Nair Arun T, Ramachandran Vadivelan, Joghee Nanjan M, Antony Shanish, Ramalingam Gopalakrishnan
Department of Pharmacology, JSS College of Pharmacy (JSS Academy of Higher Education and Research, Mysuru), Ootacamund, Tamilnadu, India.
JSS College of Pharmacy (JSS Academy of Higher Education and Research, Mysuru), Ootacamund, Tamilnadu, India.
J Neurogastroenterol Motil. 2018 Jan 30;24(1):30-42. doi: 10.5056/jnm17105.
Recent investigations suggest that gut microbiota affects the brain activity through the microbiota-gut-brain axis under both physiological and pathological disease conditions like Parkinson's disease. Further dopamine synthesis in the brain is induced by dopamine producing enzymes that are controlled by gut microbiota via the microbiota-gut-brain axis. Also alpha synuclein deposition and the associated neurodegeneration in the enteric nervous system that increase intestinal permeability, oxidative stress, and local inflammation, accounts for constipation in Parkinson's disease patients. The trigger that causes blood brain barrier leakage, immune cell activation and inflammation, and ultimately neuroinflammation in the central nervous system is believed to be due to the chronic low-grade inflammation in the gut. The non-motor symptoms that appear years before motor symptoms could be reliable early biomarkers, if they could be correlated with the established and reliable neuroimaging techniques or behavioral indices. The future directions should therefore, focus on the exploration of newer investigational techniques to identify these reliable early biomarkers and define the specific gut microbes that contribute to the development of Parkinson's disease. This ultimately should pave the way to safer and novel therapeutic approaches that avoid the complications of the drugs delivered today to the brain of Parkinson's disease patients.
最近的研究表明,在生理和病理疾病状态下,如帕金森病,肠道微生物群通过微生物-肠道-脑轴影响大脑活动。大脑中多巴胺的进一步合成是由多巴胺生成酶诱导的,这些酶通过微生物-肠道-脑轴受肠道微生物群控制。此外,肠道神经系统中α-突触核蛋白沉积及相关神经变性增加了肠道通透性、氧化应激和局部炎症,这也是帕金森病患者便秘的原因。导致血脑屏障渗漏、免疫细胞激活和炎症,并最终导致中枢神经系统神经炎症的触发因素被认为是肠道中的慢性低度炎症。如果运动症状出现前数年出现的非运动症状能够与成熟且可靠的神经成像技术或行为指标相关联,那么它们可能是可靠的早期生物标志物。因此,未来的研究方向应集中于探索更新的研究技术,以识别这些可靠的早期生物标志物,并确定导致帕金森病发展的特定肠道微生物。这最终应为更安全、新颖的治疗方法铺平道路,避免目前用于帕金森病患者大脑的药物所带来的并发症。