Protocatechuic acid modulates reproductive dysfunction linked to furan exposure in rats

• Published in: Toxicology (Amsterdam) 2020-09, Vol.442, p.152556, Article 152556
• Main Authors: Owumi, Solomon E., Adedara, Isaac A., Farombi, Ebenezer O., Oyelere, Adegboyega K.
• Format: Article
• Language: English
• Subjects: Animals; Antioxidants - metabolism; Apoptosis; Cytokines - metabolism; Furan; Furans; Hormones - blood; Hydroxybenzoates - therapeutic use; Hypothalamic-pituitary-gonadal axis; Hypothalamo-Hypophyseal System - drug effects; Infertility, Male - chemically induced; Infertility, Male - drug therapy; Inflammation; Male; Pituitary Gland - drug effects; Protocatechuic acid; Rats; Rats, Wistar; Reactive Nitrogen Species - metabolism; Reactive Oxygen Species - metabolism; Reproduction - drug effects; Spermatozoa - drug effects; Testis - drug effects; Testis - enzymology; Testis - metabolism
• ISSN: 0300-483X; 1879-3185
• DOI: 10.1016/j.tox.2020.152556

•Protocatechuic acid (PCA), a dietary polyphenol, elicits beneficial effects on male reproductive system.•PCA alleviated furan-mediated declines in sperm quality and serum reproductive hormones.•PCA attenuated furan-induced reduction in antioxidant enzyme activities and testicular function marker enzymes.•PCA effectively alleviated furan-mediated increases in myeloperoxidase activity, reactive oxygen and nitrogen species, nitric oxide, TNF-α, and IL-1β.•PCA increased anti-inflammatory cytokine IL-10, suppressed caspase-9 and caspase-3 activities and ameliorated injury in the testes, epididymis and hypothalamus of furan treated rats. The reproductive toxicity associated with furan exposure in both animals and humans has been documented. Protocatechuic acid (PCA), a dietary polyphenolic chemical, reportedly elicits beneficial effects on the male reproductive system. However, the influence of PCA on the reproductive toxicity related to furan exposure is unavailable in the literature. The current study evaluated the effects of PCA on the dysfunctional reproductive axis caused by furan exposure in rats. Experimental animals were exposed to furan (8 mg/kg) or co-treated with furan (8 mg/kg) and PCA (25 or 50 mg/kg) for twenty-eight successive days. Results revealed that PCA treatment significantly alleviated furan-mediated declines in sperm production and characteristic qualities as well as in serum levels of prolactin, luteinizing hormone, follicle-stimulating hormone, and testosterone. Further, PCA attenuated furan-induced reduction in antioxidant enzyme activities and testicular function marker enzymes, namely lactate dehydrogenase, glucose-6-phosphate dehydrogenase, acid phosphatase, and alkaline phosphatase. PCA effectively mitigated furan-mediated increases in myeloperoxidase activity, levels of reactive oxygen and nitrogen species, nitric oxide, tumour necrosis factor-alpha, and interleukin-1β in testes, epididymis, and hypothalamus of rats. Moreover, PCA increased anti-inflammatory cytokine interleukin-10 but suppressed caspase-9 and caspase-3 activities and ameliorated injuries in the testes, epididymis, and hypothalamus of furan-treated rats. In conclusion, PCA ameliorated deficits in the hypothalamic-pituitary-gonadal axis function in furan-exposed rats by suppressing oxido-inflammatory stress and apoptosis.