Food for thought: Leptin regulation of hippocampal function and its role in Alzheimer's disease

Gemma McGregor, Jenni Harvey (Lead / Corresponding author)

    Research output: Contribution to journalReview articlepeer-review

    29 Citations (Scopus)
    602 Downloads (Pure)

    Abstract

    Accumulating evidence indicates that diet and body weight are important factors associated with Alzheimer's disease (AD), with a significant increase in AD risk linked to mid-life obesity, and weight loss frequently occurring in the early stages of AD. This has fuelled interest in the hormone leptin, as it is an important hypothalamic regulator of food intake and body weight, but leptin also markedly influences the functioning of the hippocampus; a key brain region that degenerates in AD. Increasing evidence indicates that leptin has cognitive enhancing properties as it facilitates the cellular events that underlie hippocampal-dependent learning and memory. However, significant reductions in leptin's capacity to regulate hippocampal synaptic function occurs with age and dysfunctions in the leptin system are associated with an increased risk of AD. Moreover, leptin is a potential novel target in AD as leptin treatment has beneficial effects in various models of AD. Here we summarise recent advances in leptin neurobiology with particular focus on regulation of hippocampal synaptic function by leptin and the implications of this for neurodegenerative disorders like AD.

    Original languageEnglish
    Pages (from-to)298-306
    Number of pages9
    JournalNeuropharmacology
    Volume136
    Early online date5 Oct 2017
    DOIs
    Publication statusPublished - Jul 2018

    Keywords

    • Leptin
    • Alzheimer's disease
    • Hippocampus
    • Excitatory synaptic transmission
    • AMPA receptor trafficking
    • Synaptic plasticity

    Fingerprint

    Dive into the research topics of 'Food for thought: Leptin regulation of hippocampal function and its role in Alzheimer's disease'. Together they form a unique fingerprint.

    Cite this