Evidence map›Paper›PMID 40949118›Full record

ArticleFrontiers in pharmacology2025

Histopathological examination and transcriptomic profiling reveal gossypol toxicity-responsive genes related to fertility in mice.

Teame Gereziher Mehari, Maorong Jiang, Dandan Gu, Jiaxi Qian, Jungfeng Tang, Ashenafi Kiros Wubshet, Hui Fang, Kai Wang, Deng-Bing Yao, Baohua Wang

Abstract read
In one paragraph

Article in Frontiers in pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Frontiers in endocrinology · 2025
    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

10 authors.

Teame Gereziher Mehari *School of Life Sciences, Nantong University, Nantong, China.
Maorong Jiang *Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, School of Life Sciences, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, China.
Dandan GuKey Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, School of Life Sciences, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, China.
Jiaxi QianKey Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, School of Life Sciences, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, China.
Jungfeng TangSchool of Life Sciences, Nantong University, Nantong, China.
Ashenafi Kiros WubshetDepartment of Cell Engineering and Biotechnology, Shandong Province Binzhou Animal Husbandry and Veterinary Institute, Binzhou, China.
Hui FangSchool of Life Sciences, Nantong University, Nantong, China.
Kai WangSchool of Life Sciences, Nantong University, Nantong, China.
Deng-Bing YaoSchool of Life Sciences, Nantong University, Nantong, China.
Baohua WangSchool of Life Sciences, Nantong University, Nantong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gossypol impairs reproduction in both sexes, inducing mitochondrial dysfunction, irregular cycles, and fewer ovarian follicles, leading to decreased fertility rates. The present investigation was undertaken to evaluate the toxicological effects of (+)-gossypol powder, a substance derived from cottonseed in mice. Methods: The mice were divided into four groups: a control group receiving pure dimethyl sulfoxide (DMSO) and three treatment groups receiving 20, 40, or 80 mg/kg gossypol dissolved in DMSO. The mice were treated daily via oral gavage for 14 days and subjected to clinical observation. At study completion, physical, hematological, and histopathological (ovary, testis, liver, lung, kidney, and spleen) evaluations were performed. Results: Compared with the control treatment, gossypol treatment adversely affected routine blood parameters and histopathology (p < 0.05). Routine blood tests revealed significantly elevated neutrophil granulocytes and monocytes, along with a marked decrease in lymphocytes. Furthermore, gossypol treatment inhibited spermatogenesis, caused follicular degeneration in the ovaries, and induced tissue damage in the liver, kidney, lung, and spleen. Furthermore, transcriptome sequencing of ovaries, testes, and livers from mice treated with DMSO or 80 mg/kg gossypol was performed to investigate the molecular mechanisms of reproductive damage. Eighteen cDNA libraries were constructed and yielded 113.6 Gb of raw reads, which were filtered to obtain 112.4 Gb of high-quality clean reads. The analysis identified 639 differentially expressed genes (DEGs). Consecutively, weighted gene coexpression network analysis (WGCNA) revealed a strong correlation between the blue module hub gene Conclusion: Gossypol powder from cotton is toxic to mice, affecting their pathology, histology, and hematology. This study strongly links the

Indexed as

dimethyl sulfoxideDmrt2fertilitygossypolmicetranscriptome

Identifiers

PMID40949118
PMCPMC12425930

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