氨氯地平对实验性单侧隐睾大鼠睾丸组织结构和功能保护作用的研究

S. Shahraki, D. Kianifard, M. Moradi, S. Javanmardi
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引用次数: 0

摘要

目的-隐睾是男性生殖道常见的出生缺陷,是导致生育问题的原因之一。隐睾后组织温度升高可引起氧化应激,从而影响细胞和组织的变性。氨氯地平是第三代钙通道阻滞剂,具有抗氧化活性。本研究的目的是评估氨氯地平对隐睾动物模型中睾丸组织改变的保护作用。设计-实验研究动物-30只成年雄性Sprague-Dawley大鼠,体重200-220g程序-在成年大鼠中诱导实验性隐睾。氨氯地平(10 mg/kg b.w.)连续两周和四周口服给药。实验组由未治疗的隐睾(n=10)组和治疗的隐遗(n=10。在隐睾发生后第14天和第28天收集未治疗组和治疗组的睾丸组织样本。对组织样本进行组织病理学和形态计量学研究,评估精子发生的微观指标。结果:隐睾组肾小管萎缩伴生发上皮紊乱。这些变化在接受治疗的动物中呈剂量依赖性减少。与对照组相比,未治疗四周的隐睾组支持细胞平均数显著减少(p=0.025),生殖细胞谱系平均数显著降低(p<0.0001)。同样,隐睾诱导后,精子发生的所有微观指标都降低了。氨氯地平治疗组的这些改变随时间而减少。结论和临床相关性-本研究结果表明,氨氯地平作为一种抗氧化剂,可以有效地减少隐睾引起的睾丸组织细胞和组织损伤,并具有时间依赖性。这些保护作用的某些部分可能是通过其作为钙阻滞剂的活性来实现的,钙阻滞剂通过降低细胞质钙水平来减少细胞凋亡过程。
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Investigation of the Protective Effects of Amlodipine on the Structure and Function of Testicular Tissue following Experimental Unilateral Cryptorchidism in Rats
Objective- Cryptorchidism, common birth defect of the male genital tract, is one of the causes of fertility problems. The elevation of tissue temperature following of cryptorchidism could induce oxidative stress which influences the cellular and tissue degeneration. Amlodipine is a third-generation of calcium channel blockers which has antioxidant activity. The aim of this study was to evaluate the protective effects of amlodipine on testicular tissue alterations in an animal model of cryptorchidism. Design- Experimental study Animals- Thirty adult male Sprague-Dawley rats weighing 200-220g Procedure- Experimental cryptorchidism was induced in adult rats. Amlodipine (10 mg/kg b.w.) was administrated orally for two and four consecutive weeks. The experimental groups consisted of non-treated cryptorchidism (n=10) and treated cryptorchidism (n=10) groups. Testicular tissue samples were collected on days 14 and 28 following of cryptorchidism form non-treated and treated groups. Histopathological and morphometrical studies with the evaluation of microscopic indices of spermatogenesis were prepared on tissue samples. Results- Tubular atrophy with germinal epithelium disarrangement was observed in cryptorchidism groups. These changes were reduced dose-dependently in treated animals. The mean of Sertoli cells was reduced significantly (p=0.025) in four weeks non-treated and the mean of germ cells lineage was reduced significantly (p<0.0001) in four weeks non-treated and two weeks treated cryptorchidism groups compared to the control group. Similarly, all microscopic indices of spermatogenesis were reduced following the induction of cryptorchidism. These alterations were reduced time-dependently in amlodipine treated groups. Conclusion and clinical relevance- The results of this study revealed that the administration of amlodipine as an antioxidant agent, time-dependently could be effective on the reduction of cellular and tissue damages of testicular tissue induced by cryptorchidism. It seems some parts of these protective effects may be done through its activity as calcium blocker which declines apoptotic processes by reduction of cytoplasmic calcium levels.
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