Department of Neurological Sciences, Rush University Medical Center, 1735 West Harrison St, Suite 310, Chicago, IL, 60612, USA.
Division of Research and Development, Jesse Brown Veterans Affairs Medical Center, 820 South Damen Avenue, Chicago, IL, 60612, USA.
J Neuroimmune Pharmacol. 2021 Sep;16(3):592-608. doi: 10.1007/s11481-020-09955-2. Epub 2020 Sep 5.
α-Synucleinopathies in a broader sense comprise of several neurodegenerative disorders that primarily include Parkinson's disease (PD), dementia with Lewy bodies (DLB) and multiple system atrophy (MSA). These disorders are well characterized by the accumulation of aggregated insoluble α-synuclein (α-syn) protein known as Lewy bodies. Till date no effective cure is available to reduce the burden of Lewy body. The present investigation underlines the importance of a naturally used spice and flavoring agent viz. cinnamon in reducing α-syn deposits in transgenic mice expressing mutant A53T human α-syn. Upon oral administration, cinnamon markedly reduced the level of insoluble α-syn in nigra, hippocampus and brain stem of A53T mice. We also demonstrated that sodium benzoate (NaB), a metabolite of cinnamon, a widely used food additive and a FDA-approved drug for glycine encephalopathy, was also capable of reducing α-syn deposits in A53T mice. In addition, both cinnamon and NaB treatments showed improvement in their motor and cognitive functions. Glial activation plays an important role in the pathogenesis of various neurodegenerative disorders including PD, DLB and MSA, and we found suppression of microglial and astroglial activation in the nigra of A53T mice upon cinnamon treatment. Moreover, neuroprotective proteins like DJ-1 and Parkin are known to reduce the formation of Lewy bodies in the CNS. Accordingly, we observed upregulation and/or normalization of DJ-1 and Parkin in the nigra of A53T mice by treatment with cinnamon and NaB. Together, these results highlight a new therapeutic property of cinnamon and suggest that cinnamon and NaB may be used to halt the progression of α-synucleinopathies.Graphical Abstract.
广义的α-突触核蛋白病包括几种神经退行性疾病,主要包括帕金森病(PD)、路易体痴呆(DLB)和多系统萎缩(MSA)。这些疾病的特征是积累了不溶性聚集的α-突触核蛋白(α-syn),称为路易体。迄今为止,尚无有效的治疗方法可以减轻路易体的负担。本研究强调了一种天然使用的香料和调味剂肉桂在减少表达突变 A53T 人类α-syn 的转基因小鼠中α-syn 沉积的重要性。口服给药时,肉桂可显著降低 A53T 小鼠黑质、海马体和脑干中不溶性α-syn 的水平。我们还证明,肉桂的代谢产物苯甲酸钠(NaB),一种广泛使用的食品添加剂和 FDA 批准用于甘氨酸脑病的药物,也能够减少 A53T 小鼠中的α-syn 沉积。此外,肉桂和 NaB 治疗均显示出运动和认知功能的改善。神经胶质细胞激活在包括 PD、DLB 和 MSA 在内的各种神经退行性疾病的发病机制中起着重要作用,我们发现肉桂治疗可抑制 A53T 小鼠黑质中小胶质细胞和星形胶质细胞的激活。此外,DJ-1 和 Parkin 等神经保护蛋白已知可减少中枢神经系统中路易体的形成。因此,我们观察到肉桂和 NaB 治疗可上调和/或使 A53T 小鼠黑质中的 DJ-1 和 Parkin 正常化。总之,这些结果突出了肉桂的新治疗特性,并表明肉桂和 NaB 可用于阻止α-突触核蛋白病的进展。