糖精对大鼠精子、血管组织和垂体-性腺激素轴的影响

Reza Paknejad, V. H. Jahromi
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引用次数: 0

摘要

雄性Wistar在完全随机的设计中被分为5个相等的组。对照组不接受任何溶剂或对照组每天接受1ml蒸馏水作为腹膜内注射。实验组每天分别腹腔注射糖精1次、2次和3次,分别为250、500和1000mg/kg体重,持续35天。35天后从动物身上采集血样,分离睾丸组织进行组织学检查。通过SPSS软件16版和单向ANOVA和Duncan事后检验对获得的数据进行分析。与假手术组和对照组相比,实验组的精子数量显著减少;Sertoli细胞和Leydig细胞无显著性差异(P>0.05)。当然,在这方面,使用这种常用的人造甜味剂的方式和剂量是非常重要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effect of Saccharin on spermatogenes, testiscular tissue and pituitary –gonad hormones axis in rats
male Wistar classified into 5 equal groups in a completely randomized design. The control group did not receive any solvent or The control group received 1 ml distilled water per day as an intraperitoneal injection. Experimental groups received 1, 2 and 3 times daily, respectively, 250, 500 and 1000 mg / kg body weight saccharin intraperitoneal injection for 35 days, respectively. Blood samples were taken from animals after 35 days and testis tissue was isolated for histological examination. The obtained data were analyzed by SPSS software version 16 and one way ANOVA and Duncan's post hoc test. sperm in experimental groups have decreased significantly compared to the sham and control groups; but Sertoli and Leydig cells showed no any significant difference (P>0.05). Saccharin can have a harmful effects on the rate of hormone and cells, and the confirms the obtained hormonal results. Of course in this regard, the mode and dosage of using this common used artificial sweeter is very important.
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