Alzheimer's Disease 2022
DOI: 10.5772/intechopen.102762
|View full text |Cite
|
Sign up to set email alerts
|

Alzheimer’s Disease: An Insightful Review on the Future Trends of the Effective Therapeutics

Abstract: Alzheimer’s disease (AD) is a disorder of brain which progressively weakens the cognitive function. It is occur due to formation of β-amyloid plaques, neurofibrillary tangles, and degeneration of cholinergic neurotransmitter. There is no effective treatment capable of slowing down disease progression, current pharmacotherapy for AD only provides symptomatic relief and limited improvement in cognitive functions. Many molecules have been explored that show promising outcomes in AD therapy and can regulate cellul… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1

Citation Types

0
1
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(2 citation statements)
references
References 98 publications
0
1
0
Order By: Relevance
“…The first direct tau aggregation inhibitor is methylene blue, also known as methylthionine chloride [ 64 ]. Derivatives of methylene blue have revealed a specific potential to inhibit tau aggregation [ 73 ]. TRx0237 (LMTM) is the second-generation tau aggregation inhibitor (TAI) for AD and FTD and is the purified form of methylene blue.…”
Section: Tau Immunotherapiesmentioning
confidence: 99%
“…The first direct tau aggregation inhibitor is methylene blue, also known as methylthionine chloride [ 64 ]. Derivatives of methylene blue have revealed a specific potential to inhibit tau aggregation [ 73 ]. TRx0237 (LMTM) is the second-generation tau aggregation inhibitor (TAI) for AD and FTD and is the purified form of methylene blue.…”
Section: Tau Immunotherapiesmentioning
confidence: 99%
“…Several review papers related to AD that mainly present general theories of AD have been published [7,[15][16][17][18][19][20][21]. Other reviews have also overviewed AD-related inhibitors; however, most of them focused on some common target enzymes, such as acetylcholinesterase [22][23][24][25], β-secretase [26,27], and glycogen synthase kinase-3 [13], and mainly presented the sources of inhibitors through chemical synthesis, plants, or marine organisms [11][12][13][22][23][24]26,28].…”
Section: Introductionmentioning
confidence: 99%