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Atherosclerosis is the underlying cause of the majority of cardiovascular diseases, including myocardial infarction and strokes, and results in tremendous morbidity and mortality. A Western-type diet is a major risk factor for atherosclerosis because of the high saturated fat, cholesterol, and refined carbohydrate contents. Dietary strategies to reduce cardiovascular disease burden therefore focus on restriction of saturated fat, cholesterol, and refined carbohydrates whereas "lean" protein intake is recommended and has become popular. However, results from studies conducted in animal models suggest high dietary protein intake is also atherogenic. The investigators' extensive preliminary data in animal models show that dietary protein increases atherosclerotic plaque formation and size and promotes necrotic core formation, a characteristic of rupture-prone plaques. The goal of the current proposal is to provide deeper insights into the relationship between protein intake and the pathogenesis of atherosclerosis by studying the mechanisms involved in protein-mediated atherogenesis and formation of necrotic plaques. The overarching hypothesis is that high protein intake drives atherosclerosis via leucine-mediated mTORC1 signaling in macrophages, which inhibits macrophage mitophagy and aggrephagy and stimulates macrophage proliferation. Furthermore, the investigators hypothesize that proteins from animal sources are more atherogenic than proteins from plant sources, because animal proteins contain more leucine than plant proteins. The investigators will test these hypotheses by using a sophisticated array of experimental strategies, including assays in primary macrophages and human monocyte-derived macrophages and genetically engineered mouse models. In addition, they will begin to translate the results obtained in vitro and in animals to people, and explore approaches to pharmacologically target the pro-atherogenic pathways as novel cardiovascular therapeutics. This proposal represents a paradigm shift in how a Western-type diet affects vascular health which has important implications since many adults in Western societies consume excess protein and dietary protein is heavily marketed for its presumed beneficial health effects.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Standard meal | Active Comparator |
| |
| High animal protein meal | Experimental |
| |
| High plant protein meal | Experimental |
| |
| High plant protein meal with additional leucine | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Standard meal | Other | Standard meal |
| |
| High animal protein meal |
| Measure | Description | Time Frame |
|---|---|---|
| Monocyte proatherogenic pathway activation | Change in proatherogenic pathway activation | baseline before meal intake to 3 hours after the meal |
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| Measure | Description | Time Frame |
|---|---|---|
| Plasma amino acids concentrations | Change in plasma amino acid concentrations | baseline before meal intake to 3 hours after the meal |
| Plasma glucose concentration | Change in plasma glucose concentration |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Bettina Mittendorfer, PhD | Contact | 6186103465 | b.mittendorfer@missouri.edu |
| Name | Affiliation | Role |
|---|---|---|
| Bettina Mittendorfer | University of Missouri-Columbia | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Missouri School of Medicine | Recruiting | Columbia | Missouri | 65212 | United States |
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| ID | Term |
|---|---|
| D050197 | Atherosclerosis |
| ID | Term |
|---|---|
| D001161 | Arteriosclerosis |
| D001157 | Arterial Occlusive Diseases |
| D014652 | Vascular Diseases |
| D002318 | Cardiovascular Diseases |
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Randomized cross-over study
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| Other |
Meal with high animal protein content |
|
| High plant protein meal | Other | Meal with high plant protein content |
|
| High plant protein meal with additional leucine | Other | Meal with high plant protein content and additional leucine |
|
| baseline before meal intake to 3 hours after the meal |
| Plasma glucoregulatory hormone concentrations | Change in plasma concentrations of glucoregulatory hormones | baseline before meal intake to 3 hours after the meal |
| Endothelial function | Endothelial function assessed as reactive hyperemia index | baseline (before meal intake) and postprandially (after the meal) |