Evidence map›Paper›PMID 38911910›Full record

ArticleACS bio & med chem Au2024

Effects of Strigolactones on NLRP3 Activation, Nitrosative Stress, and Antioxidant Mox Phenotype: In Vitro and In Silico Evidence.

Gizem Antika, Zeynep Özlem Cinar, Serhat Dönmez, Esma Seçen, Mehmet Özbil, Cristina Prandi, Tugba Boyunegmez Tumer

Abstract read
In one paragraph

Article in ACS bio & med chem Au, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Gizem AntikaGraduate Program of Molecular Biology and Genetics, School of Graduate Studies, Canakkale Onsekiz Mart University, Canakkale 17020, Turkey.ORCID https://orcid.org/0000-0001-7069-3250
Zeynep Özlem CinarGraduate Program of Molecular Biology and Genetics, School of Graduate Studies, Canakkale Onsekiz Mart University, Canakkale 17020, Turkey.ORCID https://orcid.org/0000-0002-3553-709X
Serhat DönmezGraduate Program of Molecular Biology and Genetics, School of Graduate Studies, Canakkale Onsekiz Mart University, Canakkale 17020, Turkey.ORCID https://orcid.org/0000-0002-6301-7243
Esma SeçenGraduate Program of Molecular Medicine, Universitätsklinikum Jena, Friedrich-Schiller-Universität Jena, Jena 07740, Germany.
Mehmet ÖzbilInstitute of Biotechnology, Gebze Technical University, Kocaeli 41400, Turkey.
Cristina PrandiDepartment of Chemistry, University of Turin, Turin 10125, Italy.ORCID https://orcid.org/0000-0001-9510-8783
Tugba Boyunegmez TumerDepartment of Molecular Biology and Genetics, Faculty of Science, Canakkale Onsekiz Mart University, Canakkale 17020, Turkey.ORCID https://orcid.org/0000-0002-1740-4867

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Phytohormones have significant roles in redox metabolism, inflammatory responses, and cellular survival mechanisms within the microenvironment of the mammalian brain. Herein, we identified the mammalian molecular targets of three representative strigolactone (SL) analogues structurally derived from apocarotenoids and the functional equivalent of plant hormones. All tested SL analogues have an inhibitory effect on NLRP3 inflammasome-mediated IL-1β release in murine microglial cells. However, IND and EGO10 became prominent among them due to their high potency at low micromolar doses. All SL analogues dose-dependently suppressed the release and expression of proinflammatory factors. For EGO10 and IND, IC

Identifiers

PMID38911910
PMCPMC11191569

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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 OpenQuestion graph.