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Updated: Nov 29, 2025

Stereotaxic Infusion of Oligomeric Amyloid-beta into the Mouse Hippocampus
Published on: June 17, 2015
Graphene oxide improves postoperative cognitive dysfunction by maximally alleviating amyloid beta burden in mice
Jiqian Zhang1, Shasha Zhu2, Peipei Jin3
1Department of Anesthesiology, the First Affiliated Hospital of Anhui Medical University, Key Laboratory of Anesthesiology and Perioperative Medicine of Anhui Higher Education Institutes, Anhui Medical University.
Graphene oxide (GO) alleviates amyloid-beta (Aβ) accumulation by reducing its production and enhancing degradation. This nanomedicine improves cognitive function in postoperative mice, offering potential for Aβ-related diseases.
Area of Science:
- Nanomedicine
- Neuroscience
- Biochemistry
Background:
- Graphene oxide (GO) shows promise for Alzheimer's disease (AD) and other amyloid-beta (Aβ)-related conditions.
- The precise mechanisms of GO in reducing Aβ burden and its role in Aβ-related diseases require further investigation.
- Postoperative cognitive dysfunction (POCD), an Aβ-related complication, currently lacks effective nanomedicine treatments.
Purpose of the Study:
- To investigate the effects of graphene oxide (GO) on amyloid-beta (Aβ) levels and cognitive function.
- To explore GO's potential in treating Aβ-related central nervous system complications like postoperative cognitive dysfunction (POCD).
Main Methods:
- Established HEK293T-APP-GFP and SHSY5Y-APP-GFP cell lines to evaluate GO's impact on Aβ levels.
- Induced fear memory dysfunction in mice via intramedullary fixation surgery under inhalation anesthesia.
- Assessed fear memory using a fear conditioning test and measured hippocampal Aβ levels.
Main Results:
- GO treatment significantly reduced Aβ generation and enhanced Aβ degradation by inhibiting APP β-cleavage and improving lysosomal delivery.
- Postoperative mice exhibited increased hippocampal Aβ levels and impaired fear memory.
- GO administration decreased hippocampal Aβ levels and improved cognitive function in these mice.
Conclusions:
- Graphene oxide (GO) effectively alleviates Aβ accumulation through dual action on Aβ generation and degradation.
- GO administration improves fear memory in postoperative mice by reducing Aβ burden.
- These findings support the application of GO-based nanomedicines for Aβ-related diseases, including POCD.
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