Hearing Disorders Research Center, Loghman Hakim Hospital, Shahid Beheshti University of Medical Sciences, Iran University of Medical Sciences, Tehran, Iran.
Department of Cell Biology and Anatomical Sciences, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neurotox Res. 2021 Aug;39(4):1134-1147. doi: 10.1007/s12640-021-00354-w. Epub 2021 Apr 5.
Tramadol is a centrally acting synthetic opioid analgesic and SNRI (serotonin/norepinephrine reuptake-inhibitor) that structurally resembles codeine and morphine. Given the tramadol neurotoxic effect and the body of studies on the effect of tramadol on the cerebellum, this study aims to provide deeper insights into molecular and histological alterations in the cerebellar cortex related to tramadol administration. In this study, twenty-four adult male albino rats were randomly and equally divided into two groups: control and tramadol groups. The tramadol group received 50 mg/kg of tramadol daily for 3 weeks via oral gavage. The functional and structural change of the cerebellum under chronic exposure of tramadol were measured. Our data revealed that treating rats with tramadol not only lead to cerebellum atrophy but also resulted in the actuation of microgliosis, neuroinflammatoin, and apoptotic biomarkers. Our results illustrated a significant drop in VEGF (vascular endothelial growth factor) level in the tramadol group. Additionally, tramadol impaired motor coordination and neuromuscular activity. We also identified several signaling cascades chiefly related to neurodegenerative disease and energy metabolism that considerably deregulated in the cerebellum of tramadol-treated rats. Overall, the outcomes of this study suggest that tramadol administration has a neurodegeneration effect on the cerebellar cortex via several pathways consisting of microgliosis, apoptosis, necroptosis, and neuroinflammatoin.
曲马多是一种中枢作用的合成阿片类镇痛药和 SNRIs(血清素/去甲肾上腺素再摄取抑制剂),其结构类似于可待因和吗啡。鉴于曲马多的神经毒性作用以及大量关于曲马多对小脑影响的研究,本研究旨在深入了解与曲马多给药相关的小脑皮层的分子和组织学改变。在这项研究中,二十四只成年雄性白化大鼠被随机平均分为两组:对照组和曲马多组。曲马多组通过口服灌胃每天给予 50mg/kg 的曲马多,持续 3 周。测量小脑在慢性暴露于曲马多下的功能和结构变化。我们的数据表明,用曲马多治疗大鼠不仅导致小脑萎缩,而且还导致小胶质细胞增生、神经炎症和细胞凋亡生物标志物的激活。我们的结果表明,曲马多组的 VEGF(血管内皮生长因子)水平显著下降。此外,曲马多损害了运动协调和神经肌肉活动。我们还确定了几个主要与神经退行性疾病和能量代谢相关的信号通路,这些通路在曲马多处理的大鼠小脑内显著失调。总的来说,这项研究的结果表明,曲马多给药通过小胶质细胞增生、细胞凋亡、坏死性凋亡和神经炎症等多种途径对小脑皮层产生神经退行性作用。