Mehari Teame Gereziher, Jiang Maorong, Gu Dandan, Qian Jiaxi, Tang Jungfeng, Wubshet Ashenafi Kiros, Fang Hui, Wang Kai, Yao Deng-Bing, Wang Baohua
School of Life Sciences, Nantong University, Nantong, China.
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, School of Life Sciences, Co-Innovation Center of Neuroregeneration, Nantong University, Nantong, China.
Front Pharmacol. 2025 Aug 29;16:1654299. doi: 10.3389/fphar.2025.1654299. eCollection 2025.
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.
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.
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 () and mouse blood test results. gene expression was confirmed by RT-qPCR and GFP expression analysis. Lentivirus-mediated silencing (shRNA-Sh-a, Sh-b, and Sh-c) resulted in low expression, whereas overexpression (OE-) resulted in high expression relative to that of the controls. Gossypol stress significantly upregulated expression in ovarian tissue.
Gossypol powder from cotton is toxic to mice, affecting their pathology, histology, and hematology. This study strongly links the gene in reproductive tissues to gossypol resistance, highlighting its potential protective role and advancing the understanding of gene regulation in mouse fertility. Further research and food safety considerations are therefore crucial.
棉酚会损害两性的生殖功能,导致线粒体功能障碍、月经周期不规律以及卵巢卵泡数量减少,从而使生育率降低。本研究旨在评估从棉籽中提取的(+)-棉酚粉对小鼠的毒理学影响。
将小鼠分为四组:一组为接受纯二甲基亚砜(DMSO)的对照组,另外三组为接受溶解于DMSO中的20、40或80mg/kg棉酚的治疗组。通过每日经口灌胃对小鼠进行14天的治疗,并进行临床观察。在研究结束时,进行了体格、血液学和组织病理学(卵巢、睾丸、肝脏、肺、肾脏和脾脏)评估。
与对照治疗相比,棉酚治疗对常规血液参数和组织病理学产生了不利影响(p<0.05)。常规血液检查显示中性粒细胞和单核细胞显著升高,而淋巴细胞显著减少。此外,棉酚治疗抑制了精子发生,导致卵巢卵泡变性,并在肝脏、肾脏、肺和脾脏中诱导了组织损伤。此外,对用DMSO或80mg/kg棉酚处理的小鼠的卵巢、睾丸和肝脏进行了转录组测序,以研究生殖损伤的分子机制。构建了18个cDNA文库,产生了113.6Gb的原始读数,经过过滤后获得了112.4Gb的高质量清洁读数。分析鉴定出639个差异表达基因(DEGs)。随后,加权基因共表达网络分析(WGCNA)揭示了蓝色模块中心基因()与小鼠血液检测结果之间的强相关性。通过RT-qPCR和绿色荧光蛋白(GFP)表达分析证实了基因表达。慢病毒介导的基因沉默(shRNA-Sh-a、Sh-b和Sh-c)导致低表达,而相对于对照组,过表达(OE-)导致高表达。棉酚应激显著上调了卵巢组织中的表达。
棉籽中的棉酚粉对小鼠有毒,影响其病理学、组织学和血液学。本研究有力地将生殖组织中的基因与棉酚抗性联系起来,突出了其潜在的保护作用,并推进了对小鼠生育力基因调控的理解。因此,进一步的研究和食品安全考虑至关重要。