TY - JOUR
T1 - Alzheimer’s disease – Future therapy based on dendrimers
AU - Aliev, Gjumrakch
AU - Md Ashraf, Ghulam
AU - Tarasov, Vadim V.
AU - Chubarev, Vladimir N.
AU - Leszek, Jerzy
AU - Gąsiorowski, Kazimierz
AU - Makhmutovа, Alfiya
AU - Salem Baeesa, Saleh
AU - Avila-Rodriguez, Marco
AU - Ustyugov, Aleksey A.
AU - Bachurin, Sergey O.
N1 - Publisher Copyright:
© 2019 Bentham Science Publishers.
PY - 2019
Y1 - 2019
N2 - Alzheimer’s disease (AD) is characterized by the loss of neurons. It is the most common cause of dementia in the elderly population accompanied by pathological degeneration of neurofibrillary tangles. Senile plaques are formed with beta-amyloid, hyperphosphoryled tau protein, apolipoprotein E and presenilin associated with protease activity [amyloid beta (Aβ), gamma-secretase (γS)]. The molecular mechanisms of neurodegeneration include apoptosis, oxidative stress (free radical generation), inflammation, immune activation, and others. The lack of effective treatments for AD stems mainly from the incomplete understanding the causes of AD. Currently, there are several hypotheses explaining the early mechanisms of AD pathogenesis. Recent years witnessed an unprecedented research growth in the area of nanotechnology, which uses atomic, molecular and macromolec ular methods to create products in microscale (nanoscale) dime nsions. In this article, we have discussed the role of nanotechnology in the development and improvement of techniques for early diagnosis and effective trea tment of AD. Since AD pathology is practically irreversible, applications of disease-modifying treatments could be successful only if early diagnosis of AD is available. This review highlights various possibilities for the early diagnosis and therapy of AD and investigates potential adaptation of nanoparticles-dendrimers as a class of well-defined branched polymers that are chemically synthesized with a well-defined shape, size and nan oscopic physicochemical properties reminiscent of the proteins for the treatment of neurodegenerative diseases.
AB - Alzheimer’s disease (AD) is characterized by the loss of neurons. It is the most common cause of dementia in the elderly population accompanied by pathological degeneration of neurofibrillary tangles. Senile plaques are formed with beta-amyloid, hyperphosphoryled tau protein, apolipoprotein E and presenilin associated with protease activity [amyloid beta (Aβ), gamma-secretase (γS)]. The molecular mechanisms of neurodegeneration include apoptosis, oxidative stress (free radical generation), inflammation, immune activation, and others. The lack of effective treatments for AD stems mainly from the incomplete understanding the causes of AD. Currently, there are several hypotheses explaining the early mechanisms of AD pathogenesis. Recent years witnessed an unprecedented research growth in the area of nanotechnology, which uses atomic, molecular and macromolec ular methods to create products in microscale (nanoscale) dime nsions. In this article, we have discussed the role of nanotechnology in the development and improvement of techniques for early diagnosis and effective trea tment of AD. Since AD pathology is practically irreversible, applications of disease-modifying treatments could be successful only if early diagnosis of AD is available. This review highlights various possibilities for the early diagnosis and therapy of AD and investigates potential adaptation of nanoparticles-dendrimers as a class of well-defined branched polymers that are chemically synthesized with a well-defined shape, size and nan oscopic physicochemical properties reminiscent of the proteins for the treatment of neurodegenerative diseases.
KW - Alzheimer’s disease
KW - Dendrimers
KW - Molecular neurodegeneration
KW - Nanoparticles-dendrimers
KW - Protein misfolding
KW - Treatment strategies
UR - http://www.scopus.com/inward/record.url?scp=85062089770&partnerID=8YFLogxK
U2 - 10.2174/1570159X16666180918164623
DO - 10.2174/1570159X16666180918164623
M3 - Review article
C2 - 30227819
AN - SCOPUS:85062089770
SN - 1570-159X
VL - 17
SP - 288
EP - 294
JO - Current Neuropharmacology
JF - Current Neuropharmacology
IS - 3
ER -