Shen Yan, Guo Xingfang, Han Chao, Wan Fang, Ma Kai, Guo Shiyi, Wang Luxi, Xia Yun, Liu Ling, Lin Zhicheng, Huang Jinsha, Xiong Nian, Wang Tao
Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, 1277 Jiefang Avenue, Wuhan, 430022, Hubei, China.
Division of Alcohol and Drug Abuse, Department of Psychiatry, and Mailman Neuroscience Research Center, McLean Hospital, Harvard Medical School, Belmont, MA, 02478, USA.
Cell Mol Life Sci. 2017 Oct;74(20):3741-3768. doi: 10.1007/s00018-017-2549-2. Epub 2017 Jun 16.
Parkinson's disease (PD) is a progressive neurodegenerative disorder implicitly marked by the substantia nigra dopaminergic neuron degeneration and explicitly characterized by the motor and non-motor symptom complexes. Apart from the nigrostriatal dopamine depletion, the immune and endocrine study findings are also frequently reported, which, in fact, have helped to broaden the symptom spectrum and better explain the pathogenesis and progression of PD. Nevertheless, based on the neural, immune, and endocrine findings presented above, it is still difficult to fully recapitulate the pathophysiologic process of PD. Therefore, here, in this review, we have proposed the neuroimmunoendocrine (NIE) modulatory network in PD, aiming to achieve a more comprehensive interpretation of the pathogenesis and progression of this disease. As a matter of fact, in addition to the classical motor symptoms, NIE modulatory network can also underlie the non-motor symptoms such as gastrointestinal, neuropsychiatric, circadian rhythm, and sleep disorders in PD. Moreover, the dopamine (DA)-melatonin imbalance in the retino-diencephalic/mesencephalic-pineal axis also provides an alternative explanation for the motor complications in the process of DA replacement therapy. In conclusion, the NIE network can be expected to deepen our understanding and facilitate the multi-dimensional management and therapy of PD in future clinical practice.
帕金森病(PD)是一种进行性神经退行性疾病,其内在特征为黑质多巴胺能神经元变性,外在表现为运动和非运动症状复合体。除黑质纹状体多巴胺耗竭外,免疫和内分泌方面的研究结果也经常被报道,事实上,这些结果有助于拓宽症状谱,并更好地解释PD的发病机制和进展。然而,基于上述神经、免疫和内分泌方面的研究结果,仍难以完全概括PD的病理生理过程。因此,在本综述中,我们提出了PD中的神经免疫内分泌(NIE)调节网络,旨在对该疾病的发病机制和进展进行更全面的解释。事实上,除了经典的运动症状外,NIE调节网络也可能是PD中胃肠道、神经精神、昼夜节律和睡眠障碍等非运动症状的基础。此外,视网膜-间脑/中脑-松果体轴上的多巴胺(DA)-褪黑素失衡也为DA替代治疗过程中的运动并发症提供了另一种解释。总之,NIE网络有望加深我们的理解,并在未来临床实践中促进对PD的多维度管理和治疗。