therapeutic use. In this study, a new curcuminoid is synthesised to increase curcumin anti-inflammatory and antioxidant potential and to achieve hypoglycaemic and protective vascular effects in type 2 diabetic rats in a lower dose. In vitro, the anti-inflammatory effect was determined through the Griess reaction, and the antioxidant activity through ABTS and TBARS assays. In vivo, Goto-Kakizaki rats were treated for 2 weeks with the equimolar dose of curcumin (40 mg/kg/day) or curcuminoid (52.4 mg/kg/day). Fasting glycaemia, insulin tolerance, plasma insulin, insulin signalling, serum FFA, endothelial function and several markers of oxidative stress were evaluated. Both compounds presented a significant anti-inflammatory effect. Moreover, the curcuminoid had a marked hypoglycaemic effect, accompanied by higher GLUT4 levels in adipose tissue. Both compounds increased NO-dependent vasorelaxation, but only the curcuminoid exacerbated the response to ascorbic acid, consistent with a higher decrease in vascular oxidative and nitrosative stress. SOD1 and GLO1 levels were increased in EAT and heart, respectively. Altogether, these data suggest that the curcuminoid developed here has more pronounced effects than curcumin in low doses, improving the oxidative stress, endothelial function and glycaemic profile in type 2 diabetes.

Indexed as

CurcuminDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2AnimalsAntioxidantsBlood GlucoseDiarylheptanoidsDisease Models, AnimalHypoglycemic AgentsInsulinRatsAntioxidantsBlood GlucoseCurcuminDiarylheptanoidsHypoglycemic AgentsInsulincurcuminoidendothelial dysfunctionglycaemiaoxidative stresstype 2 diabetes mellitus

Identifiers

PMID35628465
PMCPMC9144453
OpenAlexW4280557310

What OpenQuestion holds

Textmetadata
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.