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Ghrelin controls hippocampal spine synapse density and memory performance
Abstract
The gut hormone and neuropeptide ghrelin affects energy balance and growth hormone release through hypothalamic action that involves synaptic plasticity in the melanocortin system. Ghrelin binding is also present in other brain areas, including the telencephalon, where its function remains elusive. Here we report that circulating ghrelin enters the hippocampus and binds to neurons of the hippocampal formation, where it promotes dendritic spine synapse formation and generation of long-term potentiation. These ghrelin-induced synaptic changes are paralleled by enhanced spatial learning and memory. Targeted disruption of the gene that encodes ghrelin resulted in decreased numbers of spine synapses in the CA1 region and impaired performance of mice in behavioral memory testing, both of which were rapidly reversed by ghrelin administration. Our observations reveal an endogenous function of ghrelin that links metabolic control with higher brain functions and suggest novel therapeutic strategies to enhance learning and memory processes.
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“It has been shown that ghrelin can pass through the blood–brain barrier, directly affecting brain cells [46, 48–50].”
From Protective PLCG2 variants associate with a delayed onset of Alzheimer’s disease among heterozygous APOE ε4 carriers (2026) · cites this paper as [50]
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Metadata
- Authors
- Diano, S., Farr, S. A., Benoit, S. C., McNay, E. C., da Silva, I., Horvath, B., Gaskin, F. S., Nonaka, N., Jaeger, L. B., Banks, W. A., Morley, J. E., Pinto, S., Sherwin, R. S., Xu, L., Yamada, K. A., Sleeman, M. W., Tschöp, M. H., & Horvath, T. L.
- Affiliations
- Yale University (US)
- St. Louis VA Medical Center (US)
- University of Cincinnati (US)
- Howard Hughes Medical Institute (US)
- Washington University in St. Louis (US)
- Regeneron (United States) (US)
- ORCID
- Venue
- Nature Neuroscience
- Published
- 2006-02-19
- Volume
- 9
- Issue
- 3
- Pages
- 381-388
- ISSN
- 1097-6256 (ISSN-L)
- 1546-1726
- OpenAlex
- W2154294326
- Semantic Scholar
- ed71645a1b530393f2d3862ed437ab76250f7ac4
- Cited by
- 828
- References
- 43
- Citations by year
- 2026: 9 · 2025: 18 · 2024: 24 · 2023: 19 · 2022: 46 · 2021: 39 · 2020: 29 · 2019: 38 · 2018: 48 · 2017: 49 · 2016: 33 · 2015: 48 · 2014: 46 · 2013: 75 · 2012: 48
- FWCI
- 21.15
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Neuroscience (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute on Alcohol Abuse and Alcoholism (R01AA012743, AA12743)
- National Institute on Aging (AG-22880, R01AG022880)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK7386, DK61619, DK60711, R01DK070039, DK70039, R01DK060711, R01DK061619, T35DK007386)
- National Institute of Neurological Disorders and Stroke (R01NS041725, NS-41725, R01NS040525, NS 40525)
- Topics
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- ghrelin, hippocampus, dendritic spines, synaptogenesis, long-term potentiation, spatial learning and memory, CA1 region, growth hormone secretagogue receptor, energy balance
- MeSH terms
- Animals, Cell Differentiation, Hippocampus, Learning, Male, Memory, Memory Disorders, Mice, Inbred C57BL, Synaptic Transmission, Space Perception, Synapses, Rats, Sprague-Dawley, Long-Term Potentiation, Mice, Knockout, Nootropic Agents, Peptide Hormones, Dendritic Spines, Mice, Rats, Ghrelin
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