维生素D和曲马多联合给药对Wistar大鼠血清kisspeptin、睾酮、氧化应激水平和睾丸组织学的影响:初步报告。

Revista internacional de andrologia Pub Date : 2024-12-01 Epub Date: 2024-12-30 DOI:10.22514/j.androl.2024.031
Izuchukwu Azuka Okafor, Smart Ikechukwu Mbagwu, Ikwuneme Gibson Chidera, Ezenduka Chiemeka Augustine, Ikenna Makuachukwu Anagboso, Chikwesiri Emmanuel Onyema
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引用次数: 0

摘要

背景:曲马多是一种阿片类镇痛药,已知可引起睾丸损伤并损害生殖参数。维生素D3以其抗氧化和保护特性而闻名,可能对曲马多引起的睾丸损伤有潜在的保护作用。本研究观察了维生素D3和曲马多共同给药对雄性大鼠血清kisspeptin水平、睾丸组织学、精液参数、睾酮水平和氧化应激标志物的影响。方法:体重150 ~ 250 g的雄性大鼠15只,随机分为3组,每组5只。A组为对照组,只接受蒸馏水。B组每日给予曲马多20 mg/kg体重,C组每日同时给予曲马多20 mg/kg体重和维生素D3 25 μg/kg体重。口服治疗14天。测定给药后体重、相对睾丸重量、血清kisspeptin水平、精液参数、睾酮水平和氧化应激标志物(过氧化氢酶、谷胱甘肽和丙二醛)。用显微摄影检查睾丸组织学。结果:各组大鼠体重、睾丸相对重量、血清kisspeptin水平、精液参数、睾酮水平、氧化应激指标差异均无统计学意义(p < 0.05)。组织学分析显示曲马多治疗组的精子明显退化,与对照组相比,维生素D3联合给药并没有减轻这种退化。结论:本研究表明,补充维生素D3不能显著改善曲马多诱导的睾丸损伤。需要进一步研究不同剂量和更长的持续时间,以进一步探索维生素D3的潜在保护机制。
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 coadministration of vitamin D and tramadol on serum kisspeptin, testosterone, oxidative stress levels and testicular histology in Wistar rats: a preliminary report.

Background: Tramadol, an opioid analgesic, is known to induce testicular damage and impair reproductive parameters. Vitamin D3, recognized for its antioxidant and protective properties, might offer a potential protective effect against tramadol-induced testicular damage. This study observed the effects of co-administration of vitamin D3 and tramadol on serum kisspeptin levels, testicular histology, semen parameters, testosterone levels, and oxidative stress markers in male rats.

Methods: Fifteen male rats weighing between 150 and 250 g were randomly divided into three groups (n = 5 per group). Group A was the control, receiving only distilled water. Group B was administered 20 mg/kg body weight of tramadol daily, while group C received both 20 mg/kg body weight of tramadol and 25 μg/kg body weight of vitamin D3 daily. The treatments were administered orally for 14 days. Post-administration body weight, relative testicular weight, serum kisspeptin levels, semen parameters, testosterone levels and oxidative stress markers (catalase, glutathione and malonaldehyde) were measured. Testicular histology was also examined using photomicrography.

Results: No significant differences were observed in body weights, relative testicular weights, serum kisspeptin levels, semen parameters, testosterone levels, or oxidative stress markers among the experimental groups (p > 0.05). Histological analysis in the tramadoltreated group exhibited significant degradation of spermatozoa, which was not mitigated by vitamin D3 co-administration compared to the control group.

Conclusions: The study demonstrates that vitamin D3 supplementation does not significantly ameliorate tramadol-induced testicular damage. There is a need for further research with varied doses and longer durations to further explore the potential protective mechanisms of vitamin D3.

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