Institute of Psychiatry, Psychology and Neuroscience, King's College London, Denmark Hill, London SE5 8AF, UK.
College of Medicine and Health, University of Exeter, Exeter EX1 2UL, UK.
Int J Mol Sci. 2023 Jul 7;24(13):11219. doi: 10.3390/ijms241311219.
The pan Rho-associated coiled-coil-containing protein kinase (ROCK) inhibitor fasudil acts as a vasodilator and has been used as a medication for post-cerebral stroke for the past 29 years in Japan and China. More recently, based on the involvement of ROCK inhibition in synaptic function, neuronal survival, and processes associated with neuroinflammation, it has been suggested that the drug may be repurposed for neurodegenerative diseases. Indeed, fasudil has demonstrated preclinical efficacy in many neurodegenerative disease models. To facilitate an understanding of the wider biological processes at play due to ROCK inhibition in the context of neurodegeneration, we performed a global gene expression analysis on the brains of Alzheimer's disease model mice treated with fasudil via peripheral IP injection. We then performed a comparative analysis of the fasudil-driven transcriptional profile with profiles generated from a meta-analysis of multiple neurodegenerative diseases. Our results show that fasudil tends to drive gene expression in a reverse sense to that seen in brains with post-mortem neurodegenerative disease. The results are most striking in terms of pathway enrichment analysis, where pathways perturbed in Alzheimer's and Parkinson's diseases are overwhelmingly driven in the opposite direction by fasudil treatment. Thus, our results bolster the repurposing potential of fasudil by demonstrating an anti-neurodegenerative phenotype in a disease context and highlight the potential of in vivo transcriptional profiling of drug activity.
全 Rho 相关卷曲螺旋蛋白激酶(ROCK)抑制剂法舒地尔作为血管扩张剂,在日本和中国已经被用于治疗脑卒后 29 年。最近,基于 ROCK 抑制作用在突触功能、神经元存活和神经炎症相关过程中的参与,该药物可能被重新用于神经退行性疾病。事实上,法舒地尔在许多神经退行性疾病模型中表现出了临床前疗效。为了更深入地了解 ROCK 抑制在神经退行性疾病中的广泛生物学过程,我们通过外周 IP 注射用法舒地尔处理阿尔茨海默病模型小鼠的大脑进行了全局基因表达分析。然后,我们将法舒地尔驱动的转录谱与来自多个神经退行性疾病的荟萃分析生成的谱进行了比较分析。我们的结果表明,法舒地尔倾向于以与死后神经退行性疾病大脑中相反的方式驱动基因表达。就通路富集分析而言,结果最为显著,阿尔茨海默病和帕金森病中受干扰的通路被法舒地尔治疗完全反向驱动。因此,我们的结果通过在疾病背景下证明法舒地尔的抗神经退行性表型,支持了法舒地尔的再利用潜力,并强调了药物活性的体内转录谱分析的潜力。