Sperm abnormality toxicity due to cyclosporine A and the ameliorative effect of royal jelly in male rats

IF 1.1 Q3 BIOLOGY
Azza M. Gawish , Samya ElFiky , Mary Therase , Amira AbdElraaof , Wagdi Khalil , Karima A. Mohamed
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引用次数: 14

Abstract

The immunosuppressive drug, utilized widely in Egypt, cyclosporine A was studied to evaluate its toxicity in male rats. Animals were divided into a control (untreated), 3 groups treated intraperitoneally with 20, 40 and 60 m/kg cyclosporine A for 5, 10 and 15 days, respectively and 3 groups treated intraperitoneally with 20, 40 and 60 mg/kg of cyclosporine A plus 100 mg/kg royal jelly administrated orally. Toxicity evaluation was carried out using two main endpoints: reproductive study (sperm morphology and count abnormalities) and biochemical changes in liver and testis (DNA amounts). The aim of this work is to study the protective role of royal jelly against sperm abnormalities in shape and count, and changes in DNA contents in liver and testis tissue induced in rats when treated by cyclosporine A with different doses (20–40–60 mg/kg/day) for 5, 10, and 15 days in male rats and how the royal jelly can repair this changes. Our results showed that sperm abnormalities induced by cyclosporine A included deviation from normal shape in head and tail. Abnormal heads contained amorphous head and banana-shaped head, whereas the abnormal tails included divided and coiled tails. It also induced an insignificant effect on the total sperm counts after 5 days of injection with the drug combined with royal jelly. DNA contents were determined in rat liver and testis cells to illustrate the mutagenic effect of cyclosporine A and how the royal jelly can modulate this effect. From these results we concluded that cyclosporine A toxicity was dose and time dependent and should be administrated under special precautions and medical supervision. Using of royal jelly in combination with cyclosporine A drug decreased its toxic effect, so it's considered as protector.

环孢素A对雄性大鼠精子异常毒性及蜂王浆的改善作用
环孢素A是一种在埃及广泛使用的免疫抑制药物,研究其对雄性大鼠的毒性。将动物分为对照组(未处理),3组分别腹腔注射20、40、60 m/kg环孢素a 5、10、15 d, 3组腹腔注射20、40、60 mg/kg环孢素a + 100 mg/kg蜂王浆。毒性评价采用两个主要终点:生殖研究(精子形态和计数异常)和肝脏和睾丸生化变化(DNA量)。本研究旨在研究蜂王浆对环孢素A不同剂量(20 ~ 40 ~ 60 mg/kg/天)作用5、10、15天后雄性大鼠精子形态、数量异常、肝脏和睾丸组织DNA含量变化的保护作用,以及蜂王浆如何修复这一变化。结果表明,环孢素A引起的精子畸形包括头部和尾部偏离正常形状。异常头包括无定形头和香蕉形头,异常尾包括分裂尾和盘绕尾。该药物与蜂王浆联合注射5天后,对精子总数的影响也不显著。测定了大鼠肝脏和睾丸细胞的DNA含量,以说明环孢素A的致突变作用以及蜂王浆如何调节这种作用。由此可见,环孢素A的毒性具有剂量和时间依赖性,应在特殊的预防措施和医学监督下给药。蜂王浆与环孢素A药物联用可降低其毒性作用,被认为是保护剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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