Koriem Khaled M M, Arbid Mahmoud S S
Department of Medical Physiology, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
Department of Pharmacology, Medical Research and Clinical Studies Institute, National Research Centre, Cairo, Egypt.
J Complement Integr Med. 2024 Sep 5;21(4):501-510. doi: 10.1515/jcim-2024-0161. eCollection 2024 Dec 1.
Favism is a metabolic disease while pracaxi oil is a strong antioxidant agent. This study evaluates anti-infertility activity and assists normal male fertilization of pracaxi oil in favism-induced male rats.
A total of 36 male albino rats of six equal sets were each with 6 rats; Control, Pracaxi oil (1 mL), and Pracaxi oil (2 mL), Favism-induced male rats-, Pracaxi oil (1 mL) + Favism-induced male rats, and Pracaxi oil (2 mL) + Favism-induced male rats groups. Blood parameters, liver function, serum male hormones were determined. Glucose-6-phosphate dehydrogenase, 3β-hydroxysteroid dehydrogenase, total protein, and cholesterol in testis were estimated. Sodium/potassium-ATPase and antioxidants in the hypothalamus, testis, and sperm were assessed. Sperm count, motility, and abnormality, and sperm monoclonal proliferating antibody Ki-67 were evaluated.
Favism decreased blood parameters, liver function, superoxide dismutase, glutathione, serum testosterone and dehydroepiandrosterone sulfate, sperm count and motility, sodium/potassium-ATPase activity while increased malondialdehyde, serum follicle stimulating hormone, sex hormone binding globulin, and luteinizing hormone, glucose-6-phosphatedehydrogenase, 3β-hydroxysteroid dehydrogenase, cholesterol, total protein, sperm abnormality, the percentage of spermatogonia, 1st spermatocyte, 2nd spermatocyte, and spermatid in the testis. Furthermore, two doses of pracaxi oil to favism-induced male rats back all of aforementioned parameters to be close control values where a higher dose of pracaxi oil had an efficient impact than a lower dose.
Pracaxi oil protects the hypothalamic-pituitary-gonad axis, and preserves sperm quality in favism-induced male rats.
蚕豆病是一种代谢性疾病,而普拉卡希油是一种强抗氧化剂。本研究评估普拉卡希油对蚕豆病诱导的雄性大鼠的抗不育活性及对正常雄性受精的辅助作用。
将36只雄性白化大鼠平均分为六组,每组6只;分别为对照组、普拉卡希油(1毫升)组、普拉卡希油(2毫升)组、蚕豆病诱导的雄性大鼠组、普拉卡希油(1毫升)+蚕豆病诱导的雄性大鼠组和普拉卡希油(2毫升)+蚕豆病诱导的雄性大鼠组。测定血液参数、肝功能、血清雄性激素。评估睾丸中的葡萄糖-6-磷酸脱氢酶、3β-羟基类固醇脱氢酶、总蛋白和胆固醇。评估下丘脑、睾丸和精子中的钠/钾-ATP酶和抗氧化剂。评估精子数量、活力、异常情况以及精子单克隆增殖抗体Ki-67。
蚕豆病降低了血液参数、肝功能、超氧化物歧化酶、谷胱甘肽、血清睾酮和硫酸脱氢表雄酮、精子数量和活力、钠/钾-ATP酶活性,同时增加了丙二醛、血清促卵泡激素、性激素结合球蛋白、黄体生成素、葡萄糖-6-磷酸脱氢酶、3β-羟基类固醇脱氢酶、胆固醇、总蛋白、精子异常、睾丸中生精细胞、初级精母细胞、次级精母细胞和精子细胞的百分比。此外,给蚕豆病诱导的雄性大鼠服用两剂普拉卡希油可使上述所有参数恢复到接近对照值,且高剂量的普拉卡希油比低剂量的效果更显著。
普拉卡希油可保护下丘脑-垂体-性腺轴,并维持蚕豆病诱导的雄性大鼠的精子质量。