| Literature DB >> 34436747 |
Dapinder Kaur1, Tapan Behl2, Aayush Sehgal1, Sukhbir Singh1, Neelam Sharma1, Vishnu Nayak Badavath1, Syed Shams Ul Hassan3, Mohammad Mehedi Hasan4, Saurabh Bhatia5,6, Ahmed Al-Harassi5, Haroon Khan7, Simona Bungau8.
Abstract
During the last three decades, recombinant DNA technology has produced a wide range of hematopoietic and neurotrophic growth factors, including erythropoietin (EPO), which has emerged as a promising protein drug in the treatment of several diseases. Cumulative studies have recently indicated the neuroprotective role of EPO in preclinical models of acute and chronic neurodegenerative disorders, including Alzheimer's disease (AD). AD is one of the most prevalent neurodegenerative illnesses in the elderly, characterized by the accumulation of extracellular amyloid-ß (Aß) plaques and intracellular neurofibrillary tangles (NFTs), which serve as the disease's two hallmarks. Unfortunately, AD lacks a successful treatment strategy due to its multifaceted and complex pathology. Various clinical studies, both in vitro and in vivo, have been conducted to identify the various mechanisms by which erythropoietin exerts its neuroprotective effects. The results of clinical trials in patients with AD are also promising. Herein, it is summarized and reviews all such studies demonstrating erythropoietin's potential therapeutic benefits as a pleiotropic neuroprotective agent in the treatment of Alzheimer's disease.Entities:
Keywords: Erythropoietin; Neurodegeneration; Neuroinflammation; Neuroprotection; Oxidative stress
Mesh:
Substances:
Year: 2021 PMID: 34436747 DOI: 10.1007/s11011-021-00820-6
Source DB: PubMed Journal: Metab Brain Dis ISSN: 0885-7490 Impact factor: 3.584