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Substantiation of PI3K/Akt Signaling Pathway in Alzheimer’s disease employing Pharmacological Strategies and their Nano-formulations

Implementing Organization

Chaudhary Bansi Lal University
Principal Investigator
Prof. Nitin Bansal
Chaudhary Bansi Lal University
CO-Principal Investigator
Prof. Kanwaljit Chopra
Panjab University

Project Overview

Alzheimer's disease (AD) is a progressive neurodegenerative disease characterized by memory loss in people over 60. In India, approximately 5.3 million people have dementia associated with AD, with the number set to rise to 7.6 million in 2030. Treatment of AD remains a challenge in the medicine field, with the PI-3/Akt signaling pathway being a potential therapeutic window. Insulin resistance in AD downregulates the PI3-Akt pathway, promoting apoptosis, neuroinflammation, and oxidative damage, leading to the accumulation of Aβ and hyperphosphorylation of tau protein. Normalizing the damaged PI3K/Akt pathway could be a crucial treatment plan for AD. Ellagic acid (EA), a gallic acid derivative found in plant foods, exhibits potent antioxidant, anti-inflammatory, and anti-apoptotic activity. Studies have reported that EA showed protective effects in AD via PI3/Akt pathways, but the molecular mechanisms and genes involved are not yet elucidated. This study aims to uncover the comparative nutrigenomic profile of ellagic acid alone and its nano-formulation in an experimental animal model of ICV-STZ-induced AD. Peroxisome proliferator-activated receptors (PPARs) are ligand-dependent nuclear receptors widely distributed in the brain. PPAR-α agonists exert neuroprotective properties, reducing brain damage, neuroinflammation, and oxidative stress. The objective of this study is to elucidate the effect of saroglitazar in AD rats and explore the underlying mechanisms of action.
Funding Organization
Funding Organization
Science and Engineering Research Board (SERB), New Delhi
Anusandhan National Research Foundation (ANRF)
Quick Information
Area of Research
Pharmaceutical Sciences
Focus Area
Neurology, Pharmacology
Start Year
2024
End Year
2027
Sanction Amount
₹ 30.00 L
Status
Ongoing
Output
No. of Research Paper
00
Technologies (If Any)
00
No. of PhD Produced
N/A
Startup (If Any)
00
No. of Patents
Filed :00
Grant :00
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