Neuroscience Research Center, Institute of Neuropharmacology, Kerman University of Medical Sciences, Kerman, 76198-13159, Iran.
Gastroenterology and Hepatology Research Center, Institute of Basic and Clinical Physiology Sciences, Kerman University of Medical Sciences, Kerman, Iran.
Sci Rep. 2024 Apr 29;14(1):9864. doi: 10.1038/s41598-024-60518-4.
Essential tremor (ET) is a neurological disease that impairs motor and cognitive functioning. A variant of the Lingo-1 genetic locus is associated with a heightened ET risk, and increased expression of cerebellar Lingo-1. Lingo-1 has been associated with neurodegenerative processes; however, neuroprotection from ET-associated degeneration can be conferred by the protein Sirt1. Sirt1 activity can be promoted by Resveratrol (Res) and 1,25-dihydroxyvitamin D3 (VitD3), and thus these factors may exert neuroprotective properties through a Sirt1 mechanism. As Res and VitD3 are linked to Sirt1, enhancing Sirt1 could counteract the negative effects of increased Lingo-1. Therefore, we hypothesized that a combination of Res-VitD3 in a harmaline injection model of ET would modulate Sirt1 and Lingo-1 levels. As expected, harmaline exposure (10 mg/kg/every other day; i.p.) impaired motor coordination, enhanced tremors, rearing, and cognitive dysfunction. When Res (5 mg/kg/day; i.p.) and VitD3 (0.1 mg/kg/day; i.p.) were given to adult rats (n = 8 per group) an hour before harmaline, tremor severity, rearing, and memory impairment were reduced. Individual treatment with Res and VitD3 decreased Lingo-1 gene expression levels in qPCR assays. Co-treatment with Res and VitD3 increased and decreased Sirt1 and Lingo-1 gene expression levels, respectively, and in some cases, beneficial effects on behavior were noted, which were not seen when Res or VitD3 were individually applied. Taken together, our study found that Res and VitD3 improved locomotor and cognitive deficits, modulated Sirt1 and Lingo-1. Therefore, we would recommend co-treatment of VitD3 and Res to leverage complementary effects for the management of ET symptoms.
特发性震颤(ET)是一种损害运动和认知功能的神经退行性疾病。 Lingo-1 基因座的一个变体与 ET 风险增加有关,并且小脑 Lingo-1 的表达增加。 Lingo-1 与神经退行性过程有关;然而,蛋白质 Sirt1 可以提供 ET 相关变性的神经保护。 Sirt1 活性可以通过白藜芦醇(Res)和 1,25-二羟基维生素 D3(VitD3)促进,因此这些因素可能通过 Sirt1 机制发挥神经保护作用。由于 Res 和 VitD3 与 Sirt1 相关,增强 Sirt1 可以抵消 Lingo-1 增加的负面影响。因此,我们假设 Res-VitD3 在 ET 的哈马灵注射模型中联合使用会调节 Sirt1 和 Lingo-1 水平。正如预期的那样,哈马灵暴露(10mg/kg/每隔一天;ip)会损害运动协调能力,增加震颤、竖起和认知功能障碍。当 Res(5mg/kg/天;ip)和 VitD3(0.1mg/kg/天;ip)在哈马灵前一小时给予成年大鼠(每组 8 只)时,震颤严重程度、竖起和记忆障碍减轻。 Res 和 VitD3 的单独治疗降低了 qPCR 检测中的 Lingo-1 基因表达水平。 Res 和 VitD3 的联合治疗分别增加和降低了 Sirt1 和 Lingo-1 的基因表达水平,在某些情况下,观察到行为的有益影响,而单独使用 Res 或 VitD3 则没有观察到。综上所述,我们的研究发现 Res 和 VitD3 改善了运动和认知缺陷,调节了 Sirt1 和 Lingo-1。因此,我们建议联合使用 VitD3 和 Res,以利用互补作用来管理 ET 症状。