Therapeutic Potential of Ferulic Acid in Alzheimer's Disease


Turkez H., Arslan M. E., Barboza J. N., Kahraman Ç., de Sousa D. P., Mardinoğlu A.

Current Drug Delivery, cilt.19, sa.8, ss.860-873, 2022 (SCI-Expanded) identifier identifier identifier

  • Yayın Türü: Makale / Derleme
  • Cilt numarası: 19 Sayı: 8
  • Basım Tarihi: 2022
  • Doi Numarası: 10.2174/1567201819666211228153801
  • Dergi Adı: Current Drug Delivery
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, BIOSIS, Biotechnology Research Abstracts, Chemical Abstracts Core, EMBASE, MEDLINE
  • Sayfa Sayıları: ss.860-873
  • Anahtar Kelimeler: Ferulic acid, anti-Alzheimer, Alzheimer's disease, experimental Alzheimer's model, amyloid-beta, drug candidate, neurotoxicity, neuroprotection, AMYLOID-BETA PEPTIDE, SOLID LIPID NANOPARTICLES, BLOOD-BRAIN-BARRIER, OXIDATIVE STRESS, ANTIOXIDANT ACTIVITY, PHENOLIC-COMPOUNDS, CELL-DEATH, IN-VITRO, MITOCHONDRIAL DYSFUNCTION, MULTIFUNCTIONAL AGENTS
  • Atatürk Üniversitesi Adresli: Evet

Özet

© 2022 Bentham Science Publishers.Alzheimer's Disease (AD) is one of the most important neurodegenerative diseases, ac-counting for 60% of all dementia cases. AD is a progressive neurodegenerative disease that occurs due to the production of β-amyloid (Aβ) protein and accumulation of hyper-phosphorylated tau pro-tein; it causes breakage in the synaptic bonds and neuronal deaths to a large extent. Millions of people worldwide suffer from AD because there is no definitive drug for disease prevention, treatment, or slowing down its progression. Over the last decade, multiple target applications have been devel-oped for AD treatments. These targets include Aβ accumulations, hyper-phosphorylated tau pro-teins, mitochondrial dysfunction, and oxidative stress, resulting in toxicity. Various natural or semisynthetic antioxidant formulations have been shown to protect brain cells from Aβ-induced toxicity and provide promising potentials for AD treatment. Ferulic acid (FA), a high-capacity an-tioxidant molecule, is naturally synthesized from certain plants. FA has been shown to have different substantial biological properties, such as anticancer, antidiabetic, antimicrobial, anti-inflamma-tory, hepatoprotective, and cardioprotective actions, etc. Furthermore, FA exerts neuroprotection via preventing Aβ-fibril formation, acting as an anti-inflammatory agent, and inhibiting free radical generation and acetylcholinesterase (AChE) enzyme activity. In this review, we present key biological roles of FA and several FA derivatives in preventing Aβ-induced neurotoxicity, protecting against free radical attacks, and exhibiting enzyme inhibitions and evaluate them as possible therapeutic agents for the treatment of AD.