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Vulnerability of the Hippocampus to Insults: Links to Blood-Brain Barrier Dysfunction

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Feb 24
PMID 38396670
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Abstract

The hippocampus is a critical brain substrate for learning and memory; events that harm the hippocampus can seriously impair mental and behavioral functioning. Hippocampal pathophysiologies have been identified as potential causes and effects of a remarkably diverse array of medical diseases, psychological disorders, and environmental sources of damage. It may be that the hippocampus is more vulnerable than other brain areas to insults that are related to these conditions. One purpose of this review is to assess the vulnerability of the hippocampus to the most prevalent types of insults in multiple biomedical domains (i.e., neuroactive pathogens, neurotoxins, neurological conditions, trauma, aging, neurodegenerative disease, acquired brain injury, mental health conditions, endocrine disorders, developmental disabilities, nutrition) and to evaluate whether these insults affect the hippocampus first and more prominently compared to other brain loci. A second purpose is to consider the role of hippocampal blood-brain barrier (BBB) breakdown in either causing or worsening the harmful effects of each insult. Recent research suggests that the hippocampal BBB is more fragile compared to other brain areas and may also be more prone to the disruption of the transport mechanisms that act to maintain the internal milieu. Moreover, a compromised BBB could be a factor that is common to many different types of insults. Our analysis indicates that the hippocampus is more vulnerable to insults compared to other parts of the brain, and that developing interventions that protect the hippocampal BBB may help to prevent or ameliorate the harmful effects of many insults on memory and cognition.

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References
1.
Rahman M, Rahman M, Uddin M, Mamum-Or-Rashid A, Pang M, Rhim H . Emerging risk of environmental factors: insight mechanisms of Alzheimer's diseases. Environ Sci Pollut Res Int. 2020; 27(36):44659-44672. DOI: 10.1007/s11356-020-08243-z. View

2.
den Heijer T, Tiemeier H, Luijendijk H, van der Lijn F, Koudstaal P, Hofman A . A study of the bidirectional association between hippocampal volume on magnetic resonance imaging and depression in the elderly. Biol Psychiatry. 2011; 70(2):191-7. DOI: 10.1016/j.biopsych.2011.04.014. View

3.
Zaganas I, Kapetanaki S, Mastorodemos V, Kanavouras K, Colosio C, Wilks M . Linking pesticide exposure and dementia: what is the evidence?. Toxicology. 2013; 307:3-11. DOI: 10.1016/j.tox.2013.02.002. View

4.
Sharma B, Sharma P . Arsenic toxicity induced endothelial dysfunction and dementia: pharmacological interdiction by histone deacetylase and inducible nitric oxide synthase inhibitors. Toxicol Appl Pharmacol. 2013; 273(1):180-8. DOI: 10.1016/j.taap.2013.07.017. View

5.
Ma T, Chen H, Lim D, HUME A, Ho I . Effects of subacute lead exposure on [3H]MK-801 binding in hippocampus and cerebral cortex in the adult rat. Brain Res. 1997; 760(1-2):187-92. DOI: 10.1016/s0006-8993(97)00279-5. View