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Updated: Jan 18, 2026

Quantification of Atherosclerosis in Mice
Published on: June 12, 2019
Hypercholesterolemia Duration and Brain Area Determine Inflammatory Response Intensity and Apoptotic Mediator
Ewelina Czuba-Pakuła1, Jolanta Ochocińska2, Sebastian Głowiński3
1Division of Anatomy and Neurobiology, Faculty of Medicine, Medical University of Gdansk, Dębinki 1, 80-211, Gdańsk, Poland. ewelina.czuba-pakula@gumed.edu.pl.
Insights
High cholesterol (Hch) accelerates brain inflammation and cell death, worsening with duration. This neurodegeneration impacts the hippocampus and striatum more than the prefrontal cortex.
Area of Science:
- Neuroscience
- Biomedical Research
- Pathology
Background:
- Hypercholesterolemia (Hch) is a known risk factor for cerebrovascular and neurodegenerative diseases.
- Hch is associated with neuroinflammation and programmed cell death, but the progression and regional specificity remain unclear.
Purpose of the Study:
- To investigate the impact of Hch duration and age on neuroinflammation and programmed cell death in the brain.
- To determine the intensity of these processes in specific brain regions during Hch.
Main Methods:
- Utilized Apo E-/-/LDLR-/- double-knockout mice at 3, 6, and 12 months of age, alongside age-matched wild-type controls.
- Measured cytokine (IL-1β, IL-4, IL-6) and apoptotic mediator (AIF, Cas-3) concentrations via ELISA in whole brain, prefrontal cortex (PFCx), hippocampus (HIP), and striatum (STR).
Main Results:
- Elevated IL-1β, IL-6, AIF, and Cas-3, along with decreased IL-4, correlated with the duration of Hch.
- Neuroinflammation and apoptosis were more severe in the HIP and STR compared to the PFCx.
Conclusions:
- Hch duration is directly correlated with neurodegenerative effects in the brain.
- Different brain regions exhibit varying susceptibility to Hch-induced damage, with HIP and STR being more vulnerable.
Abstract:
Hypercholesterolemia (Hch) is a risk factor for cerebrovascular and neurodegenerative diseases, manifesting with symptoms that vary depending on damage to specific brain regions. Hch triggers inflammatory responses and cell death. However, the progression of these processes in relation to the duration of Hch and the location of pathology in the central nervous system remains unclear. Therefore, we aimed to investigate (1) the impact of age and duration of Hch on neuroinflammatory responses and programmed cell death in the brain and (2) the intensity of these processes in various brain areas during Hch. In this study, we used 3-, 6-, and 12-month-old male Apo E-/-/LDLR-/- double-knockout mice and age-matched wild-type C57BL/6 mice (control group). Concentrations of cytokines IL-1β, IL-4, and IL-6, as well as apoptotic mediators AIF and Cas-3, were measured using enzyme-linked immunosorbent assay in the whole brain and separately in the prefrontal cortex (PFCx), hippocampus (HIP), and striatum (STR). The results showed that the Hch-induced release of cytokines IL-1β and IL-6, decreased expression of IL-4, and elevated level of apoptotic markers AIF and Cas-3 correlated with Hch duration. The inflammatory response and expression of apoptotic markers were more pronounced in the HIP and STR compared to the PFCx. Our results indicate a correlation between the neurodegenerative effects of Hch and its duration and highlight the varying susceptibility of different brain areas to Hch-induced damage.
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