Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, Shaqra University, Shaqra, 11961, Saudi Arabia.
Department of clinical pharmacology and therapeutic medicine, college of medicine, Mustansiriyah University, Baghdad, Iraq.
Mol Biol Rep. 2023 Jul;50(7):6107-6120. doi: 10.1007/s11033-023-08459-5. Epub 2023 May 8.
Parkinson's disease (PD) is a progressive neurodegenerative disease (NDD) caused by dopaminergic neuron degeneration in the substantia nigra (SN). Orexin is a neuropeptide that plays a role in the pathogenesis of PD. Orexin has neuroprotective properties in dopaminergic neurons. In PD neuropathology, there is also degeneration of orexinergic neurons in the hypothalamus, in addition to dopaminergic neurons. However, the loss of orexinergic neurons in PD began after the degeneration of dopaminergic neurons. Reduced activity of orexinergic neurons has been linked to developing and progressing motor and non-motor symptoms in PD. In addition, the dysregulation of the orexin pathway is linked to the development of sleep disorders. The hypothalamic orexin pathway regulates various aspects of PD neuropathology at the cellular, subcellular, and molecular levels. Finally, non-motor symptoms, particularly insomnia and disturbed sleep, promote neuroinflammation and the accumulation of neurotoxic proteins as a result of defects in autophagy, endoplasmic reticulum (ER) stress, and the glymphatic system. As a result, this review aimed to highlight the potential role of orexin in PD neuropathology.
帕金森病(PD)是一种进行性神经退行性疾病(NDD),由黑质(SN)中的多巴胺能神经元变性引起。食欲素是一种在 PD 发病机制中起作用的神经肽。食欲素对多巴胺能神经元具有神经保护作用。在 PD 神经病理学中,除了多巴胺能神经元外,下丘脑的食欲素能神经元也发生变性。然而,在 PD 中,食欲素能神经元的丧失发生在多巴胺能神经元变性之后。食欲素能神经元活性降低与 PD 运动和非运动症状的发展和进展有关。此外,食欲素途径的失调与睡眠障碍的发展有关。下丘脑食欲素途径在细胞、亚细胞和分子水平上调节 PD 神经病理学的各个方面。最后,非运动症状,特别是失眠和睡眠障碍,会导致神经炎症和神经毒性蛋白的积累,这是由于自噬、内质网(ER)应激和神经淋巴系统缺陷所致。因此,本综述旨在强调食欲素在 PD 神经病理学中的潜在作用。