Hippocampus and its involvement in Alzheimer's disease: a review
Y Lakshmisha Rao1, B Ganaraja2, B V Murlimanju1
1Department of Anatomy, Kasturba Medical College, Mangalore, Manipal Academy of Higher Education, Manipal, Karnataka India.
Insights
The hippocampus is vital for memory and learning but vulnerable to Alzheimer's disease (AD). A lifestyle promoting neurogenesis may help delay AD-related neurodegeneration and preserve cognitive function.
Area of Science:
- Neuroscience
- Neurobiology
- Gerontology
Background:
- The hippocampus, a key brain region for learning and memory, is significantly impacted by Alzheimer's disease (AD).
- Early AD stages involve rapid hippocampal tissue loss and functional disconnection, with medial temporal and hippocampal atrophy serving as MRI markers.
- Reduced sirtuin (SIRT) expression in hippocampal neurons impairs cognitive functions like spatial learning and recent memory.
Purpose of the Study:
- To explore the hippocampus's role in learning, memory, and its vulnerability in Alzheimer's disease.
- To investigate the factors influencing neural stem cell (NSC) function within the hippocampus.
- To highlight the potential of a pro-neurogenic lifestyle in mitigating neurodegeneration.
Main Methods:
- Review of existing literature on hippocampal structure and function.
- Analysis of the impact of Alzheimer's disease on hippocampal integrity.
- Examination of intrinsic and extrinsic factors affecting adult neurogenesis in the hippocampus.
Main Results:
- The hippocampus is crucial for episodic memory generation but susceptible to AD-induced atrophy and functional decline.
- Sirtuin (SIRT) expression is vital for hippocampal neuron function and cognitive processes.
- Microglia exhibit heightened immunological activity in the hippocampus, influencing the neural environment.
- Intrinsic factors (hormones, glia, vascular supply) and extrinsic factors (diet, physical activity) modulate hippocampal neural stem cell (NSC) function.
Conclusions:
- The hippocampus's vulnerability to Alzheimer's disease necessitates understanding factors that protect its structure and function.
- Modulating intrinsic and extrinsic factors can influence hippocampal neurogenesis and potentially delay neurodegeneration.
- Adopting a pro-neurogenic lifestyle may be a viable strategy to counteract cognitive decline associated with aging and neurodegenerative diseases.
Abstract:
Hippocampus is the significant component of the limbic lobe, which is further subdivided into the dentate gyrus and parts of Cornu Ammonis. It is the crucial region for learning and memory; its sub-regions aid in the generation of episodic memory. However, the hippocampus is one of the brain areas affected by Alzheimer's (AD). In the early stages of AD, the hippocampus shows rapid loss of its tissue, which is associated with the functional disconnection with other parts of the brain. In the progression of AD, atrophy of medial temporal and hippocampal regions are the structural markers in magnetic resonance imaging (MRI). Lack of sirtuin (SIRT) expression in the hippocampal neurons will impair cognitive function, including recent memory and spatial learning. Proliferation, differentiation, and migrations are the steps involved in adult neurogenesis. The microglia in the hippocampal region are more immunologically active than the other regions of the brain. Intrinsic factors like hormones, glia, and vascular nourishment are instrumental in the neural stem cell (NSC) functions by maintaining the brain's microenvironment. Along with the intrinsic factors, many extrinsic factors like dietary intake and physical activity may also influence the NSCs. Hence, pro-neurogenic lifestyle could delay neurodegeneration.
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