Abstract
ABSTRACTThis study was to explore the effect of nanoparticles on the cognitive function, learning and memory ability (LMA) of Alzheimer’s disease (AD) rats, and to analyze the changes on magnetic resonance (MR) image. Specifically, the TGN nanoparticles loading H102 (TGN-NP-H102) were prepared, and characterized first. The sprague-dawley (SD) rats were selected as the research subjects, and the AD model was constructed. They were divided into a Sham group (normal SD rats, group A), an AD model group (group B), an H102 group (treated with H102 drugs based on AD model, group C), and a TGN-NP-H102 group (treated with TGN-NP-H102 nanoparticles based on AD model, group D). The changes in T2 value in hippocampal CA1 area (T2-CA1) were analyzed, and the changes in cognitive function and LMA were tested with the Morris water maze experiment (Morris experiment). The results revealed that, the average PS (APS) of TGN-NP-H102 nanoparticles was 122.9±2.8 nm, and its average Zeta potential (AZP) was -28.8±0.2 mV. In group A, the TGN-NP-H102 nanoparticles still remained in the brain tissue homogenate by 74.3 ±4.8% after 10 hours, and the drug-release rate was 53.2 ± 3.2%. After 30 days of treatment, the T2-CA1 value of group D was lower (P <0.05), and the average escape latency (AEL) and swimming distance in the Morris experiment were shorter versus group B (P < 0.05). It indicated that, the brain-targeted TGN-NP-H102 nanoparticles prepared could act on the hippocampus of AD rats, and improve their LMA.
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