Therapeutic Potential of Ferulic Acid in Alzheimer's Disease

Author:

Turkez Hasan1,Arslan Mehmet Enes2,Barboza Joice Nascimento3,Kahraman Cigdem Yuce4,de Sousa Damiao Pergentino3,Mardinoğlu Adil5

Affiliation:

1. Department of Medical Biology, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey | Department of Pharmacy, University G. d’Annunzio Chieti-Pescara, Via dei Vestini 31, 66100 Chieti, Italy

2. Department of Molecular Biology and Genetics, Erzurum Technical University, 25200, Erzurum, Turkey

3. Department of Pharmaceutical Sciences, Federal University of Paraíba, 58051-970, João Pessoa, PB, Brazil

4. Department of Medical Genetics, Faculty of Medicine, Atatürk University, 25240, Erzurum, Turkey

5. Science for Life Laboratory, KTH-Royal Institute of Technology, Stockholm, SE-17121, Sweden | Centre for Host-Microbiome Interactions, Faculty of Dentistry, Oral & Craniofacial Sciences, King’s College London, London, SE1 9RT, United Kingdom

Abstract

Abstract: Alzheimer's Disease (AD) is one of the most important neurodegenerative diseases and it covers 60% of whole dementia cases. AD is a constantly progressing neurodegenerative disease as a result of the production of β-amyloid (Aβ) protein and the accumulation of hyper-phosphorylated Tau protein; it causes breakages 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 slowdown. Over the last decade, multiple target applications have been developed for AD treatments. These targets include Aβ accumulations, hyper-phosphorylated Tau proteins, 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 antioxidant molecule, is naturally synthesized from certain plants. FA has been shown to have different substantial biological properties, such as anticancer, antidiabetic, antimicrobial, anti-inflammatory, hepatoprotective, and cardioprotective actions, etc. Furthermore, FA exerted 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 Aβ-induced neurotoxicity, protection against free radical attacks, and enzyme inhibitions and describe them as possible therapeutic agents for the treatment of AD.

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science

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