bioRxivNeurosciencePreprint
GABAergic LRP1 is a key link between obesity and memory function
Aykut Göktürk ÜneriD, Zhi-Shuai Hou, Ahmet Aydogan, KELLEN RODRIGUES, Jennie Young, Anthony Choi, Won‐Mo YangiD, Woojin Scott KimiD, Vincent PrévotiD, Barbara J. CaldaroneiD, Bradley T. HymaniD, Hyon LeeiD, Young‐Bum KimiD
Abstract
ObjectiveLow-density lipoprotein receptor-related protein-1 (LRP1) regulates energy homeostasis, blood-brain barrier integrity, and metabolic signaling in the brain. Loss of LRP1 from inhibitory gamma-aminobutyric acid (GABA)ergic neurons causes severe obesity in mice. Its dysfunction has been associated with cognitive decline, dementia, and Alzheimers disease. However, the impact of LRP1 in inhibitory neurons on memory function and cognition in the context of obesity is poorly understood. MethodsMice lacking LRP1 in GABAergic neurons (Vgat-Cre; LRP1loxP/loxP) are subjected to conduct behavioral tests of locomotor activity and motor coordination, short/long-term and spatial memory, and fear learning/memory. We evaluated the relationships between behavior and metabolic risk factors. ResultsDeletion of LRP1 in GABAergic neurons caused a significant impairment in memory function. In the spatial Y-maze test, Vgat-Cre; LRP1loxP/loxP mice exhibited decreased travel distance and duration in the novel arm compared with controls (LRP1loxP/loxP mice). In addition, GABAergic neuron-specific LRP1-deficient mice had a diminished capacity for performing learning and memory tasks during the water T-maze test. Moreover, reduced freezing time was observed in these mice when the contextual and cued fear conditioning tests were conducted. These effects were accompanied by increased neuronal necrosis and neuroinflammation in the hippocampus. Importantly, the distance and duration in the novel arm and the performance of the reversal water T-maze test negatively correlated with metabolic risk parameters, including body weight, serum leptin, insulin, and apolipoprotein J. ConclusionsOur findings demonstrate that LRP1 from GABAergic neurons is important in normal memory function. Metabolically, obesity caused by GABAergic LRP1 deletion negatively regulates memory and cognitive function. Thus, LRP1 in GABAergic neurons may play a crucial role in maintaining normal excitatory/inhibitory balance and impacts memory function, reinforcing the potential importance of LRP1 in neural system integrity.
- Citations
- 2
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Leptin-mediated suppression of food intake by conserved Glp1r-expressing neurons prevents obesity
Alan C. Rupp, Abigail J. Tomlinson, … Martin Grosvenor Myers·bioRxiv·Dec 10, 2021
- Endotoxemia-induced inflammation in the absence of obesity decreases anxiety-like and impulsive behavior without affecting learning and memory
Molly E. Klug, Eden Crain, … Scott E. Kanoski·bioRxiv·May 19, 2025
- Obesity alters mobility and adult neurogenesis, but not hippocampal dependent learning in ob/ob mice
Alexander Bracke, Grażyna Domańska, … Oliver von Bohlen und Halbach·bioRxiv·Feb 1, 2019
- Brainstem GLP-1 neurons modulate physiological satiation and drive sustained weight loss in obese mice
Wanqing Jiang, Cecilia Skoug, … Stefan Trapp·Molecular MetabolismPeer-reviewed·Mar 4, 2026
- Reversal of obesogenic feeding and hypometabolism by a bifurcating GABAergic neural circuit
- Opposing GIPR brainstem circuits differentially control feeding behaviour
Natalie S. Figueredo Burgos, Alejandro López-Cruz, … Alice E. Adriaenssens·bioRxiv·Jul 7, 2026