Evidence map›Paper›PMID 42026174›Full record

ArticleInternational journal of impotence research2026

Protective effects of panax ginseng against bisphenol a-induced testicular toxicity in rats.

Dogancan Dorucu, Goksel Sener, Seren Ede Pazarbasi, Burcin Irem Abas, Yasemin Cesur, Ozge Cevik, Feriha Ercan, Tarik Emre Sener, Kamil Cam

Abstract read
PubMed Publisher
In one paragraph

Article in International journal of impotence research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

9 authors.

Dogancan DorucuDepartment of Urology, School of Medicine, Marmara University, Istanbul, Turkey.
Goksel SenerDepartment of Pharmacology, School of Pharmacy, Fenerbahce University, Istanbul, Turkey.
Seren Ede PazarbasiDepartment of Pharmacology, School of Pharmacy, Fenerbahce University, Istanbul, Turkey.
Burcin Irem AbasDepartment of Medical Biochemistry, School of Medicine, Adnan Menderes University, Aydin, Turkey.
Yasemin CesurDepartment of Histology & Embryology, School of Medicine, Marmara University, Istanbul, Turkey.
Ozge CevikDepartment of Medical Biochemistry, School of Medicine, Adnan Menderes University, Aydin, Turkey.ORCID http://orcid.org/0000-0002-9325-3757
Feriha ErcanDepartment of Histology & Embryology, School of Medicine, Marmara University, Istanbul, Turkey.
Tarik Emre SenerDepartment of Urology, School of Medicine, Marmara University, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-0085-7680
Kamil CamDepartment of Urology, School of Medicine, Marmara University, Istanbul, Turkey. kamil.cam@marmara.edu.tr.ORCID http://orcid.org/0000-0002-8275-5479

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bisphenol A (BPA) is an endocrine-disrupting chemical known to cause testicular toxicity through oxidative stress and apoptosis. Panax ginseng (PG) is a natural product with anti-inflammatory effects. This study aimed to evaluate the protective effect of PG against BPA-induced testicular damage in rats. Thirty-two Wistar Albino rats aged 10-12 weeks were divided into four groups: Control, PG, BPA, and BPA + PG. BPA (50 mg/kg/day) and PG (100 mg/kg/day) were orally administered for 6 weeks. BPA significantly increased serum total oxidant status and decreased antioxidant status (p < 0.001, p < 0.001). Also, the levels of superoxide dismutase (an antioxidant enzyme) (p = 0.0005) and androgen receptor-mRNA (an androgen signaling marker) decreased (p = 0.014). However, caspase 3 (an apoptosis marker) (p = 0.0067), 8-hydroxy-2'-deoxyguanosine (a marker of oxidative DNA damage) (p < 0.001), and tumor necrosis factor-α (a proinflammatory cytokine) (p < 0.001) levels increased in testicular tissues. Rats treated with PG showed improvements in all oxidative and inflammatory markers and significantly restored androgen receptor expression. Histopathological examination revealed degeneration in seminiferous tubules and reduced spermatozoa in the BPA group, while the BPA + PG group showed marked improvement. These findings suggest that PG may alleviate oxidative stress-related testicular damage at both molecular and histological levels and may offer insights for future clinical studies.

Identifiers

What OpenQuestion holds

Textmetadata
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.