Unlocking Neurogenesis: PRGF Regenerative Therapy and the role of Tau Protein in Neurodegenerative Disease Models / Aqsa Salih

By: Salih, AqsaContributor(s): Supervisor : Dr. Saima ZafarMaterial type: TextTextIslamabad: SMME- NUST; 2025Description: 71p. Soft Copy 30cmSubject(s): MS Biomedical Sciences (BMS)DDC classification: 610 Online resources: Click here to access online
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Thesis Thesis School of Mechanical & Manufacturing Engineering (SMME)
School of Mechanical & Manufacturing Engineering (SMME)
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Alzheimer's disease (AD) is a neurological condition characterized by persistent
cognitive impairment with few treatment options available. Platelet-rich plasma
(PRP) and platelet-rich growth factors (PRGF), produced from human blood, have
shown promise in treating a variety of neurological disorders. However, their use in
Alzheimer's disease is underexplored, particularly in chemically produced models.
This study looks at the therapeutic potential of PRGF and PRP in a chemically
induced Alzheimer's mouse model using aluminum chloride (AlCl3), with a
particular emphasis on the novel use of intranasal PRGF administration. This study
to explore and compare the effects of PRGF and PRP in an Alzheimer's disease
chemical model. Behavioral assessments were performed to evaluate cognitive
deficits, memory retention, and spatial learning. The Y-maze and Elevated Plus
Maze (EPM) tests demonstrated significant cognitive improvements in the PRGFtreated mice. PRGF administration resulted in enhanced memory performance and
cognitive flexibility, with higher number of alterations and entries to novel arm.
Additionally, PRGF-treated mice exhibited reduced anxiety-like behavior in the
EPM. These findings suggest that PRGF treatment significantly improves cognitive
abilities and memory retention however do not fully restore and cannot be used
confidently in treatment. Histological analysis of the frontal cortex, cerebral cortex,
hippocampus, dentate gyrus (DG) region, and liver was conducted following
behavioral assessments to There were no significant improvements in cellular
integrity observed in either the PRGF or PRP treated groups, indicating less to no
neuroprotection and potential reversal of AlCl3-induced damage.

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