Leptin: a potential cognitive enhancer?
Abstract
It is well documented that the hormone leptin signals information regarding the status of fat stores to hypothalamic nuclei, which in turn control feeding behaviour and body weight. However, leptin and its receptor are widely expressed in many extra-hypothalamic brain regions, including hippocampus, brain stem and cerebellum. Moreover, evidence is accumulating that leptin has other neuronal functions that are unrelated to its effects on energy homeostasis. Indeed a role for leptin in neuronal development has been suggested as leptin-deficient rodents display abnormal brain development and leptin actively participates in the development of the hypothalamus. In the hippocampus, leptin is a potential cognitive enhancer as genetically obese rodents with dysfunctional leptin receptors display impairments in hippocampal synaptic plasticity. Moreover, direct administration of leptin into the hippocampus can facilitate hippocampal LTP (long-term potentiation) in vivo and improve memory processing in mice. At the cellular level, we have also shown that leptin has the capacity to convert short-term potentiation into LTP. Here, we review the data that leptin influences hippocampal synaptic plasticity via enhancing NMDA (N-methyl-D-aspartate) receptor function. We also provide evidence that rapid trafficking of NMDA receptors to the plasma membrane may underlie the effects of leptin on excitatory synaptic strength.
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Neural activity in brain areas involved in cognitive processing of food representations, such as the amygdala and hippocampal complex, is modulated by leptin and ghrelin.
“Furthermore, neural activity in brain areas thought to be involved in cognitive processing of representations of food such as the amygdala and hippocampal complex is modulated by leptin ([78](#B78), [79](#B79), [105](#B105)) and ghrelin ([27](#B27), [50](#B50), [92](#B92), [109](#B109), [147](#B147), [189](#B189)).”
From Food reward, hyperphagia, and obesity (2011) · cites this paper as [78]
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References 39 · Cited by 162
- Authors
- Harvey, J., Shanley, L. J., O'Malley, D., & Irving, A. J.
- Affiliations
- University of Dundee (GB)
- Neurosciences Institute, Division of Pathology and Neuroscience, Ninewells Hospital and Medical School, University of Dundee, Dundee DD1 9SY, U.K.
- ORCID
- Irving, A.J.
- Venue
- Biochemical Society Transactions
- Publisher
- Portland Press Ltd.
- Published
- 2005-10-26
- Volume
- 33
- Issue
- 5
- Pages
- 1029-1032
- ISSN
- 0300-5127 (ISSN-L)
- 1470-8752
- OpenAlex
- W1968293808
- Cited by
- 162
- References
- 39
- Citations by year
- 2025: 7 · 2024: 4 · 2022: 4 · 2021: 4 · 2020: 3 · 2019: 9 · 2018: 3 · 2017: 7 · 2016: 7 · 2015: 6 · 2014: 16 · 2013: 11 · 2012: 19
- FWCI
- 3.12
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biochemical Society Transactions (publishedVersion)
- PubMed (publishedVersion)
- Discovery Research Portal (University of Dundee) (publishedVersion)
- Funders
- Wellcome Trust
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Regulation of Appetite and Obesity
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Keywords
- leptin, leptin receptor, hippocampus, synaptic plasticity, long-term potentiation, short-term potentiation, NMDA receptor, memory, cognitive enhancement, neuronal development, hypothalamus, energy homeostasis, ob/ob mice, obesity, receptor trafficking
- MeSH terms
- Animals, Brain, Cognition, Humans, Receptors, Cell Surface, Receptors, N-Methyl-D-Aspartate, N-Methylaspartate, Long-Term Potentiation, Leptin, Receptors, Leptin
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