Urtica dioica L. Alleviates Bisphenol A-Induced Testicular Toxicity in Rats via Modulation of Oxidative Stress, Inflammation, and Apoptosis

In this study, the aim was to investigate the effect of Urtica dioica L. (UD) on bisphenol A (BPA)-induced testicular toxicity in rats. Forty-eight male rats were divided into six groups: control, BPA (50 mg/kg), UD100 (100 mg/kg), UD200 (200 mg/kg), BPA + UD100, and BPA + UD200. UD ameliorated the BPA-induced reductions in sperm concentration and motility, membrane integrity and decreased increments in abnormalities of sperm. The results showed that BPA exposure significantly decreased testosterone levels, and moreover, co-administration of UD appeared to enhance this effect. Treatment with UD alleviated BPA-induced testicular apoptosis by attenuation of Bax and cleaved caspase-3 levels by increasing Bcl-2 level. Moreover, it was significantly reduced inflammation by decreasing the expression of TNF-α, IL-1ß, and IL-6 in the testis tissue compared to the BPA group. It was also determined that BPA-induced histopathological damage was significantly mitigated by UD co-administration. In the BPA group, CAT, SOD, and GPx levels decreased compared with those of the control group. However, co-administration of UD showed an ameliorative effect on the other antioxidant enzymes except for SOD. These findings revealed that UD can be used as a potential and effective agent to ameliorate BPA-induced testicular toxicity due to its antioxidant, anti-inflammatory and antiapoptotic properties.

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Journal
Veterinary Sciences
Published
2026-08-20
DOI
https://doi.org/10.3390/vetsci13080840
Primary Topic
Effects and risks of endocrine disrupting chemicals
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article
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article

Urtica dioica L. Alleviates Bisphenol A-Induced Testicular Toxicity in Rats via Modulation of Oxidative Stress, Inflammation, and Apoptosis

Fırat Aşir, Seydi Ahmet Şengül, Irmak İçen Taşkın, Oğuz Kaan YALÇIN et al.
Veterinary Sciences
Effects and risks of endocrine disrupting chemicals
article

Urtica dioica L. Alleviates Bisphenol A-Induced Testicular Toxicity in Rats via Modulation of Oxidative Stress, Inflammation, and Apoptosis

Fırat Aşir, Seydi Ahmet Şengül, Irmak İçen Taşkın, Oğuz Kaan YALÇIN, Nurdan COŞKUN ÇETİN, Gülsüm Pektanç Şengül
article en

Abstract

In this study, the aim was to investigate the effect of Urtica dioica L. (UD) on bisphenol A (BPA)-induced testicular toxicity in rats. Forty-eight male rats were divided into six groups: control, BPA (50 mg/kg), UD100 (100 mg/kg), UD200 (200 mg/kg), BPA + UD100, and BPA + UD200. UD ameliorated the BPA-induced reductions in sperm concentration and motility, membrane integrity and decreased increments in abnormalities of sperm. The results showed that BPA exposure significantly decreased testosterone levels, and moreover, co-administration of UD appeared to enhance this effect. Treatment with UD alleviated BPA-induced testicular apoptosis by attenuation of Bax and cleaved caspase-3 levels by increasing Bcl-2 level. Moreover, it was significantly reduced inflammation by decreasing the expression of TNF-α, IL-1ß, and IL-6 in the testis tissue compared to the BPA group. It was also determined that BPA-induced histopathological damage was significantly mitigated by UD co-administration. In the BPA group, CAT, SOD, and GPx levels decreased compared with those of the control group. However, co-administration of UD showed an ameliorative effect on the other antioxidant enzymes except for SOD. These findings revealed that UD can be used as a potential and effective agent to ameliorate BPA-induced testicular toxicity due to its antioxidant, anti-inflammatory and antiapoptotic properties.

Veterinary SciencesVol. 13(8)
Dicle University (TR), Inonu University (TR), Mustafa Kemal University (TR)
Openalex Percentile: Top 11%
Effects and risks of endocrine disrupting chemicals
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Urtica dioica L. Alleviates Bisphenol A-Induced Testicular Toxicity in Rats via Modulation of Oxidative Stress, Inflammation, and Apoptosis — Fırat Aşir, Seydi Ahmet Şengül, et al. · Veterinary Sciences (2026) | TGRS Research Map | TGRS