Evidence map›Paper›PMID 42142192›Full record

ArticleMolecular biology reports2026

Protective effects of L-theanine against bisphenol A-induced oxidative stress and gut microbiota disruption in Wistar rats.

Mahdi Marzi, Muhammet Oğuzhan Dönmez, Azize Şener, Göksel Şener

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Article in Molecular biology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

4 authors.

Mahdi MarziFaculty of Pharmacy, Department of Basic Pharmaceutical Sciences, Pharmaceutical Microbiology Division, Fenerbahçe University, Istanbul, Turkey. mahdi.marzi@fbu.edu.tr.
Muhammet Oğuzhan DönmezFaculty of Pharmacy, Department of Pharmacology, Pharmeceutical Sciences Division, Fenerbahçe University, İstanbul, Turkey.
Azize ŞenerFaculty of Pharmacy, Department of Biochemistry, Basic Pharmaceutical Sciences Division, Fenerbahçe University, Istanbul,, Turkey.
Göksel ŞenerFaculty of Pharmacy, Department of Pharmacology, Pharmeceutical Sciences Division, Fenerbahçe University, İstanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGut microbiota homeostasis plays a central role in maintaining intestinal redox balance and immune regulation. Bisphenol A (BPA), a widely distributed environmental contaminant, has been associated with oxidative stress, inflammatory responses, and disturbances in intestinal microbial communities. L-theanine (LTN), a bioactive amino acid naturally present in green tea, possesses well-documented antioxidant and anti-inflammatory properties; however, its potential protective role against BPA-induced intestinal injury has not been fully clarified. METHODS AND

resultsIn the present study, female Wistar albino rats were randomly allocated into three groups: control, BPA (50 mg/kg/day), and BPA + LTN (100 mg/kg/day) and treated for 30 days. Oxidative stress and inflammatory responses in intestinal and colonic tissues were assessed by measuring malondialdehyde (MDA), reduced glutathione (GSH) levels and myeloperoxidase (MPO), catalase (CAT) activities. BPA exposure significantly increased MDA (p < 0.001) level and MPO (p < 0.001) activity while reducing GSH content (p < 0.001) and CAT activity (p < 0.001) compared with the control group. Compared to the BPA group, LTN treatment led to significant changes in MDA, MPO, and GSH levels in both tissues. MDA and MPO levels were significantly reduced in the intestine and colon tissues of the BPA + LTN group (p < 0.001). GSH and CAT levels were significantly increased in both the intestine and colon compared to the BPA group (p < 0.001). In addition, fecal microbiota composition was analyzed using 16 S rRNA gene sequencing, with taxonomic profiling performed at the phylum, genus and species levels. BPA exposure was associated with reduced microbial stability and compositional shifts within the gut microbiota, whereas LTN treatment partially restored microbial richness and community structure.

conclusionsCollectively, these findings indicate that LTN alleviates BPA-induced intestinal oxidative stress and microbiota dysbiosis, suggesting its potential as a protective dietary compound against environmental toxicant-related intestinal injury.

Indexed as

Benzhydryl CompoundsGastrointestinal MicrobiomeGlutamatesOxidative StressPhenolsAnimalsAntioxidantsBisphenol A CompoundsCatalaseFemaleGlutathioneMalondialdehydePeroxidaseRatsRats, WistarAntioxidantsBenzhydryl Compoundsbisphenol ABisphenol A CompoundsCatalaseGlutamatesGlutathioneMalondialdehydePeroxidasePhenolstheanineBisphenol ADysbiosisGut microbiotaL-theanineOxidative stress

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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.