Ibrahim Marwan Abdel-Latif, Salah-Eldin Alaa-Eldin
Department of Biology, College of Science, Majmaah University, Majmaah, Al-Zulfi, Saudi Arabia,
Department of Biology, College of Science, Majmaah University, Majmaah, Al-Zulfi, Saudi Arabia.
Pharmacology. 2019;103(3-4):202-211. doi: 10.1159/000496424. Epub 2019 Jan 30.
The present study aimed to elucidate the effects of tramadol on the testicular functions of adult male rats due to the chronic usage of tramadol and the effect of its withdrawal.
Adult male albino rats were classified into the following 3 groups: (I) a control administered with normal saline and (II) tramadol-treated rats (40 mg/kg b.w. orally) for 21 successive days; and (III) like the rats in the second group but kept for 4 weeks after the last tramadol dose to study the effect of tramadol withdrawal. At the end of the experimental period, blood was collected and specimens from testis were taken for histopathological, biochemical, and molecular studies. A reverse transcription-polymerized chain reaction after RNA extraction from specimens was detected for the anti-apoptotic and pro-apoptotic genes in testicular tissues. Also, malondialdehyde (MDA) was measured in tissues homogenate and antioxidant enzymes activities were evaluated.
The results of this study demonstrated histological changes in testicular tissues in groups II and III compared to the control group, accompanied with increased apoptotic index and proved by increased B-cell lymphoma-2 (Bcl-2) associated-X-protein and caspase-3 expression, whereas anti-apoptotic Bcl-2 markedly decreased. Moreover, in tramadol-abused and -withdrawal groups, the MDA level increased, while the antioxidant enzymes activity decreased and revealed oxidative stress, indicating that tramadol is harmful at the cellular level and can induce apoptotic changes in testicular tissues. The withdrawal effect showed signs of improvement, but it did not return to normal levels.
It could be concluded that the administration of tramadol causes abnormalities on testicular tissues associated with oxidative stress, which confirmed the risk of increased oxidative stress on testicular tissues due to tramadol abuse.
本研究旨在阐明长期使用曲马多对成年雄性大鼠睾丸功能的影响及其戒断效应。
成年雄性白化大鼠分为以下3组:(I)给予生理盐水的对照组;(II)连续21天口服曲马多(40 mg/kg体重)的大鼠组;(III)与第二组大鼠相同,但在最后一次给予曲马多剂量后饲养4周以研究曲马多戒断效应的大鼠组。实验期结束时,采集血液并取睾丸标本进行组织病理学、生化和分子研究。从标本中提取RNA后进行逆转录聚合酶链反应,检测睾丸组织中的抗凋亡和促凋亡基因。此外,测定组织匀浆中的丙二醛(MDA)含量并评估抗氧化酶活性。
本研究结果表明,与对照组相比,第二组和第三组大鼠的睾丸组织出现组织学变化,同时凋亡指数增加,这通过B细胞淋巴瘤-2(Bcl-2)相关X蛋白和半胱天冬酶-3表达增加得到证实,而抗凋亡蛋白Bcl-2明显减少。此外,在曲马多滥用组和戒断组中,MDA水平升高,而抗氧化酶活性降低,显示出氧化应激,表明曲马多在细胞水平上具有危害性,可诱导睾丸组织发生凋亡变化。戒断效应显示出改善迹象,但未恢复到正常水平。
可以得出结论,曲马多的给药会导致与氧化应激相关的睾丸组织异常,这证实了曲马多滥用会增加睾丸组织氧化应激的风险。