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Beyond appetite: Acylated ghrelin as a learning, memory and fear behavior-modulating hormone
Niklas Reich1, Christian Hölscher2
1Faculty of Health and Medicine, Biomedical & Life Sciences Division, Lancaster University, Lancaster LA1 4YQ, UK.
Neuroscience and Biobehavioral Reviews
|November 11, 2022
Summary
Acylated ghrelin (AG), known as a hunger hormone, also plays a crucial role in memory and neuroprotection. This review explores AG's effects on memory formation, brain plasticity, and neurotransmitter systems.
Area of Science:
- Neuroscience
- Endocrinology
- Behavioral Science
Background:
- Acylated ghrelin (AG) is traditionally known as a hunger hormone.
- Emerging research reveals AG's significant neuroprotective functions.
- AG is implicated in regulating memory and fear-related behaviors.
Purpose of the Study:
- To review the specific effects of AG on different memory types and brain regions.
- To illustrate AG's role in hippocampal plasticity and neurogenesis.
- To elucidate AG's modulation of key neurotransmitter systems and its implications in stress and memory.
Main Methods:
- Literature review of studies investigating acylated ghrelin.
- Analysis of signaling pathways related to AG in the hippocampus.
- Examination of AG's influence on neurotransmitter systems (glutamate, GABA, dopamine, serotonin).
Main Results:
- AG affects specific stages and forms of memory, impacting brain areas like the hippocampus and amygdala.
- AG influences plasticity-associated signaling pathways and neurogenesis.
- AG modulates neurotransmitter systems, affecting conditioned taste aversion, novelty learning, and various fear memories.
Conclusions:
- Acylated ghrelin has diverse roles beyond appetite regulation, including significant impacts on memory and fear behavior.
- AG's interaction with the 5-HT system and its link to PTSD warrant further investigation.
- The context-dependent effects of AG on fear (suppressing or potentiating) highlight its complex role in stress responses.
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