Review article
Berberine and neurodegeneration: A review of literature
Touqeer Ahmed
a
, Anwar-ul-Hassan Gilani
b,c
, Mohammad Abdollahi
d
, Maria Daglia
e
,
Seyed Fazel Nabavi
f
, Seyed Mohammad Nabavi
f,
*
a
Atta-ur-Rahman School of Applied Biosciences, National University of Sciences and Technology, Islamabad, Pakistan
b
Department of Pharmacy, College of Health Sciences, Mekelle University, Mekelle, Ethiopia
c
Natural Product Research Division, Department of Biological and Biomedical Sciences, Aga Khan University Medical College, Karachi, Pakistan
d
Department of Toxicology and Pharmacology, Faculty of Pharmacy and Pharmaceutical Sciences Research Center, Tehran University of Medical Sciences,
Tehran, Iran
e
Department of Drug Sciences, Medicinal Chemistry and Pharmaceutical Technology Section, University of Pavia, Pavia, Italy
f
Applied Biotechnology Research Center, Baqiyatallah University of Medical Sciences, Tehran, Iran
Contents
Neurodegeneration and oxidative stress. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 971
Therapeutic potential of antioxidants in neurodegeneration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 971
Antioxidant properties of Berberine . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 971
Traditional usages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 972
Berberine chemistry. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 972
Sources and bioavailability . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 972
Completed and ongoing clinical trials. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 973
Berberine side effects . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 973
Berberine and neurodegeneration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 973
Conclusion and recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 976
Conflict of interest . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 976
Funding body . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 976
References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 976
Pharmacological Reports 67 (2015) 970–979
A R T I C L E I N F O
Article history:
Received 19 November 2014
Received in revised form 2 March 2015
Accepted 5 March 2015
Available online 18 March 2015
Keywords:
Oxidative stress
Neurodegeneration
Alzheimer and Parkinson diseases
Antioxidant compounds
Berberine
A B S T R A C T
The excessive production of reactive oxygen species in nervous tissues is considered one of the major risk
factors of neurodegenerative diseases. During the last two decades, much attention has been paid to the
antioxidant and anti-inflammatory activity of natural products and compounds isolated from natural
products which are often characterized by high efficacy and low adverse effects. Berberine is an
isoquinoline alkaloid, widely present in different medicinal herbs, especially in the genus Berberis. It is
mainly used as antidiarrhoeal, antibacterial, antifungal, and antiprotozoal agent. However, current
research has focused on its beneficial role in neurodegenerative diseases, mainly due to its powerful
antioxidant effect. The therapeutic potential of Berberine in different neurodegenerative diseases such as
Alzheimer, Parkinson and Huntington disease has been brought to evidence by numerous studies.
However, a limited number of reviews focus on the beneficial role of Berberine against
neurodegeneration. The main objective of this review is to discuss the role of oxidative stress in
neurodegeneration and the potential role of antioxidant compounds, in particular Berberine which is
analyzed in its chemical structure, source, bioavailability, therapeutic potential, with special attention to
its mechanism of action at a molecular level.
ß 2015 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights
reserved.
* Corresponding author.
E-mail address: Nabavi208@gmail.com (S.M. Nabavi).
Contents lists available at ScienceDirect
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http://dx.doi.org/10.1016/j.pharep.2015.03.002
1734-1140/ß 2015 Institute of Pharmacology, Polish Academy of Sciences. Published by Elsevier Sp. z o.o. All rights reserved.