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帕金森病介导的胃肠道疾病及联合治疗的原理

Parkinson Disease-Mediated Gastrointestinal Disorders and Rational for Combinatorial Therapies.

作者信息

Ali Syed A, Yin Ning, Rehman Arkam, Justilien Verline

机构信息

Department of Cancer Biology, Mayo Clinic Cancer Center, Jacksonville, FL 32224, USA.

Department of Pain Medicine, Baptist Medical Center, Jacksonville, FL 32258, USA.

出版信息

Med Sci (Basel). 2016 Jan 20;4(1):1. doi: 10.3390/medsci4010001.

Abstract

A gradual loss of dopamine-producing nerve cells gives rise to a common neurodegenerative Parkinson's disease (PD). This disease causes a neurotransmitter imbalance in the brain and initiates a cascade of complications in the rest of the body that appears as distressing symptoms which include gait problems, tremor, gastrointestinal (GI) disorders and cognitive decline. To aid dopamine deficiency, treatment in PD patients includes oral medications, in addition to other methods such as deep brain stimulation and surgical lesioning. Scientists are extensively studying molecular and signaling mechanisms, particularly those involving phenotypic transcription factors and their co-regulatory proteins that are associated with neuronal stem cell (SC) fate determination, maintenance and disease state, and their role in the pathogenesis of PD. Advancement in scientific research and "personalized medicine" to augment current therapeutic intervention and minimize the side effects of chemotherapy may lead to the development of more effective therapeutic strategies in the near future. This review focuses on PD and associated GI complications and summarizes the current therapeutic modalities that include stem cell studies and combinatorial drug treatment.

摘要

产生多巴胺的神经细胞逐渐丧失会引发常见的神经退行性疾病——帕金森病(PD)。这种疾病会导致大脑中的神经递质失衡,并在身体其他部位引发一系列并发症,表现为令人痛苦的症状,包括步态问题、震颤、胃肠道(GI)紊乱和认知能力下降。为了缓解多巴胺缺乏,PD患者的治疗包括口服药物,以及深部脑刺激和手术损伤等其他方法。科学家们正在广泛研究分子和信号传导机制,特别是那些涉及与神经元干细胞(SC)命运决定、维持和疾病状态相关的表型转录因子及其共调节蛋白,以及它们在PD发病机制中的作用。科学研究和“个性化医学”的进展,以增强当前的治疗干预并尽量减少化疗的副作用,可能会在不久的将来导致更有效的治疗策略的发展。本综述重点关注PD及相关的胃肠道并发症,并总结了目前的治疗方式,包括干细胞研究和联合药物治疗。

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本文引用的文献

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Pluripotent stem cell-based models of spinal muscular atrophy.基于多能干细胞的脊髓性肌萎缩症模型。
Mol Cell Neurosci. 2015 Jan;64:44-50. doi: 10.1016/j.mcn.2014.12.005. Epub 2014 Dec 12.
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Metabolism. 2015 Mar;64(3 Suppl 1):S40-6. doi: 10.1016/j.metabol.2014.10.030. Epub 2014 Oct 31.
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