Evidence map›Paper›PMID 40016714›Full record

ArticleBMC complementary medicine and therapies2025

In-vitro evaluation of the effect of okra (Abelmoschus esculentus L.) extract on periodontal cells: a comprehensive study of cellular and molecular impacts.

Umut Ulaş Tosun, Sema Tuğçe Aydın, Ayşegül Tiryaki, Dilruba Baykara, Aleyna Yakut, Erkan Rayaman, Turgut Taşkın, Canan Ekinci Doğan, Oğuzhan Gündüz, Ömer Birkan Ağralı

Abstract read
In one paragraph

Article in BMC complementary medicine and therapies, 2025. 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

10 authors.

Umut Ulaş TosunDepartment of Periodontology, Faculty of Dentistry, Marmara University, Istanbul, Türkiye.
Sema Tuğçe AydınDepartment of Medical Biochemistry, School of Medicine, Marmara University, Istanbul, Türkiye.
Ayşegül TiryakiDepartment of Materials, Metallurgical and Materials Engineering, Faculty of Technology, Marmara University, Istanbul, Türkiye.
Dilruba BaykaraDepartment of Materials, Metallurgical and Materials Engineering, Faculty of Technology, Marmara University, Istanbul, Türkiye.
Aleyna YakutDepartment of Periodontology, Faculty of Dentistry, Marmara University, Istanbul, Türkiye.
Erkan RayamanDepartment of Pharmaceutical Microbiology, Basic Pharmaceutical Sciences, Faculty of Pharmacy, Marmara University, Istanbul, Türkiye.
Turgut TaşkınDepartment of Pharmacognosy, Professional Pharmaceutical Sciences, Faculty of Pharmacy, Marmara University, Istanbul, Türkiye.
Canan Ekinci DoğanDepartment of Materials, Metallurgical and Materials Engineering, Faculty of Technology, Marmara University, Istanbul, Türkiye.
Oğuzhan GündüzDepartment of Ceramics, Metallurgical and Materials Engineering, Faculty of Technology, Marmara University, Istanbul, Türkiye.
Ömer Birkan AğralıDepartment of Periodontology, Faculty of Dentistry, Marmara University, Istanbul, Türkiye. omer.agrali@marmara.edu.tr.

Funding

Marmara University Scientific Research Projects Coordination Unit TDH-2022-10808
6 · The paper itself

Abstract

backgroundThis research assessed the potential role of okra (Abelmoschus esculentus L.) extract on periodontal tissue wound healing by evaluating its effects on human periodontal ligament fibroblast (hPDLF), human gingival fibroblast (hGF), and human osteoblast (hOB) cells in vitro.

methodsThe viability effect of okra extract on hPDLF, hGF, and hOB cells was determined using the MTT assay protocol. The highest viability concentrations were applied to hPDLF and hOB cells, and the expression levels of on type 1 collagen (COL1), bone morphogenetic protein 2 (BMP2), axis inhibition protein 2 (AXIN2), and fibroblast growth factor 2 (FGF2) proteins were determined through ELISA. The extract was also tested for antioxidant (CUPRAC, DPPH, FCR, and FRAP tests), acetylcholinesterase (AChE) inhibition, and antimicrobial properties, and its content was determined by HPLC-DAD.

resultsThe viability results showed no significant difference between the okra extract-treated and control groups for all cell types. In hPDLF cells, higher expression levels of COL1 and AXIN2 in the okra extract-treated group compared to the control group, while BMP2 expression level was lower. In hOB cells, the extract-treated group had higher levels of COL1, BMP2, and AXIN2 expression than the control group.

conclusionIt can be posited that okra extract may activate the Wnt/β-catenin signalling pathway and may have a beneficial impact on wound healing in periodontal tissues. However, extensive long-term in-vivo research on the activation of signalling pathways by okra extract in periodontal wound healing is required.

Indexed as

AbelmoschusFibroblastsOsteoblastsPeriodontal LigamentPlant ExtractsWound HealingAntioxidantsCells, CulturedCell SurvivalGingivaHumansAntioxidantsPlant ExtractsOkraPeriodontal cellsWnt/β-catenin signallingWound healing

Identifiers

PMID40016714
PMCPMC11866671

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.