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1000 Titel
  • Structural and functional consequences in the amygdala of leptin-deficient mice
1000 Autor/in
  1. Schepers, Jens |
  2. Gebhardt, Christine |
  3. Bracke, Alexander |
  4. Eiffler, Ina |
  5. von Bohlen und Halbach, Oliver |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-08-13
1000 Erschienen in
1000 Quellenangabe
  • 382(2):421-426
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00441-020-03266-x |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7584530/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • On the one hand, the emotional state can influence food intake and on the other hand, hunger can have an impact on the emotional state. Leptin, which is encoded by the ob gene, is involved in the energy homeostasis and plays a role in development of obesity. Mice deficient for leptin (ob/ob) are obese and display several behavioral alterations. It has been shown that ob/ob mice display striking changes in neuronal plasticity within the limbic system, e.g., hippocampal formation. We focus on alterations in ob/ob mice that can be related to alter processing in another part of the limbic system, the amygdala. ob/ob mice have a higher food consumption than age-matched controls, which might have an impact on the emotional state of these mice. Since the amygdala is involved in emotional processing, we analyze whether ob/ob mice display alterations in plasticity at the electrophysiological and structural level. No changes were seen in dendritic spine densities in the basolateral and lateral (LA) nucleus of the amygdala. Interestingly and in contrast to the hippocampus (Porter et al. 2013), long-term potentiation in the LA was increased in ob/ob mice. Our results indicate that amygdalar and hippocampal synaptic plasticity are regulated in different ways by leptin deficiency in accordance with the different functions of these limbic structures in stress and anxiety.
1000 Sacherschließung
lokal Amygdala/physiopathology [MeSH]
lokal Obesity
lokal LTP
lokal Leptin/deficiency [MeSH]
lokal Leptin
lokal Neuronal Plasticity/genetics [MeSH]
lokal Animals [MeSH]
lokal Amygdala
lokal Mice [MeSH]
lokal Male [MeSH]
lokal Obesity/physiopathology [MeSH]
lokal Dendritic spines
lokal Obesity/genetics [MeSH]
lokal Short Communication
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2NoZXBlcnMsIEplbnM=|https://frl.publisso.de/adhoc/uri/R2ViaGFyZHQsIENocmlzdGluZQ==|https://frl.publisso.de/adhoc/uri/QnJhY2tlLCBBbGV4YW5kZXI=|https://frl.publisso.de/adhoc/uri/RWlmZmxlciwgSW5h|https://orcid.org/0000-0002-2613-2517
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