ReviewNaunyn-Schmiedeberg's archives of pharmacology2025
A comprehensive review of medicinal plants and their beneficial roles in alleviating bisphenol A-induced organ toxicity.
Review in Naunyn-Schmiedeberg's archives of pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
4 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Endocrine disruption rewards: bisphenol-A-induced reproductive toxicity and the precision ameliorative potential of flavonoids in preclinical studies. A systematic review and meta-analysis.Frontiers in toxicology · 2025Pooled it
- Ginsenoside Rg1 alleviated testicular and sperm damage in rats exposed to bisphenol A.Biochemistry and biophysics reports · 2025Article
- Article
- Ameliorative Effects of Ethyl-Acetate Extract ofF1000Research · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Bisphenol A (BPA) is a hazardous chemical found in various products, including epoxy resins, polycarbonate plastic, canned foods, and beverage containers. Exposure to BPA can lead to organ toxicities, reproductive toxicity, hepatotoxicity, brain development disorders, and abnormal immune responses, posing a serious threat to human health. Consequently, health problems caused by continuous exposure to BPA are increasingly drawing scientists' attention as they seek solutions to alleviate BPA-induced adverse effects. Among these solutions, the use of medicinal plants has been extensively studied for this purpose. Medicinal plants exhibit protective effects against BPA toxicity through different molecular mechanisms. These mechanisms include the antioxidant defense system, enhancement of reproductive hormone synthesis, improvement in sperm quality, modification of MAPK/PI3K/akt, and insulin signaling pathways. Furthermore, another protective mechanism involves preventing neural cell death by affecting adiponectin receptors and the JNK/CREB signaling pathways. This review article outlines the studies of various medicinal plants, i.e., Crocus sativus, Asparagus officinalis, Ginkgo biloba, and Camellia sinensis, highlighting their potential to mitigate the harmful effects of BPA. Furthermore, the major signaling pathways, possible protective molecular mechanisms, and active ingredients of medicinal plants with potential for future drug discovery are discussed. It is important to note, however, that much of the existing research has focused on cell lines or laboratory animals, and thus, there is a gap in understanding the effectiveness of medicinal plants against BPA-induced toxicity in humans. In addition, the safe purification of extracts and the determination of appropriate doses for human use remain areas where clarity is needed.
Indexed as
Identifiers
39932506What Socratic holds
Registered trials
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.