Abraham Jancy Nixon, Rawat Devesh, Srikanth Priyadharshini, Sunny Lisni P, Abraham Nixon M
Laboratory of Neural Circuits and Behaviour (LNCB), Department of Biology, Indian Institute of Science Education and Research (IISER), Pune, Maharashtra, 411008, India.
Department of Life Sciences, Centre of Excellence in Epigenetics, Shiv Nadar Institution of Eminence, Gautam Buddha Nagar, Greater Noida, Uttar Pradesh, 201314, India.
Mamm Genome. 2025 Apr 28. doi: 10.1007/s00335-025-10128-w.
Olfactory dysfunction (OD) is considered one of the early signs of Parkinson's disease (PD), affecting over 90% of PD patients. OD often appears several years before the onset of motor symptoms and is therefore considered an early biomarker of PD. Recent studies have shown that COVID-19 infection might lead to worsening of symptoms and acceleration of disease progression in neurodegenerative disorders, where OD is a common symptom to both. Hence, it is essential to accurately monitor olfactory fitness in clinical settings using any of the currently available olfactory function tests. Even after a quarter of a century of the discovery of α-synuclein (α-syn) pathogenesis in PD, many aspects related to the α-syn pathogenesis in OD remain unknown. Currently, there is no definitive cure for PD; the disease management options include dopaminergic medications, deep brain stimulations, stem cells, and immunotherapy. Generating reliable PD animal models is critical for understanding the molecular pathways and neural circuits affected by disease conditions. This might contribute to the development and validation of new therapeutic approaches. This review discusses the known mechanisms of α-syn aggregated forms causing neuronal death, the recent developments in the PD preclinical models with ODs, and the treatment strategies employed.
嗅觉功能障碍(OD)被认为是帕金森病(PD)的早期症状之一,超过90%的PD患者会受到影响。OD通常在运动症状出现前数年就已出现,因此被视为PD的早期生物标志物。最近的研究表明,新型冠状病毒肺炎(COVID-19)感染可能会导致神经退行性疾病的症状恶化和疾病进展加速,而OD是这两种情况的常见症状。因此,在临床环境中使用任何现有的嗅觉功能测试准确监测嗅觉健康至关重要。即使在发现PD中α-突触核蛋白(α-syn)发病机制25年后,与OD中α-syn发病机制相关的许多方面仍不清楚。目前,PD尚无确切的治愈方法;疾病管理选项包括多巴胺能药物、深部脑刺激、干细胞和免疫疗法。生成可靠的PD动物模型对于理解受疾病状况影响的分子途径和神经回路至关重要。这可能有助于新治疗方法的开发和验证。本综述讨论了α-syn聚集形式导致神经元死亡的已知机制、伴有OD的PD临床前模型的最新进展以及所采用的治疗策略。