ORIVA2: Attenuation of Inflammatory Processes Associated With Alzheimer's Disease After Consumption of Pomace Olive Oil.
Study Details
Study Description
Brief Summary
Alzheimer's disease (AD) is the most common cause of dementia and its prevalence will multiply in the coming years, so it is urgent to establish preventive and therapeutic measures. AD it is characterized by cerebrovascular and parenchymal accumulation of protein deposits enriched in amyloid-beta (Aβ) as a consequence of alterations of the blood-brain barrier. More than 60% of plasma Aβ is associated with triglyceride-rich lipoproteins (TRL), being higher in subjects with AD. Microglia act as resident macrophages and play a crucial role in most neuropathologies, since it is activated after homeostasis impairment in the brain, and surrounds amyloid plaques in patients with AD. As a result of microglial activation, a large number of pro-inflammatory markers are released, mediated by alterations in the redox state, through the generation of ROS by the complex NADPH oxidase.
In a previous study, the investigators demonstrated in BV-2 cells that artificial TRL are capable of activating microglia and trigger an inflammatory process. In addition, the investigators showed that some of lipophilic minor components of pomace olive oil simultaneously modulate oxidative stress and the inflammatory response in microglia. The investigators suggested that these results should be replicated in humans after consumption of pomace olive oil.
Therefore, in the present study we formulate the hypothesis that human TRL are capable of activating microglia and that such activation can be attenuated when those particles are generated after consumption of pomace olive oil. The results of the study would lay the foundation for the start of clinical trials demonstrating the effect of pomace oil in reducing the risk of development and progression of AD.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Detailed Description
In a previous study, the investigators demonstrated that triglyceride-rich lipoproteins (TRL), which transport dietary lipid components, are able of activating microglia, which could be associated with the state of neuroinflammation in patients of Alzheimer's disease. In addition, the investigators also demonstrated that some of the minor fat-soluble components of olive pomace oil simultaneously modulate oxidative stress and the inflammatory response in microglia, so that these components could have the ability to protect the brain from microglial overactivation when transported in TRL.
In that study, the investigators used artificial TRL that were manufactured ad-hoc in the laboratory, in order to be able to test the effect of the compounds both individually and together. Now is the time to consolidate the results using human TRL, obtained after the consumption of olive pomace oil. The investigators expect that the results of this study will reveal that the intake of olive pomace oil can prevent the release of inflammatory markers caused by the overactivation of microglia, which could be associated to a reduction in the risk of development and progression of Alzheimer's disease.
Objectives and design
To test this hypothesis, two specific objectives will be addressed:
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To obtain and characterize human TRL obtained after the intake of olive pomace oil.
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To evaluate the mitigating effect of the microglial activation by TRL obtained after the intake of olive pomace oil.
The study has been designed as a randomized and crossover trial in the postprandial phase in healthy subjects, which will be divided into two groups to which a pomace oil and high-oleic sunflower oil will be administered.
Activities
The specific objectives set out in the project will be addressed through the execution of the activities that are detailed below:
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Selection of volunteers and administration of olive pomace oil. 1.1. Obtaining and characterizing the experimental oils. 1.2. Recruitment and selection of volunteers. 1.3. Clinical trial in the postprandial phase.
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Isolation and characterization of human TRL. 2.1. General determinations in blood serum. 2.2. Characterization of TRL.
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Microglial activation in cells treated with human TRL. 3.1. Assays in cell cultures. 3.2. Analytical determinations. 3.3. Data processing and reporting.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Active Comparator: Pomace olive oil 50 g of pomace olive oil will be administered in a single dose together with a breakfast composed of 3 slices of whole-grain bread, 5 g of tomato pureé and 200 ml of milk. |
Other: Experimental meal
Two dietary oils will be administrated as part of a single experimental meal, for the present is a postprandial phase study.
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| Active Comparator: High-oleic sunflower oil 50 g of high-sunflower oil will be administered in a single dose together with a breakfast composed of 3 slices of whole-grain bread, 5 g of tomato pureé and 200 ml of milk. |
Other: Experimental meal
Two dietary oils will be administrated as part of a single experimental meal, for the present is a postprandial phase study.
|
Outcome Measures
Primary Outcome Measures
- Inflammation markers [Postprandial (6 hours)]
Release of proinflammatory markers TNF-α, IL-6 and IL-1β by BV2 cells treated with TRL obtained after the intake of pomace olive oil or high-oleic sunflower oil.
Secondary Outcome Measures
- Redox markers [Postprandial (6 hours)]
Concentrations of the redox markers reactivo oxygen species and total and reduced glutathione in BV2 cells treated with TRL obtained after the intake of pomace olive oil or high-oleic sunflower oil.
Eligibility Criteria
Criteria
Inclusion Criteria:
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Healthy individuals.
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Subjects will be recruited after a complete biochemical and haematological analysis yields results within normal limits
Exclusion Criteria:
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Digestive or metabolic conditions.
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Overweight or obesity.
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Intolerance to food components or ingredients.
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Any condition affecting lipid metabolism.
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Any inflammatory condition.
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Habitual drug intake of any kind.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Instituto de la Grasa (IG-CSIC) | Seville | Spain | 41012 |
Sponsors and Collaborators
- National Research Council, Spain
- Hospitales Universitarios Virgen del Rocío
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 20191185 ORIVA