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Neem Derivatives Inhibits Tau Aggregation1
- Source :
- Journal of Alzheimer's Disease Reports. 3:169-178
- Publication Year :
- 2019
- Publisher :
- IOS Press, 2019.
-
Abstract
- Tau is a phosphoprotein with natively unfolded conformation that functions to stabilize microtubules in axons. Alzheimer’s disease pathology triggers several modifications in tau, which causes it to lose its affinity towards microtubule, thus, leading to microtubule disassembly and loss of axonal integrity. This elicit accumulation of tau as paired helical filaments is followed by stable neurofibrillary tangles formation. A large number of small molecules have been isolated from Azadirachta indica with varied medicinal applications. The intermediate and final limonoids, nimbin and salannin respectively, isolated from Azadirachta indica, were screened against tau aggregation. ThS and ANS fluorescence assay showed the role of intermediate and final limonoids in preventing heparin induced cross-β sheet formation and also decreased hydrophobicity, which are characteristic nature of tau aggregation. Transmission electron microscopy studies revealed that limonoids restricted the aggregation of tau to fibrils; in turn, limonoids led to the formation of short and fragile aggregates. Both the limonoids were non-toxic to HEK293T cells thus, substantiating limonoids as a potential lead in overcoming Alzheimer’s disease.
- Subjects :
- 0301 basic medicine
biology
Chemistry
General Neuroscience
HEK 293 cells
Azadirachta
biology.organism_classification
Fibril
Small molecule
Turn (biochemistry)
03 medical and health sciences
Psychiatry and Mental health
Clinical Psychology
chemistry.chemical_compound
030104 developmental biology
0302 clinical medicine
Microtubule
Phosphoprotein
Biophysics
Nimbin
Geriatrics and Gerontology
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 25424823
- Volume :
- 3
- Database :
- OpenAIRE
- Journal :
- Journal of Alzheimer's Disease Reports
- Accession number :
- edsair.doi...........31aab59bf8fbb00f16112f8b8ae3adaa
- Full Text :
- https://doi.org/10.3233/adr-190118