Department of Neurosurgery, Memorial Hospital, Istanbul, Turkey.
Department of Immunology, Istanbul University-DETAE, Istanbul, Turkey.
Biomed Pharmacother. 2016 Oct;83:635-640. doi: 10.1016/j.biopha.2016.07.018. Epub 2016 Jul 25.
There exist few efficient agents in the neurological and neurosurgical armamentarium for treatment of neurotrauma, refractory seizures and high grade glial tumors. Pathophysiological conditions of diverse neural injuries have converging common pathways including oxidative stress and apoptosis. Targeted therapies have been throughly investigated, but limited success has been achieved until now. Phytochemical drugs may provide easily achievable and cheap adjunctive sources. Thymoquinone is an edible quinone obtained from Nigella sativa seed oil and exerts powerful antiinflammatory, antioxidant and antitumor activities in experimental models. Recently emerging studies conducted with animal models suggest that thymoquinone - bearing a very simple molecular structure - significantly crosses the blood brain barrier and exerts neuromodulatory activities. Indeed, in animal studies, the following actions of thymoquinone were demonstrated: 1-Protection against ischemic brain damage. 2-Reduction of epileptic seizures and associated cerebral oxidative injury. 3-Reduction of morphine tolerance and associated oxidative brain damage. 4-Anxiolytic effects and reduction of immobility stress-associated cerebral oxidative injury. 5-Reduction of diabetes-induced cerebral oxidative stress, 6-Reduction of cerebral oxidative injuries induced by noxious exposures including toluene, lead and ionizing radiation. Substantial in vitro data suggest that thymoquinone may be beneficial in treatment of glial tumors. However, there is no clinical study investigating its antitumor effects. In fact, thymoquinone suppresses growth and invasion, and induces apoptosis of glial tumor cells via degrading tubulins and inhibiting 20S proteasome, telomerase, autophagy, FAK and metalloproteinases. A simple and easily available agent may be a promising adjunctive treatment option in neurological and neurosurgical practice.
在神经科学和神经外科学领域,用于治疗神经创伤、难治性癫痫和高级别神经胶质瘤的有效药物非常有限。各种神经损伤的病理生理条件都有趋同的共同途径,包括氧化应激和细胞凋亡。靶向治疗已经进行了深入研究,但到目前为止,收效甚微。植物化学药物可能提供易于实现和廉价的辅助来源。百里醌是从黑种草籽油中提取的一种可食用的醌,在实验模型中具有强大的抗炎、抗氧化和抗肿瘤活性。最近对动物模型进行的研究表明,百里醌——具有非常简单的分子结构——可以显著穿过血脑屏障并发挥神经调节作用。事实上,在动物研究中,百里醌表现出以下作用:1. 对抗缺血性脑损伤。2. 减少癫痫发作和相关的脑氧化损伤。3. 减少吗啡耐受和相关的脑氧化损伤。4. 抗焦虑作用和减少应激相关的脑氧化损伤。5. 减少糖尿病引起的脑氧化应激。6. 减少甲苯、铅和电离辐射等有害物质暴露引起的脑氧化损伤。大量体外数据表明,百里醌可能对治疗神经胶质瘤有益。然而,目前还没有研究其抗肿瘤作用的临床研究。事实上,百里醌通过降解微管蛋白和抑制 20S 蛋白酶体、端粒酶、自噬、FAK 和金属蛋白酶,抑制神经胶质瘤细胞的生长和侵袭,并诱导其凋亡。一种简单且易于获得的药物可能是神经科学和神经外科学实践中很有前途的辅助治疗选择。