Niloofar Bazazzadegan
1, Marzieh Dehghan Shasaltaneh
2, Kioomars Saliminejad
3, Koorosh Kamali
3, Mehdi Banan
1, Reza Nazari
2, Gholam Hossein Riazi
2, Hamid Reza Khorram Khorshid
1*1 Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.
2 Laboratory of Neuro-organic Chemistry, Institute of Biochemistry and Biophysics (IBB), University of Tehran, Tehran, Iran.
3 Reproductive Biotechnology Research Center, Avicenna Research Institute, ACECR, Tehran, Iran.
Abstract
Purpose:
Alzheimer’s disease (AD) is pathologically defined by the presence of amyloid
plaques and tangles in the brain, therefore, any drug or compound with
potential effect on lowering amyloid plaques, could be noticed for AD
management especially in the primary phases of the disease. Ectoine constitutes
a group of small molecule chaperones (SMCs). SMCs inhibit proteins and other
changeable macromolecular structures misfolding from environmental stresses.
Ectoine has been reported successfully prohibit insulin amyloid formation in
vitro.
Methods:
We selected eight genes, DAXX, NFκβ, VEGF, PSEN1, MTAP2,
SYP, MAPK3 and TNFα genes which had previously showed
significant differential expression in Alzheimer human brain and STZ- rat
model. We considered the neuroprotective efficacy by comparing the expression
of candidate genes levels in the hippocampus of rat model of Sopradic
Alzheimer’s disease (SAD), using qPCR in compound-treated and control groups as
well as therapeutic effects at learning and memory levels by using Morris Water Maze (MWM)
test.
Results:
Our results showed significant down-regulation of Syp, Mapk3 and Tnfα
and up-regulation of Vegf in rat’s hippocampus after treatment with
ectoine comparing to the STZ-induced group. In MWM, there was no significant
change in swimming distance and time for finding the hidden platform in treated
comparing to STZ-induced group. In addition, it wasn’t seen significant change
in compound-treated comparing to STZ-induced and control groups in memory level.
Conclusion:
It seems this compound may have significant effect on expression level of some
AD- related genes but not on clinical levels.