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Updated: May 31, 2026

Preparation of Naringenin Solution for In Vivo Application
Published on: August 10, 2021
Naringin, the major grapefruit flavonoid, specifically affects atherosclerosis development in diet-induced
Audrey Chanet1, Dragan Milenkovic, Christiane Deval
1INRA, UMR 1019, UNH, CRNH Auvergne, F-63000 Clermont-Ferrand, France.
Abstract:
Naringin (NAR) from grapefruit has exhibited potential protective effects against atherosclerosis development. However, specific mechanisms responsible for such effects are poorly understood. Thus, we aimed to investigate the antiatherogenic effects of NAR in different mouse models of hypercholesterolemia and decipher its molecular targets in the aorta using transcriptomic approach. Two mouse models of hypercholesterolemia, wild-type mice fed a high-fat/high-cholesterol diet and apolipoprotein E-deficient mice fed a semisynthetic diet, were studied. Mice were fed a respective control diets supplemented or not for 18 weeks with 0.02% of NAR, that is, nutritional supplementation. NAR supplementation reduced plaque progression only in wild-type mice fed the high-fat/high-cholesterol diet (-41%). Consistent with this protective effect, NAR reduced plasma non-high-density lipoprotein cholesterol concentrations as well as biomarkers of endothelial dysfunction. Microarray studies performed on aortas demonstrated differentially expressed genes encoding proteins involved in cell adhesion, actin cytoskeleton organization and cell division. Thus, the changes in gene expression induced by NAR could suggest a limited atherosclerosis progression by preventing immune cell adhesion and infiltration in the intima of vascular wall, as well as smooth muscle cell proliferation. Furthermore, this hypothesis was strengthened by in vitro experiments, which showed the ability of naringenin to reduce monocyte adhesion to endothelial cells and smooth muscle cell proliferation. In conclusion, this study revealed the antiatherogenic effect of NAR supplemented at a nutritionally achievable dose, specifically toward diet-induced atherosclerosis, and depicted its multitarget mode of action at the vascular level.
Insights
Naringin (NAR), found in grapefruit, reduces diet-induced atherosclerosis progression in mice. This natural compound limits plaque buildup by impacting vascular cell adhesion and proliferation.
Area of Science:
- Cardiovascular Research
- Nutraceuticals and Dietetics
- Molecular Biology
Background:
- Atherosclerosis is a complex vascular disease driven by hypercholesterolemia.
- Naringin (NAR), a grapefruit flavonoid, shows potential in preventing atherosclerosis, but its mechanisms are unclear.
- Understanding NAR's molecular targets is crucial for developing effective antiatherogenic strategies.
Purpose of the Study:
- To investigate the antiatherogenic effects of Naringin (NAR) in mouse models of hypercholesterolemia.
- To identify the molecular targets of NAR in the aorta using transcriptomics.
- To elucidate the mechanisms underlying NAR's protective effects against atherosclerosis.
Main Methods:
- Utilized two mouse models: wild-type mice on a high-fat/high-cholesterol diet and apolipoprotein E-deficient mice.
- Supplemented diets with 0.02% Naringin (NAR) for 18 weeks.
- Performed transcriptomic analysis (microarray) on aortas and in vitro experiments.
Main Results:
- NAR supplementation significantly reduced atherosclerotic plaque progression by 41% in wild-type mice on a high-fat/high-cholesterol diet.
- NAR lowered plasma non-high-density lipoprotein cholesterol and biomarkers of endothelial dysfunction.
- Transcriptomic analysis revealed NAR affects genes involved in cell adhesion, cytoskeleton organization, and cell division.
Conclusions:
- Naringin (NAR) exhibits significant antiatherogenic effects, particularly against diet-induced atherosclerosis.
- NAR acts through multiple molecular targets within the vascular wall, including reducing immune cell adhesion and smooth muscle cell proliferation.
- Nutritionally achievable doses of NAR demonstrate therapeutic potential for managing atherosclerosis.
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