A novel Dual GLP-1/CCK Receptor Agonist Improves Cognitive Performance and Synaptogenesis in the 5 × FAD Alzheimer Mouse Model.

Ma, He et al.·Molecular neurobiology·2025·
RPEP-123602025RETHINKTHC RESEARCH DATABASErethinkthc.com/research

Quick Facts

Study Type
Not classified
Evidence
Not graded
Sample
Not reported

What This Study Found

Key Numbers

How They Did This

Why This Research Matters

What This Study Doesn't Tell Us

Trust & Context

Original Title:
A novel Dual GLP-1/CCK Receptor Agonist Improves Cognitive Performance and Synaptogenesis in the 5 × FAD Alzheimer Mouse Model.
Published In:
Molecular neurobiology, 62(9), 11920-11934 (2025)
Database ID:
RPEP-12360

Evidence Hierarchy

Meta-Analysis / Systematic Review
Randomized Controlled Trial
Cohort / Case-Control
Cross-Sectional / ObservationalSnapshot without intervening
This study
Case Report / Animal Study
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RPEP-12360·https://rethinkpeptides.com/research/RPEP-12360

APA

Ma, He; Chang, Zhenghui; Sun, Hongyu; Ma, Dongrui; Li, Zhonghua; Hao, Li; Zhang, Zhenqiang; Hölscher, Christian; Zhang, Zijuan. (2025). A novel Dual GLP-1/CCK Receptor Agonist Improves Cognitive Performance and Synaptogenesis in the 5 × FAD Alzheimer Mouse Model.. Molecular neurobiology, 62(9), 11920-11934. https://doi.org/10.1007/s12035-025-05037-7

MLA

Ma, He, et al. "A novel Dual GLP-1/CCK Receptor Agonist Improves Cognitive Performance and Synaptogenesis in the 5 × FAD Alzheimer Mouse Model.." Molecular neurobiology, 2025. https://doi.org/10.1007/s12035-025-05037-7

RethinkPeptides

RethinkPeptides Research Database. "A novel Dual GLP-1/CCK Receptor Agonist Improves Cognitive P..." RPEP-12360. Retrieved from https://rethinkpeptides.com/research/ma-2025-a-novel-dual-glp1cck

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Study data sourced from PubMed, a service of the U.S. National Library of Medicine, National Institutes of Health.

This study breakdown was produced by the RethinkPeptides research team. We analyze and report published research findings without making health recommendations. All interpretations are based solely on the published abstract and study data.